Transcriptional changes and the role of ONECUT1 in hPSC pancreatic differentiation
peer-reviewed
Erstveröffentlichung
2021-11-17Authors
Heller, Sandra
Li, Zhijian
Lin, Qiong
Geusz, Ryan
Breunig, Markus
Wissenschaftlicher Artikel
Published in
Communications Biology ; 4 (2021). - Art.-Nr. 1298. - eISSN 2399-3642
Link to original publication
https://dx.doi.org/10.1038/s42003-021-02818-3Institutions
UKU. Klinik für Innere Medizin IExternal cooperations
RWTH AachenBayer AG
University of California
Université de Paris
Document version
published version (publisher's PDF)Abstract
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.
DFG Project THU
GRK 2254 / HEIST / Heterogenität und Evolution in soliden Tumoren (HEIST) / DFG / 288342734 [KL 2544/1-2]
Zelluläre Plastizität im Pankreas - vom Krankheitsmodell über Gewebserneuerung zur personalisierten Medizin / DFG / 426789149 [KL 2544/7-1]
Monogenetische Formen des juvenil sich manifestierenden Diabetes: neue Schritte in Richtung β-Zellentwicklung, -funktion und -überleben / DFG / 406674944
Zelluläre Plastizität im Pankreas - vom Krankheitsmodell über Gewebserneuerung zur personalisierten Medizin / DFG / 426789149 [KL 2544/7-1]
Monogenetische Formen des juvenil sich manifestierenden Diabetes: neue Schritte in Richtung β-Zellentwicklung, -funktion und -überleben / DFG / 406674944
Project uulm
BIU / Boehringer Ingelheim Ulm University BioCenter (BIU) / Forschungsverbund
Publication funding
Open-Access-Förderung durch die Medizinische Fakultät der Universität Ulm
Is supplemented by
https://www.nature.com/articles/s42003-021-02818-3#Sec21Subject headings
[GND]: Regenerative Medizin | Induzierte pluripotente Stammzelle[LCSH]: Regenerative medicine | Stem cells
[MeSH]: Pluripotent stem cells | Tissue engineering | Pancreas | Transcription, Genetic
[Free subject headings]: Differentiation | High-throughput screening | Stem-cell differentiation
[DDC subject group]: DDC 570 / Life sciences | DDC 610 / Medicine & health
Metadata
Show full item recordDOI & citation
Please use this identifier to cite or link to this item: http://dx.doi.org/10.18725/OPARU-42720
Heller, Sandra et al. (2022): Transcriptional changes and the role of ONECUT1 in hPSC pancreatic differentiation. Open Access Repositorium der Universität Ulm und Technischen Hochschule Ulm. http://dx.doi.org/10.18725/OPARU-42720
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