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Cooperative regulation of Zhx1 and hnRNPA1 drives the cardiac progenitor-specific transcriptional activation during cardiomyocyte differentiation

The zinc finger proteins (ZNFs) mediated transcriptional regulation is critical for cell fate transition. However, it is still unclear how the ZNFs realize their specific regulatory roles in the stage-specific determination of cardiomyocyte differentiation. Here, we reported that the zinc fingers an...

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Autores principales: Chen, Yang, Wu, Yukang, Li, Jianguo, Chen, Kai, Wang, Wuchan, Ye, Zihui, Feng, Ke, Yang, Yiwei, Xu, Yanxin, Kang, Jiuhong, Guo, Xudong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10349095/
https://www.ncbi.nlm.nih.gov/pubmed/37452012
http://dx.doi.org/10.1038/s41420-023-01548-1
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author Chen, Yang
Wu, Yukang
Li, Jianguo
Chen, Kai
Wang, Wuchan
Ye, Zihui
Feng, Ke
Yang, Yiwei
Xu, Yanxin
Kang, Jiuhong
Guo, Xudong
author_facet Chen, Yang
Wu, Yukang
Li, Jianguo
Chen, Kai
Wang, Wuchan
Ye, Zihui
Feng, Ke
Yang, Yiwei
Xu, Yanxin
Kang, Jiuhong
Guo, Xudong
author_sort Chen, Yang
collection PubMed
description The zinc finger proteins (ZNFs) mediated transcriptional regulation is critical for cell fate transition. However, it is still unclear how the ZNFs realize their specific regulatory roles in the stage-specific determination of cardiomyocyte differentiation. Here, we reported that the zinc fingers and homeoboxes 1 (Zhx1) protein, transiently expressed during the cell fate transition from mesoderm to cardiac progenitors, was indispensable for the proper cardiomyocyte differentiation of mouse and human embryonic stem cells. Moreover, Zhx1 majorly promoted the specification of cardiac progenitors via interacting with hnRNPA1 and co-activated the transcription of a wide range of genes. In-depth mechanistic studies showed that Zhx1 was bound with hnRNPA1 by the amino acid residues (Thr111–His120) of the second Znf domain, thus participating in the formation of cardiac progenitors. Together, our study highlights the unrevealed interaction of Zhx1/hnRNPA1 for activating gene transcription during cardiac progenitor specification and also provides new evidence for the specificity of cell fate determination in cardiomyocyte differentiation.
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spelling pubmed-103490952023-07-16 Cooperative regulation of Zhx1 and hnRNPA1 drives the cardiac progenitor-specific transcriptional activation during cardiomyocyte differentiation Chen, Yang Wu, Yukang Li, Jianguo Chen, Kai Wang, Wuchan Ye, Zihui Feng, Ke Yang, Yiwei Xu, Yanxin Kang, Jiuhong Guo, Xudong Cell Death Discov Article The zinc finger proteins (ZNFs) mediated transcriptional regulation is critical for cell fate transition. However, it is still unclear how the ZNFs realize their specific regulatory roles in the stage-specific determination of cardiomyocyte differentiation. Here, we reported that the zinc fingers and homeoboxes 1 (Zhx1) protein, transiently expressed during the cell fate transition from mesoderm to cardiac progenitors, was indispensable for the proper cardiomyocyte differentiation of mouse and human embryonic stem cells. Moreover, Zhx1 majorly promoted the specification of cardiac progenitors via interacting with hnRNPA1 and co-activated the transcription of a wide range of genes. In-depth mechanistic studies showed that Zhx1 was bound with hnRNPA1 by the amino acid residues (Thr111–His120) of the second Znf domain, thus participating in the formation of cardiac progenitors. Together, our study highlights the unrevealed interaction of Zhx1/hnRNPA1 for activating gene transcription during cardiac progenitor specification and also provides new evidence for the specificity of cell fate determination in cardiomyocyte differentiation. Nature Publishing Group UK 2023-07-14 /pmc/articles/PMC10349095/ /pubmed/37452012 http://dx.doi.org/10.1038/s41420-023-01548-1 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
Chen, Yang
Wu, Yukang
Li, Jianguo
Chen, Kai
Wang, Wuchan
Ye, Zihui
Feng, Ke
Yang, Yiwei
Xu, Yanxin
Kang, Jiuhong
Guo, Xudong
Cooperative regulation of Zhx1 and hnRNPA1 drives the cardiac progenitor-specific transcriptional activation during cardiomyocyte differentiation
title Cooperative regulation of Zhx1 and hnRNPA1 drives the cardiac progenitor-specific transcriptional activation during cardiomyocyte differentiation
title_full Cooperative regulation of Zhx1 and hnRNPA1 drives the cardiac progenitor-specific transcriptional activation during cardiomyocyte differentiation
title_fullStr Cooperative regulation of Zhx1 and hnRNPA1 drives the cardiac progenitor-specific transcriptional activation during cardiomyocyte differentiation
title_full_unstemmed Cooperative regulation of Zhx1 and hnRNPA1 drives the cardiac progenitor-specific transcriptional activation during cardiomyocyte differentiation
title_short Cooperative regulation of Zhx1 and hnRNPA1 drives the cardiac progenitor-specific transcriptional activation during cardiomyocyte differentiation
title_sort cooperative regulation of zhx1 and hnrnpa1 drives the cardiac progenitor-specific transcriptional activation during cardiomyocyte differentiation
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10349095/
https://www.ncbi.nlm.nih.gov/pubmed/37452012
http://dx.doi.org/10.1038/s41420-023-01548-1
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