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减数分裂重组起始的机制与调控

Mechanism and control of meiotic recombination initiation.

作者信息

Keeney S

机构信息

Molecular Biology Program, Memorial Sloan-Kettering Cancer Center, and Weill Graduate School of Medical Sciences of Cornell University, New York, New York 10021, USA.

出版信息

Curr Top Dev Biol. 2001;52:1-53. doi: 10.1016/s0070-2153(01)52008-6.

Abstract

Homologous recombination is essential during meiosis in most sexually reproducing organisms. In budding yeast, and most likely in other organisms as well, meiotic recombination proceeds via the formation and repair of DNA double-strand breaks (DSBs). These breaks appear to be formed by the Spo11 protein, with assistance from a large number of other gene products, by a topoisomerase-like transesterase mechanism. Recent studies in fission yeast, multicellular fungi, flies, worms, plants, and mammals indicate that the role of Spo11 in meiotic recombination initiation is highly conserved. This chapter reviews the properties of Spo11 and the other gene products required for meiotic DSB formation in a number of organisms and discusses ways in which recombination initiation is coordinated with other events occurring in the meiotic cell.

摘要

同源重组在大多数有性生殖生物的减数分裂过程中至关重要。在芽殖酵母中,很可能在其他生物中也是如此,减数分裂重组通过DNA双链断裂(DSB)的形成和修复来进行。这些断裂似乎是由Spo11蛋白在大量其他基因产物的协助下,通过一种拓扑异构酶样转酯酶机制形成的。最近在裂殖酵母、多细胞真菌、果蝇、线虫、植物和哺乳动物中的研究表明,Spo11在减数分裂重组起始中的作用高度保守。本章综述了Spo11以及许多生物中减数分裂DSB形成所需的其他基因产物的特性,并讨论了重组起始与减数分裂细胞中发生的其他事件协调的方式。

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