53BP1, a Mediator of the DNA Damage Checkpoint

Author:

Wang Bin1,Matsuoka Shuhei1,Carpenter Phillip B.2,Elledge Stephen J.134

Affiliation:

1. Verna and Mars McLean Department of Biochemistry and Molecular Biology,

2. Department of Biochemistry and Molecular Biology, University of Texas Health Sciences Center, Houston, TX 77030, USA.

3. Department of Molecular and Human Genetics,

4. Howard Hughes Medical Institute, Baylor College of Medicine, Houston, TX 77030, USA.

Abstract

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.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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