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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
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.
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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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