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酿酒酵母中的Sum1p、复制起点识别复合体以及启动子特异性阻遏物的传播

Sum1p, the origin recognition complex, and the spreading of a promoter-specific repressor in Saccharomyces cerevisiae.

作者信息

Lynch Patrick J, Fraser Hunter B, Sevastopoulos Elena, Rine Jasper, Rusche Laura N

机构信息

Department of Biochemistry and Institute for Genome Sciences and Policy, Duke University, 101 Science Drive, Box 3382, Durham, North Carolina 27708, USA.

出版信息

Mol Cell Biol. 2005 Jul;25(14):5920-32. doi: 10.1128/MCB.25.14.5920-5932.2005.

Abstract

In Saccharomyces cerevisiae, Sum1p is a promoter-specific repressor. A single amino acid change generates the mutant Sum1-1p, which causes regional silencing at new loci where wild-type Sum1p does not act. Thus, Sum1-1p is a model for understanding how the spreading of repressive chromatin is regulated. When wild-type Sum1p was targeted to a locus where mutant Sum1-1p spreads, wild-type Sum1p did not spread as efficiently as mutant Sum1-1p did, despite being in the same genomic context. Thus, the SUM1-1 mutation altered the ability of the protein to spread. The spreading of Sum1-1p required both an enzymatically active deacetylase, Hst1p, and the N-terminal tail of histone H4, consistent with the spreading of Sum1-1p involving sequential modification of and binding to histone tails, as observed for other silencing proteins. Furthermore, deletion of the N-terminal tail of H4 caused Sum1-1p to return to loci where wild-type Sum1p acts, consistent with the SUM1-1 mutation increasing the affinity of the protein for H4 tails. These results imply that the spreading of repressive chromatin proteins is regulated by their affinities for histone tails. Finally, this study uncovered a functional connection between wild-type Sum1p and the origin recognition complex, and this relationship also contributes to mutant Sum1-1p localization.

摘要

在酿酒酵母中,Sum1p是一种启动子特异性阻遏物。单个氨基酸的变化产生了突变体Sum1-1p,它会在野生型Sum1p不起作用的新位点导致区域沉默。因此,Sum1-1p是理解抑制性染色质扩散如何被调控的一个模型。当野生型Sum1p被靶向到突变体Sum1-1p扩散的位点时,尽管处于相同的基因组环境中,但野生型Sum1p的扩散效率不如突变体Sum1-1p。因此,SUM1-1突变改变了该蛋白的扩散能力。Sum1-1p的扩散需要一种具有酶活性的脱乙酰酶Hst1p和组蛋白H4的N端尾巴,这与Sum1-1p的扩散涉及对组蛋白尾巴的顺序修饰和结合一致,正如对其他沉默蛋白所观察到的那样。此外,删除H4的N端尾巴会导致Sum1-1p回到野生型Sum1p起作用的位点,这与SUM1-1突变增加了该蛋白对H4尾巴的亲和力一致。这些结果表明,抑制性染色质蛋白的扩散是由它们对组蛋白尾巴的亲和力调控的。最后,这项研究揭示了野生型Sum1p与起源识别复合体之间的功能联系,并且这种关系也有助于突变体Sum1-1p的定位。

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