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修复停滞或受损的复制叉。

Rescuing stalled or damaged replication forks.

机构信息

Molecular Biology Program, Memorial Sloan-Kettering Cancer Center, New York, NY 10065, USA.

出版信息

Cold Spring Harb Perspect Biol. 2013 May 1;5(5):a012815. doi: 10.1101/cshperspect.a012815.

Abstract

In recent years, an increasing number of studies have shown that prokaryotes and eukaryotes are armed with sophisticated mechanisms to restart stalled or collapsed replication forks. Although these processes are better understood in bacteria, major breakthroughs have also been made to explain how fork restart mechanisms operate in eukaryotic cells. In particular, repriming on the leading strand and fork regression are now established as critical for the maintenance and recovery of stalled forks in both systems. Despite the lack of conservation between the factors involved, these mechanisms are strikingly similar in eukaryotes and prokaryotes. However, they differ in that fork restart occurs in the context of chromatin in eukaryotes and is controlled by multiple regulatory pathways.

摘要

近年来,越来越多的研究表明,原核生物和真核生物都拥有复杂的机制来重新启动停滞或崩溃的复制叉。虽然这些过程在细菌中得到了更好的理解,但也取得了重大突破,解释了叉重新启动机制在真核细胞中是如何运作的。特别是,在领头链上的重新启动和叉回归现在被认为是在两个系统中维持和恢复停滞叉的关键。尽管涉及的因素之间没有保守性,但这些机制在真核生物和原核生物中非常相似。然而,它们也有不同之处,即叉重新启动发生在真核生物染色质的背景下,并受到多个调节途径的控制。

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本文引用的文献

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Translesion DNA polymerases.跨损伤 DNA 聚合酶。
Cold Spring Harb Perspect Biol. 2013 Oct 1;5(10):a010363. doi: 10.1101/cshperspect.a010363.
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Regulating DNA replication in plants.调控植物中的 DNA 复制。
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