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Transcriptional changes and the role of ONECUT1 in hPSC pancreatic differentiation
Cell type specification during pancreatic development is tightly controlled by a transcriptional and epigenetic network. The precise role of most transcription factors, however, has been only described in mice. To convey such concepts to human pancreatic development, alternative model systems such a...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8599846/ https://www.ncbi.nlm.nih.gov/pubmed/34789845 http://dx.doi.org/10.1038/s42003-021-02818-3 |
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author | Heller, Sandra Li, Zhijian Lin, Qiong Geusz, Ryan Breunig, Markus Hohwieler, Meike Zhang, Xi Nair, Gopika G. Seufferlein, Thomas Hebrok, Matthias Sander, Maike Julier, Cécile Kleger, Alexander Costa, Ivan G. |
author_facet | Heller, Sandra Li, Zhijian Lin, Qiong Geusz, Ryan Breunig, Markus Hohwieler, Meike Zhang, Xi Nair, Gopika G. Seufferlein, Thomas Hebrok, Matthias Sander, Maike Julier, Cécile Kleger, Alexander Costa, Ivan G. |
author_sort | Heller, Sandra |
collection | PubMed |
description | Cell type specification during pancreatic development is tightly controlled by a transcriptional and epigenetic network. The precise role of most transcription factors, however, has been only described in mice. To convey such concepts to human pancreatic development, alternative model systems such as pancreatic in vitro differentiation of human pluripotent stem cells can be employed. Here, we analyzed stage-specific RNA-, ChIP-, and ATAC-sequencing data to dissect transcriptional and regulatory mechanisms during pancreatic development. Transcriptome and open chromatin maps of pancreatic differentiation from human pluripotent stem cells provide a stage-specific pattern of known pancreatic transcription factors and indicate ONECUT1 as a crucial fate regulator in pancreas progenitors. Moreover, our data suggest that ONECUT1 is also involved in preparing pancreatic progenitors for later endocrine specification. The dissection of the transcriptional and regulatory circuitry revealed an important role for ONECUT1 within such network and will serve as resource to study human development and disease. |
format | Online Article Text |
id | pubmed-8599846 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-85998462021-11-19 Transcriptional changes and the role of ONECUT1 in hPSC pancreatic differentiation Heller, Sandra Li, Zhijian Lin, Qiong Geusz, Ryan Breunig, Markus Hohwieler, Meike Zhang, Xi Nair, Gopika G. Seufferlein, Thomas Hebrok, Matthias Sander, Maike Julier, Cécile Kleger, Alexander Costa, Ivan G. Commun Biol Article Cell type specification during pancreatic development is tightly controlled by a transcriptional and epigenetic network. The precise role of most transcription factors, however, has been only described in mice. To convey such concepts to human pancreatic development, alternative model systems such as pancreatic in vitro differentiation of human pluripotent stem cells can be employed. Here, we analyzed stage-specific RNA-, ChIP-, and ATAC-sequencing data to dissect transcriptional and regulatory mechanisms during pancreatic development. Transcriptome and open chromatin maps of pancreatic differentiation from human pluripotent stem cells provide a stage-specific pattern of known pancreatic transcription factors and indicate ONECUT1 as a crucial fate regulator in pancreas progenitors. Moreover, our data suggest that ONECUT1 is also involved in preparing pancreatic progenitors for later endocrine specification. The dissection of the transcriptional and regulatory circuitry revealed an important role for ONECUT1 within such network and will serve as resource to study human development and disease. Nature Publishing Group UK 2021-11-17 /pmc/articles/PMC8599846/ /pubmed/34789845 http://dx.doi.org/10.1038/s42003-021-02818-3 Text en © The Author(s) 2021 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 Heller, Sandra Li, Zhijian Lin, Qiong Geusz, Ryan Breunig, Markus Hohwieler, Meike Zhang, Xi Nair, Gopika G. Seufferlein, Thomas Hebrok, Matthias Sander, Maike Julier, Cécile Kleger, Alexander Costa, Ivan G. Transcriptional changes and the role of ONECUT1 in hPSC pancreatic differentiation |
title | Transcriptional changes and the role of ONECUT1 in hPSC pancreatic differentiation |
title_full | Transcriptional changes and the role of ONECUT1 in hPSC pancreatic differentiation |
title_fullStr | Transcriptional changes and the role of ONECUT1 in hPSC pancreatic differentiation |
title_full_unstemmed | Transcriptional changes and the role of ONECUT1 in hPSC pancreatic differentiation |
title_short | Transcriptional changes and the role of ONECUT1 in hPSC pancreatic differentiation |
title_sort | transcriptional changes and the role of onecut1 in hpsc pancreatic differentiation |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8599846/ https://www.ncbi.nlm.nih.gov/pubmed/34789845 http://dx.doi.org/10.1038/s42003-021-02818-3 |
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