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ZBTB12 is a molecular barrier to dedifferentiation in human pluripotent stem cells
Development is generally viewed as one-way traffic of cell state transition from primitive to developmentally advanced states. However, molecular mechanisms that ensure the unidirectional transition of cell fates remain largely unknown. Through exact transcription start site mapping, we report an ev...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9911396/ https://www.ncbi.nlm.nih.gov/pubmed/36759523 http://dx.doi.org/10.1038/s41467-023-36178-9 |
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author | Han, Dasol Liu, Guojing Oh, Yujeong Oh, Seyoun Yang, Seungbok Mandjikian, Lori Rani, Neha Almeida, Maria C. Kosik, Kenneth S. Jang, Jiwon |
author_facet | Han, Dasol Liu, Guojing Oh, Yujeong Oh, Seyoun Yang, Seungbok Mandjikian, Lori Rani, Neha Almeida, Maria C. Kosik, Kenneth S. Jang, Jiwon |
author_sort | Han, Dasol |
collection | PubMed |
description | Development is generally viewed as one-way traffic of cell state transition from primitive to developmentally advanced states. However, molecular mechanisms that ensure the unidirectional transition of cell fates remain largely unknown. Through exact transcription start site mapping, we report an evolutionarily conserved BTB domain-containing zinc finger protein, ZBTB12, as a molecular barrier for dedifferentiation of human pluripotent stem cells (hPSCs). Single-cell RNA sequencing reveals that ZBTB12 is essential for three germ layer differentiation by blocking hPSC dedifferentiation. Mechanistically, ZBTB12 fine-tunes the expression of human endogenous retrovirus H (HERVH), a primate-specific retrotransposon, and targets specific transcripts that utilize HERVH as a regulatory element. In particular, the downregulation of HERVH-overlapping long non-coding RNAs (lncRNAs) by ZBTB12 is necessary for a successful exit from a pluripotent state and lineage derivation. Overall, we identify ZBTB12 as a molecular barrier that safeguards the unidirectional transition of metastable stem cell fates toward developmentally advanced states. |
format | Online Article Text |
id | pubmed-9911396 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-99113962023-02-11 ZBTB12 is a molecular barrier to dedifferentiation in human pluripotent stem cells Han, Dasol Liu, Guojing Oh, Yujeong Oh, Seyoun Yang, Seungbok Mandjikian, Lori Rani, Neha Almeida, Maria C. Kosik, Kenneth S. Jang, Jiwon Nat Commun Article Development is generally viewed as one-way traffic of cell state transition from primitive to developmentally advanced states. However, molecular mechanisms that ensure the unidirectional transition of cell fates remain largely unknown. Through exact transcription start site mapping, we report an evolutionarily conserved BTB domain-containing zinc finger protein, ZBTB12, as a molecular barrier for dedifferentiation of human pluripotent stem cells (hPSCs). Single-cell RNA sequencing reveals that ZBTB12 is essential for three germ layer differentiation by blocking hPSC dedifferentiation. Mechanistically, ZBTB12 fine-tunes the expression of human endogenous retrovirus H (HERVH), a primate-specific retrotransposon, and targets specific transcripts that utilize HERVH as a regulatory element. In particular, the downregulation of HERVH-overlapping long non-coding RNAs (lncRNAs) by ZBTB12 is necessary for a successful exit from a pluripotent state and lineage derivation. Overall, we identify ZBTB12 as a molecular barrier that safeguards the unidirectional transition of metastable stem cell fates toward developmentally advanced states. Nature Publishing Group UK 2023-02-09 /pmc/articles/PMC9911396/ /pubmed/36759523 http://dx.doi.org/10.1038/s41467-023-36178-9 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 Han, Dasol Liu, Guojing Oh, Yujeong Oh, Seyoun Yang, Seungbok Mandjikian, Lori Rani, Neha Almeida, Maria C. Kosik, Kenneth S. Jang, Jiwon ZBTB12 is a molecular barrier to dedifferentiation in human pluripotent stem cells |
title | ZBTB12 is a molecular barrier to dedifferentiation in human pluripotent stem cells |
title_full | ZBTB12 is a molecular barrier to dedifferentiation in human pluripotent stem cells |
title_fullStr | ZBTB12 is a molecular barrier to dedifferentiation in human pluripotent stem cells |
title_full_unstemmed | ZBTB12 is a molecular barrier to dedifferentiation in human pluripotent stem cells |
title_short | ZBTB12 is a molecular barrier to dedifferentiation in human pluripotent stem cells |
title_sort | zbtb12 is a molecular barrier to dedifferentiation in human pluripotent stem cells |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9911396/ https://www.ncbi.nlm.nih.gov/pubmed/36759523 http://dx.doi.org/10.1038/s41467-023-36178-9 |
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