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减数分裂双链断裂和哺乳动物重组的控制。

Meiotic DSBs and the control of mammalian recombination.

机构信息

The Jackson Laboratory, Bar Harbor, ME 04609, USA.

出版信息

Cell Res. 2012 Dec;22(12):1624-6. doi: 10.1038/cr.2012.109. Epub 2012 Jul 17.

DOI:10.1038/cr.2012.109
PMID:22801475
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3515751/
Abstract

The laboratories of Galina Petukhova and R Daniel Camerini-Otero have achieved significant technical advances in determining the genome-wide sites of DNA double-strand breaks (DSBs) where the process of genetic exchange between chromatids during meiosis begins. Applying the new approaches to male meiosis in mice, their experimental results considerably increase our insights into the nature and regulation of these processes.

摘要

加利娜·彼得科娃(Galina Petukhova)和 R 丹尼尔·卡梅里尼-奥特罗(R Daniel Camerini-Otero)的实验室在确定染色体在减数分裂过程中发生遗传交换的 DNA 双链断裂(DSBs)的全基因组位点方面取得了重大技术进展。他们将新方法应用于雄性减数分裂的小鼠实验中,实验结果大大提高了我们对这些过程的本质和调控的认识。

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1
Meiotic DSBs and the control of mammalian recombination.减数分裂双链断裂和哺乳动物重组的控制。
Cell Res. 2012 Dec;22(12):1624-6. doi: 10.1038/cr.2012.109. Epub 2012 Jul 17.
2
The Landscape of Mouse Meiotic Double-Strand Break Formation, Processing, and Repair.小鼠减数分裂双链断裂的形成、处理及修复全景
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3
PRDM9 and Its Role in Genetic Recombination.PRDM9 及其在基因重组中的作用。
Trends Genet. 2018 Apr;34(4):291-300. doi: 10.1016/j.tig.2017.12.017. Epub 2018 Jan 21.
4
Scale matters: the spatial correlation of yeast meiotic DNA breaks with histone H3 trimethylation is driven largely by independent colocalization at promoters.尺度很重要:酵母减数分裂 DNA 断裂与组蛋白 H3 三甲基化的空间相关性主要是由启动子处的独立共定位驱动的。
Cell Cycle. 2012 Apr 15;11(8):1496-503. doi: 10.4161/cc.19733.
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PRDM9 Methyltransferase Activity Is Essential for Meiotic DNA Double-Strand Break Formation at Its Binding Sites.PRDM9 甲基转移酶活性对于其结合位点处减数分裂 DNA 双链断裂的形成是必不可少的。
Mol Cell. 2018 Mar 1;69(5):853-865.e6. doi: 10.1016/j.molcel.2018.01.033. Epub 2018 Feb 22.
6
Spp1, a member of the Set1 Complex, promotes meiotic DSB formation in promoters by tethering histone H3K4 methylation sites to chromosome axes.Spp1,Set1 复合物的一个成员,通过将组蛋白 H3K4 甲基化位点连接到染色体轴上,促进了启动子中的减数分裂 DSB 形成。
Mol Cell. 2013 Jan 10;49(1):43-54. doi: 10.1016/j.molcel.2012.11.008. Epub 2012 Dec 13.
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ZCWPW1 is recruited to recombination hotspots by PRDM9 and is essential for meiotic double strand break repair.ZCWPW1 通过 PRDM9 招募到重组热点,对于减数分裂双链断裂修复至关重要。
Elife. 2020 Aug 3;9:e53392. doi: 10.7554/eLife.53392.
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Meiotic recombination in mammals: localization and regulation.哺乳动物减数分裂重组:定位与调控。
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Meiotic recombination cold spots in chromosomal cohesion sites.染色体黏连位点处的减数分裂重组冷点。
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Dual histone methyl reader ZCWPW1 facilitates repair of meiotic double strand breaks in male mice.ZCWPW1 作为双重组蛋白甲基化阅读器,可促进雄性小鼠减数分裂双链断裂的修复。
Elife. 2020 Apr 30;9:e53360. doi: 10.7554/eLife.53360.

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A high-resolution map of non-crossover events reveals impacts of genetic diversity on mammalian meiotic recombination.高分辨率非交叉事件图谱揭示了遗传多样性对哺乳动物减数分裂重组的影响。
Nat Commun. 2019 Aug 29;10(1):3900. doi: 10.1038/s41467-019-11675-y.
3
Meiotic recombination in mammals: localization and regulation.哺乳动物减数分裂重组:定位与调控。
Nat Rev Genet. 2013 Nov;14(11):794-806. doi: 10.1038/nrg3573.

本文引用的文献

1
Genetic recombination is directed away from functional genomic elements in mice.遗传重组在小鼠中被定向远离功能基因组元件。
Nature. 2012 May 13;485(7400):642-5. doi: 10.1038/nature11089.
2
Clusters of ancestrally related genes that show paralogy in whole or in part are a major feature of the genomes of humans and other species.在人类和其他物种的基因组中,具有部分或全部同源关系的祖先相关基因簇是一个主要特征。
PLoS One. 2012;7(4):e35274. doi: 10.1371/journal.pone.0035274. Epub 2012 Apr 26.
3
Sensitive mapping of recombination hotspots using sequencing-based detection of ssDNA.基于测序的 ssDNA 检测技术实现重组热点的灵敏作图。
Genome Res. 2012 May;22(5):957-65. doi: 10.1101/gr.130583.111. Epub 2012 Feb 24.
4
Prdm9, a major determinant of meiotic recombination hotspots, is not functional in dogs and their wild relatives, wolves and coyotes.Prdm9 是减数分裂重组热点的主要决定因素,但在狗及其野生亲属(狼和郊狼)中没有功能。
PLoS One. 2011;6(11):e25498. doi: 10.1371/journal.pone.0025498. Epub 2011 Nov 10.
5
Death of PRDM9 coincides with stabilization of the recombination landscape in the dog genome.PRDM9 基因的缺失与犬基因组中重组景观的稳定同时发生。
Genome Res. 2012 Jan;22(1):51-63. doi: 10.1101/gr.124123.111. Epub 2011 Oct 17.
6
Genome-wide analysis reveals novel molecular features of mouse recombination hotspots.全基因组分析揭示了小鼠重组热点的新分子特征。
Nature. 2011 Apr 21;472(7343):375-8. doi: 10.1038/nature09869. Epub 2011 Apr 3.
7
Drive against hotspot motifs in primates implicates the PRDM9 gene in meiotic recombination.在灵长类动物中消除热点基序表明 PRDM9 基因参与减数分裂重组。
Science. 2010 Feb 12;327(5967):876-9. doi: 10.1126/science.1182363. Epub 2009 Dec 31.
8
PRDM9 is a major determinant of meiotic recombination hotspots in humans and mice.PRDM9 是人类和小鼠减数分裂重组热点的主要决定因素。
Science. 2010 Feb 12;327(5967):836-40. doi: 10.1126/science.1183439. Epub 2009 Dec 31.
9
Prdm9 controls activation of mammalian recombination hotspots.PRDM9 控制着哺乳动物重组热点的激活。
Science. 2010 Feb 12;327(5967):835. doi: 10.1126/science.1181495. Epub 2009 Dec 31.
10
Extraordinary molecular evolution in the PRDM9 fertility gene.PRDM9 育性基因的非凡分子进化。
PLoS One. 2009 Dec 30;4(12):e8505. doi: 10.1371/journal.pone.0008505.