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拟南芥中一个受脱落酸、脱水、高盐和冷处理快速诱导的类受体蛋白激酶基因的鉴定

Identification of a receptor-like protein kinase gene rapidly induced by abscisic acid, dehydration, high salt, and cold treatments in Arabidopsis thaliana.

作者信息

Hong S W, Jon J H, Kwak J M, Nam H G

机构信息

Department of Life Science, School of Environmental Engineering, Pohang University of Science and Technology, Kyungbuk, South Korea.

出版信息

Plant Physiol. 1997 Apr;113(4):1203-12. doi: 10.1104/pp.113.4.1203.

Abstract

A cDNA clone for a receptor-like protein kinase gene (RPK1) was isolated from Arabidopsis thaliana. The clone is 1952 bp long with 1623 bp of an open reading frame encoding a peptide of 540 amino acids. The deduced peptide (RPK1) contains four distinctive domains characteristic of receptor kinases: (a) a putative amino-terminal signal sequence domain; (b) a domain with five extracellular leucine-rich repeat sequences; (c) a membrane-spanning domain; and (d) a cytoplasmic protein kinase domain that contains all of the 11 subdomains conserved among protein kinases. The RPK1 gene is expressed in flowers, stems, leaves, and roots. Expression of the RPK1 gene is induced within 1 h after treatment with abscisic acid (ABA). The gene is also rapidly induced by several environmental stresses such as dehydration, high salt, and low temperature, suggesting that the gene is involved in a general stress response. The dehydration-induced expression is not impaired in aba-1, abi1-1, abi2-1, and abi3-1 mutants, suggesting that the dehydration-induced expression of the RPK1 gene is ABA-independent. A possible role of this gene in the signal transduction pathway of ABA and the environmental stresses is discussed.

摘要

从拟南芥中分离出一个类受体蛋白激酶基因(RPK1)的cDNA克隆。该克隆长1952 bp,有1623 bp的开放阅读框,编码一个含540个氨基酸的肽段。推导的肽段(RPK1)含有受体激酶特有的四个不同结构域:(a)一个假定的氨基末端信号序列结构域;(b)一个具有五个细胞外富亮氨酸重复序列的结构域;(c)一个跨膜结构域;以及(d)一个细胞质蛋白激酶结构域,该结构域包含蛋白激酶中保守的所有11个亚结构域。RPK1基因在花、茎、叶和根中表达。用脱落酸(ABA)处理后1小时内,RPK1基因的表达被诱导。该基因也能被脱水、高盐和低温等几种环境胁迫快速诱导,表明该基因参与一般胁迫反应。在aba - 1、abi1 - 1、abi2 - 1和abi3 - 1突变体中,脱水诱导的表达没有受损,这表明RPK1基因的脱水诱导表达不依赖ABA。本文讨论了该基因在ABA信号转导途径和环境胁迫中的可能作用。

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