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Lack of association between TDP-43 pathology and tau mis-splicing in Alzheimer's disease

A proportion of Alzheimer's disease cases displays inclusions of the RNA-binding protein, TDP-43. Considering the pathogenic role of tau mis-splicing, we compared tau isoform expression between Alzheimer's disease cases with or without TDP-43 inclusions. The average ratio of tau isoforms c...

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Detalles Bibliográficos
Autores principales: Niblock, Michael, Hortobágyi, Tibor, Troakes, Claire, Al-Sarraj, Safa, Spickett, Carl, Jones, Rebecca, Shaw, Christopher E., Gallo, Jean-Marc
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4706155/
https://www.ncbi.nlm.nih.gov/pubmed/26507309
http://dx.doi.org/10.1016/j.neurobiolaging.2015.09.022
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author Niblock, Michael
Hortobágyi, Tibor
Troakes, Claire
Al-Sarraj, Safa
Spickett, Carl
Jones, Rebecca
Shaw, Christopher E.
Gallo, Jean-Marc
author_facet Niblock, Michael
Hortobágyi, Tibor
Troakes, Claire
Al-Sarraj, Safa
Spickett, Carl
Jones, Rebecca
Shaw, Christopher E.
Gallo, Jean-Marc
author_sort Niblock, Michael
collection PubMed
description A proportion of Alzheimer's disease cases displays inclusions of the RNA-binding protein, TDP-43. Considering the pathogenic role of tau mis-splicing, we compared tau isoform expression between Alzheimer's disease cases with or without TDP-43 inclusions. The average ratio of tau isoforms containing or lacking exon 10 (4R/3R ratio) or the total level of tau mRNA was not significantly different between cases with or without TDP-43 pathology in any of the brain regions examined. Although TDP-43 functions may be affected, TDP-43 does not critically regulate expression or splicing of tau in Alzheimer's disease suggesting that TDP-43 contributes to Alzheimer's disease through mechanisms independent of tau.
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spelling pubmed-47061552016-02-08 Lack of association between TDP-43 pathology and tau mis-splicing in Alzheimer's disease Niblock, Michael Hortobágyi, Tibor Troakes, Claire Al-Sarraj, Safa Spickett, Carl Jones, Rebecca Shaw, Christopher E. Gallo, Jean-Marc Neurobiol Aging Regular Article A proportion of Alzheimer's disease cases displays inclusions of the RNA-binding protein, TDP-43. Considering the pathogenic role of tau mis-splicing, we compared tau isoform expression between Alzheimer's disease cases with or without TDP-43 inclusions. The average ratio of tau isoforms containing or lacking exon 10 (4R/3R ratio) or the total level of tau mRNA was not significantly different between cases with or without TDP-43 pathology in any of the brain regions examined. Although TDP-43 functions may be affected, TDP-43 does not critically regulate expression or splicing of tau in Alzheimer's disease suggesting that TDP-43 contributes to Alzheimer's disease through mechanisms independent of tau. Elsevier 2016-01 /pmc/articles/PMC4706155/ /pubmed/26507309 http://dx.doi.org/10.1016/j.neurobiolaging.2015.09.022 Text en © 2016 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Regular Article
Niblock, Michael
Hortobágyi, Tibor
Troakes, Claire
Al-Sarraj, Safa
Spickett, Carl
Jones, Rebecca
Shaw, Christopher E.
Gallo, Jean-Marc
Lack of association between TDP-43 pathology and tau mis-splicing in Alzheimer's disease
title Lack of association between TDP-43 pathology and tau mis-splicing in Alzheimer's disease
title_full Lack of association between TDP-43 pathology and tau mis-splicing in Alzheimer's disease
title_fullStr Lack of association between TDP-43 pathology and tau mis-splicing in Alzheimer's disease
title_full_unstemmed Lack of association between TDP-43 pathology and tau mis-splicing in Alzheimer's disease
title_short Lack of association between TDP-43 pathology and tau mis-splicing in Alzheimer's disease
title_sort lack of association between tdp-43 pathology and tau mis-splicing in alzheimer's disease
topic Regular Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4706155/
https://www.ncbi.nlm.nih.gov/pubmed/26507309
http://dx.doi.org/10.1016/j.neurobiolaging.2015.09.022
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