Literature DB >> 7635279

Suppression of a new allele of the yeast RAD52 gene by overexpression of RAD51, mutations in srs2 and ccr4, or mating-type heterozygosity.

D Schild1.   

Abstract

The RAD52 gene of Saccharomyces cerevisiae is involved both in the recombinational repair of DNA damage and in mitotic and meiotic recombination. A new allele of rad52 has been isolated that has unusual properties. Unlike other alleles of rad52, this allele (rad52-20) is partially suppressed by an srs2 deletion; srs2 mutations normally act to suppress only rad6 and rad18 mutations. In addition, although haploid rad52-20 strains are very X-ray sensitive, diploids homozygous for this allele are only slightly X-ray sensitive and undergo normal meiosis and meiotic recombination. Because rad52-20 diploids homozygous for mating type are very X-ray sensitive, mating-type heterozygosity is acting to suppress rad52-20. Mating-type heterozygosity suppresses this allele even in haploids, because sir mutations, which result in expression of the normally silent mating-type cassettes, were identified among the extragenic revertants of rad52-20. A new allele of srs2 and alleles of the transcriptional regulatory genes ccr4 and caf1 were among the other extragenic revertants of rad52-20. Because other researchers have shown that the RAD51 and RAD52 proteins interact, RAD51 on a high copy number plasmid was tested and found to suppress the rad52-20 allele, but RAD54, 55 and 57 did not suppress. The RAD51 plasmid did not suppress rad52-1. The rad52-20 allele may encode a protein that has low affinity binding to the RAD51 protein. To test whether the selected revertants suppressed rad52-20 by elevating the expression of RAD51, an integrated RAD51-lacZ fusion was genetically crossed into each revertant. Because none of the revertants increased the level of RAD51-lacZ, the revertants must exert their effect by one or more mechanisms that are not mediated by RAD51.

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Year:  1995        PMID: 7635279      PMCID: PMC1206541     

Source DB:  PubMed          Journal:  Genetics        ISSN: 0016-6731            Impact factor:   4.562


  41 in total

1.  Targeting, disruption, replacement, and allele rescue: integrative DNA transformation in yeast.

Authors:  R Rothstein
Journal:  Methods Enzymol       Date:  1991       Impact factor: 1.600

2.  The CCR4 gene from Saccharomyces cerevisiae is required for both nonfermentative and spt-mediated gene expression.

Authors:  C L Denis; T Malvar
Journal:  Genetics       Date:  1990-02       Impact factor: 4.562

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Authors:  R K Mortimer; D Schild
Journal:  Microbiol Rev       Date:  1980-12

4.  DNA damage induction of ribonucleotide reductase.

Authors:  S J Elledge; R W Davis
Journal:  Mol Cell Biol       Date:  1989-11       Impact factor: 4.272

5.  The yeast DNA repair gene RAD6 encodes a ubiquitin-conjugating enzyme.

Authors:  S Jentsch; J P McGrath; A Varshavsky
Journal:  Nature       Date:  1987 Sep 10-16       Impact factor: 49.962

6.  Similarity of the yeast RAD51 filament to the bacterial RecA filament.

Authors:  T Ogawa; X Yu; A Shinohara; E H Egelman
Journal:  Science       Date:  1993-03-26       Impact factor: 47.728

7.  Analysis of mitotic and meiotic defects in Saccharomyces cerevisiae SRS2 DNA helicase mutants.

Authors:  F Palladino; H L Klein
Journal:  Genetics       Date:  1992-09       Impact factor: 4.562

8.  Modulation of Saccharomyces cerevisiae DNA double-strand break repair by SRS2 and RAD51.

Authors:  G T Milne; T Ho; D T Weaver
Journal:  Genetics       Date:  1995-03       Impact factor: 4.562

9.  Metabolic suppressors of trimethoprim and ultraviolet light sensitivities of Saccharomyces cerevisiae rad6 mutants.

Authors:  C W Lawrence; R B Christensen
Journal:  J Bacteriol       Date:  1979-09       Impact factor: 3.490

10.  A Saccharomyces cerevisiae RAD52 allele expressing a C-terminal truncation protein: activities and intragenic complementation of missense mutations.

Authors:  K L Boundy-Mills; D M Livingston
Journal:  Genetics       Date:  1993-01       Impact factor: 4.562

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  69 in total

Review 1.  Regulation of recombination and genomic maintenance.

Authors:  Wolf-Dietrich Heyer
Journal:  Cold Spring Harb Perspect Biol       Date:  2015-08-03       Impact factor: 10.005

2.  Two pathways for removal of nonhomologous DNA ends during double-strand break repair in Saccharomyces cerevisiae.

Authors:  F Pâques; J E Haber
Journal:  Mol Cell Biol       Date:  1997-11       Impact factor: 4.272

3.  Mrc1 and Srs2 are major actors in the regulation of spontaneous crossover.

Authors:  Thomas Robert; Delphine Dervins; Francis Fabre; Serge Gangloff
Journal:  EMBO J       Date:  2006-05-25       Impact factor: 11.598

4.  DBF2, a cell cycle-regulated protein kinase, is physically and functionally associated with the CCR4 transcriptional regulatory complex.

Authors:  H Y Liu; J H Toyn; Y C Chiang; M P Draper; L H Johnston; C L Denis
Journal:  EMBO J       Date:  1997-09-01       Impact factor: 11.598

Review 5.  The consequences of Rad51 overexpression for normal and tumor cells.

Authors:  Hannah L Klein
Journal:  DNA Repair (Amst)       Date:  2008-02-01

6.  Remodeling of the Rad51 DNA strand-exchange protein by the Srs2 helicase.

Authors:  Hiroyuki Sasanuma; Yuko Furihata; Miki Shinohara; Akira Shinohara
Journal:  Genetics       Date:  2013-06-14       Impact factor: 4.562

Review 7.  Rad54, the motor of homologous recombination.

Authors:  Alexander V Mazin; Olga M Mazina; Dmitry V Bugreev; Matthew J Rossi
Journal:  DNA Repair (Amst)       Date:  2010-01-20

8.  Regulation of Rad51 recombinase presynaptic filament assembly via interactions with the Rad52 mediator and the Srs2 anti-recombinase.

Authors:  Changhyun Seong; Sierra Colavito; Youngho Kwon; Patrick Sung; Lumir Krejci
Journal:  J Biol Chem       Date:  2009-07-15       Impact factor: 5.157

9.  Role of the Saccharomyces cerevisiae Rad51 paralogs in sister chromatid recombination.

Authors:  Amy M Mozlin; Cindy W Fung; Lorraine S Symington
Journal:  Genetics       Date:  2008-01       Impact factor: 4.562

10.  Cell cycle progression in G1 and S phases is CCR4 dependent following ionizing radiation or replication stress in Saccharomyces cerevisiae.

Authors:  Tammy J Westmoreland; Jeffrey R Marks; John A Olson; Eric M Thompson; Michael A Resnick; Craig B Bennett
Journal:  Eukaryot Cell       Date:  2004-04
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