4.4 Article

Role of the Saccharomyces cerevisiae Rad51 paralogs in sister chromatid recombination

Journal

GENETICS
Volume 178, Issue 1, Pages 113-126

Publisher

GENETICS SOCIETY AMERICA
DOI: 10.1534/genetics.107.082677

Keywords

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Funding

  1. NIAID NIH HHS [T32 AI007161, T32 AI07161] Funding Source: Medline
  2. NIGMS NIH HHS [GM054099, R01 GM054099-11, T32 GM008224, T32 GM08224, R01 GM054099, R01 GM054099-12] Funding Source: Medline
  3. NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES [T32AI007161] Funding Source: NIH RePORTER
  4. NATIONAL INSTITUTE OF GENERAL MEDICAL SCIENCES [T32GM008224, R01GM054099] Funding Source: NIH RePORTER

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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.

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