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GFAP Alternative Splicing and the Relevance for Disease – A Focus on Diffuse Gliomas
Glial fibrillary acidic protein (GFAP) is an intermediate filament protein that is characteristic for astrocytes and neural stem cells, and their malignant analogues in glioma. Since the discovery of the protein 50 years ago, multiple alternative splice variants of the GFAP gene have been discovered...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9185002/ https://www.ncbi.nlm.nih.gov/pubmed/35673702 http://dx.doi.org/10.1177/17590914221102065 |
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author | van Asperen, Jessy V. Robe, Pierre A.J.T. Hol, Elly M. |
author_facet | van Asperen, Jessy V. Robe, Pierre A.J.T. Hol, Elly M. |
author_sort | van Asperen, Jessy V. |
collection | PubMed |
description | Glial fibrillary acidic protein (GFAP) is an intermediate filament protein that is characteristic for astrocytes and neural stem cells, and their malignant analogues in glioma. Since the discovery of the protein 50 years ago, multiple alternative splice variants of the GFAP gene have been discovered, leading to different GFAP isoforms. In this review, we will describe GFAP isoform expression from gene to protein to network, taking the canonical isoforms GFAPα and the main alternative variant GFAPδ as the starting point. We will discuss the relevance of studying GFAP and its isoforms in disease, with a specific focus on diffuse gliomas. |
format | Online Article Text |
id | pubmed-9185002 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-91850022022-06-11 GFAP Alternative Splicing and the Relevance for Disease – A Focus on Diffuse Gliomas van Asperen, Jessy V. Robe, Pierre A.J.T. Hol, Elly M. ASN Neuro Review Glial fibrillary acidic protein (GFAP) is an intermediate filament protein that is characteristic for astrocytes and neural stem cells, and their malignant analogues in glioma. Since the discovery of the protein 50 years ago, multiple alternative splice variants of the GFAP gene have been discovered, leading to different GFAP isoforms. In this review, we will describe GFAP isoform expression from gene to protein to network, taking the canonical isoforms GFAPα and the main alternative variant GFAPδ as the starting point. We will discuss the relevance of studying GFAP and its isoforms in disease, with a specific focus on diffuse gliomas. SAGE Publications 2022-06-07 /pmc/articles/PMC9185002/ /pubmed/35673702 http://dx.doi.org/10.1177/17590914221102065 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by-nc/4.0/This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access page (https://us.sagepub.com/en-us/nam/open-access-at-sage). |
spellingShingle | Review van Asperen, Jessy V. Robe, Pierre A.J.T. Hol, Elly M. GFAP Alternative Splicing and the Relevance for Disease – A Focus on Diffuse Gliomas |
title | GFAP Alternative Splicing and the Relevance for Disease – A Focus on Diffuse
Gliomas |
title_full | GFAP Alternative Splicing and the Relevance for Disease – A Focus on Diffuse
Gliomas |
title_fullStr | GFAP Alternative Splicing and the Relevance for Disease – A Focus on Diffuse
Gliomas |
title_full_unstemmed | GFAP Alternative Splicing and the Relevance for Disease – A Focus on Diffuse
Gliomas |
title_short | GFAP Alternative Splicing and the Relevance for Disease – A Focus on Diffuse
Gliomas |
title_sort | gfap alternative splicing and the relevance for disease – a focus on diffuse
gliomas |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9185002/ https://www.ncbi.nlm.nih.gov/pubmed/35673702 http://dx.doi.org/10.1177/17590914221102065 |
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