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酿酒酵母中α2抑制所需基因的鉴定。

Identification of genes required for alpha 2 repression in Saccharomyces cerevisiae.

作者信息

Wahi M, Johnson A D

机构信息

Department of Microbiology, University of California, San Francisco 94143-0502, USA.

出版信息

Genetics. 1995 May;140(1):79-90. doi: 10.1093/genetics/140.1.79.

Abstract

Transcriptional repression of the a-specific genes in Saccharomyces cerevisiae alpha cells involves the concerted action of several proteins. The homeodomian protein alpha 2, together with MCM1, recruits two general transcriptional repressors, SSN6 and TUP1, to the promoters of a-specific genes. SSN6 and TUP1 then mediate repression of the a-specific genes. SIN4, another general negative regulator, is required for this repression, but unlike tup1 or ssn6 deletions, sin4 deletions cause only partial loss of repression. We have screened for other genes required for a-specific gene repression in alpha cells. In addition to recovering multiple alleles of previously identified genes required for this process (referred to as alpha 2 repression), we have identified four other genes, designated ARE1, ARE2, ARE3, and ARE4 (for alpha 2 repression). Recessive mutations in the ARE genes cause partial loss of a-specific gene repression and cause pleiotropic phenotypes similar to those resulting from mutations in SSN6, TUP1, or SIN4, suggesting that the ARE genes are general negative regulators. Based on our initial analysis, we propose that two distinct classes of general negative regulators cooperate to bring about full levels of alpha 2 repression. The sequence of ARE1 revealed that it encodes a CDC28-related protein kinase, identical to UME5, and thus suggests that protein phosphorylation plays a role in alpha 2 repression.

摘要

酿酒酵母α细胞中a特异性基因的转录抑制涉及多种蛋白质的协同作用。同源结构域蛋白α2与MCM1一起,将两种通用转录抑制因子SSN6和TUP1招募到a特异性基因的启动子处。然后,SSN6和TUP1介导a特异性基因的抑制。另一种通用负调控因子SIN4是这种抑制所必需的,但与tup1或ssn6缺失不同,sin4缺失只会导致部分抑制丧失。我们筛选了α细胞中a特异性基因抑制所需的其他基因。除了获得此前鉴定的该过程所需基因(称为α2抑制)的多个等位基因外,我们还鉴定了其他四个基因,命名为ARE1、ARE2、ARE3和ARE4(用于α2抑制)。ARE基因中的隐性突变会导致a特异性基因抑制部分丧失,并导致多效性表型,类似于SSN6、TUP1或SIN4突变所产生的表型,这表明ARE基因是通用负调控因子。基于我们的初步分析,我们提出两类不同的通用负调控因子协同作用以实现α2抑制的完全水平。ARE1的序列显示它编码一种与CDC28相关的蛋白激酶,与UME5相同,因此表明蛋白质磷酸化在α2抑制中起作用。

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