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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, G2-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.
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Bin Wang
The University of Texas MD Anderson Cancer Center
Shuhei Matsuoka
Toho University
Phillip B. Carpenter
California Institute of Technology
Science
Howard Hughes Medical Institute
Baylor College of Medicine
The University of Texas Health Science Center at Houston
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Wang et al. (Thu,) studied this question.
synapsesocial.com/papers/6a1f33cf742cc02e70832c3d — DOI: https://doi.org/10.1126/science.1076182