首页> 外文会议>Proceedings of 2010' International Symposium on forage, turf-grass and biofuel germplasm research. >Cloning and expression analysis of a vacuolar Na+/H+ antiporter gene from Alfalfa
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Cloning and expression analysis of a vacuolar Na+/H+ antiporter gene from Alfalfa

机译:苜蓿液泡状Na + / H +反转运蛋白基因的克隆与表达分析

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A full-length cDNA, named MsNHXl, encoding vacuolar Na+/H+antiporter was cloned from alfalfa (Medicago sativa) , using degenerate primers, followed by 3 ' and 5 RACE. The cDNA sequence was 2225bp long and included an open reading frame encoding a deduced protein of 541 -amino -acid polypeptide. The deduced amino acid sequence showed high similarity (more than 73%) to those of the previously cloned Na+/H+antiporters form Arabidopsis thaliana, Qryza sativa, Atripkx gemlinin, Beta vulgaris and Hordeum vulgare. Southern hybridization showed that MsNHX has only one copy in alfalfa genome. Semiquantitative RT -PCR analysis indicates that the mRNA level of MsNHXl was moderate without stress and markedly up -regulated after treatment by NaCl and ABA (abscisic acid). Those results suggest that the MsNHXl product play an important role in salt tolerance of the alfalfa, and its transcript expression is possibly partially regulated through ABA -dependent signaling pathway.
机译:使用简并引物,随后是3'和5 RACE,从苜蓿(苜蓿)中克隆了编码液泡状Na + / H +反转运蛋白的全长cDNA,称为MsNHX1。 cDNA序列为2225bp长,并且包括编码541-氨基酸多肽的推导蛋白的开放阅读框。推导的氨基酸序列与拟南芥,Qryza sativa,Atripkx gemlinin,Beta vulgaris和大麦(Hordeum vulgare)先前克隆的Na + / H +反向转运蛋白具有高度相似性(超过73%)。 Southern杂交表明,MsNHX在苜蓿基因组中只有一个拷贝。半定量RT-PCR分析表明,MsNHX1的mRNA水平是中等的,没有压力,并且在用NaCl和ABA(脱落酸)处理后显着上调。这些结果表明,MsNHX1产物在紫花苜蓿的耐盐性中起重要作用,并且其转录物表达可能通过ABA依赖性信号传导途径被部分调节。

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