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Mol Cell Biol
2000 Jan 01;202:735-40. doi: 10.1128/MCB.20.2.735-740.2000.
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A cell cycle-specific requirement for the XRCC1 BRCT II domain during mammalian DNA strand break repair.
Taylor RM
,
Moore DJ
,
Whitehouse J
,
Johnson P
,
Caldecott KW
.
???displayArticle.abstract??? XRCC1 protein is essential for viability in mammals and is required for efficient DNA single-strand break repair and genetic stability following DNA base damage. We report here that XRCC1-dependent strand break repair in G(1) phase of the cell cycle is abolished by mutations created within the XRCC1 BRCT domain that interact with DNA ligase III. In contrast, XRCC1-dependent DNA strand break repair in S phase is largely unaffected by these mutations. These data describe a cell cycle-specific role for a BRCT domain, and we conclude that the XRCC1-DNA ligase III complex is required for DNA strand break repair in G(1) phase of the cell cycle but is dispensable for this process in S phase. The S-phase DNA repair process can remove both strand breaks induced in S phase and those that persist from G(1) and can in part compensate for lack of repair in G(1). This process correlates with the appearance of XRCC1 nuclear foci that colocalize with Rad51 and may thus function in concert with homologous recombination.
Aboussekhra,
Semidominant suppressors of Srs2 helicase mutations of Saccharomyces cerevisiae map in the RAD51 gene, whose sequence predicts a protein with similarities to procaryotic RecA proteins.
1992, Pubmed
Aboussekhra,
Semidominant suppressors of Srs2 helicase mutations of Saccharomyces cerevisiae map in the RAD51 gene, whose sequence predicts a protein with similarities to procaryotic RecA proteins.
1992,
Pubmed
Barlow,
Distribution of the Rad51 recombinase in human and mouse spermatocytes.
1997,
Pubmed
Barrows,
The CHO XRCC1 mutant, EM9, deficient in DNA ligase III activity, exhibits hypersensitivity to camptothecin independent of DNA replication.
1998,
Pubmed
,
Xenbase
Basile,
Nucleotide sequence and transcriptional regulation of the yeast recombinational repair gene RAD51.
1992,
Pubmed
Bork,
A superfamily of conserved domains in DNA damage-responsive cell cycle checkpoint proteins.
1997,
Pubmed
Caldecott,
XRCC1 polypeptide interacts with DNA polymerase beta and possibly poly (ADP-ribose) polymerase, and DNA ligase III is a novel molecular 'nick-sensor' in vitro.
1996,
Pubmed
,
Xenbase
Caldecott,
Characterization of the XRCC1-DNA ligase III complex in vitro and its absence from mutant hamster cells.
1995,
Pubmed
,
Xenbase
Caldecott,
Cross-sensitivity of gamma-ray-sensitive hamster mutants to cross-linking agents.
1991,
Pubmed
Caldecott,
An interaction between the mammalian DNA repair protein XRCC1 and DNA ligase III.
1994,
Pubmed
,
Xenbase
Callebaut,
From BRCA1 to RAP1: a widespread BRCT module closely associated with DNA repair.
1997,
Pubmed
Cappelli,
Involvement of XRCC1 and DNA ligase III gene products in DNA base excision repair.
1997,
Pubmed
,
Xenbase
Carrano,
Incorporated bromodeoxyuridine enhances the sister-chromatid exchange and chromosomal aberration frequencies in an EMS-sensitive Chinese hamster cell line.
1986,
Pubmed
Haaf,
Nuclear foci of mammalian Rad51 recombination protein in somatic cells after DNA damage and its localization in synaptonemal complexes.
1995,
Pubmed
Holm,
Differential requirement of DNA replication for the cytotoxicity of DNA topoisomerase I and II inhibitors in Chinese hamster DC3F cells.
1989,
Pubmed
Hsiang,
Arrest of replication forks by drug-stabilized topoisomerase I-DNA cleavable complexes as a mechanism of cell killing by camptothecin.
1989,
Pubmed
Kadkhodayan,
Construction of a functional cDNA clone of the hamster ERCC2 DNA repair and transcription gene.
1996,
Pubmed
Kubota,
Reconstitution of DNA base excision-repair with purified human proteins: interaction between DNA polymerase beta and the XRCC1 protein.
1996,
Pubmed
Lim,
A mutation in mouse rad51 results in an early embryonic lethal that is suppressed by a mutation in p53.
1996,
Pubmed
Lindahl,
Instability and decay of the primary structure of DNA.
1993,
Pubmed
Masson,
XRCC1 is specifically associated with poly(ADP-ribose) polymerase and negatively regulates its activity following DNA damage.
1998,
Pubmed
,
Xenbase
Morita,
A mouse homolog of the Escherichia coli recA and Saccharomyces cerevisiae RAD51 genes.
1993,
Pubmed
Nash,
XRCC1 protein interacts with one of two distinct forms of DNA ligase III.
1997,
Pubmed
Olive,
Heterogeneity in radiation-induced DNA damage and repair in tumor and normal cells measured using the "comet" assay.
1990,
Pubmed
Orren,
A UV-responsive G2 checkpoint in rodent cells.
1995,
Pubmed
Prasad,
Specific interaction of DNA polymerase beta and DNA ligase I in a multiprotein base excision repair complex from bovine testis.
1996,
Pubmed
Prigent,
Aberrant DNA repair and DNA replication due to an inherited enzymatic defect in human DNA ligase I.
1994,
Pubmed
Ryan,
Camptothecin cytotoxicity in mammalian cells is associated with the induction of persistent double strand breaks in replicating DNA.
1991,
Pubmed
Shen,
Mutations in hamster single-strand break repair gene XRCC1 causing defective DNA repair.
1998,
Pubmed
Shinohara,
Rad51 protein involved in repair and recombination in S. cerevisiae is a RecA-like protein.
1992,
Pubmed
Singh,
A simple technique for quantitation of low levels of DNA damage in individual cells.
1988,
Pubmed
Sonoda,
Rad51-deficient vertebrate cells accumulate chromosomal breaks prior to cell death.
1998,
Pubmed
Tashiro,
S phase specific formation of the human Rad51 protein nuclear foci in lymphocytes.
1996,
Pubmed
Taylor,
Role of a BRCT domain in the interaction of DNA ligase III-alpha with the DNA repair protein XRCC1.
1998,
Pubmed
Tebbs,
Requirement for the Xrcc1 DNA base excision repair gene during early mouse development.
1999,
Pubmed
Thompson,
Molecular cloning of the human XRCC1 gene, which corrects defective DNA strand break repair and sister chromatid exchange.
1990,
Pubmed
Thompson,
A CHO-cell strain having hypersensitivity to mutagens, a defect in DNA strand-break repair, and an extraordinary baseline frequency of sister-chromatid exchange.
1982,
Pubmed
Tsuzuki,
Targeted disruption of the Rad51 gene leads to lethality in embryonic mice.
1996,
Pubmed
Zdzienicka,
A Chinese hamster ovary cell mutant (EM-C11) with sensitivity to simple alkylating agents and a very high level of sister chromatid exchanges.
1992,
Pubmed
Zhang,
Structure of an XRCC1 BRCT domain: a new protein-protein interaction module.
1998,
Pubmed