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首页> 外文期刊>Plant Science: An International Journal of Experimental Plant Biology >Molecular cloning of glutamate dehydrogenase genes of Nicotiana plumbaginifolia: structure analysis and regulation of their expression by physiological and stress conditions
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Molecular cloning of glutamate dehydrogenase genes of Nicotiana plumbaginifolia: structure analysis and regulation of their expression by physiological and stress conditions

机译:烟草的谷氨酸脱氢酶基因的分子克隆:生理和胁迫条件下的结构分析及其表达调控

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摘要

Two Nicotiana plumbaginifolia gdh genes (gdhA and gdhB) encoding for NADH dependent glutamate dehydrogenase (GDH) were isolated by PCR and I-PCR (inverse-PCR) and sequenced. The coding sequence is interrupted by eight introns that are located in the same positions in both genes. Computer analysis of the promoter regions of gdhA (650 nt) and gdhB (1800 nt) revealed several conserved motifs and, for gdhB, the presence of an I-Box element known to have light dependent regulatory functions in plants. The response of the gdh genes to carbohydrate deprivation and to ammonium feeding and to various stress conditions (salinity, temperature shifts and heavy metals) was examined in callus culture. The results clearly showed that the carbohydrate status of the cell is the main factor affecting gdh genes expression. Stress condition may depress or increase gdh transcript levels, but theses are not always correlated to the corresponding levels of GDH activity. Altogether these results point to the existence of multiple levels of regulation (transcriptional and post-trariscriptional) of gdh genes
机译:通过PCR和I-PCR(反向PCR)分离编码NADH依赖性谷氨酸脱氢酶(GDH)的两个烟草李子gdh基因(gdhA和gdhB)并测序。编码序列被两个基因中位于相同位置的八个内含子打断。对gdhA(650 nt)和gdhB(1800 nt)启动子区域的计算机分析揭示了几个保守的基序,对于gdhB,存在一个I-Box元件,该元件已知在植物中具有光依赖性调节功能。在愈伤组织培养中检查了gdh基因对碳水化合物剥夺,对铵进食以及对各种胁迫条件(盐度,温度变化和重金属)的响应。结果清楚地表明,细胞的碳水化合物状态是影响gdh基因表达的主要因素。应激条件可能会降低或增加gdh转录水平,但这些并不总是与相应的GDH活性水平相关。总而言之,这些结果表明存在多种水平的gdh基因调控(转录和转录后)

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