Literature DB >> 26142952

Optineurin: The autophagy connection.

Hongyu Ying1, Beatrice Y J T Yue2.   

Abstract

Optineurin is a cytosolic protein encoded by the OPTN gene. Mutations of OPTN are associated with normal tension glaucoma and amyotrophic lateral sclerosis. Autophagy is an intracellular degradation system that delivers cytoplasmic components to the lysosomes. It plays a wide variety of physiological and pathophysiological roles. The optineurin protein is a selective autophagy receptor (or adaptor), containing an ubiquitin binding domain with the ability to bind polyubiquitinated cargoes and bring them to autophagosomes via its microtubule-associated protein 1 light chain 3-interacting domain. It is involved in xenophagy, mitophagy, aggrephagy, and tumor suppression. Optineurin can also mediate the removal of protein aggregates through an ubiquitin-independent mechanism. This protein in addition can induce autophagy upon overexpression or mutation. When overexpressed or mutated, the optineurin protein also serves as a substrate for autophagic degradation. In the present review, the multiple connections of optineurin to autophagy are highlighted.
Copyright © 2015 Elsevier Ltd. All rights reserved.

Entities:  

Keywords:  Aggrephagy; Amyotrophic lateral sclerosis (ALS); Autophagy; Autophagy inducer; Autophagy receptor; Mitophagy; Normal tension glaucoma (NTG); Optineurin (OPTN); Protein aggregate; Tumor suppressor; Ubiquitin–proteasome system (UPS); Xenophagy

Mesh:

Substances:

Year:  2015        PMID: 26142952      PMCID: PMC4698099          DOI: 10.1016/j.exer.2015.06.029

Source DB:  PubMed          Journal:  Exp Eye Res        ISSN: 0014-4835            Impact factor:   3.467


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