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微小染色体维持蛋白在减数分裂前DNA复制中的重要作用。

Essential role of MCM proteins in premeiotic DNA replication.

作者信息

Lindner Karola, Gregán Juraj, Montgomery Stuart, Kearsey Stephen E

机构信息

Department of Zoology, University of Oxford, Oxford, OX1 3PS United Kingdom.

出版信息

Mol Biol Cell. 2002 Feb;13(2):435-44. doi: 10.1091/mbc.01-11-0537.

Abstract

A critical event in eukaryotic DNA replication involves association of minichromosome maintenance (MCM2-7) proteins with origins, to form prereplicative complexes (pre-RCs) that are competent for initiation. The ability of mutants defective in MCM2-7 function to complete meiosis had suggested that pre-RC components could be irrelevant to premeiotic S phase. We show here that MCM2-7 proteins bind to chromatin in fission yeast cells preparing for meiosis and during premeiotic S phase in a manner suggesting they in fact are required for DNA replication in the meiotic cycle. This is confirmed by analysis of a degron mcm4 mutant, which cannot carry out premeiotic DNA replication. Later in meiosis, Mcm4 chromatin association is blocked between meiotic nuclear divisions, presumably accounting for the absence of a second round of DNA replication. Together, these results emphasize similarity between replication mechanisms in mitotic and meiotic cell cycles.

摘要

真核生物DNA复制中的一个关键事件涉及微小染色体维持蛋白(MCM2 - 7)与复制起点的结合,以形成能够起始复制的前复制复合体(pre - RCs)。MCM2 - 7功能缺陷的突变体完成减数分裂的能力表明,前复制复合体成分可能与减数分裂前的S期无关。我们在此表明,MCM2 - 7蛋白在裂殖酵母细胞准备减数分裂期间以及减数分裂前S期与染色质结合,其方式表明它们实际上是减数分裂周期中DNA复制所必需的。对一个降解标签mcm4突变体的分析证实了这一点,该突变体无法进行减数分裂前的DNA复制。在减数分裂后期,Mcm4与染色质的结合在减数分裂核分裂之间被阻断,这可能解释了第二轮DNA复制缺失的原因。总之,这些结果强调了有丝分裂和减数分裂细胞周期中复制机制之间的相似性。

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