An Allosteric Interaction Links USP7 to Deubiquitination and Chromatin Targeting of UHRF1.

Autor:	Zhang ZM; Department of Biochemistry, University of California, Riverside, Riverside, CA 92521, USA., Rothbart SB; Center for Epigenetics, Van Andel Research Institute, Grand Rapids, MI 49503, USA., Allison DF; The Lineberger Comprehensive Cancer Center, University of North Carolina at Chapel Hill School of Medicine, Chapel Hill, NC 27599, USA., Cai Q; Department of Chemistry, University of California, Riverside, Riverside, CA 92521, USA., Harrison JS; The Lineberger Comprehensive Cancer Center, University of North Carolina at Chapel Hill School of Medicine, Chapel Hill, NC 27599, USA; Department of Biochemistry and Biophysics, University of North Carolina at Chapel Hill School of Medicine, Chapel Hill, NC 27599, USA., Li L; Department of Chemistry, University of California, Riverside, Riverside, CA 92521, USA., Wang Y; Department of Chemistry, University of California, Riverside, Riverside, CA 92521, USA., Strahl BD; The Lineberger Comprehensive Cancer Center, University of North Carolina at Chapel Hill School of Medicine, Chapel Hill, NC 27599, USA; Department of Biochemistry and Biophysics, University of North Carolina at Chapel Hill School of Medicine, Chapel Hill, NC 27599, USA., Wang GG; The Lineberger Comprehensive Cancer Center, University of North Carolina at Chapel Hill School of Medicine, Chapel Hill, NC 27599, USA; Department of Biochemistry and Biophysics, University of North Carolina at Chapel Hill School of Medicine, Chapel Hill, NC 27599, USA., Song J; Department of Biochemistry, University of California, Riverside, Riverside, CA 92521, USA. Electronic address: jikui.song@ucr.edu.
Jazyk:	angličtina
Zdroj:	Cell reports [Cell Rep] 2015 Sep 01; Vol. 12 (9), pp. 1400-6. Date of Electronic Publication: 2015 Aug 20.
DOI:	10.1016/j.celrep.2015.07.046
Abstrakt:	The protein stability and chromatin functions of UHRF1 (ubiquitin-like, containing PHD and RING finger domains, 1) are regulated in a cell-cycle-dependent manner. We report a structural characterization of the complex between UHRF1 and the deubiquitinase USP7. The first two UBL domains of USP7 bind to the polybasic region (PBR) of UHRF1, and this interaction is required for the USP7-mediated deubiquitination of UHRF1. Importantly, we find that the USP7-binding site of the UHRF1 PBR overlaps with the region engaging in an intramolecular interaction with the N-terminal tandem Tudor domain (TTD). We show that the USP7-UHRF1 interaction perturbs the TTD-PBR interaction of UHRF1, thereby shifting the conformation of UHRF1 from a TTD-"occluded" state to a state open for multivalent histone binding. Consistently, introduction of a USP7-interaction-defective mutation to UHRF1 significantly reduces its chromatin association. Together, these results link USP7 interaction to the dynamic deubiquitination and chromatin association of UHRF1. (Copyright © 2015 The Authors. Published by Elsevier Inc. All rights reserved.)
Databáze:	MEDLINE
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