PUBLICATION

The prolyl isomerase Pin1 stabilizes NeuroD during differentiation of mechanoreceptors

Authors
Zhao, L., Fong, S.H., Yang, Q., Jiang, Y.J., Korzh, V., Liou, Y.C.
ID
ZDB-PUB-231004-67
Date
2023
Source
Frontiers in cell and developmental biology   11: 12251281225128 (Journal)
Registered Authors
Fong, Steven, Korzh, Vladimir
Keywords
NeuroD, Zebrafish, cis-trans isomerization, mechanoreceptors, prolyl isomerase Pin1
MeSH Terms
none
PubMed
37791075 Full text @ Front Cell Dev Biol
Abstract
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.
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