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首页> 外文期刊>The Journal of Horticultural Science & Biotechnology >DREB1A regulon expression in rd29A:DREB1A transgenic chrysanthemum under low temperature or dehydration stress.
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DREB1A regulon expression in rd29A:DREB1A transgenic chrysanthemum under low temperature or dehydration stress.

机译:低温或脱水胁迫下 rd29A:DREB1A 转基因菊花中DREB1A调节子的表达。

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Previously we reported that expression of the Arabidopsis DREB1A gene in chrysanthemum conferred increased tolerance to low-temperature and dehydration stresses, and that transgenic plants in which the DREB1A gene was driven by the abiotic stress-inducible promoter, rd29A, were more tolerant than those plants in which the DREB1A gene was driven by the 35S Cauliflower Mosaic Virus (CaMV) promoter. To understand the molecular basis for this improved tolerance, we isolated 74 DREB1A regulon genes using suppression subtractive hybridisation, then compared their expression patterns in rd29A:DREB1A transgenic plants (rd29A plants) and in 35S:DREB1A transgenic plants (35S plants) under different stress conditions. Our results showed that the increased tolerance to low temperatures and dehydration in rd29A plants was attributed to increased levels of expression of different members of the DREB1A regulon. Levels of expression of 69% or 91% for members of the DREB1A regulon that showed up-regulation in rd29A plants were highly correlated with the level of expression of DREB1A in response to low temperature or to dehydration, respectively. These results support the hypothesis that the increased tolerance of rd29A plants to abiotic stresses resulted from elevated expression of the DREB1A regulon.
机译:先前我们曾报道过拟南芥DREB1A 基因在菊花中的表达赋予了其对低温和脱水胁迫的耐受性,而 DREB1A 基因由转基因植物驱动。非生物胁迫诱导型启动子rd29A比35i花椰菜花叶病毒(CaMV)启动子驱动 DREB1A 基因的植物耐受性更高。为了了解这种耐受性提高的分子基础,我们使用抑制消减杂交技术分离了74个DREB1A regulon基因,然后比较了它们在 rd29A:DREB1A 转基因植物(rd29A植物)和 35S中的表达模式:在不同胁迫条件下的DREB1A 转基因植物(35S植物)。我们的结果表明,rd29A植物对低温和脱水的耐受性增强是由于DREB1A regulon不同成员表达水平的提高。在rd29A植物中表达上调的DREB1A regulon成员的表达水平分别为69%或91%与 DREB1A 的表达水平分别与低温或脱水反应高度相关。这些结果支持了这样的假说,即rd29A植物对非生物胁迫的耐受性增强是由于DREB1A regulon的表达升高所致。

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