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减数分裂基因表达调控因子对酿酒酵母复制起始和异染色质形成的控制

Control of replication initiation and heterochromatin formation in Saccharomyces cerevisiae by a regulator of meiotic gene expression.

作者信息

Irlbacher Horst, Franke Jacqueline, Manke Thomas, Vingron Martin, Ehrenhofer-Murray Ann E

机构信息

Otto-Warburg-Laboratorium and Department for Computational Molecular Biology, Max-Planck-Institut für Molekulare Genetik, D-14195 Berlin, Germany.

出版信息

Genes Dev. 2005 Aug 1;19(15):1811-22. doi: 10.1101/gad.334805.

Abstract

Heterochromatinization at the silent mating-type loci HMR and HML in Saccharomyces cerevisiae is achieved by targeting the Sir complex to these regions via a set of anchor proteins that bind to the silencers. Here, we have identified a novel heterochromatin-targeting factor for HML, the protein Sum1, a repressor of meiotic genes during vegetative growth. Sum1 bound both in vitro and in vivo to HML via a functional element within the HML-E silencer, and sum1Delta caused HML derepression. Significantly, Sum1 was also required for origin activity of HML-E, demonstrating a role of Sum1 in replication initiation. In a genome-wide search for Sum1-regulated origins, we identified a set of autonomous replicative sequences (ARS elements) that bound both the origin recognition complex and Sum1. Full initiation activity of these origins required Sum1, and their origin activity was decreased upon removal of the Sum1-binding site. Thus, Sum1 constitutes a novel global regulator of replication initiation in yeast.

摘要

酿酒酵母中沉默交配型基因座HMR和HML处的异染色质化是通过一组与沉默子结合的锚定蛋白将Sir复合物靶向这些区域来实现的。在此,我们鉴定出一种针对HML的新型异染色质靶向因子,即蛋白Sum1,它在营养生长期间是减数分裂基因的阻遏物。Sum1在体外和体内都通过HML-E沉默子内的一个功能元件与HML结合,并且sum1Δ导致HML去抑制。值得注意的是,HML-E的起始活性也需要Sum1,这表明Sum1在复制起始中发挥作用。在全基因组范围内搜索Sum1调控的起始位点时,我们鉴定出一组既结合起始识别复合物又结合Sum1的自主复制序列(ARS元件)。这些起始位点的完全起始活性需要Sum1,并且去除Sum1结合位点后它们的起始活性降低。因此,Sum1构成了酵母中复制起始的一种新型全局调节因子。

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