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p62/Sequestosome 1 Regulates Aggresome Formation of Pathogenic Ataxin-3 with Expanded Polyglutamine

The cellular protein quality control system in association with aggresome formation contributes to protecting cells against aggregation-prone protein-induced toxicity. p62/Sequestosome 1 (p62) is a multifunctional protein which plays an important role in protein degradation and aggregation. Although...

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Detalles Bibliográficos
Autores principales: Zhou, Liang, Wang, Hongfeng, Chen, Dong, Gao, Feng, Ying, Zheng, Wang, Guanghui
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4200763/
https://www.ncbi.nlm.nih.gov/pubmed/25158237
http://dx.doi.org/10.3390/ijms150914997
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author Zhou, Liang
Wang, Hongfeng
Chen, Dong
Gao, Feng
Ying, Zheng
Wang, Guanghui
author_facet Zhou, Liang
Wang, Hongfeng
Chen, Dong
Gao, Feng
Ying, Zheng
Wang, Guanghui
author_sort Zhou, Liang
collection PubMed
description The cellular protein quality control system in association with aggresome formation contributes to protecting cells against aggregation-prone protein-induced toxicity. p62/Sequestosome 1 (p62) is a multifunctional protein which plays an important role in protein degradation and aggregation. Although poly-ubiquitination is usually required for p62-mediated protein degradation and aggresome formation, several p62 substrates are processed to form aggregate in an ubiquitination-independent manner. In this study we demonstrate that p62 directly interacts with pathogenic Machado Joseph Disease (MJD)-associated protein ataxin-3 with polyglutamine (polyQ) expansion. Moreover, p62 could regulate the aggresome formation of pathogenic ataxin-3 and protect cells against pathogenic ataxin-3-induced cell death.
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spelling pubmed-42007632014-10-17 p62/Sequestosome 1 Regulates Aggresome Formation of Pathogenic Ataxin-3 with Expanded Polyglutamine Zhou, Liang Wang, Hongfeng Chen, Dong Gao, Feng Ying, Zheng Wang, Guanghui Int J Mol Sci Article The cellular protein quality control system in association with aggresome formation contributes to protecting cells against aggregation-prone protein-induced toxicity. p62/Sequestosome 1 (p62) is a multifunctional protein which plays an important role in protein degradation and aggregation. Although poly-ubiquitination is usually required for p62-mediated protein degradation and aggresome formation, several p62 substrates are processed to form aggregate in an ubiquitination-independent manner. In this study we demonstrate that p62 directly interacts with pathogenic Machado Joseph Disease (MJD)-associated protein ataxin-3 with polyglutamine (polyQ) expansion. Moreover, p62 could regulate the aggresome formation of pathogenic ataxin-3 and protect cells against pathogenic ataxin-3-induced cell death. MDPI 2014-08-25 /pmc/articles/PMC4200763/ /pubmed/25158237 http://dx.doi.org/10.3390/ijms150914997 Text en © 2014 by the authors; licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/).
spellingShingle Article
Zhou, Liang
Wang, Hongfeng
Chen, Dong
Gao, Feng
Ying, Zheng
Wang, Guanghui
p62/Sequestosome 1 Regulates Aggresome Formation of Pathogenic Ataxin-3 with Expanded Polyglutamine
title p62/Sequestosome 1 Regulates Aggresome Formation of Pathogenic Ataxin-3 with Expanded Polyglutamine
title_full p62/Sequestosome 1 Regulates Aggresome Formation of Pathogenic Ataxin-3 with Expanded Polyglutamine
title_fullStr p62/Sequestosome 1 Regulates Aggresome Formation of Pathogenic Ataxin-3 with Expanded Polyglutamine
title_full_unstemmed p62/Sequestosome 1 Regulates Aggresome Formation of Pathogenic Ataxin-3 with Expanded Polyglutamine
title_short p62/Sequestosome 1 Regulates Aggresome Formation of Pathogenic Ataxin-3 with Expanded Polyglutamine
title_sort p62/sequestosome 1 regulates aggresome formation of pathogenic ataxin-3 with expanded polyglutamine
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4200763/
https://www.ncbi.nlm.nih.gov/pubmed/25158237
http://dx.doi.org/10.3390/ijms150914997
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