Gao Shi-Qing, Chen Ming, Xia Lian-Qin, Xiu Hui-Jun, Xu Zhao-Shi, Li Lian-Cheng, Zhao Chang-Ping, Cheng Xian-Guo, Ma You-Zhi
National Key Facility for Crop Genetic Resources and Genetic Improvement, Key Laboratory of Crop Genetics and Breeding, Ministry of Agriculture, Institute of Crop Science, Chinese Academy of Agricultural Sciences, Beijing, China.
Plant Cell Rep. 2009 Feb;28(2):301-11. doi: 10.1007/s00299-008-0623-9. Epub 2008 Nov 13.
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.
从棉花品种泗棉3的cDNA文库中,通过酵母单杂交系统分离出一个棉花(陆地棉)脱水响应元件结合蛋白基因GhDREB,该基因编码一个含有保守AP2/EREBP结构域的153个氨基酸的蛋白质。RNA印迹分析表明,GhDREB基因在棉花幼苗中受干旱、高盐和低温胁迫诱导。电泳迁移率变动分析(EMSA)表明,GhDREB蛋白在体外能特异性结合DRE核心元件(A/GCCGAC)。构建了两个分别含有由泛素或rd29A启动子驱动的GhDREB基因的表达载体,并通过轰击法将其转入小麦(普通小麦)。通过PCR分析分别鉴定出58株扬麦(36株)和17株鲁麦(39株)的Ubi::GhDREB和rd29A::GhDREB T(0)植株。Southern印迹和RT-PCR分析表明,两个或三个拷贝的GhDREB整合到扬麦10基因组中并在转录水平表达,三个或四个拷贝整合到鲁麦23基因组中。功能分析表明,胁迫处理后,转基因植株通过在叶片中积累更高水平的可溶性糖和叶绿素,提高了对干旱、高盐和冷冻胁迫的耐受性。转基因植株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可能有助于通过基因工程提高小麦的胁迫耐受性。