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Role of the Saccharomyces cerevisiae Rad51 Paralogs in Sister Chromatid Recombination
Role of the Saccharomyces cerevisiae Rad51 Paralogs in Sister Chromatid Recombination
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Role of the Saccharomyces cerevisiae Rad51 Paralogs in Sister Chromatid Recombination
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Role of the Saccharomyces cerevisiae Rad51 Paralogs in Sister Chromatid Recombination
Role of the Saccharomyces cerevisiae Rad51 Paralogs in Sister Chromatid Recombination
Journal Article

Role of the Saccharomyces cerevisiae Rad51 Paralogs in Sister Chromatid Recombination

2008
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Overview
Rad51 requires a number of other proteins, including the Rad51 paralogs, for efficient recombination in vivo. Current evidence suggests that the yeast Rad51 paralogs, Rad55 and Rad57, are important in formation or stabilization of the Rad51 nucleoprotein filament. To gain further insights into the function of the Rad51 paralogs, reporters were designed to measure spontaneous or double-strand break (DSB)-induced sister or nonsister recombination. Spontaneous sister chromatid recombination (SCR) was reduced 6000-fold in the rad57 mutant, significantly more than in the rad51 mutant. Although the DSB-induced recombination defect of rad57 was suppressed by overexpression of Rad51, elevated temperature, or expression of both mating-type alleles, the rad57 defect in spontaneous SCR was not strongly suppressed by these same factors. In addition, the UV sensitivity of the rad57 mutant was not strongly suppressed by MAT heterozygosity, even though Rad51 foci were restored under these conditions. This lack of suppression suggests that Rad55 and Rad57 have different roles in the recombinational repair of stalled replication forks compared with DSB repair. Furthermore, these data suggest that most spontaneous SCR initiates from single-stranded gaps formed at stalled replication forks rather than DSBs.
Publisher
Genetics Soc America,Genetics Society of America
Subject

Adenosine Triphosphatases

/ chromatids

/ crossing over

/ Deoxyribonucleic acid

/ Diploidy

/ DNA

/ DNA Breaks, Double-Stranded

/ DNA Breaks, Double-Stranded - drug effects

/ DNA Breaks, Double-Stranded - radiation effects

/ DNA Breaks, Single-Stranded

/ DNA Breaks, Single-Stranded - drug effects

/ DNA Breaks, Single-Stranded - radiation effects

/ DNA repair

/ DNA Repair Enzymes

/ DNA-binding proteins

/ DNA-Binding Proteins - metabolism

/ drug effects

/ enzymology

/ Gene Conversion

/ Gene Conversion - drug effects

/ Gene Conversion - radiation effects

/ Genetics

/ Health services

/ Heterozygote

/ High temperature

/ homologous recombination

/ Investigations

/ Mating Factor

/ metabolism

/ Models, Genetic

/ Mutagens

/ Mutagens - pharmacology

/ Mutation

/ Mutation - drug effects

/ Peptides

/ Peptides - metabolism

/ pharmacology

/ Proteins

/ Rad51 Recombinase

/ Rad51 Recombinase - metabolism

/ radiation effects

/ Recombinant Fusion Proteins

/ Recombinant Fusion Proteins - metabolism

/ Repetitive Sequences, Nucleic Acid

/ Repetitive Sequences, Nucleic Acid - genetics

/ Saccharomyces cerevisiae

/ Saccharomyces cerevisiae - drug effects

/ Saccharomyces cerevisiae - enzymology

/ Saccharomyces cerevisiae - genetics

/ Saccharomyces cerevisiae - radiation effects

/ Saccharomyces cerevisiae Proteins

/ Saccharomyces cerevisiae Proteins - metabolism

/ Sequence Homology, Amino Acid

/ Sister Chromatid Exchange

/ Sister Chromatid Exchange - drug effects

/ Sister Chromatid Exchange - genetics

/ Sister Chromatid Exchange - radiation effects

/ Suppression, Genetic

/ Suppression, Genetic - drug effects

/ Suppression, Genetic - radiation effects

/ Temperature

/ Ultraviolet Rays

/ Yeast

/ Yeasts

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