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The prolyl isomerase Pin1 stabilizes NeuroD during differentiation of mechanoreceptors
The peptidyl prolyl cis-trans isomerase Pin1 plays vital roles in diverse cellular processes and pathological conditions. NeuroD is a differentiation and survival factor for a subset of neurons and pancreatic endocrine cells. Although multiple phosphorylation events are known to be crucial for Neuro...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10543749/ https://www.ncbi.nlm.nih.gov/pubmed/37791075 http://dx.doi.org/10.3389/fcell.2023.1225128 |
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author | Zhao, Liqun Fong, Steven H. Yang, Qiaoyun Jiang, Yun-Jin Korzh, Vladimir Liou, Yih-Cherng |
author_facet | Zhao, Liqun Fong, Steven H. Yang, Qiaoyun Jiang, Yun-Jin Korzh, Vladimir Liou, Yih-Cherng |
author_sort | Zhao, Liqun |
collection | PubMed |
description | The peptidyl prolyl cis-trans isomerase Pin1 plays vital roles in diverse cellular processes and pathological conditions. NeuroD is a differentiation and survival factor for a subset of neurons and pancreatic endocrine cells. Although multiple phosphorylation events are known to be crucial for NeuroD function, their mechanisms remain elusive. In this study, we demonstrate that zebrafish embryos deficient in Pin1 displayed phenotypes resembling those associated with NeuroD depletion, characterized by defects in formation of mechanosensory hair cells. Furthermore, zebrafish Pin1 interacts with NeuroD in a phosphorylation-dependent manner. In Pin1-deficient cell lines, NeuroD is rapidly degraded. However, the protein stability of NeuroD is restored upon overexpression of Pin1. These findings suggest that Pin1 functionally regulates NeuroD protein levels by post-phosphorylation cis-trans isomerization during neuronal specification. |
format | Online Article Text |
id | pubmed-10543749 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-105437492023-10-03 The prolyl isomerase Pin1 stabilizes NeuroD during differentiation of mechanoreceptors Zhao, Liqun Fong, Steven H. Yang, Qiaoyun Jiang, Yun-Jin Korzh, Vladimir Liou, Yih-Cherng Front Cell Dev Biol Cell and Developmental Biology The peptidyl prolyl cis-trans isomerase Pin1 plays vital roles in diverse cellular processes and pathological conditions. NeuroD is a differentiation and survival factor for a subset of neurons and pancreatic endocrine cells. Although multiple phosphorylation events are known to be crucial for NeuroD function, their mechanisms remain elusive. In this study, we demonstrate that zebrafish embryos deficient in Pin1 displayed phenotypes resembling those associated with NeuroD depletion, characterized by defects in formation of mechanosensory hair cells. Furthermore, zebrafish Pin1 interacts with NeuroD in a phosphorylation-dependent manner. In Pin1-deficient cell lines, NeuroD is rapidly degraded. However, the protein stability of NeuroD is restored upon overexpression of Pin1. These findings suggest that Pin1 functionally regulates NeuroD protein levels by post-phosphorylation cis-trans isomerization during neuronal specification. Frontiers Media S.A. 2023-09-18 /pmc/articles/PMC10543749/ /pubmed/37791075 http://dx.doi.org/10.3389/fcell.2023.1225128 Text en Copyright © 2023 Zhao, Fong, Yang, Jiang, Korzh and Liou. 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 | Cell and Developmental Biology Zhao, Liqun Fong, Steven H. Yang, Qiaoyun Jiang, Yun-Jin Korzh, Vladimir Liou, Yih-Cherng The prolyl isomerase Pin1 stabilizes NeuroD during differentiation of mechanoreceptors |
title | The prolyl isomerase Pin1 stabilizes NeuroD during differentiation of mechanoreceptors |
title_full | The prolyl isomerase Pin1 stabilizes NeuroD during differentiation of mechanoreceptors |
title_fullStr | The prolyl isomerase Pin1 stabilizes NeuroD during differentiation of mechanoreceptors |
title_full_unstemmed | The prolyl isomerase Pin1 stabilizes NeuroD during differentiation of mechanoreceptors |
title_short | The prolyl isomerase Pin1 stabilizes NeuroD during differentiation of mechanoreceptors |
title_sort | prolyl isomerase pin1 stabilizes neurod during differentiation of mechanoreceptors |
topic | Cell and Developmental Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10543749/ https://www.ncbi.nlm.nih.gov/pubmed/37791075 http://dx.doi.org/10.3389/fcell.2023.1225128 |
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