Agrobacterium tumefaciens-mediated transformation of Indian mulberry, Morus indica cv. K2:: a time-phased screening strategy

被引:30
作者
Bhatnagar, S [1 ]
Khurana, P [1 ]
机构
[1] Univ Delhi, Dept Plant Mol Biol, New Delhi 110021, India
关键词
Morus; regeneration; transformation; Gus; nptII;
D O I
10.1007/s00299-003-0572-2
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
An efficient and reproducible protocol for the production of transgenic plants was developed for Morus indica cv. K2 by Agrobacterium tumefaciens-mediated transformation. The hypocotyls, cotyledon, leaf and leaf callus explants precultured for 5 days on regeneration medium were co-cultivated with a bacterial suspension at 109 cells/ml for 3 days in the dark. Infectivity of A. tumefaciens strain LBA4404 was more than that of strains GV2260 and A281, and among the various plasmids tried, pBI121 and pBI101:Act1 transformed nearly 100% of the explants followed closely by p35SGUSINT. About 90-100% of the explants tested positive in the beta-glucuronidase (GUS) histochemical assay performed after 3 days of co-cultivation. This high level of transient expression, however, decreased to 20-25% after 15 days. Gus activity was most stable in the callus explants, which emerged as the explant of choice for transformation. The transformed explants were selected on 50-75 mg/l kanamycin for 1 month, and 25-50% of the explants developed adventitious buds. On the basis of kanamycin-resistant shoots produced from the total number of explants inoculated, the transformation efficiency was 44%. After 1 month, 40% of these shoots displayed high gus activity as assessed by the GUS fluorometric assay. On a selection-free root induction medium, 80% of the shoots developed roots and 90% of the potted plantlets acclimatized to the growth room conditions. The 3-month-old regenerates showed gus and nptII(neomycin phosphotransferase 11) gene activity as assayed by the GUS fluorometric assay and nptII enzyme assay, followed by PCR polymerase chain reaction (54.5%) analysis after 6-months. Transgene integration into the nuclear genome of 1-year-old regenerates was confirmed in 10 of the 18 transformants dtested by Southern analysis. The transformation efficiency as defined by the number of transgenic plants produced from the total number of explants co-cultivated was 6%.
引用
收藏
页码:669 / 675
页数:7
相关论文
共 38 条
[1]   CaMV 35S promoter directs β-glucuronidase expression in the laticiferous system of transgenic Hevea brasiliensis (rubber tree) [J].
Arokiaraj, P ;
Yeang, HY ;
Cheong, KF ;
Hamzah, S ;
Jones, H ;
Coomber, S ;
Charlwood, BV .
PLANT CELL REPORTS, 1998, 17 (08) :621-625
[2]  
BHATNAGAR S, 2000, PLANT BIOTECHNOL, V18, P61
[3]  
Bhatnagar Somika, 2002, Indian Journal of Sericulture, V41, P80
[4]  
Bhatnagar Somika, 2002, Indian Journal of Experimental Biology, V40, P1387
[5]  
BRADFORD MM, 1976, ANAL BIOCHEM, V72, P248, DOI 10.1016/0003-2697(76)90527-3
[6]   AGROBACTERIUM-MEDIATED TRANSFORMATION OF APPLE (MALUS X DOMESTICA BORKH) - AN ASSESSMENT OF FACTORS AFFECTING GENE-TRANSFER EFFICIENCY DURING EARLY TRANSFORMATION STEPS [J].
DEBONDT, A ;
EGGERMONT, K ;
DRUART, P ;
DEVIL, M ;
GODERIS, I ;
VANDERLEYDEN, J ;
BROEKAERT, WE .
PLANT CELL REPORTS, 1994, 13 (10) :587-593
[7]  
DELLAPORTA SL, 1983, PLANT MOL BIOL REP, V4, P9
[8]   Ri-plasmid mediated transformation and regeneration of Ulmus procera (English Elm) [J].
Garland, JS ;
Brasier, CM ;
Fenning, TM ;
Birch, R ;
Garland, KMA .
PLANT GROWTH REGULATION, 2001, 33 (02) :123-129
[9]   AGROBACTERIUM-TUMEFACIENS-MEDIATED TRANSFORMATION OF SEVERAL RUBUS GENOTYPES AND RECOVERY OF TRANSFORMED PLANTS [J].
HASSAN, MA ;
SWARTZ, HJ ;
INAMINE, G ;
MULLINEAUX, P .
PLANT CELL TISSUE AND ORGAN CULTURE, 1993, 33 (01) :9-17
[10]   Agrobacterium tumefaciens-mediated transformation of Pinus pinea L cotyledons:: an assessment of factors influencing the efficiency of uidA gene transfer [J].
Humara, JM ;
López, M ;
Ordás, RJ .
PLANT CELL REPORTS, 1999, 19 (01) :51-58