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Cytosolic Ptbp2 modulates axon growth in motoneurons through axonal localization and translation of Hnrnpr

The neuronal RNA-binding protein Ptbp2 regulates neuronal differentiation by modulating alternative splicing programs in the nucleus. Such programs contribute to axonogenesis by adjusting the levels of protein isoforms involved in axon growth and branching. While its functions in alternative splicin...

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Autores principales: Salehi, Saeede, Zare, Abdolhossein, Prezza, Gianluca, Bader, Jakob, Schneider, Cornelius, Fischer, Utz, Meissner, Felix, Mann, Matthias, Briese, Michael, Sendtner, Michael
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10338680/
https://www.ncbi.nlm.nih.gov/pubmed/37438340
http://dx.doi.org/10.1038/s41467-023-39787-6
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author Salehi, Saeede
Zare, Abdolhossein
Prezza, Gianluca
Bader, Jakob
Schneider, Cornelius
Fischer, Utz
Meissner, Felix
Mann, Matthias
Briese, Michael
Sendtner, Michael
author_facet Salehi, Saeede
Zare, Abdolhossein
Prezza, Gianluca
Bader, Jakob
Schneider, Cornelius
Fischer, Utz
Meissner, Felix
Mann, Matthias
Briese, Michael
Sendtner, Michael
author_sort Salehi, Saeede
collection PubMed
description The neuronal RNA-binding protein Ptbp2 regulates neuronal differentiation by modulating alternative splicing programs in the nucleus. Such programs contribute to axonogenesis by adjusting the levels of protein isoforms involved in axon growth and branching. While its functions in alternative splicing have been described in detail, cytosolic roles of Ptbp2 for axon growth have remained elusive. Here, we show that Ptbp2 is located in the cytosol including axons and growth cones of motoneurons, and that depletion of cytosolic Ptbp2 affects axon growth. We identify Ptbp2 as a major interactor of the 3’ UTR of Hnrnpr mRNA encoding the RNA-binding protein hnRNP R. Axonal localization of Hnrnpr mRNA and local synthesis of hnRNP R protein are strongly reduced when Ptbp2 is depleted, leading to defective axon growth. Ptbp2 regulates hnRNP R translation by mediating the association of Hnrnpr with ribosomes in a manner dependent on the translation factor eIF5A2. Our data thus suggest a mechanism whereby cytosolic Ptbp2 modulates axon growth by fine-tuning the mRNA transport and local synthesis of an RNA-binding protein.
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spelling pubmed-103386802023-07-14 Cytosolic Ptbp2 modulates axon growth in motoneurons through axonal localization and translation of Hnrnpr Salehi, Saeede Zare, Abdolhossein Prezza, Gianluca Bader, Jakob Schneider, Cornelius Fischer, Utz Meissner, Felix Mann, Matthias Briese, Michael Sendtner, Michael Nat Commun Article The neuronal RNA-binding protein Ptbp2 regulates neuronal differentiation by modulating alternative splicing programs in the nucleus. Such programs contribute to axonogenesis by adjusting the levels of protein isoforms involved in axon growth and branching. While its functions in alternative splicing have been described in detail, cytosolic roles of Ptbp2 for axon growth have remained elusive. Here, we show that Ptbp2 is located in the cytosol including axons and growth cones of motoneurons, and that depletion of cytosolic Ptbp2 affects axon growth. We identify Ptbp2 as a major interactor of the 3’ UTR of Hnrnpr mRNA encoding the RNA-binding protein hnRNP R. Axonal localization of Hnrnpr mRNA and local synthesis of hnRNP R protein are strongly reduced when Ptbp2 is depleted, leading to defective axon growth. Ptbp2 regulates hnRNP R translation by mediating the association of Hnrnpr with ribosomes in a manner dependent on the translation factor eIF5A2. Our data thus suggest a mechanism whereby cytosolic Ptbp2 modulates axon growth by fine-tuning the mRNA transport and local synthesis of an RNA-binding protein. Nature Publishing Group UK 2023-07-12 /pmc/articles/PMC10338680/ /pubmed/37438340 http://dx.doi.org/10.1038/s41467-023-39787-6 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Salehi, Saeede
Zare, Abdolhossein
Prezza, Gianluca
Bader, Jakob
Schneider, Cornelius
Fischer, Utz
Meissner, Felix
Mann, Matthias
Briese, Michael
Sendtner, Michael
Cytosolic Ptbp2 modulates axon growth in motoneurons through axonal localization and translation of Hnrnpr
title Cytosolic Ptbp2 modulates axon growth in motoneurons through axonal localization and translation of Hnrnpr
title_full Cytosolic Ptbp2 modulates axon growth in motoneurons through axonal localization and translation of Hnrnpr
title_fullStr Cytosolic Ptbp2 modulates axon growth in motoneurons through axonal localization and translation of Hnrnpr
title_full_unstemmed Cytosolic Ptbp2 modulates axon growth in motoneurons through axonal localization and translation of Hnrnpr
title_short Cytosolic Ptbp2 modulates axon growth in motoneurons through axonal localization and translation of Hnrnpr
title_sort cytosolic ptbp2 modulates axon growth in motoneurons through axonal localization and translation of hnrnpr
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10338680/
https://www.ncbi.nlm.nih.gov/pubmed/37438340
http://dx.doi.org/10.1038/s41467-023-39787-6
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