Title of Invention	A METHOD FOR PRODUCING A TRANSGENIC COTTON PLANT
Abstract	A method is disclosed for producing a transgenic cotton plant by Agrobacterium-mediated transformation of petiole tissue. The method comprises the steps of (a) obtaining cotton petiole explants, (b) exposing the petiole explants to a culture of Agrobacterium tumefaciens that harbors a vector comprising an exogenous gene and a selectable marker, the Agrobacterium being capable of effecting the stable transfer of the exogenous gene and selection agent resistance gene to the genome of the cells of the petiole explant, (c) culturing the petiole explants to induce callus formation, (d) selecting transformed callus that expresses the exogenous gene, (e) culturing the selected callus in suspension culture to induce formation of embryoids, (f) regenerating me embryoids into whole transgenic cotton plants.

Title of Invention

A METHOD FOR PRODUCING A TRANSGENIC COTTON PLANT

Abstract

A method is disclosed for producing a transgenic cotton plant by Agrobacterium-mediated transformation of petiole tissue. The method comprises the steps of (a) obtaining cotton petiole explants, (b) exposing the petiole explants to a culture of Agrobacterium tumefaciens that harbors a vector comprising an exogenous gene and a selectable marker, the Agrobacterium being capable of effecting the stable transfer of the exogenous gene and selection agent resistance gene to the genome of the cells of the petiole explant, (c) culturing the petiole explants to induce callus formation, (d) selecting transformed callus that expresses the exogenous gene, (e) culturing the selected callus in suspension culture to induce formation of embryoids, (f) regenerating me embryoids into whole transgenic cotton plants.

Full Text	A METHOD FOR PRODUCING A TRANSGENIC COTTON PLANT High Efficiency Agrebacterium-mediated Transformation of cotton Using Petiole Explants Technical Field The present invention relates to the general field of genetic engineering of plants, in particular to the introduction of exogenous genetic material into cotton by Agrobacterium transformation of cotton petiole explants followed by somatic embryo regeneration. packground Cotton is one of the most valuable and widely grown cash crops internationally. Its annual production worldwide is over 100 million bales valued at US$45 billion. Asia is the biggest cotton production area, with four out of five world top cotton producers located in this region. Cotton is not only the main supporter for the textile industry, but it also provides a huge and profitable market for manufacturers of chemicals for weed, disease and pest control. There are diverse opportunities for cotton molecular improvement, including improvement of yield and fiber quality and creation of new varieties that are resistant to herbicides, insects, nematodes and diseases (Steward, 1991). Tissue Culture of Cotton: In 1935, Skovsted reported the Hirst embryo culture of cotton. Beasley (1971) reported callus formation in cotton as an outgrowth from the micropylar end or fertilized ovules on Murashige & Skoog (MS) medium. Somatic embryogenesis was achieved from a suspension culture of G. klotzschianum (Price & Smith, 1979) . In 1983, Davidonis & Hamilton first succeeded in efficient and repeatable regeneration of cotton {G. hirsutum L.) plants from callus after two-year cultivation. Cotton plants were since regenerated through somatic embryogenesis from different explants (Zhang & Feng, 1992; Zhang, 1994) including cotyledon (Davidonis et al., 1987; Davidonis & Hamilton, 1983; Finer, 1988; Firoozabady et al., 1987), hypocotyl (Cousins et al., 1991; Rangan & Zavala, 1984; Rangan & Rajasekaran, 1996; Trolinder & Goodin, 1988; Umbeck et al., 1987, 1989), stem (Altman et al., 1990; Bajaj et al., 1989; Chen, et al. 1987; Finer & Smith, 1984), shoot apex (Bajaj et al., 1985; Gould et al., 1991; Turaev & Shamina, 1986), immature embryo (Beasley, 1971; Stewart & Hsu, 1977, 1978), petiole (Finer & Smith, 1984; Gawel et al., 1986; Gawel & Robacker, 1990), leaf (Finer & Smith, 1984; Gawel & Robacker, 1986), root (Chen & Xia, 1991; Kuo et al., 1989), callus (Finer & McMullen, 1990; Trolinder et al., 1991) ana protoplast (Chen et al., 1989). Transformation of cotton: Agrobacterium-mediated cotton transformation was first reported a decade ago with hypocotyl and cotyledon as explants (Firoozababy et al., 1987; Umbeck et al., 1987). Several useful genes have been introduced into cotton via Agrobacterium-mediated transformation, including insect and herbicide resistance genes (Perlak et al., 1990; Trolinder et al., 1991; Chen et al., 1994). Explants (such as hypocotyl, cotyledon, callus generated from hypocotyl and cotyledon/ as well as immature embryos) have bean used for Agrobacterium-mediated transformation and particle bombardment (de Fraxnond et al., 1983; Finer & McMullen, 1990; Firoozabady et al., 1987/ Perlak et al., 1990; Rangan & Rajasekaran, 1996; Rajasekaran et al., 1996; Trolinder et al., 1991; Umbeck et al., 1987, 1989, 1992). In addition, meristexnatic tissue of excised embryonic axes has also been used for cotton transformation by particle bombardment (Chlan et al., 1995; John, 1996; John & Keller, 1996; McCabe & Martinell, 1993). Zhou et al. (1983) transformed cotton by injecting DNA into the axile placenta one day after self-pollination. However, the transformation rates were generally low, ranging from 20 to 30% when hypocotyl were used as explant (Firoozababy et al., 1987; Cousins et al., 1991; Rajasekaran et al., 1996). A significantly higher transformation efficiency, up to 80%, was reported when cotyledon was used as explant and the ocs gene encoding octopine synthetase used as the reporter gene (Firoozababy et al., 1987). However, the validity of octopine as a marker for transformation is questionable because octopine has been found in several plant species certainly not transformed by infection with A. tumelaciens (Wendt-Gallitelli and Dobrigkeit, 1973) . A more recent report indicated that the transformation efficiency of cotyledon was about 20 to 30% (Cousins et al., 1991). The transformation efficiency was even lower when particle bombardment method was used (Keller et al., 1997). A difference in the type of explants used for transformation could have a significant effect on the efficiency of transformation and regeneration. It has been reported, for example, that for reducing false positive transformants, cotyledon was a better explant than hypocotyledon (Firoozabady et al., 1987). Cotton transformation also is highly dependent on genotype (Trolinder, 1985a, 1986; Trolinder & Goodin, 1987, 1988a, 1988b; Trolinder & Chen, 1989). Apart from a few cultivars which are regenerable and transformable, such as Gossypium hirsutum cv. Coker 312 and G. hirsutum Jin 7, most other important elite commercial cultivars, such as G. hirsutum cv. D&P 5415 and G. hirsutum cv. Zhongmian 12, are not regeneratable and transformable by these methods. The absence of a high-efficiency plant regeneration method has been regarded as a major obstacle to the application of Agrabacterium-mediated transformation to cotton (Gawel et al., 1986; Firoozabady et al., 1987). Summary of the Invention To overcome the problems associated with previously reported methods, an efficient transformation procedure using petiole as an explant has been developed, along with a set of correspondingly improved media. This method provides several advantages in comparison to the hypocotyl and cotyledon methods: (1) explants are easy to obtain; (2) transformation efficiency is higher; (3) Agrobacterium contamination is very rare; (4) efficiency in regeneration is higher; and (5) the time from transformation to regeneration of plantlets is reduced. Two cotton varieties, i.e. Coker 312 and Si-Mian 3, have been successfully transformed with this method, and more than 30 independent transgenic lines from Coker 312 showing strong activity of the marker transgene have been obtained. This method is applicable to other cotton varicties such as Jin 7 and Ji 713 from China, Siokra 1-3 from Australia, T25, Coker 201 and Coker 310 from the U.S.A. Brief Description of the Figure Figure 1 shows the plasmid pBI121GFP, containing GFP as the reporter gene and the NPT II (neomycin phosphotransferase) gene as a selectable marker, used for Agrobacterium-mediated transformation of cotton petiole according to the methods of the present invention. Detailed Description An efficient method is disclosed for genetic transformation of cotton plants, including elite lines, using cotton peticl- as an explant. By using petiole explants plus a lot of improved media, transformation efficiency is significantly enhanced and the time required from transformation to regeneration is shortened in comparison to previously reported methods. By using the methods of the present invention, the whole process from Agrobacterlum transformation to the regeneration of transgenic plantlets can take about 6-7 months. The reported hypocotyl and cotyledon methods usually required 7-9 months or longer to complete the same process (Cousins et al., 1991; Chen et al., unreported observation) . Another two months were required for growing the small plantlets to a suitable size for potting in soil. Techniques for introducing exogenous genes into Agrobacterium such that they will be transferred stably to a plant or plant tissue exposed to the Agrobacterium are well-known in the art and do not form part of the present invention. It is advantageous to use a so- called "disarmed" strain of Agrobacterium or Ti plasmid, that is, a strain or plasroid wherein the genes responsible for the formation of the tumor characteristic of the crown gall disease caused by wild-type Agrobacterium are removed or deactivated. Numerous examples of disarmed Agrobacterium strains are found in the literature (e.g., pAL4404, pEHAlOl and pEH 105 (Walkerpeach & Veltern, 1994)). It is further advantageous to use a so-called binary vector system, such as that described in Schilperoort et al., 1990, 1995. A binary vector system allows for manipulation in E. coli of the plasmid carrying the exogenous gene to be introduced into the plant, making the process of vector construction much easier to carry out. Similarly, vector construction, including the construction of chimeric genes comprising tne exogenous gene that one desires to introduce into the plant, can be carried out using techniques well-known in the art and does not form part of the present invention. Chimeric genes should comprise promoters that have activity in the host in which expression is desired. For example, it is advantageous to have a series of selectable markers for selection of transformed cells at various stages in the transformation process. A selectable marker (for example a gene conferring resistance to an antibiotic such as kanamycin, cefotaxime or streptomycin) linked to a promoter active in bacteria would permit selection of bacteria containing the marker (i.e., transformants). Another selectable marker linked to a plant-active promoter, such as the CaMV 35S promoter or a T-DNA promoter such as the NPT II NOS promoter, would allow selection of transformed plant cells. The exogenous gene that is desired to be introduced into the plant cell should comprise a plant-active promoter in functional relation to the coding sequence, so that the promoter drives expression of the gene in the transformed plant. Again, plant-active promoters, such as the CaMV 35S, the NPT II NOS promoter or any of a number of tissue- specific promoters, are well-known in the art and selection of an appropriate promoter is well within the ordinary skill in the art. The present method can be used to produce transgenic plants expressing any number of exogenous genes, and is not limited by the choice of such a gene. The selection of the desired exogenous geno depends on the goal of the researcher, and numerous examples of desirable genes that could be used with the present invention are known in the art e.g., the family of Bacillus thuringiensis toxin genes, herbicide resistance genes such as shikimate synthase genes that confer glyphosate resistance, U.S. Patent No. 5,188,642, or a 2,4-D monooxygenase gene that confers resistance to 2,4-dichlorophenoxyacetic acid (2,4-D), Bayley et al., Theoretical and Applied Genetics, vol. 82, pp. 645-4 9, male sterility genes such as the antisense genes of U.S. Patent No. 5,741,684 (Fabijanski, et al.), or even the elaborate crop protection systems described in U.S. Patent No. 5,723,765 (Oliver et al.)). Cotton regeneration is considered in the art to be heavily variety-dependant. The Coker series of cotton varieties have been shown to be relatively easy to transform. However, DP 5412, Zhongmain 12 and many other varieties still have difficulties associated with regeneration. The situation is the same for G. barbadense and other diploid species. While somatic embryogenesis and regeneration of whole plants is a highly genotype-dependent process in cotton, successful transformation and regeneration of two distinct cotton varieties, i.e. Coker 312 from U.S.A. and Si-Mian 3 from China, has been demonstrated using the methods of the present invention. It this therefor believed that the present invention has wide applicability to transformation of a variety of cotton lines. Transgene integration in the genome of cotton produced by the methods of the present invention was confirmed using standard Southern hybridization techniques, as can identification of the copy number of the inserted transgene in each transgenic line (see Example 6, below}. The F1 generation of transgenic cotton can be tested for the presence of Lhe transgene, and inheritance pattern of che transgene in tne Fl generation can be analyzed to confirm stability and inheritability. As compared with other reported protocols, the cotton transformation system of the present invention has higher transformation efficiency and survival rate. This is attributable to several factors. In the present invention, petiole was used as an explant for transformation. Different types of cotton explants can have significant effects on the efficiencies of plant transformation and regeneration (Firoozabady et al., 1987). Induction of somatic embryogenesis from petiole was reported previously. But regeneration was either unsuccessful or very poor (Finer and Smith, 1984; Gawel et al., 1986). With the present invention, the efficiency of regeneration was significantly improved by using the improved media discussed below, in a preferred embodiment, calli of high quality were obtained when tender petioles rich in parenchyma cell in primary vascular bundle tissue were cultured in the MMSI medum (described below) with low concentrations of_2,4-D_and_Kinetin. With the present invention, the Lime for embryo induction in suspension culture can be shortened to 10 - 14 days, from a previously reported 3 weeks (Cousins et al., 1991). It was found that a shortened period of suspension culture treatment is important for high frequency induction of embryogenesis. It is also important for reducing production of abnormal embryos, since a high percentage of vitreous embryos that are poor in regeneration are produced when cotton calli are maintained in suspension culture for too long (Chen et al, unpublished observation). Fr- maximum cell growth at different stages except at the young plant growing stage, glucose was used as the sole carbon source. The amount of glucose in the media can be from about 10 to about 50 g/1, preferably about 30 g/1. At the young ? '---' growing stage, glucose and sucrose at about 10 g/1 respectively as carbon sources are preferable for promotion of healthy plantlets growth. For growth of callus, embryogenesis and callus proliferation, pH range can be from 5.8 to 7.5, preferably pH 6.2 - 7.0, most preferably at pH 6.5. A medium of pH 7.0 is preferable lor healthy root growth of plantlets. For effective callus initiation and induction of the potency of embryogenesis, low concentrations of 2,4-D and kinetin in the callus induction and selection medium is important. The amount of 2,4-D can be from 0.05 to 0.5 mg/1, preferably about 0.05 mg/1. The amount of kinetin can be from 0.1 mg/1 to about 1.0 mg/1, preferably about 0.1 mg/1. In the callus differentiation stage and exnbryoid germination stage/ best result were obtained when no plant hormone was added to the media. The amino acids asparagine and glutamine are better nitrogen sources than inorganic ammonia nitrogen for specifically supporting embryoids germination and root development. In the embryoid germination medium, the amount of asparagine can be about 200 to about 1000 mg/1, preferably about 500 mg/1. The amount of glutamine can be about 500 to about 2000 mg/1, preferably about 1000 mg/1. With these optimized nitrogen sources, the growth of non-embryogenic calli was inhibited while the germination, growth and root development of embryoids were preferentially promoted. At different stages of cotton transformation except co-culture with Agrobacterium, plant tissue and callus are preferably maintained at 28°C but can be varied from 25-35°C. For effective transformation, temperature in co-culture stage should not be higher than 28°C. A light condition of 16 hrs. light (60-90, mEm-2S-1) and 8 hrs. dark per day is preferable for all stages of cotton transformation and regeneration. Unlike previously reported transformation and regeneration protocols (Umbeck et al., 1987; Firoozabady et al., 1987, Cousins et al.), the media used in the present invention are optimized in several respects: (a) glucose is used as a sole carbon source in all culture media except in the medium used to culture young plants previous to planting out in the greenhouse; (b) the media is adjusted to higher pH value (6.5-7.0); (c) lower concentration of 2,4-D (0.05mg/l) and kinetin (0.1 mg/1) is U3ed only at callus initiation stage, no hormone is used at other stages; (d) asparagine and glutamine are used to replace inorganic ammoniac nitrogen in the medium. used for embryoid germination. These modifications are adapted for the physiological requirement of cotton embryoid development and plantlet growth. It has been found that healthy embryoid development and plantlet growth, especially root system. development, are largely attributable to these optimized media. For example, it has been found that asparagine and glutamine were better nitrogen source than inorganic ammonia nitrogen for supporting embryoid germination and root development. In the preferred MMS3 medium (described below) , which contains asparagine and glutamine as the nitrogen source, the growth of non-embryogenic calli was inhibited while the germination, growth and root development of embryoids were preferentially promoted. Because of the healthy root development, the survival rate of potted transgenic cotton plants obtained by the methods of the present invention is almost 100%,. With the reported hypocotyl and cotyledon protocols (Umbeck et al., 1987; Firoozabady et al., 1967), poor root development has been regarded as the main reason accounting for poor survival rate of potted transgenic cotton plants. The following are preferred plant tissue culture media used in the Examples: (1) Seedling growing medium (per liter): ½ MS basal salt mixture (Sigma M5524) 0.9 g MgCl2 -6H2O 2.0 g gellan gum (Phytagel™, Sigma) pH 7.0 (2) Petiole pre-culture medium (per liter): MS basal salt mixture 0.9 g MgCl2-6H2O 2.0 g gellan gum (Phytagel™, Sigma) pH 7.0 (3) Co-culture medium (per liter): MS basal salt mixture 10 mg Thiamine-HCl 1 mg Pyridoxine-HCl 1 mg Nicotinic acid 100 mg Myo-inositol 0.05 mg 2,4-dichlorophenoxyacetic acid (2,4-D) 0.1 mg Kinetin 30 g Glucose 0.9 g MgCl2-6H2O 2.0 g gellan gum (Phytagel™, Sigma) pH 6.5 (4) MMS1 - callus induction and selection medium (per liter): Co-culture medium 50 mg Kanamycin 500 mg Cefotaxime (5) MMS2 - differentiation medium (per litre) : MS basal salt mixture 10 mg Thiamine-HCl 1 mg Pyridoxine-HCl. 1 mg Nicotinic acid 100 mg Myo-inositol 1.9 g KNO3 30 g Glucose 0.9 g MgCl2-6H2O 2.0 g gellan gum (Phytagel™, Sigma) pH 6.5 (5) MMS3 - embryoid germination medium (per litre) : 3.8 g KNO3 440 mg CaCl2-H2O 375 mg MgS04-7H2O 170 mg KH2PO, 1 g Glutamine 500 mg Asparagine 43 mg EDTA ferric-Na salt MS micronutrients (Murashige and Skoog, 1962) 10 mg Thiamine-HCl 1 mg Pyridoxine-HCl 1 mg Nicotinic acid 100 mg Myo-inositol 30 g Glucose 0.9 g MgCl2-6H2O 2.0 g gellan gum (Phytagel™, Sigma) pH 6.5 (7) Young plant growing medium S&H medium Macro and Micro elements (Strewart and Hsu, 1977) 10 mg Thiamine-HCl l mg Pyridoxine-HCl 1 mg Nicotinic acid 100 mg Myo-inositol 10 g Glucose 10 g Sucrose 0.9 g MgCl2-6H2O 2.0 g gellan gum (Phytagel™, Sigma) pH 7.0 The following Examples are intended to illustrate the present invention, and not in any way to limit its scope, which is solely defined by the claims. Example 1 : Agrobacterium strain and plasmids A. tumefaciens strain LBA 4404 (pBI121GFP) was used for transformation of cotton petiole and young stem. The physical map of pBI121GFP is shown in Fig.l, which contains GFP as a reporter gene and NPTII gene (encoding neomycin phosphotransferase) as a selectable marker. The GFP and NPTTT genes are under the control of CaMV 35S promoter and nos promoter respectively. For construction of pBI121GFP, a 720 bp XbaI-SstI fragment of GFP gene from the pGFP2 plasmid (from Dr. N. H. Chua, Rockefeller University, New York) was cloned into the same sites in plasmid vector pBI121 (Clontech) to replace the GUS gene. The pBI12lGFP plasmid was introduced into A. tumefaciens LBA 4404 by electroporation. Example 2: Plant material Upland cotton varieties Coker 312 from the O.S.A, and Si-Mian 3 from Shanxi Cotton Research Institute in China were used in the experiments. Tender petioles were collected from plants 8-12 weeks old grown in a greenhouse with low light conditions. The petioles were surface-sterilized with 70% ethanol for a few seconds, followed by 20% bleach solution (Clorox Co, USA, 1% available chlorine) for 20 min. After rinsing five times in sterilized water, the petioles were pre-cultured in MS medium for 3 days. Example 3: Plant transformation A single colony of A. tumefaciens strain LBA 4404 CpBI121GPP) was inoculated in liquid LB medium with 50 mg/L Rifampicin, 50 mg/L kanamycin and 100 mg/L streptomycin. The bacteria was grown overnight at 28°C in a shaker of 200 rpm. The bacterium cultures were dilute using liquid MS medium to OD600 = 0.3. The petiole and young stem were cut into about 2 cm long segments. The segments were soaked in the diluted bacterium suspension for 5 min, then transferred onto plastic plates (100 x 25 mm) containing a filter paper soaked in 50 ml of co-culture medium. The plates were kept in an incubator of 24oC under continuous light for 4 8 hrs. The co-cultured explants were transferred onto MMS1 medium and incubated at 28°C with 16 hrs light (60-90,mEm-2s-1) and 8 hrs dark per day. After 2-4 weeks calli were initiated at the cut ends of petiole segments. After 4-6 weeks kanamycin resistant calli had appeared, and the number of calli were counted and the expression of GFP gene was examined. Under the fluorescence microscope, the untransformed control callus appeared red in colour, while the transformed callus expressing GFP gene displayed distinct green fluorescence. A total of 113 putative transformed calli were examined for GFP activity, the transformation frequency of GFP gene was 39.8% (Table 1). When petioles from cotton variety Si-Mian 3 were used for transformation, 11 calli were found GFP positive from 26 calli tested, transformation efficiency was 42.3%. Table 1: Transformation frequencies or petioles from cotton Coker 312 and Si-Main 3 i Example 4: Induction of somatic embryogenesis and plant regeneration The calli with vigorous growth and strong expression of GFP were selected and transferred into liquid MMS2 medium for suspension culture tor 2 weeks. Friable cream-colored granular calli were selected and transferred to semi-solid differential medium, MMS2. After about 2 months a large number of embryoids were produced. Cytoplasmic dense embryogenic structures were gradually developed and large embryos were produced on the medium within 1-2 month. A short time of suspension culture treatment was very important, not only for high frequencies of embryogenesis induction, but also for production of embryoids of good quality. Expression of CFP gene was checked again and all were GFP positive. The embryoids and embryogenic calli with strong GFP activity were transferred onto the MMS3 medium. After 1-2 months the plantlets that were about 1-2 cm in height with 1-2 true leaves and good root development were transferred to the Young Plant Growing Medium for about one month. About one month later, young plants with 6-8 leaves and about 10-15 cm in height were potted in soil and move to the glasshouse. All 30 potted transgenic plants survived and were found expressing GFP protein. The total time required to obtain transgenic plantlets using was under 7 months, and plantlets were reading for potting out in the greenhouse in about 2 additional months (see Table 2). Table 2: The time frame from transformation of petiole segments to plant regeneration (Coker 312) Example 5: Detection of GFP Protein Activity The expression of GFP protein activity was Geteeted using a Leica MZ FLIIT Fluorescence stereo microscope with a 480/40 nM excitation filter and a 510 nM barrier filter. Green fluorescence of GFP gene can be easily distinguished in the transformed callus, embryoids, and young plantlets, with the untransformed control appeared red in colour under the fluorescence Stereo microscope. The exceptions were the untransformed roots, which appeared dim green under the fluorescence microscope, probably due to some chromophorous chemicals accumulated in roots. But the roots with GFP activity could still be identified because the green fluorescence produced by GFP protein was brighter and appeared more uniform. Under the blue light produced by the fluorescence stereo microscope, red fluorescence is clearly visible in untraneformed green plant tissues that are enriched with chlorophyll such as leaf and stem. In GFP-positive green plant tissues, yellow fluorescence also was detected because of the overlapping of red and green fluorescence. However, the expression of GFP gene in petal and anther was poorer in comparison to that in other parts of plant. Example 6: Analysis of Transgenic Plants Genomic DNA from putatively transformed lines and non-transformed control plants was purified according to Paterson et all. (1993). After digestion with EcoRI, which cuts inj-between left border of T-DNA and Nos-3' terminator of the chimerical GFP gene (Fig. 1), DNA was separated on a 0.8% TAE agarose gel and transferred to Hybond-N membrane according to manuracturer's instructions. DNA was fixed to the membrane by UV crossing linking before hybridizing to the DIG labeled coding region of the GFP gene. Hybridized probe was detected with anti-DIG-AP conjugate according to manufacturer's instructions (BOEHRINGER MANNHEIM) . The genomic DNA samples from 11 randomly selected transgenic lines and 1 untransformed control plant were analyzed Southern hybridization, using the coding region of GFP gene as the hybridization probe. The data indicate that 7 out of 11 lines have a single copy, 3 lines have 2 copies, and 1 line has 6 copies of T-DNA insertion. The high percentage of transgenic lines with a single copy of T-DNA insertion suggests that this transformation protocol has less risk of gene silencing and undesirable insertion mutants. References Cited Altman, D. W. et al. 1990. Economic Botany 40, 106. Bajaj, Y. P. S. 1985. Theor. Appl. Genet. 70, 363. Beasley, C. A. 1971. In vitro culture of fertilized cotton ovules. Biosci. 21, 906-7. Chen Z.X., Liewellyn D.J., Fan Y.L., Li S.J., Guo S.D., Jiao G.L., and Zhao J.X. 1994. 2,4-D Resistant Transgenic Cotton Plants Produced by Agrobacterium-mediated gene Transfer. Scientia Agriculture Sinica 27(2): 3 1 -37. Chen, Z. X., Li, S. J., Yue, J. X., Jiao, G. L. and Liu S. X. 1989. Plantlet regeneration from protoplasts isolated from an embryogenic suspension culture of cotton (Gossypium hirsutum L.). Acta Botanica Sinica 31, 966-9. Chen, Z. X., Trolinder, N.L. et al., 1987. Some characteristics of somatic embryogenesis and plant regeneration in cotton cell suspension culture. Scientia Agriculture Sinica 20, 6-11. Chlan, C. A., Lin, J., Cary, J. W. and Cleveland, T- E. 1995. A procedure for biolistic transformation and regeneration of transgenic cotton from meristematic tissue. Plant Mol. Biol. Rep. 13, 31-7. Cousins Y.L., Lyon B.R., and Llewellyn D.J. 1991. Transformation of Australian cotton cultivar: prospects for cotton improvement through genetic engineering Aust. J. plant physiol., 18, 481-494. Davidonis, G. H., and Hamilton, R. H. 1983. Plant regeneration from callus tissue of Gossypium hirsutum L. Plant Sci. Lett. 32, 89-93. Davidonis, G. H., Mumma, R, O. and Hamilton, R. H. 1987. Controlled regeneration of cotton plants from tissue culture. US Patent No. 4,672,035. de Framond et al. 1983. Mini-Ti; a new vector strategy for plant genetic engineering. Bio/technology 1, 262-9. Finer, J- J. and McMullen, M. D. 1990. Transformation of cotton (Gossypium hirsutum L.) via particle bombardment. Plant Cell Reports 8, 586-9. Filler, J.J., and Smith R.H. 1984. Initiation of callus and somatic embryos from explants of mature cotton (Gossypium klotzschianum Anderss). Plant Cell Reports 3, 41-43. Finer, J., 1988. Plant regeneration from somatic embryogenic suspension cultures of cotton (Gossypium hirsutum L.) . Plant Cell Rep. 7, 399-402. Firoozababy E., DeBoer D.L., Merlo D.J., Halls E.J., Anderson I.N., Raska K.A., Murray E.E. 1987, Transformation of cotton, Gossypium hirsutum L. by Agrobacterium tumefaciens and regeneration of transgenic plants. Plant Molecular Biology 10, 105 1 16 Gawel N. J., Rao A. P., and Robacker C. 1986. Somatic embryogenesis from leaf and petiole callus cultures of Gossypium hirsutum L. Plant Cell Reports 5, 457-459. Gawel, N. J. and Robacker, C. 1990. Genetic control of somatic embryogenesis in cotton petiole callus cultures. Euphytica 49, 249-53. Gould, J., Banister, S., Hasegawa, 0., Fahima, M. and Smith, R. H. 1991. Regeneration of Gossypium hirsutum and G, barbadense from shoot apex tissues for transformation. Plant Cell Reports 10, 12-6. Hoekema et al. 1983. A binary plant vector strategy based on separation of Vir- and T-Region of the Agrobacterium tumefaciena Ti-plasmid. Nature 303, 179-80. John, M. E. 19.46. Structural characterization of genes corresponding to cotton fiber mRNA, E6: reduced E6 protein in transgenic plants by antisense gene. Plant Mol. Biol.,30, 297-306. John, M. E. and Keller, G. 1996. Metabolic pathway engineering in cotton; Biosynthesis of polyhydroxybutyrate in fiber cells. Proc. Natl. Acad. Sci . USA 93, 12768-73. Keller G., Spatola L., McCabe D., Martinell s., Swain w.x. and John M.E. 1997. Transgenic cotton resistant to herbicide bialaphos. Transgenic Research 6, 385-392. Kuo, C. C. et al., 1989. Proc. Beltwide Cotton Prod. Res. Confs, 638. McCabe, D. E. and Martinell, B. J. 1993. Transformation of elite cotton cultivars via particle bombardment of meristems. Bio/technol. 11, 596-8. Murashige T., and Skoog F. 1962. A revised medium for rapid growth and bioassays with tobacco tissue culture. Physiol. Plant 15, 473-493. Paterson, A.H., Brubaker, C.L., and Wendel J.F., 1993, A rapid method for extraction of cotton (Gossypium spp.) Genomic DNA suitable for RFLP or PCR analysis. Plant Mol. Biol. Rptr. 11, 122-127. Perlak F.J., Deaton R.W., Armstrong T.A., Fuchs R.L., Sims S.R., Greenplate J.T., and Fischhoff D.A. 1990, Insect resistant cotton plants. Bio/Technology 8, 939-943. Price, H. J. and Smith, R. H. 1979. Somatic embryogenesis in suspension cultures of Gossypium klotzschianum Anderss. Planta 145, 305-6. Rangan, F. J. and Zavala, T. Ip. A. 1984. Somatic embryogenesis in tissue culture of Gossypium hirsutum L.). In Vitro 20, 256, Rangan, R. and Rajasekaran, K. 1996. Regeneration of cotton plant in cell suspension culture. OS Patent No. 5,583,036 (continued from US Patent 5,244,802, 1993 and 122,200, 1987). Rajasckaran K., Grula J.W., Hudspeth R.L., Polelis S., Anderson D.M. 1996. Herbicideresistant Acala and Coker cotton transformed with the native gene encoding mutant forms of acetohydroxyacid synthase, Mol. Breeding, 2: 307-319. Schilperoort, R.A., Hoekema, A., Hooykaas, P.J.J. 1990. Process for the incorporation of foreign DNA into the genome of dicotyledmous plants. D.S. Patent No. 4,940,838, Schilperoort, R.A., Hoekema, A., 1995. Process for the incorporation of foreign DNA into, the genome of dicotyledmous plants. U.S. Patent No. 5,4 64,763. Steward J. McD. 1991. Biotechnology of Cotton: Achievements and Perspectives. CAB International. Stewart J. McD., and Hsu C.L. 1977. In ovule embryo culture and seedling development of cotton (Gossypium hirsutum L.). Planta 137, 113-117. Stewart, J. McD. and Hsu, C. L. 1978. Hybridization of deploid and tetraploid cottons through in-ovulo embryo culture. J. Heridity 69, 404-8. Trolinder, N. L. 1985a. Somatic embryogenesis and plant regeneration in cotton (Gossypium hirsutum L.).. A Dissertation in Biology (Dec, 1985). Trolinder, N. L., Chen, Z.X., 1989. Genotype specificity of the somatic embryogenesis response in cotton. Plant Cell Reports 8, 133-6. Trolinder, N. L. and Goodin, J. E. 1987. Somatic embryogenesis and plant regeneration in cotton (Gossypium hirsutum L.). Plant Cell Reports 6, 231-4. Trolinder, N. L. and Goodin, J. E. 1988a. Somatic embryogenesis and regeneration in cotton. I. Effects of source of explant and hormone regime. Plant Cell Tissue Organ Culture 12, 31-42. Trolinder, N. L. and Goodin, J. E. 1988b. Somatic embryogenessis and regeneration in cotton. IT. Requirements for embryo development and plant regeneration. Plant Cell Tissue Organ Culture 12, 43-53. Trolinder N.L., Quisenberry J., Bayley C., Ray C, and Ow D. 1991. 2,4-D-res.i stant transgenic cotton. Proceedings, Beltwide Cotton Conferences. National Cotton Council, Memphis, Tennessee, P840. Turaev, A. M. and Shamina, Z. B. 1986. Soniet Plant Physiol. 33, 439. Umbeck P. 1992. Genetic engineering of cotton plants and lines. United States Patent: 5,159,135. Umbeck, P. F, Johnson, G., Barton, K. and Swain, W. 1987. Genetically transformed cotton (Gossypium hirsutum L.) plants. Bio/technol. 5, 263-6. Umbeck P., Johnson P., Barton K., and Swain w.. 1987. Genetically transformed cotton (Gossypium hirsutum L.) plants. Bio/Technology 5, 263-266. Walkerpeach, C.R. and Veltern, J. 1994. Agrobacterium- mediated gene transfer to plant cells: cointegrate and binary vector systems. Plant Mol. Biol. Mannuel Bl, 1-19. Wendt-Gallitelli M.F., and Dobrigkeit I. 1973. Investigations implying the invalidity of octopine as a marker for transformation by Agrobacterium tumefaciens. Zeitschrift fur Naturforschung - Section C- Biosciences 28, 768-771. Zhang, H.-B. 1994. The tissue culture of cotton (II). Plant Physiol. Commun. 30, 386-91. Zhang, H.-B, and Feng, R. 1992. The tissue culture of cotton (I). Plant Physiol- Commun. 30, 386-91. Zhou, G.-Y., Weng, J., Zeng, Y.-S., Huang, J.-G., Qian, S.-Y. and Liu, G.-L. 1983. Introduction of exogenous DNA into cotton embryos. Methods in Enzymology 101,433-81. We claim: 1. A method for producing a transgenic cotton plant comprising the steps of: (a) obtaining cotton petiole explants in the manner such as herein described; (b) exposing the petiole explants to a culture of Agrobacterium tumefaciens such as herein described, that harbors a vector comprising an exogenous gene such as herein described, and a selectable marker, such as herein described, the Agrobacterium being capable of effecting the stable transfer of the exogenous gene and selection agent resistance gene to the genome of the cells of the petiole explant, (c) culturing the petiole explants to induce callus formation, (d) selecting transformed callus that expresses the exogenous gene, (e) culturing the selected callus in suspension culture to induce formation of embryoids, (f) regenerating the embryoids into whole transgenic cotton plants. 2. The method as claimed in claim 1 wherein the petiole explants are pre-cultured for a period of time prior to exposure to the culture of Agrobacterium tumeraciens. 3.The method as claimed in claims 1 wherein the culture media used in steps (b)-(e) have glucose as the sole carbon source. 4. The method as claimed in claim 3 wherein the glucose is in an amount of about 10 g/1 to about 50 g/1. 5.The method as claimed in claim 4 wherein the glucose is in an amount of about 30 g/1. 6.The method as claimed in claim 1 wherein the culture media used in steps (b) and (d)-(f) do not contain hormones. 7.The method as claimed in claim 1 wherein embyroid germination is carried out in a medium having a source of nitrogen selected from the group consisting of asparagine, glutamine or both asparagine and glutamine. 8.The method as claimed in claim 7 wherein the source of nitrogen is in an amount of about 700 mg/1 to about 5 g/1. 9.The method as claimed in claim. 8 wherein the source of nitrogen is in an amount of about 3.6 g/1. 10.The method as claimed in claim 7 wherein the source of nitrogen is both asparagine and glutamine, and the asparagine is in an amount of about 200 mg/1 to about 1 g/l and the glutamine is in an amount of about 500 mg/1 to about 2 g/1. 11. The method as claimed in claim 10 wherein the asparagine is in an amount of about 500 mg/1 and the glutamine is in an amount of about 1 g/1. 12 The method as claimed in claim 1 wherein the suspension culture of step (e) has a duration of less than about 20 days. 13. The method as claimed in claim 12 wherein the suspension culture of step (e) has a duration of about 10 days to about 20 days. 14. The method as claimed in claim 13 whorein the suspension culture of step (e) has a duration of about 14 days. 15. The method as claimed in claim 1 wherein step (c) is carried out in the presence of low concentration of one or more hormones. 16. The method as claimed in claim 15 wherein the concentration of any on 0 to about 1 mg/1. 17. The method as claimed in 15 werein step (c) is carried out in the presence of 2,4-dichlorophenoxacetic acid in a ranging from 0 to about 0.5 mg/1 and kinetin in concentration ranging from 0 to about 1 mg/1. 18. The method as claimed in claim 17 wherein the 2, 4-dichloro- phenoxylacetic acid is in a concentration of about 0.05 mg/1 and the kinctin is in a concentration of about 0.1 mg/1. A method is disclosed for producing a transgenic cotton plant by Agrobacterium-mediated transformation of petiole tissue. The method comprises the steps of (a) obtaining cotton petiole explants, (b) exposing the petiole explants to a culture of Agrobacterium tumefaciens that harbors a vector comprising an exogenous gene and a selectable marker, the Agrobacterium being capable of effecting the stable transfer of the exogenous gene and selection agent resistance gene to the genome of the cells of the petiole explant, (c) culturing the petiole explants to induce callus formation, (d) selecting transformed callus that expresses the exogenous gene, (e) culturing the selected callus in suspension culture to induce formation of embryoids, (f) regenerating me embryoids into whole transgenic cotton plants.

Full Text

A METHOD FOR PRODUCING A TRANSGENIC COTTON PLANT
High Efficiency Agrebacterium-mediated
Transformation of cotton
Using Petiole Explants
Technical Field
The present invention relates to the general field
of genetic engineering of plants, in particular to the
introduction of exogenous genetic material into cotton
by Agrobacterium transformation of cotton petiole
explants followed by somatic embryo regeneration.
packground
Cotton is one of the most valuable and widely
grown cash crops internationally. Its annual
production worldwide is over 100 million bales valued
at US$45 billion. Asia is the biggest cotton
production area, with four out of five world top cotton
producers located in this region. Cotton is not only
the main supporter for the textile industry, but it
also provides a huge and profitable market for
manufacturers of chemicals for weed, disease and pest
control. There are diverse opportunities for cotton
molecular improvement, including improvement of yield
and fiber quality and creation of new varieties that
are resistant to herbicides, insects, nematodes and
diseases (Steward, 1991).
Tissue Culture of Cotton: In 1935, Skovsted
reported the Hirst embryo culture of cotton. Beasley
(1971) reported callus formation in cotton as an
outgrowth from the micropylar end or fertilized ovules
on Murashige & Skoog (MS) medium. Somatic
embryogenesis was achieved from a suspension culture of
G. klotzschianum (Price & Smith, 1979) . In 1983,
Davidonis & Hamilton first succeeded in efficient and
repeatable regeneration of cotton {G. hirsutum L.)
plants from callus after two-year cultivation. Cotton
plants were since regenerated through somatic
embryogenesis from different explants (Zhang & Feng,
1992; Zhang, 1994) including cotyledon (Davidonis et
al., 1987; Davidonis & Hamilton, 1983; Finer, 1988;
Firoozabady et al., 1987), hypocotyl (Cousins et al.,
1991; Rangan & Zavala, 1984; Rangan & Rajasekaran,
1996; Trolinder & Goodin, 1988; Umbeck et al., 1987,
1989), stem (Altman et al., 1990; Bajaj et al., 1989;
Chen, et al. 1987; Finer & Smith, 1984), shoot apex
(Bajaj et al., 1985; Gould et al., 1991; Turaev &
Shamina, 1986), immature embryo (Beasley, 1971; Stewart
& Hsu, 1977, 1978), petiole (Finer & Smith, 1984; Gawel
et al., 1986; Gawel & Robacker, 1990), leaf (Finer &
Smith, 1984; Gawel & Robacker, 1986), root (Chen & Xia,
1991; Kuo et al., 1989), callus (Finer & McMullen,
1990; Trolinder et al., 1991) ana protoplast (Chen et
al., 1989).
Transformation of cotton: Agrobacterium-mediated
cotton transformation was first reported a decade ago
with hypocotyl and cotyledon as explants (Firoozababy
et al., 1987; Umbeck et al., 1987). Several useful
genes have been introduced into cotton via
Agrobacterium-mediated transformation, including insect
and herbicide resistance genes (Perlak et al., 1990;
Trolinder et al., 1991; Chen et al., 1994). Explants
(such as hypocotyl, cotyledon, callus generated from
hypocotyl and cotyledon/ as well as immature embryos)
have bean used for Agrobacterium-mediated
transformation and particle bombardment (de Fraxnond et
al., 1983; Finer & McMullen, 1990; Firoozabady et al.,
1987/ Perlak et al., 1990; Rangan & Rajasekaran, 1996;
Rajasekaran et al., 1996; Trolinder et al., 1991;
Umbeck et al., 1987, 1989, 1992). In addition,
meristexnatic tissue of excised embryonic axes has also
been used for cotton transformation by particle
bombardment (Chlan et al., 1995; John, 1996; John &
Keller, 1996; McCabe & Martinell, 1993). Zhou et al.
(1983) transformed cotton by injecting DNA into the
axile placenta one day after self-pollination.
However, the transformation rates were generally
low, ranging from 20 to 30% when hypocotyl were used as
explant (Firoozababy et al., 1987; Cousins et al.,
1991; Rajasekaran et al., 1996). A significantly
higher transformation efficiency, up to 80%, was
reported when cotyledon was used as explant and the ocs
gene encoding octopine synthetase used as the reporter
gene (Firoozababy et al., 1987). However, the validity
of octopine as a marker for transformation is
questionable because octopine has been found in several
plant species certainly not transformed by infection
with A. tumelaciens (Wendt-Gallitelli and Dobrigkeit,
1973) . A more recent report indicated that the
transformation efficiency of cotyledon was about 20 to
30% (Cousins et al., 1991). The transformation
efficiency was even lower when particle bombardment
method was used (Keller et al., 1997). A difference in
the type of explants used for transformation could have
a significant effect on the efficiency of
transformation and regeneration. It has been reported,
for example, that for reducing false positive
transformants, cotyledon was a better explant than
hypocotyledon (Firoozabady et al., 1987).
Cotton transformation also is highly dependent on
genotype (Trolinder, 1985a, 1986; Trolinder & Goodin,
1987, 1988a, 1988b; Trolinder & Chen, 1989). Apart
from a few cultivars which are regenerable and
transformable, such as Gossypium hirsutum cv. Coker 312
and G. hirsutum Jin 7, most other important elite
commercial cultivars, such as G. hirsutum cv. D&P 5415
and G. hirsutum cv. Zhongmian 12, are not regeneratable
and transformable by these methods. The absence of a
high-efficiency plant regeneration method has been
regarded as a major obstacle to the application of
Agrabacterium-mediated transformation to cotton (Gawel
et al., 1986; Firoozabady et al., 1987).
Summary of the Invention
To overcome the problems associated with
previously reported methods, an efficient
transformation procedure using petiole as an explant
has been developed, along with a set of correspondingly
improved media. This method provides several
advantages in comparison to the hypocotyl and cotyledon
methods: (1) explants are easy to obtain; (2)
transformation efficiency is higher; (3) Agrobacterium
contamination is very rare; (4) efficiency in
regeneration is higher; and (5) the time from
transformation to regeneration of plantlets is reduced.
Two cotton varieties, i.e. Coker 312 and Si-Mian 3,
have been successfully transformed with this method,
and more than 30 independent transgenic lines from
Coker 312 showing strong activity of the marker
transgene have been obtained. This method is
applicable to other cotton varicties such as Jin 7 and
Ji 713 from China, Siokra 1-3 from Australia, T25,
Coker 201 and Coker 310 from the U.S.A.
Brief Description of the Figure
Figure 1 shows the plasmid pBI121GFP, containing
GFP as the reporter gene and the NPT II (neomycin
phosphotransferase) gene as a selectable marker, used
for Agrobacterium-mediated transformation of cotton
petiole according to the methods of the present
invention.
Detailed Description
An efficient method is disclosed for genetic
transformation of cotton plants, including elite lines,
using cotton peticl- as an explant. By using petiole
explants plus a lot of improved media, transformation
efficiency is significantly enhanced and the time
required from transformation to regeneration is
shortened in comparison to previously reported methods.
By using the methods of the present invention, the
whole process from Agrobacterlum transformation to the
regeneration of transgenic plantlets can take about 6-7
months. The reported hypocotyl and cotyledon methods
usually required 7-9 months or longer to complete the
same process (Cousins et al., 1991; Chen et al.,
unreported observation) . Another two months were
required for growing the small plantlets to a suitable
size for potting in soil.
Techniques for introducing exogenous genes into
Agrobacterium such that they will be transferred stably
to a plant or plant tissue exposed to the Agrobacterium
are well-known in the art and do not form part of the
present invention. It is advantageous to use a so-
called "disarmed" strain of Agrobacterium or Ti
plasmid, that is, a strain or plasroid wherein the genes
responsible for the formation of the tumor
characteristic of the crown gall disease caused by
wild-type Agrobacterium are removed or deactivated.
Numerous examples of disarmed Agrobacterium strains are
found in the literature (e.g., pAL4404, pEHAlOl and pEH
105 (Walkerpeach & Veltern, 1994)). It is further
advantageous to use a so-called binary vector system,
such as that described in Schilperoort et al., 1990,
1995. A binary vector system allows for manipulation
in E. coli of the plasmid carrying the exogenous gene
to be introduced into the plant, making the process of
vector construction much easier to carry out.
Similarly, vector construction, including the

construction of chimeric genes comprising tne exogenous
gene that one desires to introduce into the plant, can
be carried out using techniques well-known in the art
and does not form part of the present invention.
Chimeric genes should comprise promoters that have
activity in the host in which expression is desired.
For example, it is advantageous to have a series of
selectable markers for selection of transformed cells
at various stages in the transformation process. A
selectable marker (for example a gene conferring
resistance to an antibiotic such as kanamycin,
cefotaxime or streptomycin) linked to a promoter active
in bacteria would permit selection of bacteria
containing the marker (i.e., transformants). Another
selectable marker linked to a plant-active promoter,
such as the CaMV 35S promoter or a T-DNA promoter such
as the NPT II NOS promoter, would allow selection of
transformed plant cells. The exogenous gene that is
desired to be introduced into the plant cell should
comprise a plant-active promoter in functional relation
to the coding sequence, so that the promoter drives
expression of the gene in the transformed plant.
Again, plant-active promoters, such as the CaMV 35S,
the NPT II NOS promoter or any of a number of tissue-
specific promoters, are well-known in the art and
selection of an appropriate promoter is well within the
ordinary skill in the art.
The present method can be used to produce
transgenic plants expressing any number of exogenous
genes, and is not limited by the choice of such a gene.
The selection of the desired exogenous geno depends on
the goal of the researcher, and numerous examples of
desirable genes that could be used with the present
invention are known in the art e.g., the family of
Bacillus thuringiensis toxin genes, herbicide
resistance genes such as shikimate synthase genes that
confer glyphosate resistance, U.S. Patent No.
5,188,642, or a 2,4-D monooxygenase gene that confers
resistance to 2,4-dichlorophenoxyacetic acid (2,4-D),
Bayley et al., Theoretical and Applied Genetics, vol.
82, pp. 645-4 9, male sterility genes such as the
antisense genes of U.S. Patent No. 5,741,684
(Fabijanski, et al.), or even the elaborate crop
protection systems described in U.S. Patent No.
5,723,765 (Oliver et al.)).
Cotton regeneration is considered in the art to be
heavily variety-dependant. The Coker series of cotton
varieties have been shown to be relatively easy to
transform. However, DP 5412, Zhongmain 12 and many
other varieties still have difficulties associated with
regeneration. The situation is the same for G.
barbadense and other diploid species. While somatic
embryogenesis and regeneration of whole plants is a
highly genotype-dependent process in cotton, successful
transformation and regeneration of two distinct cotton
varieties, i.e. Coker 312 from U.S.A. and Si-Mian 3
from China, has been demonstrated using the methods of
the present invention. It this therefor believed that
the present invention has wide applicability to
transformation of a variety of cotton lines.
Transgene integration in the genome of cotton
produced by the methods of the present invention was
confirmed using standard Southern hybridization
techniques, as can identification of the copy number of
the inserted transgene in each transgenic line (see
Example 6, below}. The F1 generation of transgenic
cotton can be tested for the presence of Lhe transgene,
and inheritance pattern of che transgene in tne Fl
generation can be analyzed to confirm stability and
inheritability.
As compared with other reported protocols, the
cotton transformation system of the present invention
has higher transformation efficiency and survival rate.
This is attributable to several factors. In the
present invention, petiole was used as an explant for
transformation. Different types of cotton explants can
have significant effects on the efficiencies of plant
transformation and regeneration (Firoozabady et al.,
1987). Induction of somatic embryogenesis from petiole
was reported previously. But regeneration was either
unsuccessful or very poor (Finer and Smith, 1984; Gawel
et al., 1986). With the present invention, the
efficiency of regeneration was significantly improved
by using the improved media discussed below, in a
preferred embodiment, calli of high quality were
obtained when tender petioles rich in parenchyma cell
in primary vascular bundle tissue were cultured in the
MMSI medum (described below) with low concentrations
of_2,4-D_and_Kinetin.
With the present invention, the Lime for embryo
induction in suspension culture can be shortened to 10
- 14 days, from a previously reported 3 weeks (Cousins
et al., 1991). It was found that a shortened period of
suspension culture treatment is important for high
frequency induction of embryogenesis. It is also
important for reducing production of abnormal embryos,
since a high percentage of vitreous embryos that are
poor in regeneration are produced when cotton calli are
maintained in suspension culture for too long (Chen et
al, unpublished observation).
Fr- maximum cell growth at different stages except
at the young plant growing stage, glucose was used as
the sole carbon source. The amount of glucose in the
media can be from about 10 to about 50 g/1, preferably
about 30 g/1. At the young ? '---' growing stage,
glucose and sucrose at about 10 g/1 respectively as
carbon sources are preferable for promotion of healthy
plantlets growth.
For growth of callus, embryogenesis and callus
proliferation, pH range can be from 5.8 to 7.5,
preferably pH 6.2 - 7.0, most preferably at pH 6.5. A
medium of pH 7.0 is preferable lor healthy root growth
of plantlets.
For effective callus initiation and induction of
the potency of embryogenesis, low concentrations of
2,4-D and kinetin in the callus induction and selection
medium is important. The amount of 2,4-D can be from
0.05 to 0.5 mg/1, preferably about 0.05 mg/1. The
amount of kinetin can be from 0.1 mg/1 to about 1.0
mg/1, preferably about 0.1 mg/1. In the callus
differentiation stage and exnbryoid germination stage/
best result were obtained when no plant hormone was
added to the media.
The amino acids asparagine and glutamine are
better nitrogen sources than inorganic ammonia nitrogen
for specifically supporting embryoids germination and
root development. In the embryoid germination medium,
the amount of asparagine can be about 200 to about 1000
mg/1, preferably about 500 mg/1. The amount of
glutamine can be about 500 to about 2000 mg/1,
preferably about 1000 mg/1. With these optimized
nitrogen sources, the growth of non-embryogenic calli
was inhibited while the germination, growth and root
development of embryoids were preferentially promoted.
At different stages of cotton transformation
except co-culture with Agrobacterium, plant tissue and
callus are preferably maintained at 28°C but can be
varied from 25-35°C. For effective transformation,
temperature in co-culture stage should not be higher
than 28°C. A light condition of 16 hrs. light (60-90,
mEm-2S-1) and 8 hrs. dark per day is preferable for all
stages of cotton transformation and regeneration.
Unlike previously reported transformation and
regeneration protocols (Umbeck et al., 1987;
Firoozabady et al., 1987, Cousins et al.), the media
used in the present invention are optimized in several
respects: (a) glucose is used as a sole carbon source
in all culture media except in the medium used to
culture young plants previous to planting out in the
greenhouse; (b) the media is adjusted to higher pH
value (6.5-7.0); (c) lower concentration of 2,4-D
(0.05mg/l) and kinetin (0.1 mg/1) is U3ed only at
callus initiation stage, no hormone is used at other
stages; (d) asparagine and glutamine are used to
replace inorganic ammoniac nitrogen in the medium. used
for embryoid germination. These modifications are
adapted for the physiological requirement of cotton
embryoid development and plantlet growth. It has been
found that healthy embryoid development and plantlet
growth, especially root system. development, are largely
attributable to these optimized media. For example, it
has been found that asparagine and glutamine were
better nitrogen source than inorganic ammonia nitrogen
for supporting embryoid germination and root
development. In the preferred MMS3 medium (described
below) , which contains asparagine and glutamine as the
nitrogen source, the growth of non-embryogenic calli
was inhibited while the germination, growth and root
development of embryoids were preferentially promoted.
Because of the healthy root development, the survival
rate of potted transgenic cotton plants obtained by the
methods of the present invention is almost 100%,. With
the reported hypocotyl and cotyledon protocols (Umbeck
et al., 1987; Firoozabady et al., 1967), poor root
development has been regarded as the main reason
accounting for poor survival rate of potted transgenic
cotton plants.
The following are preferred plant tissue culture
media used in the Examples:
(1) Seedling growing medium (per liter):
½ MS basal salt mixture (Sigma M5524)
0.9 g MgCl2 -6H2O
2.0 g gellan gum (Phytagel™, Sigma)
pH 7.0
(2) Petiole pre-culture medium (per liter):
MS basal salt mixture
0.9 g MgCl2-6H2O
2.0 g gellan gum (Phytagel™, Sigma)
pH 7.0
(3) Co-culture medium (per liter):
MS basal salt mixture
10 mg Thiamine-HCl
1 mg Pyridoxine-HCl
1 mg Nicotinic acid
100 mg Myo-inositol
0.05 mg 2,4-dichlorophenoxyacetic acid (2,4-D)
0.1 mg Kinetin
30 g Glucose
0.9 g MgCl2-6H2O
2.0 g gellan gum (Phytagel™, Sigma)
pH 6.5
(4) MMS1 - callus induction and selection medium (per
liter):
Co-culture medium
50 mg Kanamycin
500 mg Cefotaxime
(5) MMS2 - differentiation medium (per litre) :
MS basal salt mixture
10 mg Thiamine-HCl
1 mg Pyridoxine-HCl.
1 mg Nicotinic acid
100 mg Myo-inositol
1.9 g KNO3
30 g Glucose
0.9 g MgCl2-6H2O
2.0 g gellan gum (Phytagel™, Sigma)
pH 6.5
(5) MMS3 - embryoid germination medium (per litre) :
3.8 g KNO3
440 mg CaCl2-H2O
375 mg MgS04-7H2O
170 mg KH2PO,
1 g Glutamine
500 mg Asparagine
43 mg EDTA ferric-Na salt
MS micronutrients (Murashige and Skoog, 1962)
10 mg Thiamine-HCl
1 mg Pyridoxine-HCl
1 mg Nicotinic acid
100 mg Myo-inositol
30 g Glucose
0.9 g MgCl2-6H2O
2.0 g gellan gum (Phytagel™, Sigma)
pH 6.5
(7) Young plant growing medium
S&H medium Macro and Micro elements (Strewart and
Hsu, 1977)
10 mg Thiamine-HCl
l mg Pyridoxine-HCl
1 mg Nicotinic acid
100 mg Myo-inositol
10 g Glucose
10 g Sucrose
0.9 g MgCl2-6H2O
2.0 g gellan gum (Phytagel™, Sigma)
pH 7.0
The following Examples are intended to illustrate
the present invention, and not in any way to limit its
scope, which is solely defined by the claims.
Example 1 : Agrobacterium strain and plasmids
A. tumefaciens strain LBA 4404 (pBI121GFP) was
used for transformation of cotton petiole and young
stem. The physical map of pBI121GFP is shown in Fig.l,
which contains GFP as a reporter gene and NPTII gene
(encoding neomycin phosphotransferase) as a selectable
marker. The GFP and NPTTT genes are under the control
of CaMV 35S promoter and nos promoter respectively.
For construction of pBI121GFP, a 720 bp XbaI-SstI
fragment of GFP gene from the pGFP2 plasmid (from Dr.
N. H. Chua, Rockefeller University, New York) was
cloned into the same sites in plasmid vector pBI121
(Clontech) to replace the GUS gene. The pBI12lGFP
plasmid was introduced into A. tumefaciens LBA 4404 by
electroporation.
Example 2: Plant material
Upland cotton varieties Coker 312 from the O.S.A,
and Si-Mian 3 from Shanxi Cotton Research Institute in
China were used in the experiments.
Tender petioles were collected from plants 8-12
weeks old grown in a greenhouse with low light
conditions. The petioles were surface-sterilized with
70% ethanol for a few seconds, followed by 20% bleach
solution (Clorox Co, USA, 1% available chlorine) for 20
min. After rinsing five times in sterilized water, the
petioles were pre-cultured in MS medium for 3 days.
Example 3: Plant transformation
A single colony of A. tumefaciens strain LBA 4404
CpBI121GPP) was inoculated in liquid LB medium with 50
mg/L Rifampicin, 50 mg/L kanamycin and 100 mg/L
streptomycin. The bacteria was grown overnight at 28°C
in a shaker of 200 rpm. The bacterium cultures were
dilute using liquid MS medium to OD600 = 0.3.
The petiole and young stem were cut into about 2
cm long segments. The segments were soaked in the
diluted bacterium suspension for 5 min, then
transferred onto plastic plates (100 x 25 mm)
containing a filter paper soaked in 50 ml of co-culture
medium. The plates were kept in an incubator of 24oC
under continuous light for 4 8 hrs. The co-cultured
explants were transferred onto MMS1 medium and
incubated at 28°C with 16 hrs light (60-90,mEm-2s-1) and
8 hrs dark per day. After 2-4 weeks calli were
initiated at the cut ends of petiole segments. After
4-6 weeks kanamycin resistant calli had appeared, and
the number of calli were counted and the expression of
GFP gene was examined.
Under the fluorescence microscope, the
untransformed control callus appeared red in colour,
while the transformed callus expressing GFP gene
displayed distinct green fluorescence. A total of 113
putative transformed calli were examined for GFP
activity, the transformation frequency of GFP gene was
39.8% (Table 1). When petioles from cotton variety
Si-Mian 3 were used for transformation, 11 calli were
found GFP positive from 26 calli tested, transformation
efficiency was 42.3%.
Table 1: Transformation frequencies or petioles from
cotton Coker 312 and Si-Main 3

i
Example 4: Induction of somatic embryogenesis and plant
regeneration
The calli with vigorous growth and strong
expression of GFP were selected and transferred into
liquid MMS2 medium for suspension culture tor 2 weeks.
Friable cream-colored granular calli were selected and
transferred to semi-solid differential medium, MMS2.
After about 2 months a large number of embryoids were
produced. Cytoplasmic dense embryogenic structures
were gradually developed and large embryos were
produced on the medium within 1-2 month. A short time
of suspension culture treatment was very important, not
only for high frequencies of embryogenesis induction,
but also for production of embryoids of good quality.
Expression of CFP gene was checked again and all were
GFP positive.
The embryoids and embryogenic calli with strong
GFP activity were transferred onto the MMS3 medium.
After 1-2 months the plantlets that were about 1-2 cm
in height with 1-2 true leaves and good root
development were transferred to the Young Plant Growing
Medium for about one month. About one month later,
young plants with 6-8 leaves and about 10-15 cm in
height were potted in soil and move to the glasshouse.
All 30 potted transgenic plants survived and were found
expressing GFP protein. The total time required to
obtain transgenic plantlets using was under 7 months,
and plantlets were reading for potting out in the
greenhouse in about 2 additional months (see Table 2).
Table 2: The time frame from transformation of petiole
segments to plant regeneration (Coker 312)

Example 5: Detection of GFP Protein Activity
The expression of GFP protein activity was
Geteeted using a Leica MZ FLIIT Fluorescence stereo
microscope with a 480/40 nM excitation filter and a 510
nM barrier filter.
Green fluorescence of GFP gene can be easily
distinguished in the transformed callus, embryoids, and
young plantlets, with the untransformed control
appeared red in colour under the fluorescence Stereo
microscope. The exceptions were the untransformed
roots, which appeared dim green under the fluorescence
microscope, probably due to some chromophorous
chemicals accumulated in roots. But the roots with GFP
activity could still be identified because the green
fluorescence produced by GFP protein was brighter and
appeared more uniform. Under the blue light produced
by the fluorescence stereo microscope, red fluorescence
is clearly visible in untraneformed green plant tissues
that are enriched with chlorophyll such as leaf and
stem. In GFP-positive green plant tissues, yellow
fluorescence also was detected because of the
overlapping of red and green fluorescence. However,
the expression of GFP gene in petal and anther was
poorer in comparison to that in other parts of plant.
Example 6: Analysis of Transgenic Plants
Genomic DNA from putatively transformed lines and
non-transformed control plants was purified according
to Paterson et all. (1993). After digestion with EcoRI,
which cuts inj-between left border of T-DNA and Nos-3'
terminator of the chimerical GFP gene (Fig. 1), DNA was
separated on a 0.8% TAE agarose gel and transferred to
Hybond-N membrane according to manuracturer's
instructions. DNA was fixed to the membrane by UV
crossing linking before hybridizing to the DIG labeled
coding region of the GFP gene. Hybridized probe was
detected with anti-DIG-AP conjugate according to
manufacturer's instructions (BOEHRINGER MANNHEIM) .
The genomic DNA samples from 11 randomly selected
transgenic lines and 1 untransformed control plant were
analyzed Southern hybridization, using the coding
region of GFP gene as the hybridization probe. The
data indicate that 7 out of 11 lines have a single
copy, 3 lines have 2 copies, and 1 line has 6 copies of
T-DNA insertion. The high percentage of transgenic
lines with a single copy of T-DNA insertion suggests
that this transformation protocol has less risk of gene
silencing and undesirable insertion mutants.
References Cited
Altman, D. W. et al. 1990. Economic Botany 40, 106.
Bajaj, Y. P. S. 1985. Theor. Appl. Genet. 70, 363.
Beasley, C. A. 1971. In vitro culture of fertilized
cotton ovules. Biosci. 21, 906-7.
Chen Z.X., Liewellyn D.J., Fan Y.L., Li S.J., Guo S.D.,
Jiao G.L., and Zhao J.X. 1994. 2,4-D Resistant
Transgenic Cotton Plants Produced by
Agrobacterium-mediated gene Transfer. Scientia
Agriculture Sinica 27(2): 3 1 -37.
Chen, Z. X., Li, S. J., Yue, J. X., Jiao, G. L. and Liu
S. X. 1989. Plantlet regeneration from protoplasts
isolated from an embryogenic suspension culture of
cotton (Gossypium hirsutum L.). Acta Botanica
Sinica 31, 966-9.
Chen, Z. X., Trolinder, N.L. et al., 1987. Some
characteristics of somatic embryogenesis and plant
regeneration in cotton cell suspension culture.
Scientia Agriculture Sinica 20, 6-11.
Chlan, C. A., Lin, J., Cary, J. W. and Cleveland, T- E.
1995. A procedure for biolistic transformation
and regeneration of transgenic cotton from
meristematic tissue. Plant Mol. Biol. Rep. 13,
31-7.
Cousins Y.L., Lyon B.R., and Llewellyn D.J. 1991.
Transformation of Australian cotton cultivar:
prospects for cotton improvement through genetic
engineering Aust. J. plant physiol., 18, 481-494.
Davidonis, G. H., and Hamilton, R. H. 1983. Plant
regeneration from callus tissue of Gossypium
hirsutum L. Plant Sci. Lett. 32, 89-93.
Davidonis, G. H., Mumma, R, O. and Hamilton, R. H.
1987. Controlled regeneration of cotton plants
from tissue culture. US Patent No. 4,672,035.
de Framond et al. 1983. Mini-Ti; a new vector strategy
for plant genetic engineering. Bio/technology 1,
262-9.
Finer, J- J. and McMullen, M. D. 1990. Transformation
of cotton (Gossypium hirsutum L.) via particle
bombardment. Plant Cell Reports 8, 586-9.
Filler, J.J., and Smith R.H. 1984. Initiation of
callus and somatic embryos from explants of mature
cotton (Gossypium klotzschianum Anderss). Plant
Cell Reports 3, 41-43.
Finer, J., 1988. Plant regeneration from somatic
embryogenic suspension cultures of cotton
(Gossypium hirsutum L.) . Plant Cell Rep. 7,
399-402.
Firoozababy E., DeBoer D.L., Merlo D.J., Halls E.J.,
Anderson I.N., Raska K.A., Murray E.E. 1987,
Transformation of cotton, Gossypium hirsutum L. by
Agrobacterium tumefaciens and regeneration of
transgenic plants. Plant Molecular Biology 10,
105 1 16
Gawel N. J., Rao A. P., and Robacker C. 1986. Somatic
embryogenesis from leaf and petiole callus
cultures of Gossypium hirsutum L. Plant Cell
Reports 5, 457-459.
Gawel, N. J. and Robacker, C. 1990. Genetic control of
somatic embryogenesis in cotton petiole callus
cultures. Euphytica 49, 249-53.
Gould, J., Banister, S., Hasegawa, 0., Fahima, M. and
Smith, R. H. 1991. Regeneration of Gossypium
hirsutum and G, barbadense from shoot apex tissues
for transformation. Plant Cell Reports 10, 12-6.
Hoekema et al. 1983. A binary plant vector strategy
based on separation of Vir- and T-Region of the
Agrobacterium tumefaciena Ti-plasmid. Nature 303,
179-80.
John, M. E. 19.46. Structural characterization of genes
corresponding to cotton fiber mRNA, E6: reduced E6
protein in transgenic plants by antisense gene.
Plant Mol. Biol.,30, 297-306.
John, M. E. and Keller, G. 1996. Metabolic pathway
engineering in cotton; Biosynthesis of
polyhydroxybutyrate in fiber cells. Proc. Natl.
Acad. Sci . USA 93, 12768-73.
Keller G., Spatola L., McCabe D., Martinell s., Swain
w.x. and John M.E. 1997. Transgenic cotton
resistant to herbicide bialaphos. Transgenic
Research 6, 385-392.
Kuo, C. C. et al., 1989. Proc. Beltwide Cotton Prod.
Res. Confs, 638.
McCabe, D. E. and Martinell, B. J. 1993.
Transformation of elite cotton cultivars via
particle bombardment of meristems. Bio/technol.
11, 596-8.
Murashige T., and Skoog F. 1962. A revised medium for
rapid growth and bioassays with tobacco tissue
culture. Physiol. Plant 15, 473-493.
Paterson, A.H., Brubaker, C.L., and Wendel J.F., 1993,
A rapid method for extraction of cotton
(Gossypium spp.) Genomic DNA suitable for RFLP or
PCR analysis. Plant Mol. Biol. Rptr. 11, 122-127.
Perlak F.J., Deaton R.W., Armstrong T.A., Fuchs R.L.,
Sims S.R., Greenplate J.T., and Fischhoff D.A.
1990, Insect resistant cotton plants.
Bio/Technology 8, 939-943.
Price, H. J. and Smith, R. H. 1979. Somatic
embryogenesis in suspension cultures of Gossypium
klotzschianum Anderss. Planta 145, 305-6.
Rangan, F. J. and Zavala, T. Ip. A. 1984. Somatic
embryogenesis in tissue culture of Gossypium
hirsutum L.). In Vitro 20, 256,
Rangan, R. and Rajasekaran, K. 1996. Regeneration of
cotton plant in cell suspension culture. OS
Patent No. 5,583,036 (continued from US Patent
5,244,802, 1993 and 122,200, 1987).
Rajasckaran K., Grula J.W., Hudspeth R.L., Polelis S.,
Anderson D.M. 1996. Herbicideresistant Acala and
Coker cotton transformed with the native gene
encoding mutant forms of acetohydroxyacid
synthase, Mol. Breeding, 2: 307-319.
Schilperoort, R.A., Hoekema, A., Hooykaas, P.J.J.
1990. Process for the incorporation of foreign
DNA into the genome of dicotyledmous plants. D.S.
Patent No. 4,940,838,
Schilperoort, R.A., Hoekema, A., 1995. Process for the
incorporation of foreign DNA into, the genome of
dicotyledmous plants. U.S. Patent No. 5,4 64,763.
Steward J. McD. 1991. Biotechnology of Cotton:
Achievements and Perspectives. CAB International.
Stewart J. McD., and Hsu C.L. 1977. In ovule embryo
culture and seedling development of cotton
(Gossypium hirsutum L.). Planta 137, 113-117.
Stewart, J. McD. and Hsu, C. L. 1978. Hybridization of
deploid and tetraploid cottons through in-ovulo
embryo culture. J. Heridity 69, 404-8.
Trolinder, N. L. 1985a. Somatic embryogenesis and
plant regeneration in cotton (Gossypium hirsutum
L.).. A Dissertation in Biology (Dec, 1985).
Trolinder, N. L., Chen, Z.X., 1989. Genotype
specificity of the somatic embryogenesis response
in cotton. Plant Cell Reports 8, 133-6.
Trolinder, N. L. and Goodin, J. E. 1987. Somatic
embryogenesis and plant regeneration in cotton
(Gossypium hirsutum L.). Plant Cell Reports 6,
231-4.
Trolinder, N. L. and Goodin, J. E. 1988a. Somatic
embryogenesis and regeneration in cotton. I.
Effects of source of explant and hormone regime.
Plant Cell Tissue Organ Culture 12, 31-42.
Trolinder, N. L. and Goodin, J. E. 1988b. Somatic
embryogenessis and regeneration in cotton. IT.
Requirements for embryo development and plant
regeneration. Plant Cell Tissue Organ Culture 12,
43-53.
Trolinder N.L., Quisenberry J., Bayley C., Ray C, and
Ow D. 1991. 2,4-D-res.i stant transgenic cotton.
Proceedings, Beltwide Cotton Conferences.
National Cotton Council, Memphis, Tennessee, P840.
Turaev, A. M. and Shamina, Z. B. 1986. Soniet Plant
Physiol. 33, 439.
Umbeck P. 1992. Genetic engineering of cotton plants
and lines. United States Patent: 5,159,135.
Umbeck, P. F, Johnson, G., Barton, K. and Swain, W.
1987. Genetically transformed cotton (Gossypium
hirsutum L.) plants. Bio/technol. 5, 263-6.
Umbeck P., Johnson P., Barton K., and Swain w.. 1987.
Genetically transformed cotton (Gossypium hirsutum
L.) plants. Bio/Technology 5, 263-266.
Walkerpeach, C.R. and Veltern, J. 1994. Agrobacterium-
mediated gene transfer to plant cells: cointegrate
and binary vector systems. Plant Mol. Biol.
Mannuel Bl, 1-19.
Wendt-Gallitelli M.F., and Dobrigkeit I. 1973.
Investigations implying the invalidity of octopine
as a marker for transformation by Agrobacterium
tumefaciens. Zeitschrift fur Naturforschung -
Section C- Biosciences 28, 768-771.
Zhang, H.-B. 1994. The tissue culture of cotton (II).
Plant Physiol. Commun. 30, 386-91.
Zhang, H.-B, and Feng, R. 1992. The tissue culture of
cotton (I). Plant Physiol- Commun. 30, 386-91.
Zhou, G.-Y., Weng, J., Zeng, Y.-S., Huang, J.-G., Qian,
S.-Y. and Liu, G.-L. 1983. Introduction of
exogenous DNA into cotton embryos. Methods in
Enzymology 101,433-81.
We claim:
1. A method for producing a transgenic cotton plant
comprising the steps of:
(a) obtaining cotton petiole explants in the manner such as herein described;
(b) exposing the petiole explants to a
culture of Agrobacterium tumefaciens such as herein described, that
harbors a vector comprising an exogenous gene such as herein described,
and a selectable marker, such as herein described, the Agrobacterium
being capable of effecting the stable
transfer of the exogenous gene and selection
agent resistance gene to the genome of the
cells of the petiole explant,
(c) culturing the petiole explants to induce
callus formation,
(d) selecting transformed callus that
expresses the exogenous gene,
(e) culturing the selected callus in
suspension culture to induce formation of
embryoids,
(f) regenerating the embryoids into whole
transgenic cotton plants.
2. The method as claimed in claim 1 wherein the petiole explants
are pre-cultured for a period of time prior to
exposure to the culture of Agrobacterium
tumeraciens.
3.The method as claimed in claims 1 wherein the culture media
used in steps (b)-(e) have glucose as the sole
carbon source.
4. The method as claimed in claim 3 wherein the glucose is in an
amount of about 10 g/1 to about 50 g/1.
5.The method as claimed in claim 4 wherein the glucose is in an
amount of about 30 g/1.
6.The method as claimed in claim 1 wherein the culture media
used in steps (b) and (d)-(f) do not contain
hormones.
7.The method as claimed in claim 1 wherein embyroid germination
is carried out in a medium having a source of
nitrogen selected from the group consisting of
asparagine, glutamine or both asparagine and
glutamine.
8.The method as claimed in claim 7 wherein the source of
nitrogen is in an amount of about 700 mg/1 to
about 5 g/1.
9.The method as claimed in claim. 8 wherein the source of
nitrogen is in an amount of about 3.6 g/1.
10.The method as claimed in claim 7 wherein the source of
nitrogen is both asparagine and glutamine, and the
asparagine is in an amount of about 200 mg/1 to
about 1 g/l and the glutamine is in an amount of
about 500 mg/1 to about 2 g/1.
11. The method as claimed in claim 10 wherein the asparagine is
in an amount of about 500 mg/1 and the glutamine
is in an amount of about 1 g/1.
12 The method as claimed in claim 1 wherein the suspension
culture of step (e) has a duration of less than
about 20 days.
13. The method as claimed in claim 12 wherein the suspension
culture of step (e) has a duration of about 10
days to about 20 days.
14. The method as claimed in claim 13 whorein the suspension
culture of step (e) has a duration of about 14
days.
15. The method as claimed in claim 1 wherein step (c) is carried
out in the presence of low concentration of one or
more hormones.
16. The method as claimed in claim 15 wherein the concentration
of any on 0 to about 1 mg/1.
17. The method as claimed in 15 werein step (c) is carried
out in the presence of 2,4-dichlorophenoxacetic
acid in a ranging from 0 to about
0.5 mg/1 and kinetin in concentration ranging from
0 to about 1 mg/1.
18. The method as claimed in claim 17 wherein the 2, 4-dichloro-
phenoxylacetic acid is in a concentration of about
0.05 mg/1 and the kinctin is in a concentration of
about 0.1 mg/1.
A method is disclosed for producing a transgenic cotton plant by Agrobacterium-mediated transformation of petiole
tissue. The method comprises the steps of (a) obtaining cotton petiole explants, (b) exposing the petiole explants to a culture of
Agrobacterium tumefaciens that harbors a vector comprising an exogenous gene and a selectable marker, the Agrobacterium being
capable of effecting the stable transfer of the exogenous gene and selection agent resistance gene to the genome of the cells of the
petiole explant, (c) culturing the petiole explants to induce callus formation, (d) selecting transformed callus that expresses the exogenous
gene, (e) culturing the selected callus in suspension culture to induce formation of embryoids, (f) regenerating me embryoids
into whole transgenic cotton plants.

Documents:

« Previous Patent

Next Patent »

Patent Number

225462

Indian Patent Application Number

IN/PCT/2002/00033/KOL

PG Journal Number

46/2008

Publication Date

14-Nov-2008

Grant Date

12-Nov-2008

Date of Filing

08-Jan-2002

Name of Patentee

TAMASEK LIFE SCIENCES LABORATORY LIMITED

Applicant Address

1 RESEARCH LINK, THE NATIONAL UNIVERSITY OF SINGAPORE

Inventors:

#	Inventor's Name	Inventor's Address
1	CHEN ZHI XIAN	COTTON RESEARCH INSTITUTE YUNCHENG SHANXI 044000
2	ZHANG LIANHUA	360 PASIR PANJANG # 03-11 GOLDCOAST CONDOMINIUM SINGAPORE 118699

PCT International Classification Number

C12N 15/82

PCT International Application Number

PCT/SG1999/00058

PCT International Filing date

1999-06-11

PCT Conventions:

#	PCT Application Number	Date of Convention	Priority Country
1			NA