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首页> 外文期刊>Plant Cell Reports >A cotton (Gossypium hirsutum) DRE-binding transcription factor gene, GhDREB, confers enhanced tolerance to drought, high salt, and freezing stresses in transgenic wheat
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A cotton (Gossypium hirsutum) DRE-binding transcription factor gene, GhDREB, confers enhanced tolerance to drought, high salt, and freezing stresses in transgenic wheat

机译:棉花(陆地棉)DRE结合转录因子基因GhDREB,赋予转基因小麦更高的耐旱,高盐和冰冻胁迫能力

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A cotton (G. hirsutum L.) dehydration responsive element binding protein gene, GhDREB, which encodes a 153 amino acid protein containing a conserved AP2/EREBP domain, was isolated from the cDNA library of cotton cv. Simian 3 by a yeast one-hybrid system. RNA blot analysis showed that the GhDREB gene was induced in cotton seedlings by drought, high salt and cold stresses. An electrophoretic mobility shift assay (EMSA) indicated that the GhDREB protein bound specifically to the DRE core element (A/GCCGAC) in vitro. Two expression vectors containing the GhDREB gene with either of the Ubiqutin or rd29A promoters were constructed and transferred into wheat (Triticum aestivum L.) by bombardment. Fifty-eight Ubi::GhDREB and 17 rd29A::GhDREB T(0) plants of Yangmai (36 plants) and Lumai (39 plants) were identified by PCR analysis, respectively. Southern blot and RT-PCR analyses showed that two or three copies of the GhDREB were integrated into the Yangmai 10 genome and were expressed at the transcriptional level, and three or four copies were integrated into the Lumai 23 genome. Functional analysis indicated that the transgenic plants had improved tolerance to drought, high salt, and freezing stresses through accumulating higher levels of soluble sugar and chlorophyll in leaves after stress treatments. No phenotype differences were observed between transgenic plants and their non-transgenic controls. These results indicated that GhDREB might be useful in improving wheat stress tolerance through genetic engineering.
机译:从棉花cv的cDNA文库中分离出棉花(G. hirsutum L.)脱水响应元件结合蛋白基因GhDREB,该基因编码包含保守的AP2 / EREBP域的153个氨基酸的蛋白。四面3由酵母单杂交系统组成。 RNA印迹分析表明,GhDREB基因是干旱,高盐和冷胁迫在棉花幼苗中诱导的。电泳迁移率迁移分析(EMSA)表明,GhDREB蛋白在体外与DRE核心元件(A / GCCGAC)特异性结合。构建了两个带有带有泛素启动子或rd29A启动子的GhDREB基因的表达载体,并通过轰击将其转移至小麦(Triticum aestivum L.)中。通过PCR分析分别鉴定了Yangmai(36株)和Lumai(39株)的58株Ubi :: GhDREB和17 rd29A :: GhDREB T(0)植物。 Southern印迹和RT-PCR分析表明,将两个或三个拷贝的GhDREB整合到Yangmai 10基因组中并在转录水平表达,并且将三个或四个拷贝的GhDREB整合到Lumai 23基因组中。功能分析表明,转基因植物通过在胁迫处理后在叶片中积累较高水平的可溶性糖和叶绿素,从而提高了对干旱,高盐和冷冻胁迫的耐受性。在转基因植物与其非转基因对照之间未观察到表型差异。这些结果表明,GhDREB可能通过基因工程改善小麦的抗逆性。

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