Literature DB >> 15279780

53BP1, an activator of ATM in response to DNA damage.

Tamara A Mochan1, Monica Venere, Richard A DiTullio, Thanos D Halazonetis.   

Abstract

p53 Binding protein 1 (53BP1) belongs to a family of evolutionarily conserved DNA damage checkpoint proteins with C-terminal BRCT domains and is most likely the human ortholog of the budding yeast Rad9 protein, the first cell cycle checkpoint protein to be described. 53BP1 localizes rapidly to sites of DNA double strand breaks (DSBs) and its initial recruitment to these sites has not been shown to be dependent on any other protein. Initially, 53BP1 was thought to be a mediator of DNA DSB signaling, but now it has been shown to function upstream of ataxia-telangiectasia mutated (ATM), in one of at least two parallel pathways leading to ATM activation in response to DNA damage. Currently, only a single tudor and two BRCT domains are recognized in 53BP1; however, their precise functional role is not understood. Elucidating the function of 53BP1 will be critical to understanding how cells recognize DNA DSBs and how ATM is activated.

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Year:  2004        PMID: 15279780     DOI: 10.1016/j.dnarep.2004.03.017

Source DB:  PubMed          Journal:  DNA Repair (Amst)        ISSN: 1568-7856


  61 in total

1.  PTEN loss compromises homologous recombination repair in astrocytes: implications for glioblastoma therapy with temozolomide or poly(ADP-ribose) polymerase inhibitors.

Authors:  Brian McEllin; Cristel V Camacho; Bipasha Mukherjee; Brandon Hahm; Nozomi Tomimatsu; Robert M Bachoo; Sandeep Burma
Journal:  Cancer Res       Date:  2010-06-08       Impact factor: 12.701

2.  Increased mobility of double-strand breaks requires Mec1, Rad9 and the homologous recombination machinery.

Authors:  Vincent Dion; Véronique Kalck; Chihiro Horigome; Benjamin D Towbin; Susan M Gasser
Journal:  Nat Cell Biol       Date:  2012-04-08       Impact factor: 28.824

3.  Requirement for the phospho-H2AX binding module of Crb2 in double-strand break targeting and checkpoint activation.

Authors:  Steven L Sanders; Ahmad R Arida; Funita P Phan
Journal:  Mol Cell Biol       Date:  2010-08-02       Impact factor: 4.272

Review 4.  DNA damage and repair during lymphoid development: antigen receptor diversity, genomic integrity and lymphomagenesis.

Authors:  Nahum Puebla-Osorio; Chengming Zhu
Journal:  Immunol Res       Date:  2008       Impact factor: 2.829

5.  An oligomerized 53BP1 tudor domain suffices for recognition of DNA double-strand breaks.

Authors:  Omar Zgheib; Kristopher Pataky; Juergen Brugger; Thanos D Halazonetis
Journal:  Mol Cell Biol       Date:  2008-12-08       Impact factor: 4.272

6.  53BP1 Contributes to Igh Locus Chromatin Topology during Class Switch Recombination.

Authors:  Scott Feldman; Robert Wuerffel; Ikbel Achour; Lili Wang; Phillip B Carpenter; Amy L Kenter
Journal:  J Immunol       Date:  2017-02-03       Impact factor: 5.422

Review 7.  Double-strand break repair: 53BP1 comes into focus.

Authors:  Stephanie Panier; Simon J Boulton
Journal:  Nat Rev Mol Cell Biol       Date:  2013-12-11       Impact factor: 94.444

8.  Protein phosphatase 5 regulates the function of 53BP1 after neocarzinostatin-induced DNA damage.

Authors:  Yoonsung Kang; Jung-Hee Lee; Nguyen Ngoc Hoan; Hong-Moon Sohn; In-Youb Chang; Ho Jin You
Journal:  J Biol Chem       Date:  2009-01-28       Impact factor: 5.157

9.  S-S synapsis during class switch recombination is promoted by distantly located transcriptional elements and activation-induced deaminase.

Authors:  Robert Wuerffel; Lili Wang; Fernando Grigera; John Manis; Erik Selsing; Thomas Perlot; Frederick W Alt; Michel Cogne; Eric Pinaud; Amy L Kenter
Journal:  Immunity       Date:  2007-11-01       Impact factor: 31.745

10.  53BP1 promotes ATM activity through direct interactions with the MRN complex.

Authors:  Ji-Hoon Lee; Aaron A Goodarzi; Penny A Jeggo; Tanya T Paull
Journal:  EMBO J       Date:  2009-12-10       Impact factor: 11.598

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