首页> 外文OA文献 >CHARACTERIZATION OF A DRE-BINDING TRANSCRIPTION FACTOR FROM ASPARAGUS (ASPARAGUS OFFICINALIS L.) AND ITS OVEREXPRESSION IN ARABIDOPSIS RESULTING IN SALT- AND DROUGHT-RESISTANT TRANSGENIC PLANTS
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CHARACTERIZATION OF A DRE-BINDING TRANSCRIPTION FACTOR FROM ASPARAGUS (ASPARAGUS OFFICINALIS L.) AND ITS OVEREXPRESSION IN ARABIDOPSIS RESULTING IN SALT- AND DROUGHT-RESISTANT TRANSGENIC PLANTS

机译:芦笋(aspaRaGUs OFFICINaLIs L.)一种与DaR结合的转录因子的特征及其在耐盐和抗旱转基因植物中的过度表达

摘要

A new full-length cDNA encoding an AP2/EREBP domain-containing transcription factor named AoDREB was isolated from Asparagus officinalis L. using the RACE-PCR method. It is a homolog to the dehydration-responsive element binding protein (DREB) and classified to the A6 subgroup of the DREB subfamily. Using the yeast one-hybrid system, we conducted a DRE binding assay and demonstrated that AoDREB can bind the DRE element specifically. A transcriptional activity assay showed that AoDREB is a transcription factor capable of activating expression of the reporter gene in yeast. RT-PCR analysis revealed that expression of the AoDREB gene is induced under 20% PEG and high salinity stress, whereas no obvious response to low temperature was observed. Overexpression of AoDREB in transgenic Arabidopsis caused no growth retardation and induced stronger expression of the target genes, including RD29A and COR15A, than in wild type, resulting in increased tolerance of transgenic Arabidopsis to drought and high salinity. These results suggest that introduction of an exogenous AoDREB into plants is an effective way to improve plant drought and salinity tolerance.
机译:使用RACE-PCR方法从芦笋中分离出一种新的全长cDNA,编码包含AP2 / EREBP域的转录因子AoDREB。它是脱水反应元件结合蛋白(DREB)的同源物,归类为DREB亚家族的A6亚组。使用酵母单杂交系统,我们进行了DRE结合测定,并证明AoDREB可以特异性结合DRE元件。转录活性分析表明,AoDREB是能够激活酵母中报道基因表达的转录因子。 RT-PCR分析表明,在20%PEG和高盐度胁迫下诱导了AoDREB基因的表达,而未观察到对低温的明显反应。与野生型相比,AoDREB在转基因拟南芥中的过表达不会引起生长迟缓,并且不会诱导包括RD29A和COR15A在内的目标基因表达,从而提高了转基因拟南芥对干旱和高盐度的耐受性。这些结果表明,将外源AoDREB引入植物是改善植物干旱和盐分耐受性的有效方法。

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