|Title of Invention||
"A RECOMBINANT POLYNUCLEOTIDE ENCODING A POLYPEPTIDE HAVING DESATURASE ACTIVITY"
|Abstract||A recombinant polynucleotide encoding a polypeptide having desaturase activity that desaturates a fatty acid molecule at carbon 6, wherein the polynucleotide is selected from the group consisting of: (a) a polynucleotide encoding the polypeptide sequence of SEQ ID NO:4, SEQ ID NO:5, SEQ ID NO:22, SEQ ID NO:24 SEQ ID NO:26, SEQ ID NO:46 or SEQ ID NO:48; (b) a polynucleotide comprising the nucleic acid sequence of SEQ ID NO:2, SEQ ID NO:3, SEQ ID NO:21, SEQ ID NO:23, SEQ ID NO:25, SEQ ID NO:45 or SEQ ID NO:47; (c) a polynucleotide hybridizing to SEQ ID NO:2, SEQ ID NO:3, SEQ ID NO:21, SEQ ID NO: 23, SEQ ID NO:25, SEQ ID NO:45 or SEQ ID NO:47, or a complement thereof, under conditions of 5X SSC, 50% formamide and 42°C; and (d) a polynucleotide encoding a polypeptide with at least 92% sequence identity to a polypeptide sequence of SEQ ID NO:4, SEQ ID NO:5, SEQ ID NO:22, SEQ ID NO:24, SEQ ID NO:26, SEQ ID NO:46 or SEQ ID NO:48.|
|Full Text||1. Field of the Invention
The invention relates generally to desarurase enzymes that modulate the number and location of double bonds in long chain poly-unsaturated fatty acids (LC-PUFA's). In particular, the invention relates to improvement of fatty acid profiles using desarurase enzymes and nucleic acids encoding such desarurase enzymes.
2. Description of the Related Art
The primary products of fatty acid biosynthesis in most organisms are 16- and 18-carbon compounds. The relative ratio of chain lengths and degree of unsaturation of these fatty acids vary widely among species. Mammals, for example, produce primarily saturated and monounsaturated fatty acids, while most higher plants produce fatty acids with one, two, or three double bonds, the latter two comprising polyunsaturated fatty acids (PUFA's).
Two main families of PUFAs are the omega-3 fatty acids (also represented as "n-3" fatty acids), exemplified by eicosapentaenoic acid (EPA, 20:4, n-3), and the omega-6 fatty acids (also represented as "n-6" fatty acids), exemplified by arachidonic acid (ARA, 20:4, n-6). PUFAs are important components of the plasma membrane of the cell and adipose tissue, where they maybe found in such forms as phospholipids and as triglycerides, respectively. PUFAs are necessary for proper development in mammals, particularly in the developing infant brain, and for tissue formation and repair.
Several disorders respond to treatment with fatty acids. Supplementation with PUFAs has been shown to reduce the rate of restenosis after angioplasty. The health benefits of certain dietary omega-3 fatty acids for cardiovascular disease and rheumatoid arthritis also have been well documented (Simopoulos, 1997; James et al, 2000). Further, PUFAs have been suggested
for use in treatments for asthma and psoriasis. Evidence indicates that PUFAs may be involved te calcium metabolism, suggesting that PUFAs may be useful in the treatment or prevention of osteoporosis and of kidney or urinary tract stones. The majority of evidence for health benefits applies to the long chain omega-3 fats, EPA and docosahexanenoic acid (DHA, 22:6) which are in fish and fish oil. With this base of evidence, health authorities and nutritionists in Canada (Scientific Review Committee, 1990, Nutrition Recommendations, Minister of National Health and Welfare, Canada, Ottowa), Europe (de Deckerer et al, 1998), the United Kingdom (The British Nutrition Foundation, 1992, Unsaturated fatty-acids - nutritional and physiological significance: The report of the British Nutrition Foundation's Task Force,\Chapman and Hall, London), and the United States (Simopoulos et al, 1999) have recommended increased dietary consumption of these PUFAs.
PUFAs also can be used to treat diabetes (U.S. Pat. No. 4,826,877; Horrobin et al, 1993).
Altered fatty acid metabolism and composition have been demonstrated in diabetic animals.
These alterations have been suggested to be involved in some of the long-term complications
resulting from diabetes, including retinopathy, neuropathy, nephropathy and reproductive system
damage. Primrose oil, which contains y-linolenic acid (GLA, 18:3, A6, 9, 12), has been shown to
prevent and reverse diabetic nerve damage.
PUFAs, such as linoleic acid (LA, 18:2, A9, 12) and a-linolenic acid (ALA, 18:3, A9, 12, 15), are regarded as essential fatty acids in the diet because mammals lack the ability to synthesize these acids. However, when ingested, mammals have the ability to metabolize LA and ALA to form the n-6 and n-3 families of long-chain polyunsaturated fatty acids (LC-PUFA). These LC-PUFA's are important cellular components conferring fluidity to membranes and functioning as precursors of biologically active eicosanoids such as prostaglandins, prostacyclins, and leukotrienes, which regulate normal physiological functions. Arachidonic acid is the principal precursor for the synthesis of eicosanoids, which include leukotrienes, prostaglandins, and thromboxanes, and which also play a role in the inflammation process. Administration of an omega-3 fatty acid, such as SDA, has been shown to inhibit biosynthesis of leukotrienes (U.S. Pat. No. 5,158,975). The consumption of SDA has been shown to lead to a decrease in blood levels of proinflammatory cytokines TNF-a and IL-lp (PCT US 0306870).
In mammals, the formation of LC-PUFA is rate-limited by the step of A6 desaturation, which converts LA to y-linolenic acid (GLA, 18:3, A6, 9, 12) and ALA to SDA (18:4, A6, 9, 12, 15). Many physiological and pathological conditions have been shown to depress this metabolic step even further, and consequently, the production of LC-PUFA. To overcome the rate-limiting
step and increase tissue levels of EPA, one could consume large amounts of ALA. However, ^jponsumption of just moderate amounts of SDA provides an efficient source of EPA, as SDA is about four times more efficient than ALA at elevating tissue EPA levels in humans (copending U.S. Application Ser. No. 10/384,369). In the same studies, SDA administration was also able to increase the tissue levels of docosapentaenoic acid (DPA), which is an elongation product of EPA. Alternatively, bypassing the A6-desaturation via dietary supplementation with EPA or DHA can effectively alleviate many pathological diseases associated with low levels of PUFA. However, as set forth in more detail below, currently available sources of PUFA are not desirable foj; a multitude of reasons. The need for a reliable and economical source of PUFA's has spurred interest in alternative sources of PUFA's.
Major long chain PUFAs of importance include DHA and EPA, which are primarily found in different types of fish oil, and ARA, found in filamentous fungi such as Mortierella. For DHA, a number of sources exist for commercial production including a variety of marine organisms, oils obtained from cold water marine fish, and egg yolk fractions. Commercial sources of SDA include the plant genera Trichodesma, Borago (borage) and Echium. However, there are several disadvantages associated with commercial production of PUFAs from natural sources. Natural sourtes of PUFAs, such as animals and plants, tend to have highly heterogeneous oil compositions. The oils obtained from these sources therefore can require extensive purification to separate out one or more desired PUFAs or to produce an oil which is enriched in one or more PUFAs.
Natural sources of PUFAs also are subject to uncontrollable fluctuations in availability. Fish stocks may undergo natural variation or may be depleted by overfishing. In addition, even with overwhelming evidence of their therapeutic benefits, dietary recommendations regarding omega-3 fatty acids are not heeded. Fish oils have unpleasant tastes and odors, which may be impossible to economically separate from the desired product, and can render such products unacceptable as food supplements. Animal oils, and particularly fish oils, can accumulate environmental pollutants. Foods may be enriched with fish oils, but again, such enrichment is problematic because of cost and declining fish stocks worldwide. This problem is also an impediment to consumption and intake of whole fish. Nonetheless, if the health messages to increase fish intake were embraced by communities, there would likely be a problem in meeting demand for fish. Furthermore, there are problems with sustainability of this industry, which relies heavily on wild fish stocks for aquaculture feed (Naylor et al, 2000).
Other natural limitations favor a novel approach for the production of omega-3 fatty ^ds. Weather and disease can cause fluctuation in yields from both fish and plant sources. Cropland available for production of alternate oil-producing crops is subject to competition from the steady expansion of human populations and the associated increased need for food production on the remaining arable land. Crops that do produce PUFAs, such as borage, have not been adapted to commercial growth and may not perform well in monoculture. Growth of such crops is thus not economically competitive where more profitable and better-established crops can be grown. Large scale fermentation of organisms such as Mortierella is also expensive. Natural animal tissues contain low amountsxof ARA and are difficult to process. Microorganisms such as Porphyridium and Mortierella are difficult to cultivate on a commercial scale.
A number of enzymes are involved in the biosynthesis of PUFAs. LA (18:2, A9, 12) is produced from oleic acid (OA, 18:1, A9) by a A12-desaturase while ALA (18:3, A9, 12, 15) is produced from LA by a A15-desaturase. SDA (18:4, A6, 9, 12, 15) and GLA (18:3, A6, 9, 12) are produced from LA and ALA by a A6-desaturase. However, as stated above, mammals cannot desaturate beyond the A9 position and therefore cannot convert oleic acid into LA. Likewise, ALA cannot be synthesized by mammals. Other eukaryOtes, including fungi and plants, have enzymes which desaturate at the carbon 12 and carbon 15 position. The major polyunsaturated fatty acids of animals therefore are derived from diet via the subsequent desaturation and elongation of dietary LA and ALA.
Various genes encoding desaturases have been described. For example, U.S. Pat. No. 5,952,544 describes nucleic acid fragments isolated and cloned from Brassica napus that encode fatty acid desaturase enzymes. Expression of the nucleic acid fragments of the '544 patent resulted in accumulation of ALA. However, in transgenic plants expressing the B. napus A15-desaturase, substantial LA remains unconverted by the desaturase. More active enzymes that convert greater amounts of LA to ALA would be advantageous. Increased ALA levels allow a A6-desaturase, when co-expressed with a nucleic acid encoding for the A15-desaturase, to act upon the ALA, thereby producing greater levels of SDA. Because of the multitude of beneficial uses for SDA, there is a need to create a substantial increase in the yield of SDA.
Nucleic acids from a number of sources have been sought for use in increasing SDA yield. However, innovations that would allow for improved commercial production in land-based crops are still needed (see, e.g., Reed et al., 2000). Furthermore, the use of desaturase polynucleotides derived from organisms such as Caenorhabditis elegans (Meesapyodsuk et al.,
2000) is not ideal for the commercial production of enriched plant seed oils. Genes encoding pi6-desaturases have been isolated from two species of Primula, P. farinosa and P. vialii, and these found to be active in yeast, but the function in plants was not shown (Sayanova et al., 2003).
Therefore, it would be advantageous to obtain genetic material involved in PUFA biosynthesis and to express the isolated material in a plant system, in particular, a land-based terrestrial crop plant system, which can be manipulated to provide production of commercial quantities of one or more PUFA's. There is also a need to increase omega-3 fat intake in humans and animals. Thus there is a need to provide a wide range of omega-3 enriched foods and food supplements so that subjects can choose feed, feed ingredients, food and food ingredients which suit their usual dietary habits. Particularly advantageous would be seed oils with increased SDA.
Currently there is only one omega-3 fatty acid, ALA, available in vegetable oils. However, there is poor conversion of ingested ALA to the longer-chain omega-3 fatty acids such as EPA and DHA. It has been demonstrated in copending U.S. Application Ser. No. 10/384,369 for "Treatment And Prevention Of Inflammatory Disorders," that elevating ALA intake from the community average of 1/g day to 14 g/day by use of flaxseed oil only modestly increased plasma phospholipid EPA levels. A 14-fold increase in ALA intake resulted in a 2-fold increase in plasma phospholipid EPA (Manzioris et al, 1994). Thus, to that end, there is a need for efficient and commercially viable production of PUFAs using fatty acid desaturases, genes encoding them, and recombinant methods of producing them. A need also exists for oils containing higher relative proportions of specific PUFAs, and food compositions and supplements containing them. A need also exists for reliable economical methods of producing specific PUFA's.
Despite inefficiencies and low yields as described above, the production of omega-3 fatty acids via the terrestrial food chain is an enterprise beneficial to public health and, in particular, the production of SDA. SDA is important because, as described above, there is low conversion of ALA to EPA. This is because the initial enzyme in the conversion, A6-desaturase, has low activity in humans and is rate-limiting. Evidence that A6-desaturase is rate-limiting is provided by studies which demonstrate that the conversion of its substrate, ALA, is less efficient than the conversion of its product, SDA to EPA in mice and rats (Yamazaki et al, 1992; Huang, 1991).
Based on such studies, it is seen that in commercial oilseed crops, such as canola, soybean, corn, sunflower, safflower, or flax, the conversion of some fraction of the mono and polyunsaturated fatty acids that typify their seed oil to SDA requires the seed-specific expression of multiple desaturase enzymes, that includes A6-, A12-and/or A15-desaturases. Oils derived
from plants expressing elevated levels of A6, A12, and A15-desaturases are rich in SDA and fitter omega-3 fatty acids. Such oils can be utilized to produce foods and food supplements enriched in omega-3 fatty acids and consumption of such foods effectively increases tissue levels of EPA and DHA. Foods and foodstuffs, such as milk, margarine and sausages, all made or prepared with omega-3 enriched oils, will result in therapeutic benefits. It has been shown that subjects can have an omega-3 intake comparable to EPA and DHA of at least 1.8 g/day without altering their dietary habits by utilizing foods containing oils enriched with omega-3 fatty acids. Thus, there exists a strong need for novel nucleic acids of A6-desaturases for use in transgenic crop plants with oils enriched in PUFAs, as well as the improved oils produced thereby.
SUMMARY OF THE INVENTION
In one aspect, the invention provides isolated nucleic acids encoding a polypeptide capable of desaturating a fatty acid molecule at carbon 6 (A6-desaturase). These may be used to transform cells or modify the fatty acid composition of a plant or the oil produced by a plant. One embodiment of the invention is an isolated polynucleotide sequence isolated from a Primula species having unique desaturase activity. In certain embodiments, the isolated polynucleotides are isolated, for example, from Primula juliae, P. alpicola, P. waltonii, P. farinosa or P. florindae. In certain further embodiments of the invention, the polynucleotides encode a polypeptide having at least 90% sequence identity to the polypeptide sequence of SEQ ID NO:4, SEQ ID NO:5, SEQ ID NO:22, SEQ ID NO:24, SEQ ID NO:26, SEQ ID NO:46 or SEQ ID NO:48, including at least about 92%, 95%, 98% and 99% homology to these sequences. Those of skill in the art will recognize that, as these sequences are related, a given polypeptide may simultaneously share 90% or greater homology to more than one of these polypeptide sequences. In certain embodiments, a sequence provided by the invention has a substrate selectivity for a-linolenic acid relative to linoleic acid, as described herein. In further embodiments, there is at least 2:1 substrate selectivity for a-linolenic acid relative to linoleic acid, including from about 2:1 to about 2.9:1.
In another aspect, the invention provides an isolated polynucleotide that encodes a polypeptide having desaturase activity that desaturates a fatty acid molecule at carbon 6, comprising a sequence selected from the group consisting of: (a) a polynucleotide encoding the polypeptide of SEQ ID N0:4, SEQ ID NO:5, SEQ ID NO:22, SEQ ID NO:24, SEQ ID NO:26, SEQ ID NO:46 or SEQ ID NO:48; (b) a polynucleotide comprising the nucleic acid sequence of SEQ ID N0:2, SEQ ID N0:3, SEQ ID NO:21, SEQ ID NO:23, SEQ ID NO:25, SEQ ID N0:45 or SEQ ID NO:47; (c) a polynucleotide hybridizing to SEQ ID N0:2, SEQ ID NO:3, SEQ ID
NO:21, SEQ ID NO:23, SEQ ID NO:25, SEQ ID NO:45 or SEQ ID N0:47, or a complement ||iereof, under conditions of 5X SSC, 50% formamide and 42°C; and (d) a polynucleotide encoding a polypeptide with at least 90% sequence identity to a polypeptide sequence of SEQ ID N0:4, SEQ ID NO:5, SEQ ID NO:22, SEQ ID N0:24, SEQ ID N0:26, SEQ ID NO:46 or SEQ ID NO:48.
In yet another aspect, the invention provides a recombinant vector comprising an isolated polynucleotide in accordance with the invention. The term "recombinant vector" as used herein, includes any recombinant segment of DNA that one desires to introduce into a host cell, tissue and/or organism, and specifically includes expression cassettes isolated from- a starting polynucleotide. A recombinant vector may be linear or circular. In various aspects, a recombinant vector may comprise at least one additional sequence chosen from the group consisting of: regulatory sequences operatively coupled to the polynucleotide; selection markers operatively coupled to the polynucleotide; marker sequences operatively coupled to the polynucleotide; a purification moiety operatively coupled to the polynucleotide; and a targeting sequence operatively coupled to the polynucleotide.
In still yet another aspect, the invention provides cells, such as mammal, plant, insect,
further embodiment, the cells are transformed with recombinant vectors containing constitutive and tissue-specific promoters in addition to the polynucleotides of the instant invention, hi certain embodiments of the invention, such cells may be further defined as transformed with a nucleic acid sequence encoding a polypeptide having desaturase activity that desaturates a fatty acid molecule at carbon 12 and/or 15.
The invention also provides a polypeptide comprising the amino acid sequence of SEQ ID N0:4, SEQ ID NO:5, SEQ ID NO:22, SEQ ID NO:24, SEQ ID NO:26, SEQ ID N0:46 or SEQ ID NO:48; or a fragment thereof having desaturase activity that desaturates a fatty acid molecule at carbon 6.
Still yet another aspect of the invention provides a method of producing seed oil containing omega-3 fatty acids from plant seeds, comprising the steps of (a) obtaining seeds of a plant according to the invention; and (b) extracting the oil from said seeds. Examples of such a plant include canola, soy, soybeans, rapeseed, sunflower, cotton, cocoa, peanut, safflower, coconut, flax, oil palm, oilseed Brassica napus, and corn. Preferred methods of transforming such plant cells include the use of Ti and Ri plasmids of Agrobacterium, electroporation, and high-velocity ballistic bombardment.
In still yet another aspect, the invention provides a method of producing a plant
Comprising seed oil containing altered levels of omega-3 fatty acids comprising introducing a
recombinant vector of the invention into an oil-producing plant. In the method, introducing the
recombinant vector may comprise genetic transformation. In embodiment, transformation
comprises the steps of: (a) transforming a plant cell with a recombinant vector of the invention;
and (b) regenerating the plant from the plant cell, wherein the plant has altered levels of omega-3
fatty acids relative to a corresponding plant of the same genotype that was not transformed with
the vector. In the method, the plant may, for example, be selected from the group consisting of
Arabidopsis thaliana, oilseed Brassica, rapeseed, sunflower, safflower, canola, corn, soybean,
cotton, flax, jojoba, Chinese tallow tree, tobacco, cocoa, peanut, fruit plants, citrus plants, and
plants producing nuts and berries. The plant may be further defined as transformed with a
nucleic acid sequence encoding a polypeptide having desaturase activity that desaturates a fatty
acid molecule at carbon 12 and/or 15. The plant may comprise increased SDA. The method
may further comprise introducing the recombinant vector into a plurality of oil-producing plants
and screening the plants or progeny thereof having inherited the recombinant vector for a plant
having a desired profile of omega-3 fatty acids.
In still yet another aspect, the invention provides an endogenous soybean seed oil having a SDA content of from about 5% to about 50% and a gamma-linoleic acid content of less than about 10%. The SDA content may, in certain embodiments, be further defined as from about 5% to about 32%, from about 5% to about 35%, from about 15% to about 30%, from about 22% to about 30%, and from about 22% to about 40%. The gamma-linoleic acid content may, in further embodiments, be defined as less than about 10, 8, 5 and/or about 3%. In particular embodiments, the stearidonic acid content may be from about 15% to about 35% and the gamma-linoleic acid content less than 5%. In still further embodiments, the seed may comprise a ratio of omega-3 to omega-6 fatty acids of from about 0.35:1 to about 3.5:1, including from about 1:1 to about 3.5:1 and from about 2:1 to about 3.5:1.
In still yet another aspect, the invention provides a method of increasing the nutritional value of an edible product for human or animal consumption, comprising adding a soybean seed oil provided by the invention to the edible product. In certain embodiments, the product is human and/or animal food. The edible product may also be animal feed and/or a food supplement. In the method, the soybean seed oil may increase the SDA content of the edible product and/or may increase the ratio of omega-3 to omega-6 fatty acids of the edible product. The edible product may lack SDA prior to adding the soybean seed oil.
In still yet another aspect, the invention provides a method of manufacturing food or |ped, comprising adding a soybean seed oil provided by the invention to starting food or feed ingredients to produce the food or feed. In certain embodiments, the method is further defined as a method of manufacturing food and/or feed. The invention also provides food or feed made by the method.
In still yet another aspect, the invention comprises a method of providing SDA to a human or animal, comprising administering the soybean seed oil of claim 1 to said human or
animal. In the method, the soybean seed oil may be administered in an edible composition,
Examples of food include beverages, infused foods, sauces, condiments,
salad dressings, fruit juices, syrups, desserts, icings and fillings, soft frozen products, confections or intermediate food. The edible composition may be substantially a liquid or solid. The edible composition may also be a food supplement and/or nutraceutical. In the method, the soybean seed oil may be administered to a human and/or an animal. Examples of animals the oil may be administered to include livestock or poultry.
BRIEF DESCRIPTION OF THE FIGURES
The following drawings form part of the present specification and are included to further demonstrate certain aspects of the present invention. The invention may be better understood by reference to one or more of these drawings in combination with the detailed description of specific embodiments presented herein.
FIG. 1 shows alignment of Primula juliae A6 desaturases PJD6D-1 and PJD6D-2 (SEQ ID NOs:4 and 5), Primula alpicola Pa6D-l and Pa6D-2 (SEQ ID NOs: 22 and 24), Primula waltonii PwD6D (SEQ ID NO:26), Primula farinosa D6D-2 (SEQ ID NO:46), Primula florindae D6D (SEQ ID NO:48), Borago oficinalis D6D (SEQ ID NO:59) and Echium gentianoides D6D (SEQ ID NO:60).
FIG. 2 shows map of vector pMON67011. FIG. 3 shows map of vector pMON83950. FIG. 4 shows map of vector pMON77245. FIG. 5 shows map of vector pMON77247. FIG. 6 shows map of vector pMON82821.
FIG. 7 shows map of vector pMON82822. FIG. 8 shows map of vector pMON83961. FIG. 9 shows map of vectorpMON83962. FIG. 10 shows map of vector pMON83963. FIG. 11 shows map of vector pMON83964. FIG. 12 shows map of vector pMON83 965. FIG. 13 shows map of vector pMON83966.
DETAILED DESCRIPTION OF THE INVENTION
The invention overcomes the limitations of the prior art by providing methods and compositions for creation of plants with improved PUFA content. The modification of fatty acid content of an organism such as a plant presents many advantages, including improved nutrition and health benefits. Modification of fatty acid content can be used to achieve beneficial levels or profiles of desired PUFA's in plants, plant parts, and plant products, including plant seed oils. For example, when the desired PUFA's are produced in the seed tissue of a plant, the oil may be isolated from the seeds typically resulting in an oil high in desired PUFAs or an oil having a desired fatty acid content or profile, which may in turn be used to provide beneficial characteristics in food stuffs and other products. The invention in particular embodiments provides endogenous soybean oil having SDA while also containing a beneficial oleic acid content.
Various aspects of the invention include methods and compositions for modification of PUFA content of a cell, for example, modification of the PUFA content of a plant cell(s). Compositions related to the invention include novel isolated polynucleotide sequences, polynucleotide constructs and plants and/or plant parts transformed by polynucleotides of the invention. The isolated polynucleotide may encode Primula fatty acid desaturases and, in particular, may encode a Primula A6-desaturase. Host cells may be manipulated to express a polynucleotide encoding a desaturase polypeptide(s) which catalyze desaturation of a fatty acid(s).
Some aspects of the invention include desaturase polypeptides and polynucleotides encoding the same. Various embodiments of the invention may use combinations of desaturase
polynucleotides and the encoded polypeptides that typically depend upon the host cell, the |p«ailability of substrate(s), and the desired end product(s). "Desaturase" refers to a polypeptide that can desaturate or catalyze formation of a double bond between consecutive carbons of one or more fatty acids to produce a mono- or poly-unsaturated fatty acid or a precursor thereof. Of particular interest are polypeptides that can catalyze the conversion of oleic acid to LA, LA to ALA, or ALA to SDA, which includes enzymes which desaturate at the 12, 15, or 6 positions. The term "polypeptide" refers to any chain of amino acids, regardless of length or post-translational modification (e.g., glycosylation or phosphorylation). Considerations for choosing a specific polypeptide having desaturase activity include, but are not limited to, the pH optimum of the polypeptide, whether the polypeptide is a rate limiting enzyme or a component thereof, whether the desaturase used is essential for synthesis of a desired PUFA, and/or whether a co-factor is required by the polypeptide. The expressed polypeptide preferably has characteristics that are compatible with the biochemical environment of its location in the host cell. For example, the polypeptide may have to compete for substrate(s).
Analyses of the Km and specific activity of a polypeptide in question may be considered in determining the suitability of a given polypeptide for modifying PUFA(s) production, level, or profile in a given host cell. The polypeptide used in a particular situation is one which typically can function under the conditions present in the intended host cell, but otherwise may be any desaturase polypeptide having a desired characteristic or being capable of modifying the relative production, level or profile of a desired PUFA(s) or any other desired characteristics as discussed herein. The substrate(s) for the expressed enzyme may be produced by the host cell or may be exogenously supplied. To achieve expression, the polypeptide(s) of the instant invention are encoded by polynucleotides as described below.
The inventors have isolated and produced enzymes from Primula that exhibit A6-desaturase activity. The sequences encoding the A6-desaturase may be expressed in transgenic plants, microorganisms or animals to effect greater synthesis of SDA. Other polynucleotides which are substantially identical to the A6-desaturase polynucleotides provided herein, or which encode polypeptides which are substantially identical to the A6-desaturase polypeptides, also can be used. "Substantially identical" refers to an amino acid sequence or nucleic acid sequence exhibiting in order of increasing preference at least 90% , 95%, 98 or 99% identity to the A6-desaturase polypeptide sequence in SEQ ID NO:4, SEQ ID NO:5, SEQ ID NO:22, SEQ ID NO:24, SEQ ID NO:26, SEQ ID N0:46 or SEQ ID NO:48 or sequences encoding these polypeptides. Polypeptide or polynucleotide comparisons may be carried out using sequence
analysis software, for example, the Sequence Analysis software package of the GCG Wisconsin package (Accelrys, San Diego, CA), MEGAlign (DNAStar, Inc., 1228 S. Park St., Madison, Wis. 53715), and MacVector (Oxford Molecular Group, 2105 S. Bascom Avenue, Suite 200, Campbell, Calif. 95008). Such software matches similar sequences by assigning degrees of similarity or identity.
Encompassed by the present invention are related desaturases, including variants of the disclosed A6-desaturases naturally occurring within the same or different species of Primula. Related desaturases can be identified by their ability to function substantially the same as the disclosed desaturases; that is, having A6-desaturase activity. Related desaturases alsoxcan be identified by screening sequence databases for sequences homologous to the disclosed desaturases, by hybridization of a probe based on the disclosed desaturases to a library constructed from the source organism, or by RT-PCR using mRNA from the source organism and primers based on the disclosed desaturases. The invention therefore provides nucleic acids hybridizing under stringent conditions to a desaturase coding sequences described herein. One of skill in the art understands that conditions may be rendered less stringent by increasing salt concentration and decreasing temperature. Thus, hybridization conditions can be readily manipulated, and thus will generally be a method of choice depending on the desired results. An example of high stringency conditions is 5X SSC, 50% formamide and 42°C. By conducting a wash under such conditions, for example, for 10 minutes, those sequences not hybridizing to a particular target sequence under these conditions can be removed.
In another aspect of the invention, vectors containing a nucleic acid, or fragment thereof, containing a promoter, a A6-desaturase coding sequence and a termination region may be transferred into an organism in which the promoter and termination regions are functional. Accordingly, organisms producing recombinant A6-desaturase are provided by this invention. Yet another aspect of this invention provides isolated A6-desaturase, which can be purified from the recombinant organisms by standard methods of protein purification. (For example, see Ausubelefa/., 1994).
Various aspects of the invention include nucleic acid sequences that encode desaturases, described herein. Nucleic acids may be isolated from Primula including SEQ ID NO:2, SEQ ID NO:3, SEQ ID NO:21, SEQ ID NO:23, SEQ ID N0:25, SEQ ID NO:45 or SEQ ID NO:47 and the like. A cloning strategy based on oligonucleotide primers designed to amplify sequences identified as potential fatty acid desaturases, based on BLAST searches of genomic DNA
databases, may be used to sequence individual clones. These clones may then be functionally ^.aracterized.
Nucleic acid constructs may be provided that integrate into the genome of a host cell or
are autonomously replicated (e.g., episomally replicated) in the host cell. For production of
ALA and/or SDA, the expression cassettes (i.e., a polynucleotide encoding a protein that is
operatively linked to nucleic acid sequence(s) that directs the expression of the polynucleotide)
generally used include an expression cassette which provides for expression of a polynucleotide
encoding a A6-desaturase. In certain embodiments a host cell may have wild type oleic acid
Methods and compositions for the construction of expression vectors, when taken in light of the teachings provided herein, for expression of Primula desaturase enzymes will be apparent to one of ordinary skill in the art. Expression vectors, as described herein, are DNA or RNA molecules engineered for controlled expression of a desired polynucleotide, e.g., the A6-desaturase-encoding polynucleotide. Examples of vectors include plasmids, bacteriophages, cosmids or viruses. Shuttle vectors, e.g. (Wolk et al. 1984; Bustos et al, 1991) are also contemplated in accordance with the present invention. Reviews of vectors and methods of preparing and using them can be found in Sambrook et al. (2001); Goeddel (1990); and Perbal (1988). Sequence elements capable of effecting expression of a polynucleotide include promoters, enhancer elements, upstream activating sequences, transcription termination signals and polyadenylation sites.
Polynucleotides encoding desaturases may be placed under transcriptional control of a strong promoter. In some cases this leads to an increase in the amount of desaturase enzyme expressed and concomitantly an increase in the fatty acid produced as a result of the reaction catalyzed by the enzyme. There are a wide variety of plant promoter sequences which may be used to drive tissue-specific expression of polynucleotides encoding desaturases in transgenic plants. Indeed, in particular embodiments of the invention, the promoter used is a seed specific promoter. Examples of such promoters include the 5' regulatory regions from such genes as napin (Kridl et al, Seed Sci. Res. 1:209:219, 1991), phaseolin (Bustos, et al, Plant Cell, l(9):839-853, 1989), soybean trypsin inhibitor (Riggs, et al, Plant Cell 1(6):609-621, 1989), ACP (Baerson et al, Plant Mol Biol, 22(2):255-267, 1993), stearoyl-ACP desaturase (Slocombe et al, Plant Physiol 104(4): 167-176, 1994), soybean a' subunit of/3-conglycinin (P-Gm7S, see for example, Chen et al, Proc. Natl. Acad. Sci. 83:8560-8564, 1986), Viciafaba USP (P-Vf.Usp, see for example, SEQ ID N0:l, 2, and 3, U.S. Patent Application 10/429,516), the
globulin promoter (see for example Belanger and Kriz, Genet. 129: 863-872 (1991), soybean Jipha subunit of |8-conglycinin (7S alpha) (U.S. Patent Application 10/235,618, incorporated by reference) and Zea mays L3 oleosin promoter (P-Zm.L3, see, for example, Hong et al, Plant Mol Biol, 34(3):549-555, 1997). Also included are the zeins, which are a group of storage proteins found in corn endosperm. Genomic clones for zein genes have been isolated (Pedersen et al, Cell 2P:1015-1026 (1982), and Russell et al., Trans-genie Res. tf(2):157-168) and the promoters from these clones, including the 15 kD, 16 kD, 19 kD, 22 kD, 27 kD and genes, could also be used.
The ordinarily skilled artisan can determine vectors and regulatory elements (including operably linked promoters and coding regions) suitable for expression in a particular host cell. "Operably linked" in this Context means that the promoter and terminator sequences effectively function to regulate transcription. As a further example, a vector appropriate for expression of A6-desaturase in transgenic plants can comprise a seed-specific promoter sequence derived from helianthinin, napin, or glycinin operably linked to the A6-desaturase coding region and further operably linked to a seed storage protein termination signal or the nopaline synthase termination signal. As a still further example, a vector for use in expression of A6-desaturase in plants can comprise a constitutive promoter or a tissue specific promoter operably linked to the A6-desaturase coding region and further operably linked to a constitutive or tissue specific terminator or the nopaline synthase termination signal.
Modifications of the nucleotide sequences or regulatory elements disclosed herein which maintain the functions contemplated herein are within the scope of this invention. Such modifications include insertions, substitutions and deletions, and specifically substitutions which reflect the degeneracy of the genetic code.
Standard techniques for the construction of such recombinant vectors are well-known to those of ordinary skill in the art and can be found in references such as Sambrook et al (2001), or any of the myriad of laboratory manuals on recombinant DNA technology that are widely available. A variety of strategies are available for ligating fragments of DNA, the choice of which depends on the nature of the termini of the DNA fragments. It is further contemplated in accordance with the present invention to include in a nucleic acid vector other nucleotide sequence elements which facilitate cloning, expression or processing, for example sequences encoding signal peptides, a sequence encoding KDEL, which is required for retention of proteins in the endoplasmic reticulum or sequences encoding transit peptides which direct A6-desaturase to the chloroplast. Such sequences are known to one of ordinary skill in the art. An optimized
transit peptide is described, for example, by Van den Broeck et al. (1985). Prokaryotic and tfekaryotic signal sequences are disclosed, for example, by Michaelis et al. (1982).
Polynucleotides encoding desired desaturases can be identified in a variety of ways. As an example, a source of the desired desaturase, for example genomic or cDNA libraries from Primula, is screened with detectable enzymatically- or chemically-synthesized probes, which can be made from DNA, RNA, or non-naturally occurring nucleotides, or mixtures thereof. Probes may be enzymatically synthesized from polynucleotides of known desaturases for normal or reduced-stringency hybridization methods. Oligonucleotide probes also can be used to screen sources Nand can be based on sequences of known desaturases, including sequences conserved among known desaturases, or on peptide sequences obtained from the desired purified protein. Oligonucleotide probes based on amino acid sequences can be degenerate to encompass the degeneracy of the genetic code, or can be biased in favor of the preferred codons of the source organism. Oligonucleotides also can be used as primers for PCR from reverse transcribed mRNA from a known or suspected source; the PCR product can be the full length cDNA or can be used to generate a probe to obtain the desired full length cDNA. Alternatively, a desired protein can be entirely sequenced and total synthesis of a DNA encoding that polypeptide performed.
Once the desired genomic or cDNA has been isolated, it can be sequenced by known methods. It is recognized in the art that such methods are subject to errors, such that multiple sequencing of the same region is routine and is still expected to lead to measurable rates of mistakes in the resulting deduced sequence, particularly in regions having repeated domains, extensive secondary structure, or unusual base compositions, such as regions with high GC base content. When discrepancies arise, resequencing can be done and can employ special methods. Special methods can include altering sequencing conditions by using: different temperatures; different enzymes; proteins which alter the ability of oligonucleotides to form higher order structures; altered nucleotides such as ITP or methylated dGTP; different gel compositions, for example adding formamide; different primers or primers located at different distances from the problem region; or different templates such as single stranded DNAs. Sequencing of mRNA also can be employed.
Some or all of the coding sequence for a polypeptide having desaturase activity may be from a natural source. In some situations, however, it is desirable to modify all or a portion of the codons, for example, to enhance expression, by employing host preferred codons. Host-preferred codons can be determined from the codons of highest frequency in the proteins expressed in the largest amount in a particular host species and/or tissue of interest. Thus, the
coding sequence for a polypeptide having desaturase activity can be synthesized in whole or in fflMt All or portions of the DNA also can be synthesized to remove any destabilizing sequences or regions of secondary structure which would be present in the transcribed mRNA. All or portions of the DNA also can be synthesized to alter the base composition to one more preferable in the desired host cell. Methods for synthesizing sequences and bringing sequences together are well established in the literature. In vitro mutagenesis and selection, site-directed mutagenesis, or other means can be employed to obtain mutations of naturally-occurring desaturase genes to produce a polypeptide having desaturase activity in vivo with more desirable physical and kinetic parameters for function in the host cell, such as a longer half-life or a higher rate of production of a desired polyunsaturated fatty acid.
Once the polynucleotide encoding a desaturase polypeptide has been obtained, it is placed in a vector capable of replication in a host cell, or is propagated in vitro by means of techniques such as PCR or long PCR. Replicating vectors can include plasmids, phage, viruses, cosmids and the like. Desirable vectors include those useful for mutagenesis of the gene of interest or for expression of the gene of interest in host cells. The technique of long PCR has made in vitro propagation of large constructs possible, so that modifications to the gene of interest, such as mutagenesis or addition of expression signals, and propagation of the resulting constructs can occur entirely in vitro without the use of a replicating vector or a host cell.
For expression of a desaturase polypeptide, functional transcriptional and translational initiation and termination regions are operably linked to the polynucleotide encoding the desaturase polypeptide. Expression of the polypeptide coding region can take place in vitro or in a host cell. Transcriptional and translational initiation and termination regions are derived from a variety of nonexclusive sources, including the polynucleotide to be expressed, genes known or suspected to be capable of expression in the desired system, expression vectors, chemical synthesis, or from an endogenous locus in a host cell.
Expression in a host cell can be accomplished in a transient or stable fashion. Transient expression can occur from introduced constructs which contain expression signals functional in the host cell, but which constructs do not replicate and rarely integrate in the host cell, or where the host cell is not proliferating. Transient expression also can be accomplished by inducing the activity of a regulatable promoter operably linked to the gene of interest, although such inducible systems frequently exhibit a low basal level of expression. Stable expression can be achieved by introduction of a construct that can integrate into the host genome or that autonomously replicates in the host cell. Stable expression of the gene of interest can be selected for through
the use of a selectable marker located on or transfected with the expression construct, followed selection for cells expressing the marker. When stable expression results from integration, integration of constructs can occur randomly within the host genome or can be targeted through the use of constructs containing regions of homology with the host genome sufficient to target recombination with the host locus. Where constructs are targeted to an endogenous locus, all or some of the transcriptional and translational regulatory regions can be provided by the endogenous locus.
When increased expression of the desaturase polypeptide in the source organism is desired, several methods can be employed. Additional genes encoding the desaturase polypeptide can be introduced into the host organism. Expression from the native desaturase locus also can be increased through homologous recombination, for example by inserting a stronger promoter into the host genome to cause increased expression, by removing destabilizing sequences from either the mRNA or the encoded protein by deleting that information from the host genome, or by adding stabilizing sequences to the mRNA (U.S. Pat. No. 4,910,141).
It is contemplated that more than one polynucleotide encoding a desaturase or a polynucleotide encoding more than one desaturase may be introduced and propagated in a host cell through the use of episomal or integrated expression vectors. Where two or more genes are expressed from separate replicating vectors, it is desirable that each vector has a different means of replication. Each introduced construct, whether integrated or not, should have a different means of selection and should lack homology to the other constructs to maintain stable expression and prevent reassortment of elements among constructs. Judicious choices of regulatory regions, selection means and method of propagation of the introduced construct can be experimentally determined so that all introduced polynucleotides are expressed at the necessary levels to provide for synthesis of the desired products.
When necessary for transformation, the A6-desaturase coding sequences of the present invention can be inserted into a plant transformation vector, e.g. the binary vector described by Bevan (1984). Plant transformation vectors can be derived by modifying the natural gene transfer system of Agrobacterium tumefaciens. The natural system comprises large Ti (tumor-inducing)-plasmids containing a large segment, known as T-DNA, which is transferred to transformed plants. Another segment of the Ti plasmid, the vir region, is responsible for T-DNA transfer. The T-DNA region is bordered by terminal repeats. In the modified binary vectors the tumor-inducing genes have been deleted and the functions of the vir region are utilized to transfer foreign DNA bordered by the T-DNA border sequences. The T-region also contains a
selectable marker for antibiotic resistance, and a multiple cloning site for inserting sequences for ^pansfer. Such engineered strains are known as "disarmed" A. tumefaciens strains, and allow the efficient transformation of sequences bordered by the T-region into the nuclear genomes of plants.
The subject invention finds many applications. Probes based on the polynucleotides of the present invention may find use in methods for isolating related molecules or in methods to detect organisms expressing desaturases. When used as probes, the polynucleotides or
oligonucleotides must be detectable. This is usually accomplished by attaching a label either at an internal site, for example via incorporation of a modified residue, or at the 5' or 3' terminus. Such labels can be directly detectable, can bind to a secondary molecule that is detectably labeled, or can bind to an unlabelled secondary molecule and a detectably labeled tertiary molecule; this process can be extended as long as is practical to achieve a satisfactorily detectable signal without unacceptable levels of background signal. Secondary, tertiary, or bridging systems can include use of antibodies directed against any other molecule, including labels or other antibodies, or can involve any molecules which bind to each other, for example a biotin-streptavidin/avidin system. Detectable labels typically include radioactive isotopes, - molecules which chemically or enzymatically produce or alter light, enzymes which produce detectable reaction products, magnetic molecules, fluorescent molecules or molecules whose fluorescence or light-emitting characteristics change upon binding. Examples of labeling methods can be found in U.S. Pat. No. 5,011,770. Alternatively, the binding of target molecules can be directly detected by measuring the change in heat of solution on binding of probe to target via isothermal titration calorimetry, or by coating the probe or target on a surface and detecting the change in scattering of light from the surface produced by binding of target or probe, respectively, as may be done with the BIAcore system.
Constructs comprising the gene of interest may be introduced into a host cell by standard techniques. For convenience, a host cell which has been manipulated by any method to take up a DNA sequence or construct will be referred to as "transformed" or "recombinant" herein. The subject host will have at least have one copy of the expression construct and may have two or more, for example, depending upon whether the gene is integrated into the genome, amplified, or is present on an extrachromosomal element having multiple copy numbers.
The transformed host cell can be identified by selection for a marker contained on the introduced construct. Alternatively, a separate marker construct may be introduced with the desired construct, as many transformation techniques introduce many DNA molecules into host
cells. Typically, transformed hosts are selected for their ability to grow on selective media. Elective media may incorporate an antibiotic or lack a factor necessary for growth of the untransformed host, such as a nutrient or growth factor. An introduced marker gene therefore may confer antibiotic resistance, or encode an essential growth factor or enzyme, and permit growth on selective media when expressed in the transformed host. Selection of a transformed host can also occur when the expressed marker protein can be detected, either directly or indirectly. The marker protein may be expressed alone or as a fusion to another protein. The marker protein can be detected by its enzymatic activity; for example, beta-galactosidase can convert the substrate X-gal to a colored product, and luciferase can convert; luciferin to a light-emitting product. The marker protein can be detected by its light-producing or modifying characteristics; for example, the green fluorescent protein ofAequorea victoria fluoresces when illuminated with blue light. Antibodies can be used to detect the marker protein or a molecular tag on, for example, a protein of interest. Cells expressing the marker protein or tag can be selected, for example, visually, or by techniques such as FACS or panning using antibodies. Desirably, resistance to kanamycin and the amino glycoside G418 are of interest, as well as ability to grow on media lacking uracil, leucine, lysine or tryptophan.
Of particular interest is the A6-desaturase-mediated production of PUFA's in eukarydtic host cells. Eukaryotic cells include plant cells, such as those from oil-producing crop plants, and other cells amenable to genetic manipulation including fungal cells. The cells may be cultured or formed as part or all of a host organism including a plant. In a preferred embodiment, the host is a plant cell which produces and/or can assimilate exogenously supplied substrate(s) for a A6-desaturase, and preferably produces large amounts of one or more of the substrates.
The transformed host cell is grown under appropriate conditions adapted for a desired end result. For host cells grown in culture, the conditions are typically optimized to produce the greatest or most economical yield of PUFA's, which relates to the selected desaturase activity. Media conditions which may be optimized include: carbon source, nitrogen source, addition of substrate, final concentration of added substrate, form of substrate added, aerobic or anaerobic growth, growth temperature, inducing agent, induction temperature, growth phase at induction, growth phase at harvest, pH, density, and maintenance of selection.
Another aspect of the present invention provides transgenic plants or progeny of plants containing the isolated DNA of the invention. Both monocotyledonous and dicotyledonous plants are contemplated. Plant cells are transformed with an isolated DNA encoding A6-desaturase by any plant transformation method. The transformed plant cell, often in a callus
culture or leaf disk, is regenerated into a complete transgenic plant by methods well-known to %ie of ordinary skill in the art (e.g. Horsch et al, 1985). In one embodiment, the transgenic plant is selected from the group consisting of Arabidopsis thaliana, canola, soy, soybean, rapeseed, sunflower, cotton, cocoa, peanut, safflower, coconut, flax, oil palm, oilseed Brassica napus, corn, jojoba, Chinese tallow tree, tobacco, fruit plants, citrus plants or plants producing nuts and berries. Since progeny of transformed plants inherit the polynucleotide encoding A6-desaturase, seeds or cuttings from transformed plants may be used to maintain the transgenic plant line.
The present invention further provides a method for providing transgenic plants with an increased content of ALA and/or SDA. This method includes, for example, introducing DNA encoding A6-desaturase into plant cells which lack or have low levels SDA but contain ALA, and regenerating plants with increased SDA content from the transgenic cells. In certain embodiments of the invention, a DNA encoding a A15- and/or A12-desaturase may also be introduced into the plant cells. Such plants may or may not also comprise endogenous A12-and/or A15-desaturase activity. In certain embodiments, modified commercially grown crop plants are contemplated as the transgenic organism, including, but not limited to, Arabidopsis thaliana, canola, soy, soybean, rapeseed, sunflower, cotton, cocoa, peanut, safflower, coconut, flax, oil palm, oilseed Brassica napus, corn, jojoba, Chinese tallow tree, tobacco, fruit plants, citrus plants or plants producing nuts and berries.
The present invention further provides a method for providing transgenic plants which may contain elevated levels of ALA and/or SDA, wherein said elevated levels are greater than levels found in non-transformed plants. Expression vectors comprising DNA encoding a A6-desaturase, and/or a A12-desaturase and/or a A15-desaturase, can be constructed by methods of recombinant technology known to one of ordinary skill in the art (Sambrook et al., 2001). In particular, commercially grown crop plants are contemplated as the transgenic organism, including, but not limited to, Arabidopsis thaliana, canola, soy, soybean, rapeseed, sunflower, cotton, cocoa, peanut, safflower, coconut, flax, oil palm, oilseed Brassica napus, and corn.
For dietary supplementation, the purified PUFAs, transformed plants or plant parts, or derivatives thereof, may be incorporated into cooking oils, fats or margarines formulated so that in normal use the recipient would receive the desired amount. The PUFAs may also be incorporated into infant formulas, nutritional supplements or other food products, and may find use as anti-inflammatory or cholesterol lowering agents.
As used herein, "edible composition" is defined as compositions which may be ingested a mammal such as foodstuffs, nutritional substances and pharmaceutical compositions. As used herein "foodstuffs" refer to substances that can be used or prepared for use as food for a mammal and include substances that may be used in the preparation of food (such as frying oils) or food additives. For example, foodstuffs include animals used for human consumption or any product therefrom, such as, for example, eggs. Typical foodstuffs include but are not limited to beverages, (e.g., soft drinks, carbonated beverages, ready to mix beverages), infused foods (e.g. fruits and vegetables), sauces, condiments, salad dressings, fruit juices, syrups, desserts (e.g., puddings, gelatin, icings and fillings, baked goods and frozen desserts such as ice creams and sherbets), soft frozen products (e.g., soft frozen creams, soft frozen ice creams and yogurts, soft frozen toppings such as dairy or non-dairy whipped toppings), oils and emulsified products (e.g., shortening, margarine, mayonnaise, butter, cooking oil, and salad dressings) and intermediate moisture foods (e.g., rice and dog foods).
Furthermore, edible compositions described herein can also be ingested as an additive or supplement contained in foods and drinks. These can be formulated together with a nutritional substance such as various vitamins and minerals and incorporated into substantially liquid compositions such as nutrient drinks, soymilks and soups; substantially s6lid compositions; and gelatins or used in the form of a powder to be incorporated into various foods. The content of the effective ingredient in such a functional or health food can be similar to the dose contained in a typical pharmaceutical agent.
The purified PUFAs, transformed plants or plant parts may also be incorporated into animal, particularly livestock, feed. In this way, the animals themselves may benefit from a PUFA rich diet, while human consumers of food products produced from such livestock may benefit as well. It is expected in certain embodiments that SDA will be converted to EPA in animals and thus such animals may benefit from an increase in EPA by consumption of SDA.
For pharmaceutical use (human or veterinary), the compositions may generally be administered orally but can be administered by any route by which they may be successfully absorbed, e.g., parenterally (i.e. subcutaneously, intramuscularly or intravenously), rectally, vaginally or topically, for example, as a skin ointment or lotion. The PUFAs transformed plants or plant parts of the present invention may be administered alone or in combination with a pharmaceutically acceptable carrier or excipient. Where available, gelatin capsules are the preferred form of oral administration. Dietary supplementation as set forth above can also provide an oral route of administration. The unsaturated acids of the present invention may be
administered in conjugated forms, or as salts, esters, amides or prodrugs of the fatty acids. Any •pharmaceutically acceptable salt is encompassed by the present invention; especially preferred are the sodium, potassium or lithium salts. Also encompassed are the N-alkylpolyhydroxamine salts, such as N-methyl glucamine, found in PCX publication WO 96/33155. The preferred esters are the ethyl esters. As solid salts, the PUFAs also can be administered in tablet form. For intravenous administration, the PUFAs or derivatives thereof may be incorporated into commercial formulations such as Intralipids.
If desired, the regions of a desaturase polypeptide important for desaturase activity can be determined through routine mutagenesis followed by expression of the resulting mutant polypeptides and determination of their activities. Mutants may include substitutions, deletions, insertions and point mutations, or combinations thereof. Substitutions may be made on the basis of conserved hydrophobicity or hydrophilicity (Kyte and Doolittle, 1982), or on the basis of the ability to assume similar polypeptide secondary structure (Chou and Fasman, 1978). A typical functional analysis begins with deletion mutagenesis to determine the N- and C-terminal limits of the protein necessary for function, and then internal deletions, insertions or point mutants are made to further determine regions necessary for function. Other techniques such as cassette mutagenesis or total synthesis also can be used. Deletion mutagenesis is accomplished, for example, by using exonucleases to sequentially remove the 5' or 3' coding regions. Kits are available for such techniques. After deletion, the coding region is completed by ligating oligonucleotides containing start or stop codons to the deleted coding region after 5' or 3' deletion, respectively. Alternatively, oligonucleotides encoding start or stop codons are inserted into the coding region by a variety of methods including site-directed mutagenesis, mutagenic PCR or by ligation onto DNA digested at existing restriction sites.
Internal deletions can similarly be made through a variety of methods including the use of existing restriction sites in the DNA, by use of mutagenic primers via site directed mutagenesis or mutagenic PCR. Insertions are made through methods such as linker-scanning mutagenesis, site-directed mutagenesis or mutagenic PCR. Point mutations are made through techniques such as site-directed mutagenesis or mutagenic PCR. Chemical mutagenesis may also be used for identifying regions of a desaturase polypeptide important for activity. Such structure-function analysis can determine which regions may be deleted, which regions tolerate insertions, and which point mutations allow the mutant protein to function in substantially the same way as the native desaturase. All such mutant proteins and nucleotide sequences encoding them are within the scope of the present invention.
As described herein above, certain embodiments of the current invention concern plant Jipransformation constructs. For example, one aspect of the current invention is a plant transformation vector comprising one or more desaturase gene(s) or cDNA(s). Exemplary coding sequences for use with the invention include Primula juliae A6-desaturase (SEQ ID NOs:2-3). In certain embodiments, antisense desaturase sequences can also be employed with the invention. Exemplary desaturase encoding nucleic acids include-at least 20, 40, 80, 120, 300 and up to the full length of the nucleic acid sequences of SEQ ID NO:2, SEQ ID NO:3, SEQ ID NO:21, SEQ ID NO:23, SEQ ID NO:25, SEQ ID NO:45 or SEQ ID NO:47. In certain aspects, a nucleic acid may encode 1, 2, 3, 4, or more desaturase enzymes. In particular embodiments, a nucleic acid may encode a A6- and a A15-desaturase.
Vectors used for plant transformation may include, for example, plasmids, cosmids, YACs (yeast artificial chromosomes), BACs (bacterial artificial chromosomes) or any other suitable cloning system, as well as fragments of DNA therefrom. Thus when the term "vector" or "expression vector" is used, all of the foregoing types of vectors, as well as nucleic acid sequences isolated therefrom, are included. It is contemplated that utilization of cloning systems with large insert capacities will allow introduction of large DNA sequences comprising more than one selected gene. In accordance with the invention, this could be used to introduce various desaturase encoding nucleic acids. Introduction of such sequences may be facilitated by use of bacterial or yeast artificial chromosomes (BACs or YACs, respectively), or even plant artificial chromosomes. For example, the use of BACs for Agrobacterium-mediated transformation was disclosed by Hamilton et al. (1996).
Particularly useful for transformation are expression cassettes which have been isolated from such vectors. DNA segments used for transforming plant cells will, of course, generally comprise the cDNA, gene or genes which one desires to introduce into and have expressed in the host cells. These DNA segments can further include structures such as promoters, enhancers, polylinkers, or even regulatory genes as desired. The DNA segment or gene chosen for cellular introduction will often encode a protein which will be expressed in the resultant recombinant cells resulting in a screenable or selectable trait and/or which will impart an improved phenotype to the resulting transgenic plant. However, this may not always be the case, and the present invention also encompasses transgenic plants incorporating non-expressed transgenes. Preferred components likely to be included with vectors used in the current invention are as follows.
In one embodiment the instant invention utilizes certain promoters. Examples of such promoters that may be used with the instant invention include, but are not limited to, the 35S
CaMV (cauliflower mosaic virus), 34S FMV (figwort mosaic virus) (see, e.g., U.S. Patent No. %• 378,619, the contents of which are herein incorporated in their entirety), Napin (from Brassica), 7S (from soybean), Globulin and Lee (from com). The napin promoter and promoters, which are regulated during plant seed maturation, are of particular interest for use with the instant invention. All such promoter and transcriptional regulatory elements, singly or in combination, are contemplated for use in the present replicable expression vectors and are known to one of ordinary skill in the art..
The DNA sequence between the transcription initiation site and the start of the coding sequence, i.e., the untranslated leader sequence, can also influence gene expression. X)ne may thus wish to employ a particular leader sequence with a transformation construct of the invention. Preferred leader sequences are contemplated to include those which comprise sequences predicted to direct optimum expression of the attached gene, i.e., to include a preferred consensus leader sequence which may increase or maintain mRNA stability and prevent inappropriate initiation of translation. The choice of such sequences will be known to those of skill in the art in light of the present disclosure. Sequences that are derived from genes that are highly expressed in plants will typically be preferred.
Transformation constructs prepared in accordance with the invention will typically include a 3' end DNA sequence that acts as a signal to terminate transcription and allow for the poly-adenylation of the mRNA produced by coding sequences operably linked to a desaturase gene (e.g., cDNA). In one embodiment of the invention, the native terminator of a desaturase gene is used. Alternatively, a heterologous 3' end may enhance the expression of desaturase coding regions. Examples of terminators deemed to be useful include those from the nopaline synthase gene of Agrobacterium tumefaciens (nos 3' end) (Bevan et al., 1983), the terminator for the T7 transcript from the octopine synthase gene of Agrobacterium tumefaciens, the 3' end of the protease inhibitor I or II genes from potato or tomato and the CaMV 35S terminator (tm!3'). Regulatory elements such as an Adh intron (Callis et al., 1987), sucrose synthase intron (Vasil et al., 1989) or TMV omega element (Gallie et al., 1989), may further be included where desired.
By employing a selectable or screenable marker protein, one can provide or enhance the ability to identify transformants. "Marker genes" are genes that impart a distinct phenotype to cells expressing the marker protein and thus allow such transformed cells to be distinguished from cells that do not have the marker. Such genes may encode either a selectable or screenable marker, depending on whether the marker confers a trait which one can "select" for by chemical means, i.e., through the use of a selective agent (e.g., a herbicide, antibiotic, or the like), or
whether it is simply a trait that one can identify through observation or testing, i.e., by Screening" (e.g., the green fluorescent protein). Of course, many examples of suitable marker proteins are known to the art and can be employed in the practice of the invention.
Suitable methods for transformation of plant or other cells for use with the current invention are believed to include virtually any method by which DNA can be introduced into a cell, such as by direct delivery of DNA such as by PEG-mediated transformation of protoplasts (Omirulleh et al., 1993), by desiccation/inhibition-mediated DNA uptake (Potrykus et al., 1985), by electroporation (U.S. Patent No. 5,384,253, specifically incorporated herein by reference in its entirety), by agitation with silicon carbide fibers (Kaeppler et al., 1990; U.S. Patent No. 5,302,523, specifically incorporated herein by reference in its entirety; and U.S. Patent No. 5,464,765, specifically incorporated herein by reference in its entirety), by Agrobacterium-mediated transformation (U.S. Patent No. 5,591,616 and U.S. Patent No. 5,563,055; both specifically incorporated herein by reference) and by acceleration of DNA coated particles (U.S. Patent No. 5,550,318; U.S. Patent No. 5,538,877; and U.S. Patent No. 5,538,880; each specifically incorporated herein by reference in its entirety), etc. Through the application of techniques such as these, the cells of virtually any plant species may be stably transformed, and these cells developed into transgenit plants.
After effecting delivery of exogenous DNA to recipient cells, the next steps generally concern identifying the transformed cells for further culturing and plant regeneration. In order to improve the ability to identify transformants, one may desire to employ a selectable or screenable marker gene with a transformation vector prepared in accordance with the invention. In this case, one would then generally assay the potentially transformed cell population by exposing the cells to a selective agent or agents, or one would screen the cells for the desired marker gene trait.
Cells that survive the exposure to the selective agent, or cells that have been scored positive in a screening assay, may be cultured in media that supports regeneration of plants. In an exemplary embodiment, MS and N6 media may be modified by including further substances such as growth regulators. One such growth regulator is dicamba or 2,4-D. However, other growth regulators may be employed, including NAA, NAA + 2,4-D or picloram. Media improvement in these and like ways has been found to facilitate the growth of cells at specific developmental stages. Tissue may be maintained on a basic media with growth regulators until sufficient tissue is available to begin plant regeneration efforts, or following repeated rounds of manual selection, until the morphology of the tissue is suitable for regeneration, typically at least
2 weeks, then transferred to media conducive to maturation of embryoids. Cultures are ilh-ansferred every 2 weeks on this medium. Shoot development will signal the time to transfer to medium lacking growth regulators.
To confirm the presence of the exogenous DNA or "transgene(s)" in the regenerating plants, a variety of assays may be performed. Such assays include, for example, "molecular biological" assays, such as Southern and Northern blotting and PCR™; "biochemical" assays, such as detecting the presence of a protein product, e.g., by immunological means (ELISAs and Western blots) or by enzymatic function; plant part assays, such as leaf or root assays; and also, by analyzing the phenotype of the whole regenerated plant.
In addition to direct transformation of a particular plant genotype with a construct prepared according to the current invention, transgenic plants may be made by crossing a plant having a selected DNA of the invention to a second plant lacking the DNA. Plant breeding techniques may also be used to introduce a multiple desaturases, for example A6, A12, and/or AlS-desaturase(s) into a single plant. In this manner, A6-desaturase can be effectively up-regulated. By creating plants homozygous for a A6-desaturase activity and/or other desaturase activity (e.g., A12- and/or A15-desaturase activity) beneficial metabolites can be increased in the plant.
As set forth above, a selected desaturase gene can be introduced into a particular plant variety by crossing, without the need for ever directly transforming a plant of that given variety. Therefore, the current invention not only encompasses a plant directly transformed or regenerated from cells which have been transformed in accordance with the current invention, but also the progeny of such plants. As used herein the term "progeny" denotes the offspring of any generation of a parent plant prepared in accordance with the instant invention, wherein the progeny comprises a selected DNA construct prepared in accordance with the invention. "Crossing" a plant to provide a plant line having one or more added transgenes or alleles relative to a starting plant line, as disclosed herein, is defined as the techniques that result in a particular sequence being introduced into a plant line by crossing a starting line with a donor plant line that comprises a trans gene or allele of the invention. To achieve this one could, for example, perform the following steps: (a) plant seeds of the first (starting line) and second (donor plant line that comprises a desired transgene or allele) parent plants; (b) grow the seeds of the first and second parent plants into plants that bear flowers; (c) pollinate a flower from the first parent plant with pollen from the second parent plant; and (d) harvest seeds produced on the parent plant bearing the fertilized flower.
Backcrossing is herein defined as the process including the steps of: (a) crossing a plant a first genotype containing a desired gene, DNA sequence or element to a plant of a second genotype lacking said desired gene, DNA sequence or element; (b) selecting one or more progeny plant containing the desired gene, DNA sequence or element; (c) crossing the progeny plant to a plant of the second genotype; and (d) repeating steps (b) and (c) for the purpose of transferring a desired DNA sequence from a plant of a first genotype to a plant of a second genotype.
Introgression of a DNA element into a plant genotype is defined as the result of the process of backcross conversion. A plant genotype into which a DNA sequence has been introgressed may be referred to as a backcross converted genotype, line, inbred, or hybrid. Similarly a plant genotype lacking the desired DNA sequence may be referred to as an unconverted genotype, line, inbred, or hybrid.
The following examples are included to illustrate embodiments of the invention. It should be appreciated by those of skill in the art that the techniques disclosed in the examples that follow represent techniques discovered by the inventor to function well in the practice of the invention. However, those of skill in the art should, in light of the present disclosure, appreciate that many changes can be made in the specific embodiments which are disclosed and still obtain a like or similar result without departing from the concept, spirit and scope of the invention. More specifically, it will be apparent that certain agents which are both chemically and physiologically related may be substituted for the agents described herein while the same or similar results would be achieved. All such similar substitutes and modifications apparent to those skilled in the art are deemed to be within the spirit, scope and concept of the invention as defined by the appended claims.
Cloning of Primula juliae A6 Desaturase Sequences
Cloning of the Primula juliae A6 desaturase (PJD6D) was achieved by PCR amplification of a partial internal genomic DNA region using degenerate oligonucleotides, followed by bidirectional genomic walking. Total genomic DNA was isolated from P. juliae (Collector's
Nursery, Battleground WA) using the DNeasy Plant Mini Kit (Qiagen, Valencia, CA), following manufacturer's procedure. Initially, a 552 bp fragment corresponding to positions 687 to 1238 of SEQ ID NO:1 was isolated using degenerate oligonucleotides BO-1 For and BO-2 Rev as described by Garcia-Maroto et al. (2002). The fragment was cloned into pCR®4-TOPO® (Invitrogen, Carlsbad, CA) to yield the vector pMON83955 and the insert was sequenced. Primer sequences BO-1 For and BO-2 Rev were as follows:
BO-1 For: 5'-ATMAGYATYGGTTGGTGGAARTGG-3' (SEQIDNO:6)
BO-2 Rev: 5'-AATCCACCRTGRAACCARTCCAT-3' (SEQ ID NO:7)
To determine the genomic flanking sequence of the insert of pMON83955, a Universal Genome Walker Kit™ (BD Biosciences, Palo Alto, CA) was utilized, following the manufacture's procedure. Four P. juliae genomic libraries were generated by digesting the DNA with four restriction enzymes: EcoRV, PvuII, StuI, and Dral. After a purification step, the digestions were ligated to an adapter provided in the kit. The procedure then involved two PCR reactions, each with a gene-specific primer and an adapter-primer. The secondary PCR reaction used a dilution of the primary PCR reaction products as a template. For the 5' direction, primers PD6D R8 and PD6D R2 were used for the primary and secondary PCR reactions, respectively. For the 3' direction, primers PD6D F8 and PD6D F3 were used for the primary and secondary PCR reactions, respectively. The primer sequences are given below:
PD6D R8: 5'-CACACATGACCGGATAAAACGACCAGT-3' (SEQ ID NO:8) PD6D R2: 5'-GGGAATGTACTGGAGGTCAGGGTCGTA-3' (SEQ ID NO:9) PD6D F8: 5'-CGTGCAGTTCAGCTTGAACCATTTCTC -3' (SEQ ID NO: 10) PD6D F3: 5'-TGCAGGGACACTCAACATATCGTGCCC-3' (SEQ ID NO:11)
Genome walking in the 5' direction yielded a 574 bp fragment from the EcoRV library. This product was cloned into pCR®4-TOPO® (Invitrogen) giving pMON83956, and the insert was sequenced. The resulting sequence did not contain a start codon of the putative delta 6 desaturase gene and thus another set of PCR reactions was performed using gene specific primers designed to walk in the 5' direction from the pMON83956 insert. The primers used for the second genome walking set in the 5' direction were PD6D R15 and PD6D R14 for the primary and secondary PCR reactions, respectively. The sequences are given below:
PD6D R15: 5'- GTAGGTTGGTGGAGAAGGGAGGGAGGA-3' (SEQ ID NO:12)
PD6D R14: 5'-GGAAGGGGGATGGTAAGCGAGGAAAGC-3' (SEQ ID NO: 13)
A product of 328 bp in length from the StuI library was cloned into pCR®4-TOPO® (Invitrogen) giving pMON83958 and the insert was sequenced. This insert contained 2 potential start codons, 44 bases apart. The first start codon corresponds to position 87 and the second to position 135 of SEQ ID NO:1. Genome walking in the 3' direction resulted in a 773 bp fragment from the Oral library. This product was cloned into pCR®4-TOPO®, giving pMON83957. The insert was sequenced and found to contain 292 bp of the coding region for the putative delta 6 desaturase gene, followed by a stop codon at position 1473 with respect to SEQ ID N0:l.
The inserts of pMON83955, pMON83956, pMON83957, and pMON83958 were aligned to form a composite sequence, SEQ ID NO:1. Three primers were designed to PCR amplify 2 different lengths of coding sequence from P. juliae genomic DNA, reflecting the two start codons found in pMON83958. The longer of the two sequences, PJD6D-1, was amplified using forward primer Pj D6D F2 and reverse primer Pj D6D Rl. The shorter of the two, PJD6D-2, was amplified using forward primer Pj D6D Fl and reverse primer Pj D6D Rl. The two putative delta 6 desaturase coding sequences were each then ligated into the yeast expression vector pYES2.1-TOPO. Upon sequencing, the plasmid containing PJD6D-1 was designated pMON83950 (SEQ ID NO:3) and the plasmid containing PJD6D-2 was designated pMON67011 (SEQ ID NO:2). The primer sequences are given below:
Pj D6D F2: 5'-GTCGACATGGAAAACACATTTTCACCACCACCT-3' (SEQ ID
Pj D6D Fl: 5'-GTCGACATGACTAAGACCATTTACATAACCAGC-3' (SEQ ID NO: 15)
Pj D6D Rl: 5'-CCTGCAGGTCACCCGACATTTTTAACAGCCTCCC-3' (SEQ ID NO: 16)
The two PjA6 desaturase clones, PJD6D-2 and PJD6D-1, encode potential polypeptides of 446 amino acids and 462 amino acids, given in SEQ ID NO:4 and SEQ ID N0:5, respectively. The initial MET site of the shorter peptide sequence (PJD6D-2) is located 16 amino acids downstream from the first MET site of the longer sequence (PJD6D-1). 3' of the second MET, the sequences are identical. These sequences have high similarity to other plant A 6 desaturases (FIG. 1), including an N-terminal cytochrome 65 domain which is found in all front-end desaturases (Napier et al., 2003). Within the cytochrome b$ domain is found the eight invariant residues characteristic of the cytochrome b$ superfamily and the H-P-G-G heme-binding motif,
which has been shown to be essential for enzymatic activity (Napier et al, 1997, Sayanova et al, fe99, Sperling and Heinz 2001). Within the desaturase domain of the putative PJD6D desaturase are three conserved histidine boxes that are characteristic of all membrane-bound desaturases (Shanklin et al, 1994). A distinguishing feature found in all front-end desaturases is that the third histidine box contains a glutamine residue in the first position (Q-x-x-H-H) instead of a histidine (Napier et al, 1997, Napier et al, 2003, Sperling and Heinz 2001). The deduced amino acid sequence of the PJD6D had approximately 88% identity to the Primula vialii and P. farinosa desaturases and approximately 64% identity to the Echium pitardii and E. gentianoides desaturases. Visual inspection^ the multiple sequence alignment shown in FIG. 1 suggests that the P.juliae A6 desaturase sequence does not contain any introns. This has been observed in A6 desaturases from Primula and Echium species (Sayanova et al, 2003, Garcia-Maroto et al, 2002).
Example 2 Yeast Transformation and Expression
Constructs pMON83950 (FIG. 3) and pMON67011 (FIG. 2) were introduced into the host strain Saccharomyces cerevisiae INVScl (Invitrogen), which is auxotrophic for uracil, using the PEG/Li Ac protocol as described in the Invitrogen manual for pYES2.1/V5-His-TOPO. Transformants were selected on plates made of SC minimal media minus uracil with 2% glucose. Colonies of transformants were used to inoculate 5 ml of SC minimal media minus uracil and 2% glucose and were grown overnight at 30°C. For induction, stationary phase yeast cells were pelleted and re-suspended in SC minimal media minus uracil supplemented with 2% galactose and grown for 3 days at 15°C. When exogenous fatty acids were provide to the cultures, 0.01% LA (A9,12-18:2) was added with the emulsifier 0.1% Tergitol. The cultures were grown for 3 days at 15°C, and subsequently harvested by centrifugation. Cell pellets were washed once with sterile TE buffer pH 7.5, to remove the media, and lyophilized for 24 h. The host strain transformed with the vector containing the LacZ gene was used as a negative control in all studies.
Lipids were extracted from lyophilized yeast pellets by adding 0.1 mL toluene and incubating over night at room temperature. Extracted lipids were converted to fatty acid methyl esters (FAMEs) in situ by addition of 0.5 mL 0.6N sodium methoxide in methanol and incubating for 45 min. The FAMEs were extracted by addition of 0.8 mL 10% (w/v) NaCl and
0.15 mL of heptane. The heptane layer containing FAMEs was removed and used directly for ^SSLS chromatography (GC). The FAMEs were identified on a Hewlett-Packard 5890 II Plus GC (Hewlett-Packard, Palo Alto, CA) equipped with a flame-ionization detector and a capillary column (omegawax 250; 30m x 0.25mm i.d. x 0.25|j,m; Supelco, Bellefonte, PA). A 100:1 split ratio was used for injections. The injector was maintained at 250°C and the flame ionization detector was maintained at 270°C. The column temperature was maintained at 180°C for 1.5 min following injection, increased to 240°C at 40°C/min, and held at 245°C for 3.38 min.
Table 1 shows the fatty acid composition for yeast expressing P. juliae clones pMON67011 (PJD6D-2), pMON83950 (PJD6D-1) or Mortierella alpina A6 desaturase, pMON77205. Expected products for A6 desaturation of LA and ALA were observed for both P. juliae clones (Table 1, GLA and SD A, respectively), demonstrating that the clones contained in pMON67011 and pMON83950 are A6 desaturases. The substrate selectivity was determined by feeding equal quantities of LA and ALA. M. alpina is a filamentous fungus that accumulates high levels of the n-6 fatty acid arachidonic acid and was expected to have a A6 desaturase with an n-6 selectivity. Table 2 shows the n-3:n-6 substrate selectivities of the P. juliae and M. alpina
A6 desaturases. An n-3:n-6 selectivity of ~0.8 was observed for the M. alpina A6 desaturase.
An n-3:n-6 selectivity of -1.5-1.9 was observed for both P. juliae A6 desaturase clones.
Table 1: Comparison of fatty acid composition of yeast expressing different A6 desaturases
** Reported as a % of the total for all analytes included in the GC-FID chromatogram, including but not shown (16:0, 16:1,18:0, 20:0, 20:1, 20:2, 22:0, 22:1,22:2
Table 2. Comparison of n-3:n-6 substrate selectivities for P. juliae and M. alpina A6 desaturases.
* The percentage conversion to GLA was calculated by dividing the value for GLA (Table 1) by the sum of the values for LA and GLA (Table 1). The same calculation was made for SDA using the sum of ALA and SDA (Table 1).
**The n-3:n-6 ratio was calculated by dividing the % conv. SDA by % conv. GLA.
Example 3 Plant Transformation and Expression of Primula juliae A6-desaturase
The activity of the P. juliae A6-desaturase was evaluated in soybean by combining it with a A15-desaturase from either Neurospora crassa (NcDISD), pMON77245 (FIG. 4), or Aspergillus nidulans (AnDlSD), pMON77247 (FIG. 5). The vector pMON77245 was constructed in three steps. First P. juliae A6-desaturase (PJD6D-2) was placed behind the seed-specific 7S alpha' promoter by digesting pMON67011 with Sse8387 I, followed by removal of the 3' overhangs, and Sal I, and then ligating the resulting fragment into the EcoRI and filled-in Xhol sites of the expression vector pMON68527, generating the vector pMON77243. Second, the PJD6D-2 expression cassette was removed from pMON77243 by digesting with NotI, followed by a fill-in reaction, and then the resulting fragment was ligated into the EcoRV site of the 2T binary vector pMON77244. Finally, a codon-optimized NcD15D (SEQ ID NO: 17) under the control of a 7S alpha seed-specific promoter was combined with the PJD6D-2 by digesting pMON77227 with NotI and then ligating the resulting NcD15D expression cassette fragment into NotI digested pMON77344 to give pMON77245 (FIG. 4). The vector pMON77247 (FIG.
5) was constructed by digesting vector pMON77242 with Not I and ligating the resulting
expression cassette fragment comprising a codon-optimized AnD15D (SEQ ID NO:18) linked to %the 7S alpha promoter into the NotI site of pMON77244. The vectors pMON77245 and pMON77247 were transformed into soybean using the method of Martinell et al. (U.S. Patent No. 6,384,301, the disclosure of which is incorporated herein by reference in the entirety).
Expression of the PJD6D-2 coding sequence was measured by determining the fatty acid composition of immature (approximately 30 days after flowering) Rl transgenic soybean seeds, including both homozygotes and heterozygotes, by gas chromatography of lipid methyl ester derivatives (PCT US03/16144, filed May 21, 2003, the entire disclosure of which is specifically incorporated herein by reference). The levels of PA (palmitic acid, 16:0), SA (stearic acid, 18:0), OA, LA, GLA, ALA, and SDA are expressed as a percentage of the total weight of measured fatty acids and are shown in Tables 3 and 4 below. The non-transgenic control line was A3525. Whenever possible, five individual seeds were analyzed from each event.
Individual seed from a majority of the pMON77245 transgenic events were found to accumulate measurable amounts of SDA. hi all cases, the levels of SDA were greater than those of GLA, with an average SDA:GLA ratio for each event ranging from 2:1 to a high of 8:1. The highest single seed value was observed from event GM_A38083, which contained 32.0% SDA and 2.6% GLA, with a SDA:GLA ratio of 12:1. Of the 12 events shown below, 9 had SDA values >10% in at least one seed out of five. As SDA values increased, the levels of PA, SA and OA did not vary significantly from control levels; however, there is a strong negative correlation for LA. hi seeds that accumulated SDA, the levels of GLA remains low, between 2.3 to 5.5%. The ALA levels increased along the SDA levels.
TABLE 3: Relative Area Percent Results (Approx. wt percent) from single pMON77245-transformed Rl seeds
Individual seed from the pMON77247 transgenic events accumulated similar amounts of SDA as compared to pMON77245, with the exception of event GM_A38083 that accumulated significantly higher levels of SDA. The levels of PA, SA, OA, and LA were similar to the control levels shown in Table 3. Generally, the levels of SDA were greater than those of GLA with an average SDA:GLA ratio for each event ranging from 1:1 to 1.6:1, which was less than that observed for pMON77245.
TABLE 4: Relative Area Percent Results (Approx. wt percent) from single pMON77247 Rl seeds
Activity of the Primula juliae A6-desaturase in combination with the Neurospora cmssa
A15-desaturase in canola
The activity of the Primula juliae A6-desaturase in combination with Neurospora crassa A15-desaturase was evaluated by transforming canola with the MON82822 (FIG. 7). pMON82822 contained a native NcDISD (SEQ ID NO: 19) as well as PJD6D-2, both inserted into a seed-specific expression cassette under the control of the napin promoter (PCT, US03/16144, the disclosure of which is specifically incorporated herein by reference).
The pMON82822 vector was constructed by first digesting pMON77214 (PCT US03/16144) with Pmel and BamHI (filled-in) and ligating the resulting native NcDISD napin cassette into the EcoRV site of the 2T binary vector pMON71801 to generate pMON82820. Next, pMON82819 was digested with NotI, the ends were filled in and the resulting PJD6D-2 napin expression cassette was ligated into the filled-in AscI site of pMON82820 to generate pMON82822.
A second vector, pMON82821, was also constructed containing the codon-optimized NcDISD (SEQ ID NO: 17) and PJD6D-2 pMON82821 by first digesting pMON67011 with Sail and Sse8387I and ligating the resulting PJD6D-2 fragment into the Sail and Xhol (filled-in) sites of the napin expression cassette in pMON82800 giving pMON82819. The napin cassette containing a codon-optimized NcDISD was constructed by digesting pMON67024 with Pmel and BamHI (filled-in) and ligating the resulting fragment into an EcoRV-digested 2T binary vector, pMON71801, giving pMON82801. Finally, pMON82819 was digested with NotI, filled-in and the resulting PJD6D-2 napin expression cassette was ligated into the filled in NotI site of pMON82801 giving pMON82821.
pMON82822 was transformed into canola (Brassica napus) using a modification of the ^Protocol described by Radke et al, (Plant Cell Reports 11:499-505, 1992). Briefly canola seed of the cultivar 'Ebony' (Monsanto Canada, Inc., Winnipeg, Canada) were disinfected and germinated in vitro as described in Radke et al, 1992. Precocultivation with tobacco feeder plates, explant preparation and inoculation of explants with Agrobacterium tumefaciens strain ABI (Koncz and Schell, Mol Gen Genet 204:383-396 (1986)) containing the desired vector were as described with the Agrobacterium being maintained in LB media (solid or liquid) containing 75 mg/1 spectinomycin, 25 mg/1 chloramphenicol and 50 mg/1 kanamycin. For plant transformation including callus induction, shoot regeneration, maturation and rooting, glyphosate selection was used rather than the kanamycin selection as described in Radke et al, 1992. Specifically, the B5-1 callus induction medium was supplemented with 500 mg/1 carbenicillin and 50 mg/1 Timentin (Duchefa Biochemie BV) to inhibit the Agrobacterium growth and kanamycin was omitted from the media. B5BZ shoot regeneration medium contained, in addition, 500 mg/1 carbenicillin, 50 mg/1 Timentin and 45 mg/1 glyphosate with explants being transferred to fresh medium every two weeks.
Glyphosate selected shoots were transferred to hormone-free B5-0 shoot maturation medium containing 300 mg/1 carbenicillin and 45 mg/1 glyphosate for two weeks and finally shoots were transferred to B5 root induction medium containing 45 mg/1 glyphosate. Rooted green plantlets were transplanted to potting soil and acclimated to green house conditions. Plants were maintained in a greenhouse under standard conditions. The fatty acid composition of mature seed was determined by GC analysis of methyl ester derived lipids as done above for soybean transformants. The GC analysis of canola seed from plants transformed with pMON82822 yielded 199 events with SDA levels ranging from 0.12 to 4.49% (weight %, 100 seed pool).
Example 5 Construction and transformation of PJD6D expression vectors for Soy, Corn and Canola
The expression of the PJD6D sequences alone is evaluated in planta for canola, corn and soybean under the expression a seed-specific promoter. A soybean expression vector is constructed by digesting pMON77243 with Not I, and ligating the resulting fragment containing PJD6D-2 into the Not I site of the binary vector pMON17227. A canola expression vector is constructed by digesting pMON83950 with Sail and Sse8387I (made blunt) and ligating the
resulting fragment, which contains the coding region of PJD6D-1 into the Sail and Xhol (filled-
in) sites of the seed-specific napin expression cassette vector pMON82800. The resulting asmid is then digested with Not I followed by ligating the resulting napin-PjD6D-l expression cassette into the Not I site of the binary vector pMON17227. A corn expression vector is constructed by digesting pMON83950 with Sal I (filled-in) and Sse83872I (made blunt) and ligating the resulting PJD6D-1 fragment into the Sfil (made blunt) site of the globulin expression cassette in pMON71084. The resulting vector is then digested with Pmel and Hindlll and the expression cassette is then ligated into the Hpal and Hindlll sites of the binary vector pMON30167.
The activity of the P. juliae A6-desaturase in corn is evaluated in combination with a Neurospora crassa A15-desaturase codon-optimized for corn (NcDISDnno) (SEQ ID NO:20). The vector pMON67011 is digested with Sail and Sse8387I (made blunt) and the resulting PJD6D-2 fragment is ligated into the Sfil (fill-in) site of the globulin expression cassette in pMON71084 to give pMON82823. Next, pMON82806 (PCT US03/16144) is digested with Pmel and Hindlll and the resulting globulin NcDISDnno cassette is ligated into the NotI (fill-in) and Hindlll sites of the IT binary vector pMON30167 to give pMON82824. Finally the globulin PJD6D-2 cassette is combined with globulin NcDISDnno by digesting pMON82823 with Pmel and Hindlll and ligating the resulting fragment into the Smal and Hindlll sites of pMON82824 giving pMON82825. The resulting vector is introduced into maize via Agrobacterium tumefaciens-mediated transformation as known to one of skill in the art, e.g., U.S. Patent No. 6,603,061.
Example 6 Cloning of Primula \valtonll and Primula alpicola A6 Desaturase Sequences
Cloning of the Primula waltonii A6 desaturase (PwD6D) and P. alpicola A6 desaturase (PaD6D) genes was achieved by PCR amplification of a partial internal genomic DNA region using degenerate oligonucleotides, followed by bi-directional genomic walking. Total genomic DNA was isolated from P. waltonii and P. alpicola (Collector's Nursery) using the DNeasy Plant Mini Kit (Qiagen), following the manufacturer's procedure. Two fragments were isolated from the P. alpicola genomic DNA using the degenerate oligonucleotides BO-1 For and BO-2 Rev as described by Garcia-Maroto et al. 2002:
BO-1 For: 5'-ATMAGYATYGGTTGGTGGAARTGG-3' (SEQIDNO:6) BO-2 Rev: 5'-AATCCACCRTGRAACCARTCCAT-3' (SEQ ID NO:7)
The first P. alpicola fragment was 550 bp in length and corresponded to positions 553 to of SEQ ID NO:21. This fragment was cloned into pCR®4-TOPO® (Invitrogen) to yield the vector pMON83977 (no intron). The second P. alpicola fragment was 550 bp in length and corresponded to positions 763 to 1313 of SEQ ID N0:23. This fragment was cloned into pCR®4-TOPO® (Invitrogen) to yield the vector pMON83975 (contains intron). One fragment was obtained from P. waltonii that was 550 bp in length and -corresponded to positions 763 to 1313 of SEQ ID NO:25. This fragment was cloned into pCR®4-TOPO® (Invitrogen) to yield the vector pMON83976. The polypeptide sequences encoded by SEQ ID NOs:21, 23 and 25 are given in SEQ ID NOs:22, 24 and 26, respectively.
To determine the genomic flanking sequences of the pMON83975, pMON83976, and pMON83977 inserts, a Universal Genome Walker Kit™ (BD Biosciences) was utilized, following the manufacture's procedure. Four genomic libraries for each Primula species were generated by digesting the DNA with four restriction enzymes: EcoRV, Pvull, Stui, and Dral. After a purification step, the digestions were ligated to an adapter provided in the kit. The procedure then involved two PCR reactions, each with a gene-specific primer and an adapter-primer. The secondary PCR reaction used a dilution of the primary PCR reaction products as a template.
A. pMON83975 (PaD6D-2)
For the 5' direction, primers PD6D R7 and PD6D Rl were used for the primary and secondary PCR reactions, respectively. For the 3' direction, primers PD6D F7 and PD6D Fl were used for the primary and secondary PCR reactions, respectively. The primer sequences are given below:
PD6D R7: 5'-CACACATGACCGGATAAAACGTCCAGT-3' (SEQ ID NO:27) PD6D Rl: 5'-AGGGATATACTGGAGGTCGGGGTCGTA-3' (SEQ ID NO:28) PD6D F7: 5'- GAGCTATTCCGTTACGGGGATACAACA -3' (SEQ ID NO:29) PD6D Fl: 5'- TGCAGGGACACTTAACATATCGTGCCC-3' (SEQ ID NO:30)
Genome walking in the 5' direction yielded a 751 bp fragment from the EcoRV library. This product was cloned into pCR®4-TOPO® (Invitrogen) giving pMON83978, and the insert was sequenced. The resulting sequence did not contain a start codon of the putative delta 6 desaturase gene and thus another set of PCR reactions was performed using gene specific primers designed to walk in the 5' direction from the pMON83978 insert. The primers used for
the second genome walking set in the 5' direction were PD6D R17 and PD6D R16 for the mary and secondary PCR reactions, respectively. The sequences are given below:
PD6D R17: 5'- GTGAAAGTTGTTGAGGAGGGATCGGTA-3' (SEQ ID NO: 31) PD6D R16: 5'-GTGGAAGGAGGATGGTAAGCGAGGAAA-3' (SEQ ID NO: 32)
A product of 473 bp in length from the PvuII library was cloned into pCR®4-TOPO® giving pMON83980 and the insert was sequenced. This insert contained a start codon corresponding to position 1 of SEQ ID NO:23. Genome walking in the 3' direction resulted in a 942 bp fragment from the Dral library. This^ product was cloned into pCR 4-TOPO®, giving pMON83979. The insert was sequenced and found to contain 294 bp of the coding region for the putative delta 6 desaturase gene, followed by a stop codon at position 1549 with respect to SEQ LD NO:23.
The inserts of pMON83975, pMON83978, pMON83980 and pMON83979 were aligned to form a composite sequence of a putative A6 desaturase gene for P. alpicola giving PaD6D-2, SEQ ID NO:23. Two primers were designed to PCR amplify the complete open reading frame from P. alpicola genomic DNA. The primer sequences are given below:
PaD6D Fl: 5'- GTCGACATGGCTAACAAATCfCAAACAGGTTAC-3' (SEQ ID NO: 33)
Pa D6D Rl: 5'- CCTGCAGGTCACCCGAGAGTTTTAACAGCCTCC-3" (SEQ ID NO: 34)
The PCR amplified fragment (SEQ ID NO:23) was then ligated into the yeast expression vector pYES2.1-TOPO giving the vector pMON83968.
B. pMON83976 (PwD6D)
A putative A6 desaturase was PCR amplified from P. waltonii genomic DNA using the primers Pa D6D Fl (SEQ ID NO:33) and Pa D6D Rl (SEQ ID NO:34) shown above. The PCR amplified fragment (SEQ ID NO:25) was then ligated into the yeast expression vector pYES2.1-TOPO giving the vector pMON83967.
C. pMON83977 (PaD6D-l)
For the 5' direction, primers PD6D R9 and PD6D R4 were used for the primary and secondary PCR reactions, respectively. For the 3' direction, primers PD6D F9 and PD6D F4 were used for the primary and secondary PCR reactions, respectively. The primer sequences are given below:
PD6D R9: 5'-CACACATTACCGGATAAAACGTCCAGT -3' (SEQ ID NO:35) PD6D R4: 5'-AGGAATATACTGGAGGTCTGGGTCGTA-3' (SEQ ID NO:36) PD6D F9: 5'- ATTTTTCTTCGGACGTATACATGGGCC -3' (SEQ ID N0:37) PD6D F4: 5'- TTCGGGGACACTGAACATATCGTGCCC-3' (SEQ ID NO:38)
Genome walking in the 5s direction yielded a 979 bp fragment from the StuI library. This product was cloned into pCR®4-TOPO® (Invitrogen) giving pMON83981, and the insert was sequenced. The resulting sequence contained the start codon of the putative delta 6 desaturase at position 1 with respect to SEQ ID NO:21. Genome walking in the 3' direction resulted in a 1028 bp fragment from the Oral library. This product was cloned into pCR®4-TOPO® (Invitrogen), giving pMON83982. The insert was sequenced and found to contain 295 bp of the coding region for the putative delta 6 desaturase gene, followed by a stop codon at position 1339 with respect to SEQ ID N0:21.
The inserts of pMON83977, pMON83981 and pMON83982 were aligned to form a composite sequence of a second putative A6 desaturase gene for P. alpicola giving PaD6D-l, SEQ ID NO:21. Two primers were designed to PCR amplify the complete open reading frame from P. alpicola genomic DNA. The primer sequences are given below.
Pf D6D-F2: 5'-GTCGACATGGCCAACACTAGTTACATTTCCAGCT-3' (SEQ ID NO:39)
Pf D6D-R2: 5'- GATATCACCCCAGAGTGTTAACAGCTTCCCAG-3' (SEQ ID NO: 40)
The PCR amplified fragment was then ligated into the yeast expression vector pYES2.1-TOPO giving the vector pMON67026 (SEQ ID NO 21).
Alignment of PaD6D-2 and PwD6D (also abbreviated PRIwaD6D) with other characterized plant A6 desaturase genes revealed that these two genes contained a single intron corresponding to positions 476 to 676 in SEQ ID NO:23 and positions 476 to 651 in SEQ ID N0:25. This has been observed in A6 desaturases from Primula and Echium species (Sayanova et al, 2003, Garcia-Maroto et al, 2002).
The three A6 desaturase clones encode potential polypeptides of 446 amino acids for PaD6D-l (SEQ ID NO:22), 449 amino acids for PaD6D-2 (SEQ ID NO: 24) and 449 amino acids for PwD6D (SEQ ID NO: 26). These sequences have high similarity to other plant A6 desaturases (FIG. 1), including an N-terminal cytochrome 65 domain, which is found in all front-
end desaturases (Napier et al., 2003). Within the cytochrome 65 domain is found the eight invariant residues characteristic of the cytochrome 65 superfamily and the H-P-G-G heme-binding motif, which has been shown to be essential for enzymatic activity (Napier et al., 1997, Sayanova et al, 1999, Sperling and Heinz 2001). Within the desaturase domain of the PaD6D-l, PaD6D-2, and PwD6D desaturases are three conserved histidine boxes that are characteristic of all membrane-bound desaturases (Shanklin et al, 1994). A distinguishing feature found in all front-end desaturases is that the third histidine box contains a glutamine residue in the first position (Q-x-x-H-H) instead of a histidine (Napier et al., 1997, Napier et al., 2003, Sperling and Heinz 2001). The deducedsamino acid sequence of the PaD6D-l had approximately 80% identity to PaD6D-2 and approximately 80% identity to PwD6D. However, the two intron containing genes, PaD6D-2 and PwD6D, are more similar to each other with approximately 97% identity, than the two P. alpicola genes, PaD6D-l and PaD6D are to each other.
Example 7 Cloning Additional Primula A6 Desaturase Sequences
Genomic DNA was isolated from P. farinosa and P. florindae using a Sarkosyl/CTAB lysis system. Five grams of tissue frprn each species was ground in a mortar and pestle with liquid nitrogen until ground into a fine powder. The powdered tissue was then resuspended in lysis buffer (140 mM sorbitol, 220 mM Tris-HCl, pH 8.0, 22 mM ethylenediaminetetraacetic acid (EDTA), 800 mM sodium chloride (NaCl), 1% N-laurylsarcosine and 0.8% hexadecyltrimethyl ammonium bromide (CTAB)) and incubated for 1 hour at 65°C with gentle inversion every 10 minutes. After incubation, 10 ml of chloroform was added to the lysis suspension and incubated at room temperature with gentle rocking for 20 minutes. The lysis suspension was centrifuged for 10 minutes at 12,000 X g. The aqueous layer was transferred to a clean tube and the nucleic acid precipitated with 0.6% isopropanol. The nucleic acid pellet was resuspended in 4 ml of a solution containing 10 mM Tris-HCl, pH 8.0, ImM EDTA, 1 M NaCl and 20 mg Proteinase K. The resuspended nucleic acid was then incubated for 2 hours at 63°C. The Proteinase K was then heat inactivated by incubation at 75°C for 20 minutes. RNase (2.5 (ig) was added to the solution and incubated at 37°C for 1 hour. The solution was extracted with an equal volume of phenol:chloroform:isoamylalcohol (25:24:1) 2 times. The purified genomic DNA was then ethanol precipitated.
Approximately, 3 jag of genomic DNA was digested in separate reactions with the restriction endonucleases, EcoRI, Hindlll, Kpnl, Sail and Xhol. After digestion, each reaction
was purified using a QIAquick® PCR Purification Kit (Qiagen, Valencia, CA), following the
manufacturer's protocol. The digested genomic DNA was eluted from the purification columns t&ing 100 (J.1 of elution buffer supplied in the kit. Ligation favoring intramolecular interactions was performed in a 200 ul volume using 20 (J.1 of the eluted digested genomic DNA in a PEG-free ligation reaction with 800 units of ligase (M0202L) (New England Biolabs, Beverly MA) overnight at 16°C, followed by heat inactivation at 75°C for 10 minutes. After ligation, the reaction was again purified using a QIAquick® PCR Purification Kit. Inverse PCR was performed using 6-20 ng of purified ligated DNA and from 10-20 pg of primer and the Expand Long Template PCR System (Roche Applied Science, Indianapolis, IN). Primers are shown in Table 5 and were designed using a combination of available sequence data and data covering the desaturase domain. Thermal cycle conditions consisted of an initial incubation at 94 °C for 2 minutes; 10 cycles of 94 °C for 20 seconds, 52 °C for 30 seconds and 68 °C for 8 minutes; followed by 25 cycles of 94 °C for 30 seconds, 52 °C for 30 seconds and 68 °C for 8 minutes plus 10 seconds per cycle. After cycling was complete, a further incubation at 68 °C for 7 minutes was performed. Inverse PCR library products visible after agarose electrophoresis were cloned into either pCR®2.1-TOPO or pCR®4Blunt-TOPO (Invitrogen) following the manufacturer's protocol. The following inverse library fragments (with approximate size) were cloned: P. farinosa-EcoRl (6 kb) and P florindae-Hindlll (3 kb). The DNA sequencing was performed on an Applied Biosystems 3730x1 DNA Analyzer, using Big Dye® Terminator v3.0.
Table 5. Primers and fragments used in inverse PCR determination of the 5' and 3' regions of the delta 6 desaturase genes.
Species Primer Sequence SEQ ID NO:
P.farinosa Pfll07Fl TGGAGGTCTGGGTCGTAATC 41
PH107R1 CTTCGGACGTATACATGGGC 42
P.florindae Pflll3-lF2 TCGTAATCCAGGCTATTGCA 43
Pflll3-lR2 TTTTCTTCGGACGTCCATGT 44
Putative sequences were aligned with public data to determine the approximate region of the open reading frame (ORF) covered for each gene. Primers to amplify the ORF of each gene were designed based upon the aligned inverse PCR data. Proofreading polymerases were used to amplify the putative delta 6 genes to insure fidelity of the final product. The primers used in the final cloning of the putative delta 6 desaturase genes are shown in Table 6. The products were cloned into either pUC19 or pCR®4Blunt-TOPO (Invitrogen). DNA sequencing was performed on an Applied Biosystems 3730x1 DNA Analyzer, using Big Dye® Terminator v3.0. Two
putative delta 6 desaturase genes were cloned: P. farinosa (PfaD6D) (pMON84809) (SEQ ID
lto:45) andP.florindae (PflD6D) (PMON84810) (SEQ ID NO:47).
Table 6. Primers used to amplify delta 6 desaturase genes.
Primer Sequence SEQ ID NO:
Pfarinosa754F GACGATTTTTGAGTGAGAGTTAATTTGAGTCAATAATA 49
Pfarinosa2447R CGACATCATAGACAATCATCAAGACACCGT 50
PflorindaestartF ATACCCCCTCAAAACACCCCCAAAT 51
PflorindaestopR CTCAATATCACCCGAGAGTTTTAACAGCCT 52
Two primers were designed to amplify the complete PfaD6D open reading frame from pMON84809. The resulting fragment was ligated into the yeast expression vector pYES2.1-TOPO giving pMON67065. The two primers are given below.
Pfar Fl: 5'- GTCGACAACAATGTCCAACACATATCCACCAAATC -3' (SEQ ID NO:53)
Pfar Rl: 5'- CCTGCAGGTCACCCCAGAGTGTTAACAGCTTC -3' (SEQ ID NO:54)
Two primers 'were designed to amplify the complete PflD6D gene containing two exons and one intron from pMON84810. The resulting fragment was ligated into vector pYES2.1-TOPO giving pMON67067. The two primers are given below.
Pw Fl: 5'- GTCGACATGGCTAACAAATCTCAAAC -3' (SEQ ID N0:55)
Pw R2: 5'- CCTGCAGGTCACCCGAGAGT -3' (SEQ ID N0:56)
The two A6 desaturase clones encode potential polypeptides of 454 amino acids for PfaD6D (SEQ ID NO:46) and 449 amino acids for PflD6D (SEQ ID NO:48). These sequences have high similarity to other plant A6 desaturases (FIG. 1), including an N-terminal cytochrome bs domain, which is found in all front-end desaturases (Napier et al., 2003). Within the cytochrome bs domain is found the eight invariant residues characteristic of the cytochrome b5 superfamily and the H-P-G-G heme-binding motif, which has been shown to be essential for enzymatic activity (Napier et al., 1997, Sayanova et al, 1999, Sperling and Heinz 2001). Within the desaturase domain of the putative PflD6D and PfaD6D desaturases are three conserved histidine boxes that are characteristic of all membrane-bound desaturases (Shanklin et al., 1994). A distinguishing feature found in all front-end desaturases is that the third histidine box contains
a glutamine residue in the first position (Q-x-x-H-H) instead of a histidine (Napier et al, 1997, Napier et al, 2003, Sperling and Heinz 2001).
Alignment of the three Primula clones PaD6D-2 (SEQ ID NO:22), PwD6D (SEQ ID N0:25), and PflD6D (SEQ ID NO:47) revealed extensive similarity between the DNA sequences. PaD6D-2 had approximately 97% identity to PwD6D and approximately 98% identity to PflD6D. PwD6D had approximately 98% identity to PflD6D. A 2-step PCR procedure was utilized to remove the intron region from each gene. Briefly, the procedure entails the amplification of the two exons in separate PCRs, followed by a second round of PCR amplification to combine the two exons together. The same set of primers was used for each gene amplification because of the extensive similarity between the three A6 desaturase genes.
Two sets of primers were designed to amplify exonl from the PwD6D insert in pMON83967. The size of the amplified product was 475 bp and corresponded to exon 1 of PwD6D. The two primers are given below.
Pw Fl: 5'- GTCGACATGGCTAACAAATCTCAAAC -3'
Exon 2 was PCR amplified from pMON83967 using the primer sequences shown below. The size of the amplified product was 875 bp.
Pw F2: 5'- GATCCAGTGCGGATGGATAGGTCACGACTCTGGGCATTACCG -3' (SEQIDNO:58)
Pw R2: 5'- CCTGCAGGTCACCCGAGAGT-3' (SEQ ID NO:56)
The amplified exonl and exon2 products were then combined together with the primers Pw Fl and Pw R2 to PCR amplify the complete ORF minus the original intron. The resulting 1350 bp fragment was ligated into the yeast expression vector pYES2.1-TOPO giving pMON67062.
The removal of the intron region from PaD6D-2 in pMON83968 and PflD6D in pMON84810 was done utilizing the same procedure as described above for PwD6D. The sizes of the exons were the same as that of PwD6D. The resulting 1350bp combined exon fragments
were ligated into the yeast expression vector pYES2.1-TOPO giving pMON67063 for PaD6D-2 alid pMON67064 for PflD6D.
Example 9 Yeast Transformation and Expression
Constructs pMON83950 (FIG. 3), pMON67011 (FIG. 2), pMON67026, pMON67062, pMON67064, and pMON67065 were introduced into the uracil auxotrophic Saccharomyces cerevisiae strain INVScl (Invitrogen) using the S. cerevisiae EasyComp Transformation Kit (Invitrogen). Transformants were selected on plates made of SC minimal media minus uracil \ with 2% glucose. Colonies of transformants were used to inoculate 5 ml of SC minimal media minus uracil and 2% glucose and were grown overnight at 30°C. For induction, stationary phase yeast cells were pelleted and re-suspended in SC minimal media minus uracil supplemented with 2% galactose and grown for 1 day at 25°C followed by 3 days at 15°C. When exogenous fatty acids were provide to the cultures, 0.01% (v/v) LA (A9, 12-18:2) and 0.01% ALA (A9, 12, 15-18:3) were added with the emulsifier 0.1% (w/v) Tergitol. The cultures were grown 1 day at 25°C followed by 3 days at 15°C, and subsequently harvested by centrifugation. Cell pellets were washed once with sterile TE buffer pH 7.5, to remove the media, and lyophilized for 24 h. The host strain transformed with the vector containing the LacZ gene was used as a negative control in all studies.
FAMEs were prepared from lyophilized yeast pellets by transmethylation with 0.5 mL 5% (v/v) E^SCM in methanol containing 0.075 mg/mL 2,6-Di-terr-butyl-4-methoxyphenol for 90 min at 90°C. The FAMEs were extracted by addition of 0.9 mL 10% (w/v) NaCl and 0.3 mL of heptane. The heptane layer containing FAMEs was removed and used directly for GC as described in Example 2.
The results shown in Table 7 demonstrate that P. juliae clones pMON67011 and pMON83950, P. alpicola clones pMON67026 and pMON67063, P. waltonii clone pMON67062, P. florindae clone pMON67064, and P. farinosa clone pMON67065 exhibit A6 desaturase activity in a yeast expression system. The data in Table 8 demonstrate that each Primula clone encodes a protein with selectivity for either n-3 or n-6 substrate fatty acids.
Table 7: A6 desaturase activity of Primula clones in a yeast expression system.
*Reported as a % of the total for all analytes included in the GC-FID chromatogram, including (16:0,16:1,18:0,20:0,20:1,20:2,22:0,22:1,22:2)
Table 8: Comparison of n-3:n-6 substrate selectivities for Primula A6 desaturases.
The percentage conversion to GLA was calculated by dividing the value for GLA (Table 1) by |the sum of the values for LA and GLA (Table 1). The same calculation was made for SDA using the sum of ALA and SDA (Table 1).
**The n-3:n-6 ratio was calculated by dividing the % conv. SDA by % conv. GLA.
Example 10 Arabidopsis Cloning, Transformation and Expression
After confirming activity of the Primula A6 desaturases in yeast, the genes were then cloned into pMON73273 (a binary vector containing the constitutive 35S CaMV promoter) for expression in Arabidopsis thaliana to determine activity in planta. PwD6D and PaD6D-2 were cloned with introns intact. The following vectors were transformed into Arabidopsis: pMON83961 (MaD6D) (FIG. 8), pMON83962 (PJD6D-1) (FIG. 9), pMQN83963 (PaD6D-2) (FIG. 10), pMON84964 (PJD6D-2) (FIG. 11), pMON84965 (PaD6D-l) (FIG. 12), and pMON83966 (PwD6D) (FIG. 13).
Arabidopsis plants were grown by sowing seeds onto 4 inch pots containing reverse osmosis water (ROW) saturated MetroMix 200 (The Scotts Company, Columbus, OH). The plants were vernalized by placing the pots in a covered flat, in a growth chamber at 4-7°C, 8
hours light/day for 4-7 days. The flats were transferred to a growth chamber at 22°C, 55% relative humidity, and 16 hours light/day at an average intensity of 160-200 jjEinstein/s/m2. The cover was lifted and slid back 1 inch after germination, and then was removed when the true leaves had formed. The plants were bottom watered, as needed, with ROW until 2-3 weeks after germination. Plants were then bottom watered, as needed, with Plantex 15-15-18 solution (Plantex Corporation Ottawa, Canada) at 50 ppm N2. Pots were thinned so that 1 plant remained per pot at 2-3 weeks after germination. Once the plants began to bolt, the primary inflorescence was trimmed to encourage the growth of axillary bolts.
Transgenic Arabidopsis thaliana plants were obtained as described by Bent et al., Science, 265:1856-1860, 1994 or Bechtold et al, C.R.Acad.Sci, Life Sciences, 316:1194-1199, 1993. Cultures of Agrobacterium tumefaciens strain ABI containing one of the transformation vectors pMON69804, pMON69812, or pMON69815 were grown overnight in LB (10% bacto-tryptone, 5% yeast extract, and 10% NaCl with kanamycin (75 mg/L), chloramphenicol (25 mg/L), and spectinomycin (100 mg/L)). The bacterial culture was centrifuged and resuspended in 5% sucrose + .05% Silwet-77 solution. The aerial portions of whole Arabidopsis thaliana Columbia plants (at about 5-7 weeks of age) were immersed in the resulting solution for 2-3 seconds. The excess solution was removed by blotting the plants on paper towels. The dipped
plants were placed on their side in a covered flat and transferred to a growth chamber at 19°C. ?ffter 16 to 24 hours the dome was removed and the plants were set upright. When plants had reached maturity, water was withheld for 2-7 days prior to seed harvest. Harvested seed was passed through a stainless steel mesh screen (40 holes/inch) to remove debris.
The harvested seeds described above were.sown onto flats containing ROW saturated MetroMix 200 (The Scotts Company). The plants were vernalized and germinated as described above. After true leaves had emerged, the seedlings were sprayed with Roundup to select for
\ The fatty acid composition of mature seed (R2) was determined by GC analysis of
methyl ester derived lipids as done above for soybean seed. Values for pooled seed from each transgenic event are shown in Table 9. The n-3 or n-6 substrate selectivities that were observed in the yeast assays were confirmed in planta.
Table 9 Fatty Acid Analysis of Arabidopsis Seed
Canola Transformation and Expression
The vectors pMON83961, pMON83962, pMON83963, and pMON83964 described in Example 9 were also transformed into Canola according to the methods in Example 4. pMON70500 was included as a negative control. The fatty acid composition of leaves was determined by GC analysis of methyl ester derived lipids. The data is shown in Table 10. Again the substrate selectivities observed in yeast and Arabidopsis were confirmed.
Table 10 Fatty Acid Analysis of Canola Leaf Tissue
All of the compositions and methods disclosed and claimed herein can be made and executed without undue experimentation in light of the present disclosure. While the compositions and methods of this invention have been described in terms of preferred embodiments, it will be apparent to those of skill in the art that variations may be applied to the compositions and methods and in the steps or in the sequence of steps of the method described herein without departing from the concept, spirit and scope of the invention. More specifically, it will be apparent that certain agents which are both chemically and physiologically related may be substituted for the agents described herein while the same or similar results would be achieved. All such similar substitutes and modifications apparent to those skilled in the art are deemed to be within the spirit, scope and concept of the invention as defined by the appended claims.
The references listed below are incorporated herein by reference to the extent that they supplement, explain, provide a background for, or teach methodology, techniques, and/or compositions employed herein.
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1. A recombinant polynucleotide encoding a polypeptide having desaturase activity that desaturates a fatty acid molecule at carbon 6, wherein the polynucleotide is selected from the group consisting of:
(a) a polynucleotide encoding the polypeptide sequence of SEQ ID NO:4, SEQ ID NO:5;
(b) a polynucleotide comprising the nucleic acid sequence of SEQ ID NO:3;
(c) a polynucleotide hybridizing to SEQ ID NO:3, or a complement thereof, under conditions of 5X SSC, 50% formamide and 42°C; and
(d) a polynucleotide encoding a polypeptide with at least 92% sequence identity to a polypeptide sequence of SEQ ID NO:4, SEQ ID NO:5.
2. The recombinant polynucleotide as claimed in claim 1, wherein the polynucleotide encodes the polypeptide of SEQ ID NO:4, SEQ ID NO:5.
3..The recombinant polynucleotide as claimed in claim 1, further defined as operably linked to a heterologous promoter.
4.A recombinant polypeptide comprising the polypeptide sequence of SEQ ID NO:4, SEQ ID NO:5, or a fragment thereof having desaturase activity that desaturates a fatty acid molecule at carbon 6.
5. A recombinant vector comprising the isolated polynucleotide sequence as claimed in claim 1.
6.The recombinant vector as claimed in claim 5, optionally comprising at least one additional sequence from the group consisting of:
(a) regulatory sequences operatively linked to the polynucleotide;
(b) selection markers operatively linked to the polynucleotide;
(c) marker sequences operatively linked to the polynucleotide;(d) a purification moiety operatively linked to the polynucleotide; and
(e) a targeting sequence operatively linked to the polynucleotide.
7. The recombinant vector as claimed in claim 5, optionally defined as comprising a promoter operably linked to said isolated polynucleotide.
8. The recombinant vector as claimed in claim 7, wherein the promoter is a developmentally-regulated, organelle-specific, tissue-specific, constitutive or cell-specific promoter.
9. The recombinant vector as claimed in claim 7, wherein said promoter is selected from the group consisting of 35S CaMV, 348 FMV, Napin, 78 alpha, 7S alpha', Glob, and Lee.
10.The recombinant vector as claimed in claim 5, defined as an isolated expression cassette.
11. A method of producing a transgenic plant comprising seed oil containing altered levels of omega-3 acids comprising introducing the recombinant vector as claimed in claim 5 into an oil-producing plant.
12. The method as claimed in claim 11, wherein the plant is a plant selected from the group consisting of Arabidopsis thaliana, oilseed Brassica, rapeseed, sunflower, safflower, canola, corn, soybean, cotton, flax, jojoba, Chinese tallow tree, tobacco, cocoa, peanut, fruit plants, citrus plants, and plants producing nuts and berries.
13. The method as claimed in claim 11, wherein the plant is further defined as transformed with a nucleic acid sequence encoding a polypeptide having desaturase activity that desaturates a fatty acid molecule at carbon 15.
14. The method as claimed in claim 13, wherein stearidonic acid is increased.
15. The method as claimed in claim 11, further defined as comprising introducing the recombinant vector of claim 5 into a plurality of oil-producing plants and screening said plants or progeny thereof having inherited the recombinant vector for a plant having a desired profile of omega-3 fatty acids.
16. The method as claimed in claim 11, wherein the plant is soybean and the seed oil has a stearidonic acid content of from 5% to 50% and a gamma-linoleic acid content of less than 10%.
17. The method as claimed in claim 11, wherein
(i) the seed oil comprises less than 10% combined alpha-linoleic acid, linoleic acid and gamma-linoleic acid; or
(ii) has a stearidonic acid content from 15% to 35%; or
(iii) has a stearidonic acid content from 22% to 30%; or
(iv) has less than 5% gamma-linoleic acid; or
(v) has a stearidonic acid content from 15% to 35% and a gamma-linoleic acid content of less than 5%; or
(vi) has a ratio of omega-3 to omega-6 fatty acids from 0.35: 1 to 3.5: 1; or
(vii) has a ratio of omega-3 to omega-6 fatty acids from 1: 1 to 3.5: 1.
|Indian Patent Application Number||631/DELNP/2006|
|PG Journal Number||12/2011|
|Date of Filing||07-Feb-2006|
|Name of Patentee||MONSANTO TECHNOLOGY, LLC.|
|Applicant Address||800 NORTH LINDBERGH BLVD., ST, LOUIS, MO 63167,USA.|
|PCT International Classification Number||C12N 15/53|
|PCT International Application Number||PCT/US2004/026944|
|PCT International Filing date||2004-08-20|