Takata Hideki, Tanaka Yayoi, Matsuura Akira
Department of Geriatric Research, National Institute for Longevity Sciences, Obu, Aichi 474-8522, Japan.
Mol Cell. 2005 Feb 18;17(4):573-83. doi: 10.1016/j.molcel.2005.01.014.
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.
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。