| Literature DB >> 11934988 |
Arkady Celeste1, Simone Petersen, Peter J Romanienko, Oscar Fernandez-Capetillo, Hua Tang Chen, Olga A Sedelnikova, Bernardo Reina-San-Martin, Vincenzo Coppola, Eric Meffre, Michael J Difilippantonio, Christophe Redon, Duane R Pilch, Alexandru Olaru, Michael Eckhaus, R Daniel Camerini-Otero, Lino Tessarollo, Ferenc Livak, Katia Manova, William M Bonner, Michel C Nussenzweig, André Nussenzweig.
Abstract
Higher order chromatin structure presents a barrier to the recognition and repair of DNA damage. Double-strand breaks (DSBs) induce histone H2AX phosphorylation, which is associated with the recruitment of repair factors to damaged DNA. To help clarify the physiological role of H2AX, we targeted H2AX in mice. Although H2AX is not essential for irradiation-induced cell-cycle checkpoints, H2AX-/- mice were radiation sensitive, growth retarded, and immune deficient, and mutant males were infertile. These pleiotropic phenotypes were associated with chromosomal instability, repair defects, and impaired recruitment of Nbs1, 53bp1, and Brca1, but not Rad51, to irradiation-induced foci. Thus, H2AX is critical for facilitating the assembly of specific DNA-repair complexes on damaged DNA.Entities:
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Year: 2002 PMID： 11934988 PMCID： PMC4721576 DOI： 10.1126/science.1069398
Source DB: PubMed Journal: Science ISSN： 0036-8075 Impact factor: 47.728