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Mouse and Human Tau Expression in Different Brain Areas
BACKGROUND: An increase in tau protein is believed to be necessary for tau aggregation. However, whether this is due to increased expression of the endogenous tau promoter or protein accumulation due to proteostasis failure remains uncertain. OBJECTIVE: To analyze the expression of GFP protein under...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
IOS Press
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9696674/ https://www.ncbi.nlm.nih.gov/pubmed/36506485 http://dx.doi.org/10.3233/ADR-220051 |
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author | Vallés-Saiz, Laura Ruiz-Gabarre, Daniel García-Escudero, Vega Perry, George Avila, Jesús Hernández, Félix |
author_facet | Vallés-Saiz, Laura Ruiz-Gabarre, Daniel García-Escudero, Vega Perry, George Avila, Jesús Hernández, Félix |
author_sort | Vallés-Saiz, Laura |
collection | PubMed |
description | BACKGROUND: An increase in tau protein is believed to be necessary for tau aggregation. However, whether this is due to increased expression of the endogenous tau promoter or protein accumulation due to proteostasis failure remains uncertain. OBJECTIVE: To analyze the expression of GFP protein under endogenous tau promoter across different ages and within different brain areas. METHODS: We have measured direct expression of Mapt gene promotor by western blot and immunofluorescence, by means of a commercial tau knock-out mice generated by integrating GFP-encoding cDNA into exon 1 of the Mapt gene. Besides, we have analyzed the MAPT gene expression in human samples. RESULTS: Mapt expression is similar in the cortex, hippocampus, and cerebellum in mice and in human samples although some differences exist between dentate gyrus and CA1 hippocampal areas in mice. Besides, we have analyzed the murine Mapt gene expression during aging (at 2, 6, 12, and 18 moths) and no differences in endogenous tau promoter expression were observed. CONCLUSION: Our results suggest that Mapt promoter activity is similar in the brain areas studied and, therefore, tau accumulation due to aging is likely due to proteostasis failure rather than occurring at the transcriptional level. |
format | Online Article Text |
id | pubmed-9696674 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | IOS Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-96966742022-12-08 Mouse and Human Tau Expression in Different Brain Areas Vallés-Saiz, Laura Ruiz-Gabarre, Daniel García-Escudero, Vega Perry, George Avila, Jesús Hernández, Félix J Alzheimers Dis Rep Research Report BACKGROUND: An increase in tau protein is believed to be necessary for tau aggregation. However, whether this is due to increased expression of the endogenous tau promoter or protein accumulation due to proteostasis failure remains uncertain. OBJECTIVE: To analyze the expression of GFP protein under endogenous tau promoter across different ages and within different brain areas. METHODS: We have measured direct expression of Mapt gene promotor by western blot and immunofluorescence, by means of a commercial tau knock-out mice generated by integrating GFP-encoding cDNA into exon 1 of the Mapt gene. Besides, we have analyzed the MAPT gene expression in human samples. RESULTS: Mapt expression is similar in the cortex, hippocampus, and cerebellum in mice and in human samples although some differences exist between dentate gyrus and CA1 hippocampal areas in mice. Besides, we have analyzed the murine Mapt gene expression during aging (at 2, 6, 12, and 18 moths) and no differences in endogenous tau promoter expression were observed. CONCLUSION: Our results suggest that Mapt promoter activity is similar in the brain areas studied and, therefore, tau accumulation due to aging is likely due to proteostasis failure rather than occurring at the transcriptional level. IOS Press 2022-11-03 /pmc/articles/PMC9696674/ /pubmed/36506485 http://dx.doi.org/10.3233/ADR-220051 Text en © 2022 – The authors. Published by IOS Press https://creativecommons.org/licenses/by-nc/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution Non-Commercial (CC BY-NC 4.0) License (https://creativecommons.org/licenses/by-nc/4.0/) , which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Report Vallés-Saiz, Laura Ruiz-Gabarre, Daniel García-Escudero, Vega Perry, George Avila, Jesús Hernández, Félix Mouse and Human Tau Expression in Different Brain Areas |
title | Mouse and Human Tau Expression in Different Brain Areas |
title_full | Mouse and Human Tau Expression in Different Brain Areas |
title_fullStr | Mouse and Human Tau Expression in Different Brain Areas |
title_full_unstemmed | Mouse and Human Tau Expression in Different Brain Areas |
title_short | Mouse and Human Tau Expression in Different Brain Areas |
title_sort | mouse and human tau expression in different brain areas |
topic | Research Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9696674/ https://www.ncbi.nlm.nih.gov/pubmed/36506485 http://dx.doi.org/10.3233/ADR-220051 |
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