Drosophila Hold'em Is Required for a Subset of Meiotic Crossovers and Interacts With the DNA Repair Endonuclease Complex Subunits MEI-9 and ERCC1

被引:21
作者
Joyce, Eric F.
Tanneti, S. Nikhila
McKim, Kim S. [1 ]
机构
[1] Rutgers State Univ, Waksman Inst, Piscataway, NJ 08854 USA
基金
美国国家科学基金会;
关键词
EXCISION-REPAIR; RECOMBINATION; MELANOGASTER; MECHANISM; HOMOLOG; ENCODES; YEAST;
D O I
10.1534/genetics.108.093104
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
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.
引用
收藏
页码:335 / 340
页数:6
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