We report an improved method for white clover (Trifolium repens) transformation using Agrobacterium tumefaciens. High efficiencies of transgenic plant production were achieved using cotyledons of imbibed mature seed. Transgenic plants were recovered routinely from over 50% of treated cotyledons. The bar gene and phosphinothricin selection was shown to be a more effective selection system than nptII (kanamycin selection) or aadA (spectinomycin selection). White clover was transformed with the soybean auxin responsive promoter, GH3, fused to the GUS gene (beta-glucuronidase) to study the involvement of auxin in root development. Analysis of 12 independent transgenic plants showed that the location and pattern of GUS expression was consistent but the levels of expression varied. The level of GH3:GUS expression in untreated plants was enhanced specifically by auxin-treatment but the pattern of expression was not altered. Expression of the GH3:GUS fusion was not enhanced by other phytohormones. A consistent GUS expression pattern was evident in untreated plants presumably in response to endogenous auxin or to differences in auxin sensitivity in various clover tissues. In untreated plants, the pattern of GH3:GUS expression was consistent with physiological responses which are regarded as being auxin-mediated. For the first time it is shown that localised spots of GH3:GUS activity occurred in root cortical tissue opposite the sites where lateral roots subsequently were initiated. Newly formed lateral roots grew towards and through these islands of GH3:GUS expression, implying the importance of auxin in controlling lateral root development. Similarly, it is demonstrated for the first time that gravistimulated roots developed a rapid (within 1 h) induction of GH3:GUS activity in tissues on the non-elongating side of the responding root and this induction occurred concurrently with root curvature. These transgenic plants could be useful tools in determining the physiological and biochemical changes that occur during auxin-mediated responses.
机构:Seoul Natl Univ, Dept Plant Sci, Plant Genom & Breeding Inst, Seoul, South Korea
Yoo, Soo-Cheul
Cho, Sung-Hwan
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机构:Seoul Natl Univ, Dept Plant Sci, Plant Genom & Breeding Inst, Seoul, South Korea
Cho, Sung-Hwan
Paek, Nam-Chon
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Seoul Natl Univ, Dept Plant Sci, Plant Genom & Breeding Inst, Seoul, South KoreaSeoul Natl Univ, Dept Plant Sci, Plant Genom & Breeding Inst, Seoul, South Korea
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Chinese Acad Sci, State Key Lab Plant Cell & Chromosome Engn, Ctr Agr Res Resources, Inst Genet & Dev Biol, Shijiazhuang 050021, Hebei, Peoples R China
Chinese Acad Sci, Grad Univ, Beijing 100039, Peoples R ChinaChinese Acad Sci, State Key Lab Plant Cell & Chromosome Engn, Ctr Agr Res Resources, Inst Genet & Dev Biol, Shijiazhuang 050021, Hebei, Peoples R China
Zhao, Yankun
Wang, Tao
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Chinese Acad Sci, State Key Lab Plant Cell & Chromosome Engn, Ctr Agr Res Resources, Inst Genet & Dev Biol, Shijiazhuang 050021, Hebei, Peoples R China
Chinese Acad Sci, Grad Univ, Beijing 100039, Peoples R ChinaChinese Acad Sci, State Key Lab Plant Cell & Chromosome Engn, Ctr Agr Res Resources, Inst Genet & Dev Biol, Shijiazhuang 050021, Hebei, Peoples R China
Wang, Tao
Zhang, Wensheng
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Chinese Acad Sci, State Key Lab Plant Cell & Chromosome Engn, Ctr Agr Res Resources, Inst Genet & Dev Biol, Shijiazhuang 050021, Hebei, Peoples R ChinaChinese Acad Sci, State Key Lab Plant Cell & Chromosome Engn, Ctr Agr Res Resources, Inst Genet & Dev Biol, Shijiazhuang 050021, Hebei, Peoples R China
Zhang, Wensheng
Li, Xia
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Chinese Acad Sci, State Key Lab Plant Cell & Chromosome Engn, Ctr Agr Res Resources, Inst Genet & Dev Biol, Shijiazhuang 050021, Hebei, Peoples R ChinaChinese Acad Sci, State Key Lab Plant Cell & Chromosome Engn, Ctr Agr Res Resources, Inst Genet & Dev Biol, Shijiazhuang 050021, Hebei, Peoples R China