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Identification and functional comparison of novel alternatively spliced isoforms of human YAP
As a key effector of the Hippo pathway, yes‐associated protein (YAP) is a major regulator of cell proliferation and apoptosis. In this study, 23 hYAP isoforms were identified in HEK293 cells, with 14 isoforms being reported for the first time. These isoforms were classified into hYAP‐a and hYAP‐b is...
Autores principales: | , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10240341/ https://www.ncbi.nlm.nih.gov/pubmed/37098971 http://dx.doi.org/10.1002/2211-5463.13618 |
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author | Liu, Lianlian Zhang, Junlei Wang, Jiaqi Tian, Yanping Wang, Jiali Xu, Yixiao Cheng, Yuda Yu, Meng Wang, Jiangjun Yang, Yi Wang, Xueyue Yang, Ran Wu, Wei Zhang, Chen Hu, Yan Jian, Rui Xiao, Lan Ruan, Yan |
author_facet | Liu, Lianlian Zhang, Junlei Wang, Jiaqi Tian, Yanping Wang, Jiali Xu, Yixiao Cheng, Yuda Yu, Meng Wang, Jiangjun Yang, Yi Wang, Xueyue Yang, Ran Wu, Wei Zhang, Chen Hu, Yan Jian, Rui Xiao, Lan Ruan, Yan |
author_sort | Liu, Lianlian |
collection | PubMed |
description | As a key effector of the Hippo pathway, yes‐associated protein (YAP) is a major regulator of cell proliferation and apoptosis. In this study, 23 hYAP isoforms were identified in HEK293 cells, with 14 isoforms being reported for the first time. These isoforms were classified into hYAP‐a and hYAP‐b isoforms based on the variation in exon 1. The two groups of isoforms showed distinctly different subcellular localizations. hYAP‐a isoforms could activate TEAD‐ or P73‐mediated transcription, affect the proliferation rate, and enhance the cellular chemosensitivity of HEK293 cells. Moreover, different activation abilities and pro‐cytotoxic effects were observed among hYAP‐a isoforms. However, hYAP‐b isoforms were not found to exert any significant biological effects. Our findings add to the knowledge of YAP gene structure and protein‐coding capacity and will help in the elucidation of the function and related molecular mechanisms of the Hippo‐YAP signaling pathway. |
format | Online Article Text |
id | pubmed-10240341 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-102403412023-06-06 Identification and functional comparison of novel alternatively spliced isoforms of human YAP Liu, Lianlian Zhang, Junlei Wang, Jiaqi Tian, Yanping Wang, Jiali Xu, Yixiao Cheng, Yuda Yu, Meng Wang, Jiangjun Yang, Yi Wang, Xueyue Yang, Ran Wu, Wei Zhang, Chen Hu, Yan Jian, Rui Xiao, Lan Ruan, Yan FEBS Open Bio Research Articles As a key effector of the Hippo pathway, yes‐associated protein (YAP) is a major regulator of cell proliferation and apoptosis. In this study, 23 hYAP isoforms were identified in HEK293 cells, with 14 isoforms being reported for the first time. These isoforms were classified into hYAP‐a and hYAP‐b isoforms based on the variation in exon 1. The two groups of isoforms showed distinctly different subcellular localizations. hYAP‐a isoforms could activate TEAD‐ or P73‐mediated transcription, affect the proliferation rate, and enhance the cellular chemosensitivity of HEK293 cells. Moreover, different activation abilities and pro‐cytotoxic effects were observed among hYAP‐a isoforms. However, hYAP‐b isoforms were not found to exert any significant biological effects. Our findings add to the knowledge of YAP gene structure and protein‐coding capacity and will help in the elucidation of the function and related molecular mechanisms of the Hippo‐YAP signaling pathway. John Wiley and Sons Inc. 2023-05-08 /pmc/articles/PMC10240341/ /pubmed/37098971 http://dx.doi.org/10.1002/2211-5463.13618 Text en © 2023 The Authors. FEBS Open Bio published by John Wiley & Sons Ltd on behalf of Federation of European Biochemical Societies. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Articles Liu, Lianlian Zhang, Junlei Wang, Jiaqi Tian, Yanping Wang, Jiali Xu, Yixiao Cheng, Yuda Yu, Meng Wang, Jiangjun Yang, Yi Wang, Xueyue Yang, Ran Wu, Wei Zhang, Chen Hu, Yan Jian, Rui Xiao, Lan Ruan, Yan Identification and functional comparison of novel alternatively spliced isoforms of human YAP |
title | Identification and functional comparison of novel alternatively spliced isoforms of human YAP
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title_full | Identification and functional comparison of novel alternatively spliced isoforms of human YAP
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title_fullStr | Identification and functional comparison of novel alternatively spliced isoforms of human YAP
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title_full_unstemmed | Identification and functional comparison of novel alternatively spliced isoforms of human YAP
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title_short | Identification and functional comparison of novel alternatively spliced isoforms of human YAP
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title_sort | identification and functional comparison of novel alternatively spliced isoforms of human yap |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10240341/ https://www.ncbi.nlm.nih.gov/pubmed/37098971 http://dx.doi.org/10.1002/2211-5463.13618 |
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