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二色补血草液泡膜H~+-ATP酶C亚基(LbVHA-C)基因克隆和表达分析
Cloning and Expression Analysis of LbVHA-C Gene from Limonium bicolor (Bunge) Kuntze
【摘要】 从二色补血草cDNA文库中分离出一个V-H+-ATP酶C亚基(LbVHA-C)基因全长cDNA序列。该基因全长为729bp。其中,开放读码框(ORF)为498bp,编码165个氨基酸,预测编码蛋白的分子量为16.6kDa,理论等电点为8.62。用实时定量RT-PCR方法进一步研究二色补血草在NaCl、NaHCO3和NaCO3胁迫下的不同时间内该基因表达模式的结果表明,NaCl强烈诱导二色补血草叶组织中LbVHA-C基因的表达,但其根部的表达变化不明显。NaHCO3胁迫下LbVHA-C基因在根部组织的表达受抑制。Na2CO3胁迫24h时的LbVHA-C基因在根和叶部组织中的表达都强烈受抑制,随后在根和叶组织的表达量逐步升高。
【Abstract】 A novel vacuolar H+-ATPase gene (LbVHA-C) was cloned from a cDNA library of Limonium bicolor. Sequence analysis showed that the LbVHA-C gene was 729 bp in length, including 498 bp of open reading frame (ORF), and encodes a protein of 165 amino acids with a predicted molecular mass of 16.6 kDa and pI of 8.62. The expression of LbVHA-C gene of L. bicolor in response to NaCl, NaHCO3 and Na2CO3 were investi-gated by real-time RT-PCR. The result showed that the expression of LbVHA-C gene was strongly induced by NaCl in leaves of L. bicolor, but not highly changed in roots. Under NaHCO3 stress, the expression of LbVHA-C gene was inhibited in roots. And the expression of LbVHA-C gene were also strongly inhibited in both roots and leaves under NaCO3 stress for 24 h, then the expression increased.
【Key words】 Limonium bicolor; vacuolar H+-ATPase gene (LbVHA-C); real time RT-PCR; gene expression;
- 【文献出处】 植物生理学通讯 ,Plant Physiology Communications , 编辑部邮箱 ,2009年12期
- 【分类号】S688.4
- 【被引频次】6
- 【下载频次】171