Literature DB >> 27880896

RNF166 Determines Recruitment of Adaptor Proteins during Antibacterial Autophagy.

Robert J Heath1, Gautam Goel2, Leigh A Baxt2, Jason S Rush3, Vishnu Mohanan2, Geraldine L C Paulus2, Vijay Jani2, Kara G Lassen4, Ramnik J Xavier5.   

Abstract

Xenophagy is a form of selective autophagy that involves the targeting and elimination of intracellular pathogens through several recognition, recruitment, and ubiquitination events. E3 ubiquitin ligases control substrate selectivity in the ubiquitination cascade; however, systematic approaches to map the role of E3 ligases in antibacterial autophagy have been lacking. We screened more than 600 putative human E3 ligases, identifying E3 ligases that are required for adaptor protein recruitment and LC3-bacteria colocalization, critical steps in antibacterial autophagy. An unbiased informatics approach pinpointed RNF166 as a key gene that interacts with the autophagy network and controls the recruitment of ubiquitin as well as the autophagy adaptors p62 and NDP52 to bacteria. Mechanistic studies demonstrated that RNF166 catalyzes K29- and K33-linked polyubiquitination of p62 at residues K91 and K189. Thus, our study expands the catalog of E3 ligases that mediate antibacterial autophagy and identifies a critical role for RNF166 in this process. Copyright Â
© 2016 The Authors. Published by Elsevier Inc. All rights reserved.

Entities:  

Keywords:  E3 ligases; RNF166; antibacterial autophagy; autophagy; p62; p62 ubiquitination; xenophagy

Mesh:

Substances:

Year:  2016        PMID: 27880896      PMCID: PMC5192565          DOI: 10.1016/j.celrep.2016.11.005

Source DB:  PubMed          Journal:  Cell Rep            Impact factor:   9.423


  71 in total

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  33 in total

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Review 2.  Molecular definitions of autophagy and related processes.

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Review 4.  Autophagy and microbial pathogenesis.

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Review 6.  Genetic control of autophagy underlies pathogenesis of inflammatory bowel disease.

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7.  Keap1/Cullin3 Modulates p62/SQSTM1 Activity via UBA Domain Ubiquitination.

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8.  The ubiquitin-specific protease USP8 directly deubiquitinates SQSTM1/p62 to suppress its autophagic activity.

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Review 10.  Ubiquitin, SUMO, and NEDD8: Key Targets of Bacterial Pathogens.

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