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Biochem Biophys Res Commun. 2011 Aug 12;411(4):762-7. doi: 10.1016/j.bbrc.2011.07.021. Epub 2011 Jul 18.

Recruitment of the cohesin loading factor NIPBL to DNA double-strand breaks depends on MDC1, RNF168 and HP1γ in human cells.

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1
Department of Radiation Medical Sciences, Atomic Bomb Disease Institute, Nagasaki University, Graduate School of Biomedical Sciences, Japan. dm06188j@cc.nagasaki-u.ac.jp

Abstract

The cohesin loading factor NIPBL is required for cohesin to associate with chromosomes and plays a role in DNA double-strand break (DSB) repair. Although the NIPBL homolog Scc2 is recruited to an enzymatically generated DSB and promotes cohesin-dependent DSB repair in yeast, the mechanism of the recruitment remains poorly understood. Here we show that the human NIPBL is recruited to the sites of DNA damage generated by micro-irradiation as well as to the sites of DSBs induced by homing endonuclease, I-PpoI. The recruitment of NIPBL was impaired by RNAi-mediated knockdown of MDC1 or RNF168, both of which also accumulate at DSBs. We also show that the recruitment of NIPBL to the sites of DNA damage is mediated by its C-terminal region containing HEAT repeats and Heterochromatin protein 1 (HP1) interacting motif. Furthermore, NIPBL accumulation at damaged sites was also compromised by HP1γ depletion. Taken together, our study reveals that human NIPBL is a novel protein recruited to DSB sites, and the recruitment is controlled by MDC1, RNF168 and HP1γ.

PMID:
21784059
DOI:
10.1016/j.bbrc.2011.07.021
[Indexed for MEDLINE]
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