Affiliation:
1. Department of Microbiology and Institute of Cancer Research, Columbia University College of Physicians and Surgeons, New York, New York 10032
Abstract
ABSTRACT
Rad51 can promote extensive strand exchange in vitro in the absence of ATP hydrolysis, and the Rad51-K191R mutant protein, which can bind but poorly hydrolyze ATP, also promotes strand exchange. A haploid strain expressing the
rad51-K191R
allele showed an equivalent sensitivity at low doses of ionizing radiation to
rad51-K191A
or
rad51
null mutants and was defective in spontaneous and double-strand break-induced mitotic recombination. However, the
rad51-K191R/rad51-K191R
diploid sporulated and the haploid spores showed high viability, indicating no apparent defect in meiotic recombination. The DNA repair defect caused by the
rad51-K191R
allele was suppressed in diploids and by mating-type heterozygosity in haploids.
RAD54
expressed from a high-copy-number plasmid also suppressed the γ-ray sensitivity of
rad51-K191R
haploids. The suppression by mating-type heterozygosity of the DNA repair defect conferred by the
rad51-K191R
allele could occur by elevated expression of factors that act to stabilize, or promote catalysis, by the partially functional Rad51-K191R protein.
Publisher
American Society for Microbiology
Subject
Cell Biology,Molecular Biology
Cited by
55 articles.
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