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hnRNP A1B, a Splice Variant of HNRNPA1, Is Spatially and Temporally Regulated
RNA binding proteins (RBPs) play a key role in cellular growth, homoeostasis and survival and are tightly regulated. A deep understanding of their spatiotemporal regulation is needed to understand their contribution to physiology and pathology. Here, we have characterized the spatiotemporal expressi...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8498194/ https://www.ncbi.nlm.nih.gov/pubmed/34630013 http://dx.doi.org/10.3389/fnins.2021.724307 |
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author | Gagné, Myriam Deshaies, Jade-Emmanuelle Sidibé, Hadjara Benchaar, Yousri Arbour, Danielle Dubinski, Alicia Litt, Gurleen Peyrard, Sarah Robitaille, Richard Sephton, Chantelle F. Vande Velde, Christine |
author_facet | Gagné, Myriam Deshaies, Jade-Emmanuelle Sidibé, Hadjara Benchaar, Yousri Arbour, Danielle Dubinski, Alicia Litt, Gurleen Peyrard, Sarah Robitaille, Richard Sephton, Chantelle F. Vande Velde, Christine |
author_sort | Gagné, Myriam |
collection | PubMed |
description | RNA binding proteins (RBPs) play a key role in cellular growth, homoeostasis and survival and are tightly regulated. A deep understanding of their spatiotemporal regulation is needed to understand their contribution to physiology and pathology. Here, we have characterized the spatiotemporal expression pattern of hnRNP A1 and its splice variant hnRNP A1B in mice. We have found that hnRNP A1B expression is more restricted to the CNS compared to hnRNP A1, and that it can form an SDS-resistant dimer in the CNS. Also, hnRNP A1B expression becomes progressively restricted to motor neurons in the ventral horn of the spinal cord, compared to hnRNP A1 which is more broadly expressed. We also demonstrate that hnRNP A1B is present in neuronal processes, while hnRNP A1 is absent. This finding supports a hypothesis that hnRNP A1B may have a cytosolic function in neurons that is not shared with hnRNP A1. Our results demonstrate that both isoforms are differentially expressed across tissues and have distinct localization profiles, suggesting that the two isoforms may have specific subcellular functions that can uniquely contribute to disease progression. |
format | Online Article Text |
id | pubmed-8498194 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-84981942021-10-09 hnRNP A1B, a Splice Variant of HNRNPA1, Is Spatially and Temporally Regulated Gagné, Myriam Deshaies, Jade-Emmanuelle Sidibé, Hadjara Benchaar, Yousri Arbour, Danielle Dubinski, Alicia Litt, Gurleen Peyrard, Sarah Robitaille, Richard Sephton, Chantelle F. Vande Velde, Christine Front Neurosci Neuroscience RNA binding proteins (RBPs) play a key role in cellular growth, homoeostasis and survival and are tightly regulated. A deep understanding of their spatiotemporal regulation is needed to understand their contribution to physiology and pathology. Here, we have characterized the spatiotemporal expression pattern of hnRNP A1 and its splice variant hnRNP A1B in mice. We have found that hnRNP A1B expression is more restricted to the CNS compared to hnRNP A1, and that it can form an SDS-resistant dimer in the CNS. Also, hnRNP A1B expression becomes progressively restricted to motor neurons in the ventral horn of the spinal cord, compared to hnRNP A1 which is more broadly expressed. We also demonstrate that hnRNP A1B is present in neuronal processes, while hnRNP A1 is absent. This finding supports a hypothesis that hnRNP A1B may have a cytosolic function in neurons that is not shared with hnRNP A1. Our results demonstrate that both isoforms are differentially expressed across tissues and have distinct localization profiles, suggesting that the two isoforms may have specific subcellular functions that can uniquely contribute to disease progression. Frontiers Media S.A. 2021-09-24 /pmc/articles/PMC8498194/ /pubmed/34630013 http://dx.doi.org/10.3389/fnins.2021.724307 Text en Copyright © 2021 Gagné, Deshaies, Sidibé, Benchaar, Arbour, Dubinski, Litt, Peyrard, Robitaille, Sephton and Vande Velde. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Neuroscience Gagné, Myriam Deshaies, Jade-Emmanuelle Sidibé, Hadjara Benchaar, Yousri Arbour, Danielle Dubinski, Alicia Litt, Gurleen Peyrard, Sarah Robitaille, Richard Sephton, Chantelle F. Vande Velde, Christine hnRNP A1B, a Splice Variant of HNRNPA1, Is Spatially and Temporally Regulated |
title | hnRNP A1B, a Splice Variant of HNRNPA1, Is Spatially and Temporally Regulated |
title_full | hnRNP A1B, a Splice Variant of HNRNPA1, Is Spatially and Temporally Regulated |
title_fullStr | hnRNP A1B, a Splice Variant of HNRNPA1, Is Spatially and Temporally Regulated |
title_full_unstemmed | hnRNP A1B, a Splice Variant of HNRNPA1, Is Spatially and Temporally Regulated |
title_short | hnRNP A1B, a Splice Variant of HNRNPA1, Is Spatially and Temporally Regulated |
title_sort | hnrnp a1b, a splice variant of hnrnpa1, is spatially and temporally regulated |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8498194/ https://www.ncbi.nlm.nih.gov/pubmed/34630013 http://dx.doi.org/10.3389/fnins.2021.724307 |
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