Suppr超能文献

酵母鸟嘌呤核苷酸交换因子Rom2p的PH结构域在体内发挥着重要功能。

The PH domain of the yeast GEF Rom2p serves an essential function in vivo.

作者信息

Lorberg A, Jacoby J J, Schmitz H P, Heinisch J J

机构信息

Institut für Mikrobiologie, Heinrich-Heine-Universität Düsseldorf, Universitätsstr.1, Geb. 26.12, D-40225 Düsseldorf, Germany.

出版信息

Mol Genet Genomics. 2001 Nov;266(3):505-13. doi: 10.1007/s004380100579.

Abstract

In a screen designed to identify new upstream components of the Pkc1p-MAP kinase signal transduction pathway that responds to cell wall damage in yeast, we identified a new mutant allele of the ROM2 gene, which encodes a GDP/GTP exchange factor that acts on Rho1p. This allele, originally termed ubk1 (upstream of Bck1p) encodes a truncated protein that lacks the putative PH domain. Complementation experiments showed that genes coding for several known components of the pathway are able to suppress the ubk1 mutation to various degrees when introduced on low- or high-copy-number vectors. Analysis of several rom2 mutants showed that mutants in which the PH domain is deleted result in a phenotype indistinguishable from that of a strain deleted for the entire gene, indicating that this domain fulfills an essential function in vivo. Furthermore, we found that the growth phenotype of rom2 mutants is highly dependent on the strain background. Surprisingly, analysis of the phosphorylation status of Mpk1p in these mutants showed an elevated level of doubly phosphorylated Mpk1 protein, indicating that the growth defect of rom2 mutants is not due to an inability to activate the MAP kinase module, but rather to lack of a function of the Rom2 protein that has yet to be identified precisely.

摘要

在一项旨在鉴定参与酵母细胞壁损伤应答的Pkc1p-丝裂原活化蛋白激酶信号转导途径新上游组分的筛选中,我们鉴定出ROM2基因的一个新突变等位基因,该基因编码一种作用于Rho1p的鸟苷二磷酸/鸟苷三磷酸交换因子。这个等位基因最初被命名为ubk1(Bck1p上游),编码一种缺失假定PH结构域的截短蛋白。互补实验表明,当将编码该途径几个已知组分的基因导入低拷贝或高拷贝载体时,它们能够不同程度地抑制ubk1突变。对几个rom2突变体的分析表明,缺失PH结构域的突变体产生的表型与整个基因缺失的菌株无法区分,这表明该结构域在体内发挥着重要功能。此外,我们发现rom2突变体的生长表型高度依赖于菌株背景。令人惊讶的是,对这些突变体中Mpk1p磷酸化状态的分析显示,双磷酸化Mpk1蛋白水平升高,这表明rom2突变体的生长缺陷不是由于无法激活丝裂原活化蛋白激酶模块,而是由于Rom2蛋白缺乏尚未精确鉴定的功能。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验