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Role of SUMOylation in Neurodegenerative Diseases
Neurodegenerative diseases (NDDs) are irreversible, progressive diseases with no effective treatment. The hallmark of NDDs is the aggregation of misfolded, modified proteins, which impair neuronal vulnerability and cause brain damage. The loss of synaptic connection and the progressive loss of neuro...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9654019/ https://www.ncbi.nlm.nih.gov/pubmed/36359791 http://dx.doi.org/10.3390/cells11213395 |
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author | Mandel, Nicolas Agarwal, Nitin |
author_facet | Mandel, Nicolas Agarwal, Nitin |
author_sort | Mandel, Nicolas |
collection | PubMed |
description | Neurodegenerative diseases (NDDs) are irreversible, progressive diseases with no effective treatment. The hallmark of NDDs is the aggregation of misfolded, modified proteins, which impair neuronal vulnerability and cause brain damage. The loss of synaptic connection and the progressive loss of neurons result in cognitive defects. Several dysregulated proteins and overlapping molecular mechanisms contribute to the pathophysiology of NDDs. Post-translational modifications (PTMs) are essential regulators of protein function, trafficking, and maintaining neuronal hemostasis. The conjugation of a small ubiquitin-like modifier (SUMO) is a reversible, dynamic PTM required for synaptic and cognitive function. The onset and progression of neurodegenerative diseases are associated with aberrant SUMOylation. In this review, we have summarized the role of SUMOylation in regulating critical proteins involved in the onset and progression of several NDDs. |
format | Online Article Text |
id | pubmed-9654019 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-96540192022-11-15 Role of SUMOylation in Neurodegenerative Diseases Mandel, Nicolas Agarwal, Nitin Cells Review Neurodegenerative diseases (NDDs) are irreversible, progressive diseases with no effective treatment. The hallmark of NDDs is the aggregation of misfolded, modified proteins, which impair neuronal vulnerability and cause brain damage. The loss of synaptic connection and the progressive loss of neurons result in cognitive defects. Several dysregulated proteins and overlapping molecular mechanisms contribute to the pathophysiology of NDDs. Post-translational modifications (PTMs) are essential regulators of protein function, trafficking, and maintaining neuronal hemostasis. The conjugation of a small ubiquitin-like modifier (SUMO) is a reversible, dynamic PTM required for synaptic and cognitive function. The onset and progression of neurodegenerative diseases are associated with aberrant SUMOylation. In this review, we have summarized the role of SUMOylation in regulating critical proteins involved in the onset and progression of several NDDs. MDPI 2022-10-27 /pmc/articles/PMC9654019/ /pubmed/36359791 http://dx.doi.org/10.3390/cells11213395 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Mandel, Nicolas Agarwal, Nitin Role of SUMOylation in Neurodegenerative Diseases |
title | Role of SUMOylation in Neurodegenerative Diseases |
title_full | Role of SUMOylation in Neurodegenerative Diseases |
title_fullStr | Role of SUMOylation in Neurodegenerative Diseases |
title_full_unstemmed | Role of SUMOylation in Neurodegenerative Diseases |
title_short | Role of SUMOylation in Neurodegenerative Diseases |
title_sort | role of sumoylation in neurodegenerative diseases |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9654019/ https://www.ncbi.nlm.nih.gov/pubmed/36359791 http://dx.doi.org/10.3390/cells11213395 |
work_keys_str_mv | AT mandelnicolas roleofsumoylationinneurodegenerativediseases AT agarwalnitin roleofsumoylationinneurodegenerativediseases |