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酿酒酵母中由钙调神经磷酸酶/Crz1p信号通路调控的基因表达的全基因组分析。

Genome-wide analysis of gene expression regulated by the calcineurin/Crz1p signaling pathway in Saccharomyces cerevisiae.

作者信息

Yoshimoto Hiroyuki, Saltsman Kirstie, Gasch Audrey P, Li Hong Xia, Ogawa Nobuo, Botstein David, Brown Patrick O, Cyert Martha S

机构信息

Department of Biological Sciences, Stanford University, 371 Serra Mall, Stanford, CA 94305-5020, USA.

出版信息

J Biol Chem. 2002 Aug 23;277(34):31079-88. doi: 10.1074/jbc.M202718200. Epub 2002 Jun 10.

Abstract

In Saccharomyces cerevisiae, the Ca(2+)/calmodulin-dependent protein phosphatase, calcineurin, is activated by specific environmental conditions, including exposure to Ca(2+) and Na(+), and induces gene expression by regulating the Crz1p/Tcn1p transcription factor. We used DNA microarrays to perform a comprehensive analysis of calcineurin/Crz1p-dependent gene expression following addition of Ca(2+) (200 mm) or Na(+) (0.8 m) to yeast. 163 genes exhibited increased expression that was reduced 50% or more by calcineurin inhibition. These calcineurin-dependent genes function in signaling pathways, ion/small molecule transport, cell wall maintenance, and vesicular transport, and include many open reading frames of previously unknown function. Three distinct gene classes were defined as follows: 28 genes displayed calcineurin-dependent induction in response to Ca(2+) and Na(+), 125 showed calcineurin-dependent expression following Ca(2+) but not Na(+) addition, and 10 were regulated by calcineurin in response to Na(+) but not Ca(2+). Analysis of crz1Delta cells established Crz1p as the major effector of calcineurin-regulated gene expression in yeast. We identified the Crz1p-binding site as 5'-GNGGC(G/T)CA-3' by in vitro site selection. A similar sequence, 5'-GAGGCTG-3', was identified as a common sequence motif in the upstream regions of calcineurin/ Crz1p-dependent genes. This finding is consistent with direct regulation of these genes by Crz1p.

摘要

在酿酒酵母中,Ca(2+)/钙调蛋白依赖性蛋白磷酸酶钙调神经磷酸酶可被特定环境条件激活,包括暴露于Ca(2+)和Na(+),并通过调节Crz1p/Tcn1p转录因子诱导基因表达。我们使用DNA微阵列对向酵母中添加Ca(2+)(200 mM)或Na(+)(0.8 M)后钙调神经磷酸酶/Crz1p依赖性基因表达进行了全面分析。163个基因表现出表达增加,而钙调神经磷酸酶抑制可使其表达降低50%或更多。这些钙调神经磷酸酶依赖性基因在信号通路、离子/小分子转运、细胞壁维持和囊泡转运中发挥作用,并且包括许多功能未知的开放阅读框。定义了三个不同的基因类别如下:28个基因在响应Ca(2+)和Na(+)时表现出钙调神经磷酸酶依赖性诱导,125个在添加Ca(2+)后而非添加Na(+)后表现出钙调神经磷酸酶依赖性表达,10个在响应Na(+)而非Ca(2+)时受钙调神经磷酸酶调节。对crz1Delta细胞的分析确定Crz1p是酵母中钙调神经磷酸酶调节基因表达的主要效应物。我们通过体外位点选择将Crz1p结合位点鉴定为5'-GNGGC(G/T)CA-3'。一个相似序列5'-GAGGCTG-3'被鉴定为钙调神经磷酸酶/Crz1p依赖性基因上游区域中的一个共同序列基序。这一发现与Crz1p对这些基因的直接调节一致。

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