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减数分裂重组:一种追踪和消除突变的机制?

Meiotic recombination: a mechanism for tracking and eliminating mutations?

作者信息

McKee B D

机构信息

Department of Biochemistry and Molecular and Cellular Biology, University of Tennessee, Knoxville 37996, USA.

出版信息

Bioessays. 1996 May;18(5):411-9. doi: 10.1002/bies.950180511.

DOI:10.1002/bies.950180511
PMID:8639164
Abstract

The function of meiotic recombination has remained controversial, despite recent inroads into mechanisms. Ideas concerning a possible role of recombination in the elimination or efficient incorporation of mutations have been backed by theoretical studies but have lacked empirical support. Recent investigations into the basis for local variations in recombination frequency in yeast have uncovered a strong association between recombination initiation sites and transcriptional regulatory sequences. Other recent studies indicate a strong correlation between transcription and mutation rates in yeast genes. Taken together, these data imply that distributions of recombination and mutation frequencies may be strongly correlated. This suggests that recombination may be targeted to genomic sites of high mutation frequency; such a 'mutation-tracking' function would clearly aid in the shuffling of mutations to break up unfavorable and create favorable allelic combinations. Moreover, recent insights into the mechanism of gene conversion in yeast reveal a very strong inherent bias in favor of alleles on the non-initiating homolog. Combined with mutation tracking, these findings suggest a novel and general mechanism by which allelic gene conversion may act to eliminate mutations.

摘要

尽管最近在减数分裂重组机制方面取得了进展,但其功能仍存在争议。关于重组在消除或有效整合突变中可能发挥的作用的观点,得到了理论研究的支持,但缺乏实证依据。最近对酵母中重组频率局部变异基础的研究发现,重组起始位点与转录调控序列之间存在强烈关联。其他近期研究表明,酵母基因中的转录与突变率之间存在很强的相关性。综合这些数据表明,重组频率和突变频率的分布可能密切相关。这表明重组可能靶向高突变频率的基因组位点;这样一种“突变追踪”功能显然有助于突变的洗牌,以打破不利组合并创造有利的等位基因组合。此外,最近对酵母基因转换机制的深入了解揭示了一种非常强烈的固有偏向,即有利于非起始同源染色体上的等位基因。结合突变追踪,这些发现提示了一种新的通用机制,等位基因基因转换可能通过该机制来消除突变。

相似文献

1
Meiotic recombination: a mechanism for tracking and eliminating mutations?减数分裂重组:一种追踪和消除突变的机制?
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2
Molecular mechanisms of recombination in Saccharomyces cerevisiae: testing mitotic and meiotic models by analysis of hypo-rec and hyper-rec mutations.酿酒酵母中重组的分子机制:通过分析低重组和高重组突变来检验有丝分裂和减数分裂模型。
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The influence of sequence divergence between alleles of the human MS205 minisatellite incorporated into the yeast genome on length-mutation rates and lethal recombination events during meiosis.整合到酵母基因组中的人类MS205微卫星等位基因间序列差异对减数分裂期间长度突变率和致死性重组事件的影响。
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Effects of mismatch repair and Hpr1 on transcription-stimulated mitotic recombination in the yeast Saccharomyces cerevisiae.错配修复和Hpr1对酿酒酵母中转录刺激的有丝分裂重组的影响。
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The yeast MSH1 gene is not involved in DNA repair or recombination during meiosis.酵母MSH1基因在减数分裂过程中不参与DNA修复或重组。
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Can tetraplex recombination models explain observations in induced mitotic gene conversion?四重重组模型能否解释诱导有丝分裂基因转换中的观察结果?
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Meiotic instability of human minisatellite CEB1 in yeast requires DNA double-strand breaks.人类小卫星CEB1在酵母中的减数分裂不稳定性需要DNA双链断裂。
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[Mechanisms and control of meiotic recombination in the yeast Saccharomyces cerevisiae].[酿酒酵母减数分裂重组的机制与调控]
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Mechanisms of human minisatellite mutation in yeast.酵母中人类微卫星突变的机制。
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The signal from the initiation of meiotic recombination to the first division of meiosis.从减数分裂重组起始到减数第一次分裂的信号。
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引用本文的文献

1
Persistence and loss of meiotic recombination hotspots.减数分裂重组热点的持续性与丧失
Genetics. 2005 Apr;169(4):2319-33. doi: 10.1534/genetics.104.034363. Epub 2005 Jan 31.
2
The hotspot conversion paradox and the evolution of meiotic recombination.热点转换悖论与减数分裂重组的进化
Proc Natl Acad Sci U S A. 1997 Jul 22;94(15):8058-63. doi: 10.1073/pnas.94.15.8058.
3
The extent, mechanism, and consequences of genetic variation, for recombination rate.基因变异在重组率方面的程度、机制及后果。
Am J Hum Genet. 1996 Dec;59(6):1175-83.