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修饰组蛋白并启动减数分裂重组;一个老问题的新答案。

Modifying histones and initiating meiotic recombination; new answers to an old question.

作者信息

Maleki Shohreh, Keeney Scott

机构信息

Molecular Biology Program, Memorial Sloan-Kettering Cancer Center, 1275 York Avenue, Box 97, New York, NY 10021, USA.

出版信息

Cell. 2004 Aug 20;118(4):404-6. doi: 10.1016/j.cell.2004.08.008.

DOI:10.1016/j.cell.2004.08.008
PMID:15315752
Abstract

It is well documented that the formation of the DNA double-strand breaks (DSBs) that initiate meiotic recombination is influenced by chromatin and larger scale chromosome organization, but the molecular nature of this influence has remained elusive. Several recent studies, including (this issue of Cell), shed light on this issue by revealing roles for posttranslational histone modifications in promoting DSB formation.

摘要

有充分的文献记载,引发减数分裂重组的DNA双链断裂(DSB)的形成受染色质和更大规模的染色体组织影响,但其影响的分子本质仍不清楚。最近的几项研究,包括(本期《细胞》杂志),通过揭示翻译后组蛋白修饰在促进DSB形成中的作用,为这个问题提供了线索。

相似文献

1
Modifying histones and initiating meiotic recombination; new answers to an old question.修饰组蛋白并启动减数分裂重组;一个老问题的新答案。
Cell. 2004 Aug 20;118(4):404-6. doi: 10.1016/j.cell.2004.08.008.
2
Tails and cuts: the role of histone post-translational modifications in the formation of programmed double-strand breaks.尾巴与切割:组蛋白翻译后修饰在程序性双链断裂形成中的作用
Biochimie. 2005 Jul;87(7):603-12. doi: 10.1016/j.biochi.2004.11.017. Epub 2004 Dec 23.
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DNA double-strand breaks in meiosis: checking their formation, processing and repair.减数分裂中的DNA双链断裂:检查其形成、加工和修复
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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。
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Initiation of meiotic recombination by formation of DNA double-strand breaks: mechanism and regulation.通过形成DNA双链断裂启动减数分裂重组:机制与调控
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HTP-3 links DSB formation with homolog pairing and crossing over during C. elegans meiosis.HTP-3在秀丽隐杆线虫减数分裂过程中将双链断裂的形成与同源配对及交叉联系起来。
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Histone modifications and DNA double-strand break repair.组蛋白修饰与DNA双链断裂修复。
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Spermatocyte responses in vitro to induced DNA damage.体外精子细胞对诱导性DNA损伤的反应。
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H4K44 Acetylation Facilitates Chromatin Accessibility during Meiosis.H4K44乙酰化在减数分裂过程中促进染色质可及性。
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Mnd1/Hop2 facilitates Dmc1-dependent interhomolog crossover formation in meiosis of budding yeast.Mnd1/Hop2促进芽殖酵母减数分裂中依赖Dmc1的同源染色体交叉形成。
Mol Cell Biol. 2006 Apr;26(8):2913-23. doi: 10.1128/MCB.26.8.2913-2923.2006.

引用本文的文献

1
A Co-Expression Network in Hexaploid Wheat Reveals Mostly Balanced Expression and Lack of Significant Gene Loss of Homeologous Meiotic Genes Upon Polyploidization.六倍体小麦中的共表达网络揭示了多倍体化后同源减数分裂基因的表达大多平衡且缺乏显著的基因丢失。
Front Plant Sci. 2019 Oct 18;10:1325. doi: 10.3389/fpls.2019.01325. eCollection 2019.
2
Meiotic recombination hotspots of fission yeast are directed to loci that express non-coding RNA.裂殖酵母的减数分裂重组热点定位于表达非编码RNA的基因座。
PLoS One. 2008 Aug 6;3(8):e2887. doi: 10.1371/journal.pone.0002887.
3
Poly(ADP-ribose) polymerase-2 contributes to the fidelity of male meiosis I and spermiogenesis.
聚(ADP - 核糖)聚合酶 - 2有助于雄性减数分裂I和精子发生的保真度。
Proc Natl Acad Sci U S A. 2006 Oct 3;103(40):14854-9. doi: 10.1073/pnas.0604252103. Epub 2006 Sep 25.
4
EGO-1, a putative RNA-dependent RNA polymerase, is required for heterochromatin assembly on unpaired dna during C. elegans meiosis.EGO-1是一种假定的RNA依赖性RNA聚合酶,在秀丽隐杆线虫减数分裂期间,未配对DNA上的异染色质组装需要该酶。
Curr Biol. 2005 Nov 8;15(21):1972-8. doi: 10.1016/j.cub.2005.09.049.