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本文引用的文献

1
Evolution of an MCM complex in flies that promotes meiotic crossovers by blocking BLM helicase.果蝇 MCM 复合物的进化通过阻止 BLM 解旋酶来促进减数分裂交叉。
Science. 2012 Dec 7;338(6112):1363-5. doi: 10.1126/science.1228190.
2
Preaching about the converted: how meiotic gene conversion influences genomic diversity.宣讲转化:减数分裂基因转换如何影响基因组多样性。
Ann N Y Acad Sci. 2012 Sep;1267:95-102. doi: 10.1111/j.1749-6632.2012.06595.x.
3
FANCM limits meiotic crossovers.FANCM 限制减数分裂交叉。
Science. 2012 Jun 22;336(6088):1588-90. doi: 10.1126/science.1220381.
4
The Fanconi anemia ortholog FANCM ensures ordered homologous recombination in both somatic and meiotic cells in Arabidopsis.范可尼贫血症相关蛋白 FANCM 确保拟南芥体细胞和减数分裂细胞中同源重组的有序进行。
Plant Cell. 2012 Apr;24(4):1448-64. doi: 10.1105/tpc.112.096644. Epub 2012 Apr 30.
5
Delineation of joint molecule resolution pathways in meiosis identifies a crossover-specific resolvase.减数分裂中联合分子解析途径的描绘确定了一个特定位点的交叉特异性核酸酶。
Cell. 2012 Apr 13;149(2):334-47. doi: 10.1016/j.cell.2012.03.023.
6
BLM helicase ortholog Sgs1 is a central regulator of meiotic recombination intermediate metabolism.BLM 解旋酶同源物 Sgs1 是减数分裂重组中间代谢的核心调节剂。
Mol Cell. 2012 Apr 13;46(1):43-53. doi: 10.1016/j.molcel.2012.02.020.
7
COSA-1 reveals robust homeostasis and separable licensing and reinforcement steps governing meiotic crossovers.COSA-1 揭示了稳健的同源重组调控,以及分离的起始和加强步骤。
Cell. 2012 Mar 30;149(1):75-87. doi: 10.1016/j.cell.2012.01.052.
8
Homeostatic control of recombination is implemented progressively in mouse meiosis.同源重组的体内平衡控制在小鼠减数分裂中逐步实施。
Nat Cell Biol. 2012 Mar 4;14(4):424-30. doi: 10.1038/ncb2451.
9
Processing of joint molecule intermediates by structure-selective endonucleases during homologous recombination in eukaryotes.真核生物同源重组过程中结构选择性核酸内切酶对联合分子中间体的加工处理。
Chromosoma. 2011 Apr;120(2):109-27. doi: 10.1007/s00412-010-0304-7. Epub 2011 Jan 11.
10
Temporally and biochemically distinct activities of Exo1 during meiosis: double-strand break resection and resolution of double Holliday junctions.减数分裂中 Exo1 的时空和生化活性:双链断裂切除和双链 Holliday 连接的解析。
Mol Cell. 2010 Dec 22;40(6):1001-15. doi: 10.1016/j.molcel.2010.11.032.

减数分裂中的减数分裂和有丝分裂重组。

Meiotic and mitotic recombination in meiosis.

机构信息

Curriculum in Genetics and Molecular Biology, University of North Carolina, Chapel Hill, NC 27599, USA.

出版信息

Genetics. 2013 Jun;194(2):327-34. doi: 10.1534/genetics.113.150581.

DOI:10.1534/genetics.113.150581
PMID:23733849
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3664844/
Abstract

Meiotic crossovers facilitate the segregation of homologous chromosomes and increase genetic diversity. The formation of meiotic crossovers was previously posited to occur via two pathways, with the relative use of each pathway varying between organisms; however, this paradigm could not explain all crossovers, and many of the key proteins involved were unidentified. Recent studies that identify some of these proteins reinforce and expand the model of two meiotic crossover pathways. The results provide novel insights into the evolutionary origins of the pathways, suggesting that one is similar to a mitotic DNA repair pathway and the other evolved to incorporate special features unique to meiosis.

摘要

减数分裂交叉促进同源染色体的分离并增加遗传多样性。减数分裂交叉的形成以前被认为是通过两种途径发生的,每种途径的相对使用在生物体之间有所不同;然而,这种模式并不能解释所有的交叉,而且许多涉及的关键蛋白质尚未被识别。最近的研究确定了其中一些蛋白质,这加强和扩展了两种减数分裂交叉途径的模型。这些结果为这些途径的进化起源提供了新的见解,表明其中一种途径类似于有丝分裂 DNA 修复途径,另一种途径则进化为包含减数分裂特有的特殊特征。