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Drosophila PCH2 is required for a pachytene checkpoint that monitors double-strand-break-independent events leading to meiotic crossover formation.果蝇PCH2是粗线期检查点所必需的,该检查点监测导致减数分裂交叉形成的双链断裂非依赖性事件。
Genetics. 2009 Jan;181(1):39-51. doi: 10.1534/genetics.108.093112. Epub 2008 Oct 28.
2
Exploring the extremes of sequence/structure space with ensemble fold recognition in the program Phyre.在Phyre程序中使用集成折叠识别方法探索序列/结构空间的极限。
Proteins. 2008 Feb 15;70(3):611-25. doi: 10.1002/prot.21688.
3
On the Control of the Distribution of Meiotic Exchange in DROSOPHILA MELANOGASTER.在控制黑腹果蝇减数分裂交换分布中的作用。
Genetics. 1982 May;101(1):81-9. doi: 10.1093/genetics/101.1.81.
4
Temporal analysis of meiotic DNA double-strand break formation and repair in Drosophila females.果蝇雌性减数分裂中DNA双链断裂形成与修复的时间分析。
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REC, Drosophila MCM8, drives formation of meiotic crossovers.果蝇MCM8的REC蛋白驱动减数分裂交叉的形成。
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6
Drosophila ERCC1 is required for a subset of MEI-9-dependent meiotic crossovers.果蝇ERCC1是MEI-9依赖的减数分裂交叉的一个子集所必需的。
Genetics. 2005 Aug;170(4):1737-45. doi: 10.1534/genetics.104.036178. Epub 2005 Jun 8.
7
Mutational analysis of the Drosophila DNA repair and recombination gene mei-9.果蝇DNA修复与重组基因mei-9的突变分析
Genetics. 2004 May;167(1):263-73. doi: 10.1534/genetics.167.1.263.
8
Relationship of DNA double-strand breaks to synapsis in Drosophila.果蝇中DNA双链断裂与联会的关系。
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9
Drosophila MUS312 interacts with the nucleotide excision repair endonuclease MEI-9 to generate meiotic crossovers.果蝇MUS312与核苷酸切除修复内切核酸酶MEI-9相互作用以产生减数分裂交叉。
Mol Cell. 2002 Dec;10(6):1503-9. doi: 10.1016/s1097-2765(02)00782-7.
10
Meiotic recombination and chromosome segregation in Drosophila females.果蝇雌性减数分裂中的重组与染色体分离。
Annu Rev Genet. 2002;36:205-32. doi: 10.1146/annurev.genet.36.041102.113929. Epub 2002 Jun 11.

果蝇梭哈蛋白是减数分裂交叉互换的一个子集中所必需的,并且与DNA修复内切核酸酶复合体亚基MEI-9和ERCC1相互作用。

Drosophila hold'em is required for a subset of meiotic crossovers and interacts with the dna repair endonuclease complex subunits MEI-9 and ERCC1.

作者信息

Joyce Eric F, Tanneti S Nikhila, McKim Kim S

机构信息

Department of Genetics, Rutgers, the State University of New Jersey, Piscataway, New Jersey 08854-8020, USA.

出版信息

Genetics. 2009 Jan;181(1):335-40. doi: 10.1534/genetics.108.093104. Epub 2008 Oct 28.

DOI:10.1534/genetics.108.093104
PMID:18957705
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2621184/
Abstract

Three Drosophila proteins, ERCC1, MUS312, and MEI-9, function in a complex proposed to resolve double-Holliday-junction intermediates into crossovers during meiosis. We report here the characterization of hold'em (hdm), whose protein product belongs to a single-strand-DNA-binding superfamily of proteins. Mutations in hdm result in reduced meiotic crossover formation and sensitivity to the DNA-damaging agent methyl methanesulfonate. Furthermore, HDM physically interacts with both MEI-9 and ERCC1 in a yeast two-hybrid assay. We conclude that HDM, MEI-9, MUS312, and ERCC1 form a complex that resolves meiotic recombination intermediates into crossovers.

摘要

三种果蝇蛋白,即ERCC1、MUS312和MEI-9,在一个复合物中发挥作用,该复合物被认为在减数分裂过程中将双Holliday连接中间体转化为交叉。我们在此报告“梭哈”(hdm)的特征,其蛋白质产物属于蛋白质的单链DNA结合超家族。hdm中的突变导致减数分裂交叉形成减少以及对DNA损伤剂甲磺酸甲酯的敏感性增加。此外,在酵母双杂交试验中,HDM与MEI-9和ERCC1都发生物理相互作用。我们得出结论,HDM、MEI-9、MUS312和ERCC1形成一个将减数分裂重组中间体转化为交叉的复合物。