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错配修复,但不是异源双链体排斥,与 DNA 复制在时间上偶联。

Mismatch repair, but not heteroduplex rejection, is temporally coupled to DNA replication.

机构信息

Ludwig Institute for Cancer Research, Departments of Medicine and Cellular and Molecular Medicine and Cancer Center, Moores-UCSD Cancer Center, University of California School of Medicine-San Diego, 9500 Gilman Drive, La Jolla, CA 92093-0669, USA.

出版信息

Science. 2011 Dec 23;334(6063):1713-6. doi: 10.1126/science.1210770.

Abstract

In eukaryotes, it is unknown whether mismatch repair (MMR) is temporally coupled to DNA replication and how strand-specific MMR is directed. We fused Saccharomyces cerevisiae MSH6 with cyclins to restrict the availability of the Msh2-Msh6 mismatch recognition complex to either S phase or G2/M phase of the cell cycle. The Msh6-S cyclin fusion was proficient for suppressing mutations at three loci that replicate at mid-S phase, whereas the Msh6-G2/M cyclin fusion was defective. However, the Msh6-G2/M cyclin fusion was functional for MMR at a very late-replicating region of the genome. In contrast, the heteroduplex rejection function of MMR during recombination was partially functional during both S phase and G2/M phase. These results indicate a temporal coupling of MMR, but not heteroduplex rejection, to DNA replication.

摘要

在真核生物中,尚不清楚错配修复 (MMR) 是否与 DNA 复制具有时间相关性,以及链特异性 MMR 是如何定向的。我们将酿酒酵母 MSH6 与细胞周期蛋白融合,将 Msh2-Msh6 错配识别复合物的可用性限制在细胞周期的 S 期或 G2/M 期。Msh6-S 细胞周期蛋白融合在抑制三个在中 S 期复制的基因座的突变方面非常有效,而 Msh6-G2/M 细胞周期蛋白融合则有缺陷。然而,Msh6-G2/M 细胞周期蛋白融合在基因组的一个很晚复制的区域具有 MMR 功能。相比之下,在 S 期和 G2/M 期,MMR 的异源双链体排斥功能部分发挥作用。这些结果表明 MMR 与 DNA 复制具有时间相关性,但异源双链体排斥功能没有。

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