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从菜豆(Phaseolus vulgaris L.)中克隆编码应激诱导蛋白磷酸酶1(PP1)催化亚基的cDNA的分子克隆。

Molecular cloning of the cDNA encoding a stress-inducible protein phosphatase 1 (PP1) catalytic subunit from French bean (Phaseolus vulgaris L.).

作者信息

Zimmerlin A, Jupe S C, Bolwell G P

机构信息

Dept of Biochemistry, Royal Holloway and Bedford New College, University of London, Egham, Survey, UK.

出版信息

Plant Mol Biol. 1995 Jun;28(3):363-8. doi: 10.1007/BF00020386.

Abstract

A cDNA showing high sequence similarity (> 70%) to plant protein phosphatase 1 catalytic subunit variants from other species has been isolated from a cDNA library derived from mRNAs expressed in elicitor-treated suspension-cultured cells. The clone appears to be a near full-length 1431 bp with a 172 bp 5'-untranslated region and a 317 bp 3'-untranslated region. The open reading frame, determined by sequence similarity, codes for a protein with predicted M(r) of 35,552. Alternatively an ATG situated to the 5' end of the putative start site would increase the protein size by 6 amino acids. The mRNA for Pvpp1 was shown to be rapidly induced by elicitor treatment of suspension-cultured cells of French bean. The cloned cDNA represents one of the few examples of a gene product that is probably involved in dephosphorylation events arising after the initial responses to biotic stress.

摘要

从激发子处理的悬浮培养细胞中表达的mRNA构建的cDNA文库中,分离出了一个与其他物种的植物蛋白磷酸酶1催化亚基变体具有高度序列相似性(> 70%)的cDNA。该克隆似乎是一个近全长的1431 bp,具有172 bp的5'-非翻译区和317 bp的3'-非翻译区。通过序列相似性确定的开放阅读框编码一个预测分子量为35,552的蛋白质。另外,位于推定起始位点5'端的一个ATG会使蛋白质大小增加6个氨基酸。研究表明,菜豆悬浮培养细胞经激发子处理后,Pvpp1的mRNA会迅速被诱导。克隆的cDNA代表了少数几个可能参与生物胁迫初始反应后去磷酸化事件的基因产物实例之一。

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