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盐碱胁迫下生长的 Virginiasporobolus 中发育调控的质膜多肽 1(DREPP1)的分离、表达及功能分析

Isolation, expression, and functional analysis of developmentally regulated plasma membrane polypeptide 1 (DREPP1) in Sporobolus virginicus grown under alkali salt stress.

作者信息

Theerawitaya Cattarin, Yamada-Kato Nana, Singh Harminder Pal, Cha-Um Suriyan, Takabe Teruhiro

机构信息

National Center for Genetic Engineering and Biotechnology (BIOTEC), National Science and Technology Development Agency (NSTDA), Pathum Thani, 12120, Thailand.

Research Institute, Meijo University, Tenpaku-ku, Nagoya, Aichi, 468-8502, Japan.

出版信息

Protoplasma. 2018 Sep;255(5):1423-1432. doi: 10.1007/s00709-018-1242-0. Epub 2018 Mar 25.

Abstract

The plant specific DREPP proteins have been shown to bind Ca and regulate the N-myristoylation signaling and microtubule polymerization in Arabidopsis thaliana. The information about DREPP proteins in other plants is, however, scarce. In the present study, we isolated the DREPP gene from a halophytic grass, Sporobolus virginicus, and tested whether the gene was involved in alkaline salt stress responses. The SvDREPP1 was cloned from S. virginicus by RACE methods. The isolated gene showed high homology to DREPP homologs from C grasses, Setaria italica, and Panicum hallii as well as rice (OsDREPP1). The encoded protein contained 202 amino acid residues. It was expressed in E. coli, and its biochemical properties were studied. It was observed that SvDREPP1 was not only Ca-binding protein, but also bind to calmodulin and microtubules. The SvDREPP1 mRNA expression in plants grown under alkaline salt stress was upregulated by 3.5 times over the control in leaf tissues after 48-h treatment, whereas it was increased for 6.0 times in the root tissues at 36 h. The data suggests the importance of SvDREPP1 in regulating alkali salt stress responses in the leaf tissues.

摘要

植物特有的DREPP蛋白已被证明能结合钙离子,并调节拟南芥中的N-肉豆蔻酰化信号传导和微管聚合。然而,关于其他植物中DREPP蛋白的信息却很少。在本研究中,我们从盐生草类植物 Virginiasporobolus 中分离出DREPP基因,并测试该基因是否参与碱性盐胁迫反应。通过RACE方法从 Virginiasporobolus 中克隆出SvDREPP1。分离出的基因与C4禾本科植物狗尾草、哈利稗以及水稻(OsDREPP1)的DREPP同源物具有高度同源性。编码的蛋白质含有202个氨基酸残基。它在大肠杆菌中表达,并对其生化特性进行了研究。观察到SvDREPP1不仅是一种钙结合蛋白,还能与钙调蛋白和微管结合。在碱性盐胁迫下生长的植物中,SvDREPP1 mRNA在叶组织中经48小时处理后表达量比对照上调了3.5倍,而在根组织中36小时时增加了6.0倍。数据表明SvDREPP1在调节叶组织中的碱性盐胁迫反应中具有重要作用。

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