Literature DB >> 15989975

Localization of checkpoint and repair proteins in eukaryotes.

Michael Lisby1, Rodney Rothstein.   

Abstract

In eukaryotes, the cellular response to DNA damage depends on the type of DNA structure being recognized by the checkpoint and repair machinery. DNA ends and single-stranded DNA are hallmarks of double-strand breaks and replication stress. These two structures are recognized by distinct sets of proteins, which are reorganized into a focal assembly at the lesion. Moreover, the composition of these foci is coordinated with cell cycle progression, reflecting the favoring of end-joining in the G1 phase and homologous recombination in S and G2. The assembly of proteins at sites of DNA damage is largely controlled by a network of protein-protein interactions, with the Mre11 complex initiating assembly at DNA ends and replication protein A directing recruitment to single-stranded DNA. This review summarizes current knowledge on the cellular organization of DSB repair and checkpoint proteins focusing on budding yeast and mammalian cells.

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Year:  2004        PMID: 15989975     DOI: 10.1016/j.biochi.2004.10.023

Source DB:  PubMed          Journal:  Biochimie        ISSN: 0300-9084            Impact factor:   4.079


  27 in total

1.  MCL-1 localizes to sites of DNA damage and regulates DNA damage response.

Authors:  Sarwat Jamil; Cezar Stoica; Tillie-Louise Hackett; Vincent Duronio
Journal:  Cell Cycle       Date:  2010-07-11       Impact factor: 4.534

2.  Proteomic analysis of the Kaposi's sarcoma-associated herpesvirus terminal repeat element binding proteins.

Authors:  Huaxin Si; Subhash C Verma; Erle S Robertson
Journal:  J Virol       Date:  2006-09       Impact factor: 5.103

3.  Histone modification-dependent and -independent pathways for recruitment of checkpoint protein Crb2 to double-strand breaks.

Authors:  Li-Lin Du; Toru M Nakamura; Paul Russell
Journal:  Genes Dev       Date:  2006-06-15       Impact factor: 11.361

4.  Synchronization in the cell cycle by inhibitors of DNA replication induces histone H2AX phosphorylation: an indication of DNA damage.

Authors:  A Kurose; T Tanaka; X Huang; F Traganos; Z Darzynkiewicz
Journal:  Cell Prolif       Date:  2006-06       Impact factor: 6.831

5.  How to exchange your partner. Workshop on recombination mechanisms and the maintenance of genomic stability.

Authors:  Andrés Aguilera; Simon J Boulton
Journal:  EMBO Rep       Date:  2006-12-15       Impact factor: 8.807

6.  Nucleoporins prevent DNA damage accumulation by modulating Ulp1-dependent sumoylation processes.

Authors:  Benoit Palancade; Xianpeng Liu; Maria Garcia-Rubio; Andrès Aguilera; Xiaolan Zhao; Valérie Doye
Journal:  Mol Biol Cell       Date:  2007-05-30       Impact factor: 4.138

Review 7.  Replication fork stalling at natural impediments.

Authors:  Ekaterina V Mirkin; Sergei M Mirkin
Journal:  Microbiol Mol Biol Rev       Date:  2007-03       Impact factor: 11.056

8.  Visualization of local DNA unwinding by Mre11/Rad50/Nbs1 using single-molecule FRET.

Authors:  Brian Cannon; Jeffrey Kuhnlein; Soo-Hyun Yang; Anita Cheng; Detlev Schindler; Jeremy M Stark; Rick Russell; Tanya T Paull
Journal:  Proc Natl Acad Sci U S A       Date:  2013-11-04       Impact factor: 11.205

Review 9.  ATM-like kinases and regulation of telomerase: lessons from yeast and mammals.

Authors:  Michelle Sabourin; Virginia A Zakian
Journal:  Trends Cell Biol       Date:  2008-05-22       Impact factor: 20.808

10.  Forkhead-associated domain of yeast Xrs2, a homolog of human Nbs1, promotes nonhomologous end joining through interaction with a ligase IV partner protein, Lif1.

Authors:  Kenichiro Matsuzaki; Akira Shinohara; Miki Shinohara
Journal:  Genetics       Date:  2008-05-05       Impact factor: 4.562

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