2006
DOI: 10.1007/s10535-006-0082-5
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Identification of a novel elite genotype for in vitro culture and genetic transformation of cotton

Abstract: Hypocotyls of cotton (Gossypium hirsutum L.) cultivars cv. YZ-1, Coker 312 and Coker 201 were inoculated on Murashige and Skoog callus induction medium. YZ-1 exhibited a very high regeneration potential, with 81.9 % of the explants inoculated differentiated into embryogenic callus within 8 -10 weeks. During the process of callus maintenance (subculture for 1 to 3 years), the total embryos number in Coker 312 and Coker 201 calli dropped sharply, and the percentage of embryo germination decreased. On the contrar… Show more

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Cited by 124 publications
(100 citation statements)
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References 30 publications
(22 reference statements)
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“…The RNAi region containing a partially conserved domain and the specific 39 region of GbWRKY1 was cloned into the RNAi vector pHellsgate 4 through recombination reaction (Tan et al, 2013). The overexpression vector and RNAi vectors were introduced into G. hirsutum 'YZ1' plants by A. tumefaciens (strain EHA105)-mediated transformation as described previously (Jin et al, 2006). The overexpression vector was transferred into A. tumefaciens strain GV3101 to transform the Arabidopsis (Arabidopsis thaliana) ecotype Columbia-0 using the floral dip method .…”
Section: Gene Cloning Vector Construction and Plant Transformationmentioning
confidence: 99%
“…The RNAi region containing a partially conserved domain and the specific 39 region of GbWRKY1 was cloned into the RNAi vector pHellsgate 4 through recombination reaction (Tan et al, 2013). The overexpression vector and RNAi vectors were introduced into G. hirsutum 'YZ1' plants by A. tumefaciens (strain EHA105)-mediated transformation as described previously (Jin et al, 2006). The overexpression vector was transferred into A. tumefaciens strain GV3101 to transform the Arabidopsis (Arabidopsis thaliana) ecotype Columbia-0 using the floral dip method .…”
Section: Gene Cloning Vector Construction and Plant Transformationmentioning
confidence: 99%
“…The conserved region of the four published F3H genes was selected as the RNAi target and cloned into the RNAi vector pHellsgate 4 through the Gateway system to produce pHG4-F3H (Helliwell et al, 2002). Transformation was performed via Agrobacterium tumefaciens (EHA105) according to a previously described method (Jin et al, 2006b). Because several regenerated transgenic seedlings failed in healthy root growth, a grafting method was performed to rescue these seedlings (Jin et al, 2006a).…”
Section: Plasmid Construction and Plant Transformationmentioning
confidence: 99%
“…The overexpression vector, RNAi vectors, PGbPDF1::GUS, DBCD, DCD, DD, and PGbPDF1-1::GFP were introduced into cotton (YZ1) plants by A. tumefaciens-mediated (EHA105 and LBA4404) transformation as described by Jin et al (2006) and Li et al (2010). After regeneration, transformed cotton lines were checked by PCR (V-RNAi-F/R for RNAi constructs and V-gus-F/R for GUS-fused vectors) and Southern blotting.…”
Section: Plasmid Construction and Plant Transformationmentioning
confidence: 99%