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The Auto-Generated Fragment of the Usp1 Deubiquitylase Is a Physiological Substrate of the N-End Rule Pathway

Piatkov, Konstantin I. and Colnaghi, Luca and Békés, Miklos and Varshavsky, Alexander and Huang, Tony T. (2012) The Auto-Generated Fragment of the Usp1 Deubiquitylase Is a Physiological Substrate of the N-End Rule Pathway. Molecular Cell, 48 (6). pp. 926-933. ISSN 1097-2765. PMCID PMC3889152. doi:10.1016/j.molcel.2012.10.012. https://resolver.caltech.edu/CaltechAUTHORS:20130211-154805502

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Abstract

Deamidation of N-terminal Gln by the Ntaq1 Nt^Q-amidase is a part of the Arg/N-end rule pathway, a ubiquitin-dependent proteolytic system. Here we identify Gln-Usp1^(Ct), the C-terminal fragment of the autocleaved Usp1 deubiquitylase, as the first physiological Arg/N-end rule substrate that is targeted for degradation through deamidation of N-terminal Gln. Usp1 regulates genomic stability, in part through the deubiquitylation of monoubiquitylated PCNA, a DNA polymerase processivity factor. The autocleaved Usp1 remains a deubiquitylase because its fragments remain associated with Uaf1, an enhancer of Usp1 activity, until the Gln-Usp1^(Ct) fragment is selectively destroyed by the Arg/N-end rule pathway. We also show that metabolic stabilization of Gln-Usp1^(Ct) results in a decreased monoubiquitylation of PCNA and in a hypersensitivity of cells to ultraviolet irradiation. Thus, in addition to its other functions in DNA repair and chromosome segregation, the Arg/N-end rule pathway regulates genomic stability through the degradation-mediated control of the autocleaved Usp1 deubiquitylase.


Item Type:Article
Related URLs:
URLURL TypeDescription
https://doi.org/10.1016/j.molcel.2012.10.012 DOIArticle
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3889152PubMed CentralArticle
ORCID:
AuthorORCID
Varshavsky, Alexander0000-0002-4011-258X
Additional Information:© 2012 Elsevier Inc. Received: July 16, 2012; Revised: September 21, 2012; Accepted: October 2, 2012; Published online: November 15, 2012. We are grateful to A. D’Andrea for the anti-USP1Cterm antibody. We thank members of the Varshavsky, Huang, Bar-Sagi, and Reinberg laboratories for their reagents, advice, assistance, and equipment. This study was supported by NIH grants to A.V. (DK039520 and GM031530) and T.H. (GM084244) and by an American Cancer Society grant to T.H. (RSG-12-158-01-DMC).
Funders:
Funding AgencyGrant Number
NIHDK039520
NIHGM031530
NIHGM084244
American Cancer SocietyRSG-12-158-01-DMC
Issue or Number:6
PubMed Central ID:PMC3889152
DOI:10.1016/j.molcel.2012.10.012
Record Number:CaltechAUTHORS:20130211-154805502
Persistent URL:https://resolver.caltech.edu/CaltechAUTHORS:20130211-154805502
Official Citation:Konstantin I. Piatkov, Luca Colnaghi, Miklos Békés, Alexander Varshavsky, Tony T. Huang, The Auto-Generated Fragment of the Usp1 Deubiquitylase Is a Physiological Substrate of the N-End Rule Pathway, Molecular Cell, Volume 48, Issue 6, 28 December 2012, Pages 926-933, ISSN 1097-2765, 10.1016/j.molcel.2012.10.012.
Usage Policy:No commercial reproduction, distribution, display or performance rights in this work are provided.
ID Code:36855
Collection:CaltechAUTHORS
Deposited By: Tony Diaz
Deposited On:25 Feb 2013 21:50
Last Modified:09 Nov 2021 23:25

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