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Non-Proteasomal UbL-UbA Family of Proteins in Neurodegeneration

Ubiquitin-like/ubiquitin-associated proteins (UbL-UbA) are a well-studied family of non-proteasomal ubiquitin receptors that are evolutionarily conserved across species. Members of this non-homogenous family facilitate and support proteasomal activity by promoting different effects on proteostasis b...

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Detalles Bibliográficos
Autores principales: Jantrapirom, Salinee, Lo Piccolo, Luca, Yamaguchi, Masamitsu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6514573/
https://www.ncbi.nlm.nih.gov/pubmed/30999567
http://dx.doi.org/10.3390/ijms20081893
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author Jantrapirom, Salinee
Lo Piccolo, Luca
Yamaguchi, Masamitsu
author_facet Jantrapirom, Salinee
Lo Piccolo, Luca
Yamaguchi, Masamitsu
author_sort Jantrapirom, Salinee
collection PubMed
description Ubiquitin-like/ubiquitin-associated proteins (UbL-UbA) are a well-studied family of non-proteasomal ubiquitin receptors that are evolutionarily conserved across species. Members of this non-homogenous family facilitate and support proteasomal activity by promoting different effects on proteostasis but exhibit diverse extra-proteasomal activities. Dysfunctional UbL-UbA proteins render cells, particularly neurons, more susceptible to stressors or aging and may cause earlier neurodegeneration. In this review, we summarized the properties and functions of UbL-UbA family members identified to date, with an emphasis on new findings obtained using Drosophila models showing a direct or indirect role in some neurodegenerative diseases.
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spelling pubmed-65145732019-05-30 Non-Proteasomal UbL-UbA Family of Proteins in Neurodegeneration Jantrapirom, Salinee Lo Piccolo, Luca Yamaguchi, Masamitsu Int J Mol Sci Review Ubiquitin-like/ubiquitin-associated proteins (UbL-UbA) are a well-studied family of non-proteasomal ubiquitin receptors that are evolutionarily conserved across species. Members of this non-homogenous family facilitate and support proteasomal activity by promoting different effects on proteostasis but exhibit diverse extra-proteasomal activities. Dysfunctional UbL-UbA proteins render cells, particularly neurons, more susceptible to stressors or aging and may cause earlier neurodegeneration. In this review, we summarized the properties and functions of UbL-UbA family members identified to date, with an emphasis on new findings obtained using Drosophila models showing a direct or indirect role in some neurodegenerative diseases. MDPI 2019-04-17 /pmc/articles/PMC6514573/ /pubmed/30999567 http://dx.doi.org/10.3390/ijms20081893 Text en © 2019 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 (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Jantrapirom, Salinee
Lo Piccolo, Luca
Yamaguchi, Masamitsu
Non-Proteasomal UbL-UbA Family of Proteins in Neurodegeneration
title Non-Proteasomal UbL-UbA Family of Proteins in Neurodegeneration
title_full Non-Proteasomal UbL-UbA Family of Proteins in Neurodegeneration
title_fullStr Non-Proteasomal UbL-UbA Family of Proteins in Neurodegeneration
title_full_unstemmed Non-Proteasomal UbL-UbA Family of Proteins in Neurodegeneration
title_short Non-Proteasomal UbL-UbA Family of Proteins in Neurodegeneration
title_sort non-proteasomal ubl-uba family of proteins in neurodegeneration
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6514573/
https://www.ncbi.nlm.nih.gov/pubmed/30999567
http://dx.doi.org/10.3390/ijms20081893
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