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首页> 外文期刊>Plant Molecular Biology >Organization and expression of two Arabidopsis DREB2 genes encoding DRE-binding proteins involved in dehydration- and high-salinity-responsive gene expression
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Organization and expression of two Arabidopsis DREB2 genes encoding DRE-binding proteins involved in dehydration- and high-salinity-responsive gene expression

机译:组织和表达两个拟南芥DREB2基因的编码与干旱和高盐度响应基因表达有关的DRE结合蛋白的表达。

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摘要

In plants, a cis-acting element, DRE/CRT, is involved in ABA-independent gene expression in response to dehydration and low-temperature stress. To understand signal transduction pathways from perception of the dehydration stress signal to gene expression, we characterized a gene family for DRE/CRT-binding proteins DREB2A and DREB2B in Arabidopsis thaliana. Northern analysis showed that both genes are induced by dehydration and high-salt stress. Organ-specific northern analysis with gene-specific probes showed that these genes are strongly induced in roots by high-salt stress and in stems and roots by dehydration stress. The DREB2A gene is located on chromosome 5, and DREB2B on chromosome 3. We screened an Arabidopsis genomic DNA library with cDNA fragments of DREB2A and DREB2B as probes, and isolated DNA fragments that contained 5'-flanking regions of these genes. Sequence analysis showed that both genes are interrupted by a single intron at identical positions in their leader sequence. Several conserved sequences were found in the promoter regions of both genes. The beta-glucuronidase (GUS) reporter gene driven by the DREB2 promoters was induced by dehydration and high-salt stress in transgenic Arabidopsis plants. [References: 27]
机译:在植物中,顺式作用元件DRE / CRT响应脱水和低温胁迫而与ABA无关的基因表达。为了理解从脱水胁迫信号的感知到基因表达的信号转导途径,我们表征了拟南芥中DRE / CRT结合蛋白DREB2A和DREB2B的基因家族。 Northern分析表明,这两个基因都是由脱水和高盐胁迫诱导的。用基因特异性探针进行的器官特异性Northern分析表明,这些基因在高盐胁迫下强烈诱导根系,而在脱水胁迫下强烈诱导茎和根系。 DREB2A基因位于5号染色体上,DREB2B基因位于3号染色体上。我们用DREB2A和DREB2B的cDNA片段作为探针筛选了拟南芥基因组DNA文库,并分离了包含这些基因5'侧翼区域的DNA片段。序列分析表明,两个基因在其前导序列的相同位置被一个内含子打断。在两个基因的启动子区域中发现了几个保守序列。由DREB2启动子驱动的β-葡萄糖醛酸苷酶(GUS)报告基因是通过脱水和高盐胁迫在转基因拟南芥植物中诱导的。 [参考:27]

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