Affiliation:
1. The Stowers Institute for Medical Research, 1000 E. 50th St., Kansas City, Missouri 64110
2. University of Kansas Medical Center, Department of Biochemistry and Molecular Biology, 4011 Wahl Hall East, 3901 Rainbow Blvd., Kansas City, Kansas 66160
Abstract
ABSTRACT
During meiosis, each chromosome must pair with its homolog and undergo meiotic crossover recombination in order to segregate properly at the first meiotic division. Recombination in meiosis in
Saccharomyces cerevisiae
relies on two
Escherichia coli
recA homologs, Rad51 and Dmc1, as well as the more recently discovered heterodimer Mnd1/Hop2. Meiotic recombination in
S. cerevisiae mnd1
and
hop2
single mutants is initiated via double-strand breaks (DSBs) but does not progress beyond this stage; heteroduplex DNA, joint molecules, and crossovers are not detected. Whereas
hop2
and
mnd1
single mutants are profoundly recombination defective, we show that
mnd1 rad51
,
hop2 rad51
, and
mnd1 rad17
double mutants are able to carry out crossover recombination. Interestingly, noncrossover recombination is absent, indicating a role for Mnd1/Hop2 in the designation of DSBs for noncrossover recombination. We demonstrate that in the
rad51 mnd1
double mutant, recombination is more likely to occur between repetitive sequences on nonhomologous chromosomes. Our results support a model in which Mnd1/Hop2 is required for DNA-DNA interactions that help ensure Dmc1-mediated stable strand invasion between homologous chromosomes, thereby preserving genomic integrity.
Publisher
American Society for Microbiology
Subject
Cell Biology,Molecular Biology
Cited by
44 articles.
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