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Permanent URL to this publication: http://dx.doi.org/10.5167/uzh-50378

Meerang, M; Ritz, D; Paliwal, S; Garajova, Z; Bosshard, M; Mailand, N; Janscak, P; Hübscher, U; Meyer, H; Ramadan, K (2011). The ubiquitin-selective segregase VCP/p97 orchestrates the response to DNA double-strand breaks. Nature Cell Biology, 13(11):1376-1382.

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Abstract

Unrepaired DNA double-strand breaks (DSBs) cause genetic instability that leads to malignant transformation or cell death. Cells respond to DSBs with the ordered recruitment of signalling and repair proteins to the site of lesion. Protein modification with ubiquitin is crucial for the signalling cascade, but how ubiquitylation coordinates the dynamic assembly of these complexes is poorly understood. Here, we show that the human ubiquitin-selective protein segregase p97 (also known as VCP; valosin-containing protein) cooperates with the ubiquitin ligase RNF8 to orchestrate assembly of signalling complexes and efficient DSB repair after exposure to ionizing radiation. p97 is recruited to DNA lesions by its ubiquitin adaptor UFD1-NPL4 and Lys-48-linked ubiquitin (K48-Ub) chains, whose formation is regulated by RNF8. p97 subsequently removes K48-Ub conjugates from sites of DNA damage to orchestrate proper association of 53BP1, BRCA1 and RAD51, three factors critical for DNA repair and genome surveillance mechanisms. Impairment of p97 activity decreases the level of DSB repair and cell survival after exposure to ionizing radiation. These findings identify the p97-UFD1-NPL4 complex as an essential factor in ubiquitin-governed DNA-damage response, highlighting its importance in guarding genome stability.

Item Type:Journal Article, refereed, original work
Communities & Collections:04 Faculty of Medicine > Institute of Molecular Cancer Research
07 Faculty of Science > Institute of Molecular Cancer Research

05 Vetsuisse Faculty > Institute of Veterinary Pharmacology and Toxicology
DDC:570 Life sciences; biology
Language:English
Date:2011
Deposited On:28 Oct 2011 12:19
Last Modified:29 Nov 2013 14:20
Publisher:Nature Publishing Group
ISSN:1465-7392
Publisher DOI:10.1038/ncb2367
PubMed ID:22020440
Citations:Web of Science®. Times Cited: 60
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Scopus®. Citation Count: 65

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