Interaction of excision repair gene products and mitotic recombination functions in yeast.

We have tested the ability of mutants of three additional genes in the excision repair pathway of Saccharomyces cerevisiae to suppress the hyper-recombination and rad52 double-mutant lethality phenotypes of the rad3-102 (formerly rem1-2) mutation. Such suppression has previously been observed with mutant alleles of RAD1 and RAD4. We had hypothesized ...
that the rad3-102 mutation created elevated levels of DNA lesions which could be processed by the products of the RAD1 and RAD4 genes into recombinogenic double-strand breaks requiring the RAD52 product for repair. In this report, we show that the RAD2, RAD7, and RAD10 genes are also necessary for this processing. We discuss our observations of varying levels of mitotic crossing-over in Rem- rad double-mutant strains.
Mesh Terms:
Crosses, Genetic, DNA Repair, Diploidy, Genes, Fungal, Genes, Lethal, Genotype, Mitosis, Phenotype, Recombination, Genetic, Saccharomyces cerevisiae
Curr. Genet.
Date: Dec. 01, 1993
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