Literature DB >> 11709049

Detecting, signalling and repairing DNA double-strand breaks.

S P Jackson1.   

Abstract

DNA double-strand breaks (DSBs) can be generated by a variety of genotoxic agents, including ionizing radiation and radiomimetic chemicals. They can also occur when DNA replication complexes encounter other forms of DNA damage, and are produced as intermediates during certain site-specific recombination processes. It is crucial that cells recognize DSBs and bring about their efficient repair, because a single unrepaired cellular DSB can induce cell death, and defective DSB repair can lead to mutations or the loss of significant segments of chromosomal material. Eukaryotic cells have evolved a variety of systems to detect DNA DSBs, repair them, and signal their presence to the transcription, cell cycle and apoptotic machineries. In this review, I describe how work on mammalian cells and also on model organisms such as yeasts has revealed that such systems are highly conserved throughout evolution, and has provided insights into the molecular mechanisms by which DNA DSBs are recognized, signalled and repaired. I also explain how defects in the proteins that function in these pathways are associated with a variety of human pathological states.

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Year:  2001        PMID: 11709049     DOI: 10.1042/0300-5127:0290655

Source DB:  PubMed          Journal:  Biochem Soc Trans        ISSN: 0300-5127            Impact factor:   5.407


  36 in total

1.  A genomics-based screen for yeast mutants with an altered recombination/end-joining repair ratio.

Authors:  Thomas E Wilson
Journal:  Genetics       Date:  2002-10       Impact factor: 4.562

2.  Carcinogenic lead chromate induces DNA double-strand breaks in human lung cells.

Authors:  Hong Xie; Sandra S Wise; Amie L Holmes; Bo Xu; Timothy P Wakeman; Stephen C Pelsue; Narendra P Singh; John Pierce Wise
Journal:  Mutat Res       Date:  2005-10-03       Impact factor: 2.433

Review 3.  Constitutive histone H2AX phosphorylation and ATM activation, the reporters of DNA damage by endogenous oxidants.

Authors:  Toshiki Tanaka; H Dorota Halicka; Xuan Huang; Frank Traganos; Zbigniew Darzynkiewicz
Journal:  Cell Cycle       Date:  2006-09-01       Impact factor: 4.534

Review 4.  Radiation-induced bystander signalling in cancer therapy.

Authors:  Kevin M Prise; Joe M O'Sullivan
Journal:  Nat Rev Cancer       Date:  2009-04-20       Impact factor: 60.716

5.  Response to multiple radiation doses of fibroblasts over-expressing dominant negative Ku70.

Authors:  Muneyasu Urano; Yunhong Huang; Fuqiu He; Akiko Minami; C Clifton Ling; Gloria C Li
Journal:  Int J Radiat Oncol Biol Phys       Date:  2008-04-18       Impact factor: 7.038

6.  Extent of constitutive histone H2AX phosphorylation on Ser-139 varies in cells with different TP53 status.

Authors:  T Tanaka; A Kurose; X Huang; F Traganos; W Dai; Z Darzynkiewicz
Journal:  Cell Prolif       Date:  2006-08       Impact factor: 6.831

7.  Frequency of DNA end joining in trans is not determined by the predamage spatial proximity of double-strand breaks in yeast.

Authors:  Sham Sunder; Thomas E Wilson
Journal:  Proc Natl Acad Sci U S A       Date:  2019-04-24       Impact factor: 11.205

8.  Multiple recombination pathways for sister chromatid exchange in Saccharomyces cerevisiae: role of RAD1 and the RAD52 epistasis group genes.

Authors:  Zheng Dong; Michael Fasullo
Journal:  Nucleic Acids Res       Date:  2003-05-15       Impact factor: 16.971

9.  H2AX Phosphorylation: Its Role in DNA Damage Response and Cancer Therapy.

Authors:  Monika Podhorecka; Andrzej Skladanowski; Przemyslaw Bozko
Journal:  J Nucleic Acids       Date:  2010-08-03

10.  Suppression of DNA-damage checkpoint signaling by Rsk-mediated phosphorylation of Mre11.

Authors:  Chen Chen; Liguo Zhang; Nai-Jia Huang; Bofu Huang; Sally Kornbluth
Journal:  Proc Natl Acad Sci U S A       Date:  2013-12-02       Impact factor: 11.205

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