Ubiquitin-Binding Protein RAP80 Mediates BRCA1-Dependent DNA Damage Response

Author:

Kim Hongtae12,Chen Junjie12,Yu Xiaochun12

Affiliation:

1. Department of Therapeutic Radiology, Yale University School of Medicine, Post Office Box 208040, New Haven, CT 06520, USA.

2. Division of Molecular Medicine and Genetics, Department of Internal Medicine, University of Michigan Medical School, 109 Zina Pitcher Place, 1520 Biomedical Science Research Building, Ann Arbor, MI 48109, USA.

Abstract

Mutations in the breast cancer susceptibility gene 1 ( BRCA1 ) are associated with an increased risk of breast and ovarian cancers. BRCA1 participates in the cellular DNA damage response. We report the identification of receptor-associated protein 80 (RAP80) as a BRCA1-interacting protein in humans. RAP80 contains a tandem ubiquitin-interacting motif domain, which is required for its binding with ubiquitin in vitro and its damage-induced foci formation in vivo. Moreover, RAP80 specifically recruits BRCA1 to DNA damage sites and functions with BRCA1 in G 2 /M checkpoint control. Together, these results suggest the existence of a ubiquitination-dependent signaling pathway involved in the DNA damage response.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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