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C9orf72 loss-of-function: a trivial, stand-alone or additive mechanism in C9 ALS/FTD?
A repeat expansion in C9orf72 is responsible for the characteristic neurodegeneration in amyotrophic lateral sclerosis (ALS) and frontotemporal dementia (FTD) in a still unresolved manner. Proposed mechanisms involve gain-of-functions, comprising RNA and protein toxicity, and loss-of-function of the...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7547039/ https://www.ncbi.nlm.nih.gov/pubmed/32876811 http://dx.doi.org/10.1007/s00401-020-02214-x |
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author | Braems, Elke Swinnen, Bart Van Den Bosch, Ludo |
author_facet | Braems, Elke Swinnen, Bart Van Den Bosch, Ludo |
author_sort | Braems, Elke |
collection | PubMed |
description | A repeat expansion in C9orf72 is responsible for the characteristic neurodegeneration in amyotrophic lateral sclerosis (ALS) and frontotemporal dementia (FTD) in a still unresolved manner. Proposed mechanisms involve gain-of-functions, comprising RNA and protein toxicity, and loss-of-function of the C9orf72 gene. Their exact contribution is still inconclusive and reports regarding loss-of-function are rather inconsistent. Here, we review the function of the C9orf72 protein and its relevance in disease. We explore the potential link between reduced C9orf72 levels and disease phenotypes in postmortem, in vitro, and in vivo models. Moreover, the significance of loss-of-function in other non-coding repeat expansion diseases is used to clarify its contribution in C9orf72 ALS/FTD. In conclusion, with evidence pointing to a multiple-hit model, loss-of-function on itself seems to be insufficient to cause neurodegeneration in C9orf72 ALS/FTD. |
format | Online Article Text |
id | pubmed-7547039 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-75470392020-10-19 C9orf72 loss-of-function: a trivial, stand-alone or additive mechanism in C9 ALS/FTD? Braems, Elke Swinnen, Bart Van Den Bosch, Ludo Acta Neuropathol Review A repeat expansion in C9orf72 is responsible for the characteristic neurodegeneration in amyotrophic lateral sclerosis (ALS) and frontotemporal dementia (FTD) in a still unresolved manner. Proposed mechanisms involve gain-of-functions, comprising RNA and protein toxicity, and loss-of-function of the C9orf72 gene. Their exact contribution is still inconclusive and reports regarding loss-of-function are rather inconsistent. Here, we review the function of the C9orf72 protein and its relevance in disease. We explore the potential link between reduced C9orf72 levels and disease phenotypes in postmortem, in vitro, and in vivo models. Moreover, the significance of loss-of-function in other non-coding repeat expansion diseases is used to clarify its contribution in C9orf72 ALS/FTD. In conclusion, with evidence pointing to a multiple-hit model, loss-of-function on itself seems to be insufficient to cause neurodegeneration in C9orf72 ALS/FTD. Springer Berlin Heidelberg 2020-09-02 2020 /pmc/articles/PMC7547039/ /pubmed/32876811 http://dx.doi.org/10.1007/s00401-020-02214-x Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Review Braems, Elke Swinnen, Bart Van Den Bosch, Ludo C9orf72 loss-of-function: a trivial, stand-alone or additive mechanism in C9 ALS/FTD? |
title | C9orf72 loss-of-function: a trivial, stand-alone or additive mechanism in C9 ALS/FTD? |
title_full | C9orf72 loss-of-function: a trivial, stand-alone or additive mechanism in C9 ALS/FTD? |
title_fullStr | C9orf72 loss-of-function: a trivial, stand-alone or additive mechanism in C9 ALS/FTD? |
title_full_unstemmed | C9orf72 loss-of-function: a trivial, stand-alone or additive mechanism in C9 ALS/FTD? |
title_short | C9orf72 loss-of-function: a trivial, stand-alone or additive mechanism in C9 ALS/FTD? |
title_sort | c9orf72 loss-of-function: a trivial, stand-alone or additive mechanism in c9 als/ftd? |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7547039/ https://www.ncbi.nlm.nih.gov/pubmed/32876811 http://dx.doi.org/10.1007/s00401-020-02214-x |
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