53BP1 binds to the tumor suppressor protein p53 and has a potential role in DNA damage responses. We used small interfering RNA (siRNA) directed against 53BP1 in mammalian cells to demonstrate that 53BP1 is a key transducer of the DNA damage checkpoint signal. 53BP1 was required for p53 accumulation, G(2)-M checkpoint arrest, and the intra-S-phase checkpoint in response to ionizing radiation. 53BP1 played a partially redundant role in phosphorylation of the downstream checkpoint effector proteins Brca1 and Chk2 but was required for the formation of Brca1 foci in a hierarchical branched pathway for the recruitment of repair and signaling proteins to sites of DNA damage.
机构:
UNIV PARIS 07, CNRS URA 09, LAB MINERAL CRISTALLOG, F-75252 PARIS 05, FRANCEUNIV PARIS 07, CNRS URA 09, LAB MINERAL CRISTALLOG, F-75252 PARIS 05, FRANCE
Callebaut, I
Mornon, JP
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机构:
UNIV PARIS 07, CNRS URA 09, LAB MINERAL CRISTALLOG, F-75252 PARIS 05, FRANCEUNIV PARIS 07, CNRS URA 09, LAB MINERAL CRISTALLOG, F-75252 PARIS 05, FRANCE
机构:
UNIV PARIS 07, CNRS URA 09, LAB MINERAL CRISTALLOG, F-75252 PARIS 05, FRANCEUNIV PARIS 07, CNRS URA 09, LAB MINERAL CRISTALLOG, F-75252 PARIS 05, FRANCE
Callebaut, I
Mornon, JP
论文数: 0引用数: 0
h-index: 0
机构:
UNIV PARIS 07, CNRS URA 09, LAB MINERAL CRISTALLOG, F-75252 PARIS 05, FRANCEUNIV PARIS 07, CNRS URA 09, LAB MINERAL CRISTALLOG, F-75252 PARIS 05, FRANCE