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利马豆的获得性耐热性及HSP100/ClpB基因的表达

Acquired thermotolerance and expression of the HSP100/ClpB genes of lima bean.

作者信息

Keeler S J, Boettger C M, Haynes J G, Kuches K A, Johnson M M, Thureen D L, Keeler C L, Kitto S L

机构信息

Department of Plant and Soil Sciences, University of Delaware, Newark, Delaware 19717, USA.

出版信息

Plant Physiol. 2000 Jul;123(3):1121-32. doi: 10.1104/pp.123.3.1121.

Abstract

Acquired thermotolerance (AT) is the ability of cells to survive a normally lethal temperature treatment as a consequence of pretreatment at an elevated but sublethal temperature. In yeast and cyanobacteria, the expression of the HSP100/ClpB protein is required for the AT response. To determine whether the HSP100/ClpB protein is associated with this response in lima bean (Phaseolus lunatus), we have cloned an HSP100/ClpB homolog and assessed expression of the two gene copies under heat stress conditions, which induce AT. Transcription of the cytoplasmically localized HSP100/ClpB protein genes is stringently controlled by heat stress in both of the laboratory and field heat stress conditions. From a heat-induced cDNA library, we identified a clone of a putative chloroplast-targeted (cp) HSP100/ClpB protein gene sequence. The cp HSP100/ClpB protein genes are constitutively expressed, but transcript levels increase post-heat stress in laboratory heat stress experiments. In field conditions the genes for the cp HSP100/ClpB are constitutively expressed. Although we were unable to correlate differences in the timing of AT response with the expression or genetic structure of the HSP100/ClpB genes in heat-tolerant or -sensitive varieties of lima bean, we clearly demonstrate the association of expression of HSP100/ClpB proteins with heat response in this species.

摘要

获得性耐热性(AT)是指细胞由于在升高但亚致死温度下进行预处理而能够在通常致死的温度处理中存活的能力。在酵母和蓝细菌中,AT反应需要HSP100/ClpB蛋白的表达。为了确定HSP100/ClpB蛋白是否与利马豆(菜豆)中的这种反应相关,我们克隆了一个HSP100/ClpB同源物,并评估了在诱导AT的热胁迫条件下两个基因拷贝的表达。在实验室和田间热胁迫条件下,细胞质定位的HSP100/ClpB蛋白基因的转录都受到热胁迫的严格控制。从一个热诱导的cDNA文库中,我们鉴定出一个假定的叶绿体靶向(cp)HSP100/ClpB蛋白基因序列的克隆。cp HSP100/ClpB蛋白基因组成性表达,但在实验室热胁迫实验中,转录水平在热胁迫后增加。在田间条件下,cp HSP100/ClpB的基因组成性表达。尽管我们无法将AT反应时间的差异与耐热或敏感利马豆品种中HSP100/ClpB基因的表达或遗传结构相关联,但我们清楚地证明了该物种中HSP100/ClpB蛋白的表达与热反应之间的关联。

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