Literature DB >> 9200329

The RAD52 epistasis group in mammalian double strand break repair.

J H Petrini1, D A Bressan, M S Yao.   

Abstract

The S. cerevisiae RAD52 epistasis group gene products mediate DNA double strand break repair and recombination. These proteins and their modes of action have been extensively characterized. The existence of highly conserved mammalian RAD52 epistasis group homologues suggests that information regarding the functions and mechanisms of double strand break repair proteins in yeast may be applicable to mammalian recombinational DNA repair. Herein, we provide an overview of the S. cerevisiae RAD52 epistasis group and describe the characterization of the five mammalian RAD52 epistasis group homologues identified to date. In the context of their expression patterns and other functional analyses, we discuss potential roles for these proteins in mammalian recombinational DNA repair and specialized recombination events such as V(D)J recombination.

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Year:  1997        PMID: 9200329     DOI: 10.1006/smim.1997.0067

Source DB:  PubMed          Journal:  Semin Immunol        ISSN: 1044-5323            Impact factor:   11.130


  24 in total

1.  Homologous and non-homologous recombination differentially affect DNA damage repair in mice.

Authors:  J Essers; H van Steeg; J de Wit; S M Swagemakers; M Vermeij; J H Hoeijmakers; R Kanaar
Journal:  EMBO J       Date:  2000-04-03       Impact factor: 11.598

Review 2.  The mammalian Mre11-Rad50-nbs1 protein complex: integration of functions in the cellular DNA-damage response.

Authors:  J H Petrini
Journal:  Am J Hum Genet       Date:  1999-05       Impact factor: 11.025

3.  Deficiency of human BRCA2 leads to impaired homologous recombination but maintains normal nonhomologous end joining.

Authors:  F Xia; D G Taghian; J S DeFrank; Z C Zeng; H Willers; G Iliakis; S N Powell
Journal:  Proc Natl Acad Sci U S A       Date:  2001-07-10       Impact factor: 11.205

4.  Mre11 and Rad50 from Pyrococcus furiosus: cloning and biochemical characterization reveal an evolutionarily conserved multiprotein machine.

Authors:  K P Hopfner; A Karcher; D Shin; C Fairley; J A Tainer; J P Carney
Journal:  J Bacteriol       Date:  2000-11       Impact factor: 3.490

5.  Sister chromatid-based DNA repair is mediated by RAD54, not by DMC1 or TID1.

Authors:  A Arbel; D Zenvirth; G Simchen
Journal:  EMBO J       Date:  1999-05-04       Impact factor: 11.598

6.  The Rad50 genes of diploid and polyploid wheat species. Analysis of homologue and homoeologue expression and interactions with Mre11.

Authors:  R Pérez; A Cuadrado; I P Chen; H Puchta; N Jouve; A De Bustos
Journal:  Theor Appl Genet       Date:  2010-09-09       Impact factor: 5.699

7.  The Drosophila melanogaster DmRAD54 gene plays a crucial role in double-strand break repair after P-element excision and acts synergistically with Ku70 in the repair of X-ray damage.

Authors:  R Kooistra; A Pastink; J B Zonneveld; P H Lohman; J C Eeken
Journal:  Mol Cell Biol       Date:  1999-09       Impact factor: 4.272

8.  hMre11 and hRad50 nuclear foci are induced during the normal cellular response to DNA double-strand breaks.

Authors:  R S Maser; K J Monsen; B E Nelms; J H Petrini
Journal:  Mol Cell Biol       Date:  1997-10       Impact factor: 4.272

9.  Strand pairing by Rad54 and Rad51 is enhanced by chromatin.

Authors:  Vassilios Alexiadis; James T Kadonaga
Journal:  Genes Dev       Date:  2002-11-01       Impact factor: 11.361

Review 10.  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
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