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酿酒酵母中端粒和HML沉默中Rap1p/Sir3p相互作用的遗传分析。

Genetic analysis of Rap1p/Sir3p interactions in telomeric and HML silencing in Saccharomyces cerevisiae.

作者信息

Liu C, Lustig A J

机构信息

Cornell University, Graduate School of Medical Sciences, New York, New York 10021, USA.

出版信息

Genetics. 1996 May;143(1):81-93. doi: 10.1093/genetics/143.1.81.

Abstract

We have identified three SIR3 suppressors of the telomeric silencing defects conferred by missense mutations within the Rap1p C-terminal tail domain (aa 800-827). Each SIR3 suppressor was also capable of suppressing a rap1 allele (rap1-21), which deletes the 28 aa C-terminal tail domain, but none of the suppressors restored telometric silencing to a 165 amino acid truncation allele. These data suggest a Rap1p site for Sir3p association between the two truncation points (aa 664-799). In SIR3 suppressor strains lacking the Rap1p C-terminal tail domain, the presence of a second intragenic mutation within the rap1s domain (aa 727-747), enhanced silencing 30-300-fold. These data suggest a competition between Sir3p and factors that interfere with silencing for association in the rap1s domain. Rap1-21 strains containing both wild-type Sir3p and either of the Sir3 suppressor proteins displayed a 400-4000-fold increase in telomeric silencing over rap1-21 strains carrying either Sir3p suppressor in the absence of wild-type Sir3p. We propose that this telomere-specific synergism is mediated in part through stabilization of Rap1p/Sir3p telometric complexes by Sir3p-Sir3p interactions.

摘要

我们已经鉴定出三种SIR3抑制子,它们能够抑制由Rap1p C末端尾巴结构域(氨基酸800 - 827)内的错义突变所导致的端粒沉默缺陷。每个SIR3抑制子也能够抑制一个rap1等位基因(rap1 - 21),该等位基因缺失了28个氨基酸的C末端尾巴结构域,但没有一个抑制子能将端粒沉默恢复到一个165个氨基酸截短等位基因的水平。这些数据表明在两个截短点(氨基酸664 - 799)之间存在一个Sir3p与Rap1p结合的位点。在缺乏Rap1p C末端尾巴结构域的SIR3抑制子菌株中,rap1s结构域(氨基酸727 - 747)内第二个基因内突变的存在使沉默增强了30 - 300倍。这些数据表明在rap1s结构域中,Sir3p与干扰沉默的因子之间存在结合竞争。与在没有野生型Sir3p时携带任一Sir3p抑制子的rap1 - 21菌株相比,同时含有野生型Sir3p和任一Sir3抑制子蛋白的Rap1 - 21菌株的端粒沉默增加了400 - 4000倍。我们提出这种端粒特异性协同作用部分是通过Sir3p - Sir3p相互作用稳定Rap1p / Sir3p端粒复合物来介导的。

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