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PRDM9将其锌指结构插入重组热点以及物种之间。

PRDM9 sticks its zinc fingers into recombination hotspots and between species.

作者信息

Sandovici Ionel, Sapienza Carmen

出版信息

F1000 Biol Rep. 2010 May 24;2:37. doi: 10.3410/B2-37.

DOI:10.3410/B2-37
PMID:20948797
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2950028/
Abstract

Meiotic recombination events typically cluster within narrow regions of the genome termed hotspots. A series of recent papers reveals that PRDM9, a C2H2-type zinc-finger protein with histone H3 lysine 4 methyltransferase activity, plays a major role in the specification of hotspots. The zinc fingers that contact DNA in a sequence-dependent manner evolve rapidly and are under positive selection, leading to differences in the location of recombination hotspots as well as hybrid sterility.

摘要

减数分裂重组事件通常聚集在基因组中被称为热点的狭窄区域内。最近的一系列论文表明,PRDM9是一种具有组蛋白H3赖氨酸4甲基转移酶活性的C2H2型锌指蛋白,在热点的指定中起主要作用。以序列依赖性方式与DNA接触的锌指快速进化并处于正选择之下,导致重组热点位置以及杂种不育的差异。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9e24/2950028/a101f2e9c7f6/1757-594X-0002-0000000037-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9e24/2950028/a101f2e9c7f6/1757-594X-0002-0000000037-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9e24/2950028/a101f2e9c7f6/1757-594X-0002-0000000037-g001.jpg

相似文献

1
PRDM9 sticks its zinc fingers into recombination hotspots and between species.PRDM9将其锌指结构插入重组热点以及物种之间。
F1000 Biol Rep. 2010 May 24;2:37. doi: 10.3410/B2-37.
2
The consequences of sequence erosion in the evolution of recombination hotspots.序列侵蚀在重组热点进化中的后果。
Philos Trans R Soc Lond B Biol Sci. 2017 Dec 19;372(1736). doi: 10.1098/rstb.2016.0462.
3
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.
4
The Meiotic Recombination Activator PRDM9 Trimethylates Both H3K36 and H3K4 at Recombination Hotspots In Vivo.减数分裂重组激活因子PRDM9在体内对重组热点处的H3K36和H3K4进行三甲基化修饰。
PLoS Genet. 2016 Jun 30;12(6):e1006146. doi: 10.1371/journal.pgen.1006146. eCollection 2016 Jun.
5
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6
Zinc Finger Domain of the PRDM9 Gene on Chromosome 1 Exhibits High Diversity in Ruminants but Its Paralog PRDM7 Contains Multiple Disruptive Mutations.1号染色体上PRDM9基因的锌指结构域在反刍动物中表现出高度多样性,但其旁系同源基因PRDM7含有多个破坏性突变。
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Accelerated evolution of the Prdm9 speciation gene across diverse metazoan taxa.Prdm9 种系基因在不同后生动物类群中的加速进化。
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The long zinc finger domain of PRDM9 forms a highly stable and long-lived complex with its DNA recognition sequence.PRDM9的长锌指结构域与其DNA识别序列形成高度稳定且寿命长的复合物。
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PRDM9 drives evolutionary erosion of hotspots in Mus musculus through haplotype-specific initiation of meiotic recombination.PRDM9通过减数分裂重组的单倍型特异性起始驱动小家鼠热点区域的进化侵蚀。
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引用本文的文献

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The formation and repair of DNA double-strand breaks in mammalian meiosis.哺乳动物减数分裂中 DNA 双链断裂的形成和修复。
Asian J Androl. 2021 Nov-Dec;23(6):572-579. doi: 10.4103/aja202191.
2
Ruminant-specific multiple duplication events of PRDM9 before speciation.物种形成之前PRDM9的反刍动物特异性多次重复事件。
BMC Evol Biol. 2017 Mar 14;17(1):79. doi: 10.1186/s12862-017-0892-4.
3
Genome-Wide Association Study of Meiotic Recombination Phenotypes.减数分裂重组表型的全基因组关联研究

本文引用的文献

1
Mammalian recombination hot spots: properties, control and evolution.哺乳动物重组热点:特性、调控与进化。
Nat Rev Genet. 2010 Mar;11(3):221-33. doi: 10.1038/nrg2712.
2
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.
3
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。
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PR Domain-containing Protein 7 (PRDM7) Is a Histone 3 Lysine 4 Trimethyltransferase.含PR结构域蛋白7(PRDM7)是一种组蛋白3赖氨酸4三甲基转移酶。
J Biol Chem. 2016 Jun 24;291(26):13509-19. doi: 10.1074/jbc.M116.721472. Epub 2016 Apr 29.
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Nutr Rev. 2013 Jul;71(7):441-57. doi: 10.1111/nure.12030. Epub 2013 May 15.
6
High diversity at PRDM9 in chimpanzees and bonobos.黑猩猩和倭黑猩猩中 PRDM9 具有高度多样性。
PLoS One. 2012;7(7):e39064. doi: 10.1371/journal.pone.0039064. Epub 2012 Jul 2.
7
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.
Science. 2010 Feb 12;327(5967):836-40. doi: 10.1126/science.1183439. Epub 2009 Dec 31.
4
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.
5
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.
6
Accelerated evolution of the Prdm9 speciation gene across diverse metazoan taxa.Prdm9 种系基因在不同后生动物类群中的加速进化。
PLoS Genet. 2009 Dec;5(12):e1000753. doi: 10.1371/journal.pgen.1000753. Epub 2009 Dec 4.
7
Distinct histone modifications define initiation and repair of meiotic recombination in the mouse.不同的组蛋白修饰决定了小鼠减数分裂重组的起始和修复。
EMBO J. 2009 Sep 2;28(17):2616-24. doi: 10.1038/emboj.2009.207. Epub 2009 Jul 30.
8
Genome-wide control of the distribution of meiotic recombination.减数分裂重组分布的全基因组控制
PLoS Biol. 2009 Feb 17;7(2):e35. doi: 10.1371/journal.pbio.1000035.
9
A common sequence motif associated with recombination hot spots and genome instability in humans.一种与人类重组热点和基因组不稳定性相关的常见序列基序。
Nat Genet. 2008 Sep;40(9):1124-9. doi: 10.1038/ng.213.
10
HapMap methylation-associated SNPs, markers of germline DNA methylation, positively correlate with regional levels of human meiotic recombination.HapMap甲基化相关单核苷酸多态性,即种系DNA甲基化的标记,与人类减数分裂重组的区域水平呈正相关。
Genome Res. 2009 Apr;19(4):581-9. doi: 10.1101/gr.086181.108. Epub 2009 Jan 21.