Mre11复合物在S期晚期的特异性募集触发酿酒酵母端粒复制蛋白的分级组装。

Late S phase-specific recruitment of Mre11 complex triggers hierarchical assembly of telomere replication proteins in Saccharomyces cerevisiae.

作者信息

Takata Hideki, Tanaka Yayoi, Matsuura Akira

机构信息

Department of Geriatric Research, National Institute for Longevity Sciences, Obu, Aichi 474-8522, Japan.

出版信息

Mol Cell. 2005 Feb 18;17(4):573-83. doi: 10.1016/j.molcel.2005.01.014.

Abstract

In Saccharomyces cerevisiae, telomere replication occurs in late S phase and is accompanied by dynamic remodeling of its protein components. Here, we show that MRX (Mre11-Rad50-Xrs2), an evolutionarily conserved protein complex involved in DNA double-strand break (DSB) repair, is recruited to the telomeres in late S phase. MRX is required for the late S phase-specific recruitment of ATR-like kinase Mec1 to the telomeres. Mec1, in turn, contributes to the assembly of the telomerase regulators Cdc13 and Est1 at the telomere ends. Our results provide a model for the hierarchical assembly of telomere-replication proteins in late S phase; this involves triggering by the loading of MRX onto the chromosome termini. The recruitment of DNA repair-related proteins to the telomeres at particular times in the cell cycle suggests that the normal terminus of a chromosome is recognized as a DSB during the course of replication.

摘要

在酿酒酵母中,端粒复制发生在S期晚期,并伴随着其蛋白质组分的动态重塑。在此,我们表明MRX(Mre11-Rad50-Xrs2),一种参与DNA双链断裂(DSB)修复的进化保守蛋白复合物,在S期晚期被招募到端粒。MRX是S期晚期ATR样激酶Mec1特异性招募到端粒所必需的。反过来,Mec1有助于端粒酶调节因子Cdc13和Est1在端粒末端的组装。我们的结果提供了一个S期晚期端粒复制蛋白分级组装的模型;这涉及通过将MRX加载到染色体末端来触发。在细胞周期的特定时间将DNA修复相关蛋白招募到端粒表明,染色体的正常末端在复制过程中被识别为DSB。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索