Document Detail


Accumulation of checkpoint protein 53BP1 at DNA breaks involves its binding to phosphorylated histone H2AX.
MedLine Citation:
PMID:  12697768     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
53BP1 participates in the cellular response to DNA damage. Like many proteins involved in the DNA damage response, 53BP1 becomes hyperphosphorylated after radiation and colocalizes with phosphorylated H2AX in megabase regions surrounding the sites of DNA strand breaks. However, it is not yet clear whether the phosphorylation status of 53BP1 determines its localization or vice versa. In this study we mapped a region upstream of the 53BP1 C terminus that is required and sufficient for the recruitment of 53BP1 to these DNA break areas. In vitro assays revealed that this region binds to phosphorylated but not unphosphorylated H2AX. Moreover, using H2AX-deficient cells reconstituted with wild-type or a phosphorylation-deficient mutant of H2AX, we have shown that phosphorylation of H2AX at serine 140 is critical for efficient 53BP1 foci formation, implying that a direct interaction between 53BP1 and phosphorylated H2AX is required for the accumulation of 53BP1 at DNA break sites. On the other hand, radiation-induced phosphorylation of the 53BP1 N terminus by the ATM (ataxia-telangiectasia mutated) kinase is not essential for 53BP1 foci formation and takes place independently of 53BP1 redistribution. Thus, these two damage-induced events, hyperphosphorylation and relocalization of 53BP1, occur independently in the cell.
Authors:
Irene M Ward; Kay Minn; Katherine G Jorda; Junjie Chen
Related Documents :
21047968 - Bocavirus infection induces a dna damage response that facilitates viral dna replicatio...
11303908 - The molecular control of dna damage-induced cell death.
12663048 - Activation of p53 by the cytoprotective aminothiol wr1065: dna-damage-independent pathw...
16400328 - Role of genomic instability and p53 in aid-induced c-myc-igh translocations.
2750788 - Quantitative calibration and use of dna probes for investigating chromosome abnormaliti...
24404958 - Biochemical characterisation and comparison of two closely related active mariner trans...
Publication Detail:
Type:  Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, Non-P.H.S.; Research Support, U.S. Gov't, P.H.S.     Date:  2003-04-15
Journal Detail:
Title:  The Journal of biological chemistry     Volume:  278     ISSN:  0021-9258     ISO Abbreviation:  J. Biol. Chem.     Publication Date:  2003 May 
Date Detail:
Created Date:  2003-05-26     Completed Date:  2003-07-10     Revised Date:  2006-11-15    
Medline Journal Info:
Nlm Unique ID:  2985121R     Medline TA:  J Biol Chem     Country:  United States    
Other Details:
Languages:  eng     Pagination:  19579-82     Citation Subset:  IM    
Affiliation:
Department of Oncology, Mayo Clinic and Foundation, Rochester, Minnesota 55905, USA.
Export Citation:
APA/MLA Format     Download EndNote     Download BibTex
MeSH Terms
Descriptor/Qualifier:
Carrier Proteins / genetics,  metabolism*
Cell Line
DNA / metabolism*
DNA Damage*
Histones / metabolism*
Intracellular Signaling Peptides and Proteins*
Mutagenesis, Site-Directed
Phosphoproteins*
Phosphorylation
Protein Binding
Chemical
Reg. No./Substance:
0/Carrier Proteins; 0/Histones; 0/Intracellular Signaling Peptides and Proteins; 0/Phosphoproteins; 9007-49-2/DNA

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


Previous Document:  Induction of osteoclast differentiation by Runx2 through receptor activator of nuclear factor-kappa ...
Next Document:  Ferritoid, a tissue-specific nuclear transport protein for ferritin in corneal epithelial cells.