Literature DB >> 1411547

Removal of nonhomologous DNA ends in double-strand break recombination: the role of the yeast ultraviolet repair gene RAD1.

J Fishman-Lobell1, J E Haber.   

Abstract

Double-strand breaks (DSBs) in Saccharomyces cerevisiae can be repaired by gene conversions or by deletions resulting from single-strand annealing between direct repeats of homologous sequences. Although rad1 mutants are resistant to x-rays and can complete DSB-mediated mating-type switching, they could not complete recombination when the ends of the break contained approximately 60 base pairs of nonhomology. Recombination was restored when the ends of the break were made homologous to donor sequences. Additionally, the absence of RAD1 led to the frequent appearance of a previously unobserved type of recombination product. These data suggest RAD1 is required to remove nonhomologous DNA from the 3' ends of recombining DNA, a process analogous to the excision of photodimers during repair of ultraviolet-damaged DNA.

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Year:  1992        PMID: 1411547     DOI: 10.1126/science.1411547

Source DB:  PubMed          Journal:  Science        ISSN: 0036-8075            Impact factor:   47.728


  202 in total

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Authors:  Y Bellaiche; V Mogila; N Perrimon
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2.  The Saccharomyces cerevisiae DNA recombination and repair functions of the RAD52 epistasis group inhibit Ty1 transposition.

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Journal:  Genetics       Date:  2000-02       Impact factor: 4.562

3.  DNA interstrand cross-links induce futile repair synthesis in mammalian cell extracts.

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4.  Visualization of repair of double-strand breaks in the bacteriophage T7 genome without normal DNA replication.

Authors:  Y T Lai; W Masker
Journal:  J Bacteriol       Date:  2000-01       Impact factor: 3.490

Review 5.  Roles for mismatch repair factors in regulating genetic recombination.

Authors:  E Evans; E Alani
Journal:  Mol Cell Biol       Date:  2000-11       Impact factor: 4.272

6.  The structure-specific endonuclease Ercc1-Xpf is required for targeted gene replacement in embryonic stem cells.

Authors:  L J Niedernhofer; J Essers; G Weeda; B Beverloo; J de Wit; M Muijtjens; H Odijk; J H Hoeijmakers; R Kanaar
Journal:  EMBO J       Date:  2001-11-15       Impact factor: 11.598

7.  The active site of the DNA repair endonuclease XPF-ERCC1 forms a highly conserved nuclease motif.

Authors:  Jacqueline H Enzlin; Orlando D Schärer
Journal:  EMBO J       Date:  2002-04-15       Impact factor: 11.598

8.  Activity of individual ERCC1 and XPF subunits in DNA nucleotide excision repair.

Authors:  Pierre-Henri L Gaillard; R D Wood
Journal:  Nucleic Acids Res       Date:  2001-02-15       Impact factor: 16.971

9.  Defining the roles of nucleotide excision repair and recombination in the repair of DNA interstrand cross-links in mammalian cells.

Authors:  I U De Silva; P J McHugh; P H Clingen; J A Hartley
Journal:  Mol Cell Biol       Date:  2000-11       Impact factor: 4.272

10.  DNA interstrand cross-link repair in the Saccharomyces cerevisiae cell cycle: overlapping roles for PSO2 (SNM1) with MutS factors and EXO1 during S phase.

Authors:  Louise J Barber; Thomas A Ward; John A Hartley; Peter J McHugh
Journal:  Mol Cell Biol       Date:  2005-03       Impact factor: 4.272

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