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Heterochromatin protein 1 promotes self-renewal and triggers regenerative proliferation in adult stem cells
Adult stem cells (ASCs) capable of self-renewal and differentiation confer the potential of tissues to regenerate damaged parts. Epigenetic regulation is essential for driving cell fate decisions by rapidly and reversibly modulating gene expression programs. However, it remains unclear how epigeneti...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Rockefeller University Press
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3639387/ https://www.ncbi.nlm.nih.gov/pubmed/23629965 http://dx.doi.org/10.1083/jcb.201207172 |
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author | Zeng, An Li, Yong-Qin Wang, Chen Han, Xiao-Shuai Li, Ge Wang, Jian-Yong Li, Dang-Sheng Qin, Yong-Wen Shi, Yufang Brewer, Gary Jing, Qing |
author_facet | Zeng, An Li, Yong-Qin Wang, Chen Han, Xiao-Shuai Li, Ge Wang, Jian-Yong Li, Dang-Sheng Qin, Yong-Wen Shi, Yufang Brewer, Gary Jing, Qing |
author_sort | Zeng, An |
collection | PubMed |
description | Adult stem cells (ASCs) capable of self-renewal and differentiation confer the potential of tissues to regenerate damaged parts. Epigenetic regulation is essential for driving cell fate decisions by rapidly and reversibly modulating gene expression programs. However, it remains unclear how epigenetic factors elicit ASC-driven regeneration. In this paper, we report that an RNA interference screen against 205 chromatin regulators identified 12 proteins essential for ASC function and regeneration in planarians. Surprisingly, the HP1-like protein SMED–HP1-1 (HP1-1) specifically marked self-renewing, pluripotent ASCs, and HP1-1 depletion abrogated self-renewal and promoted differentiation. Upon injury, HP1-1 expression increased and elicited increased ASC expression of Mcm5 through functional association with the FACT (facilitates chromatin transcription) complex, which consequently triggered proliferation of ASCs and initiated blastema formation. Our observations uncover an epigenetic network underlying ASC regulation in planarians and reveal that an HP1 protein is a key chromatin factor controlling stem cell function. These results provide important insights into how epigenetic mechanisms orchestrate stem cell responses during tissue regeneration. |
format | Online Article Text |
id | pubmed-3639387 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-36393872013-10-29 Heterochromatin protein 1 promotes self-renewal and triggers regenerative proliferation in adult stem cells Zeng, An Li, Yong-Qin Wang, Chen Han, Xiao-Shuai Li, Ge Wang, Jian-Yong Li, Dang-Sheng Qin, Yong-Wen Shi, Yufang Brewer, Gary Jing, Qing J Cell Biol Research Articles Adult stem cells (ASCs) capable of self-renewal and differentiation confer the potential of tissues to regenerate damaged parts. Epigenetic regulation is essential for driving cell fate decisions by rapidly and reversibly modulating gene expression programs. However, it remains unclear how epigenetic factors elicit ASC-driven regeneration. In this paper, we report that an RNA interference screen against 205 chromatin regulators identified 12 proteins essential for ASC function and regeneration in planarians. Surprisingly, the HP1-like protein SMED–HP1-1 (HP1-1) specifically marked self-renewing, pluripotent ASCs, and HP1-1 depletion abrogated self-renewal and promoted differentiation. Upon injury, HP1-1 expression increased and elicited increased ASC expression of Mcm5 through functional association with the FACT (facilitates chromatin transcription) complex, which consequently triggered proliferation of ASCs and initiated blastema formation. Our observations uncover an epigenetic network underlying ASC regulation in planarians and reveal that an HP1 protein is a key chromatin factor controlling stem cell function. These results provide important insights into how epigenetic mechanisms orchestrate stem cell responses during tissue regeneration. The Rockefeller University Press 2013-04-29 /pmc/articles/PMC3639387/ /pubmed/23629965 http://dx.doi.org/10.1083/jcb.201207172 Text en © 2013 Zeng et al. This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 3.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/3.0/). |
spellingShingle | Research Articles Zeng, An Li, Yong-Qin Wang, Chen Han, Xiao-Shuai Li, Ge Wang, Jian-Yong Li, Dang-Sheng Qin, Yong-Wen Shi, Yufang Brewer, Gary Jing, Qing Heterochromatin protein 1 promotes self-renewal and triggers regenerative proliferation in adult stem cells |
title | Heterochromatin protein 1 promotes self-renewal and triggers regenerative proliferation in adult stem cells |
title_full | Heterochromatin protein 1 promotes self-renewal and triggers regenerative proliferation in adult stem cells |
title_fullStr | Heterochromatin protein 1 promotes self-renewal and triggers regenerative proliferation in adult stem cells |
title_full_unstemmed | Heterochromatin protein 1 promotes self-renewal and triggers regenerative proliferation in adult stem cells |
title_short | Heterochromatin protein 1 promotes self-renewal and triggers regenerative proliferation in adult stem cells |
title_sort | heterochromatin protein 1 promotes self-renewal and triggers regenerative proliferation in adult stem cells |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3639387/ https://www.ncbi.nlm.nih.gov/pubmed/23629965 http://dx.doi.org/10.1083/jcb.201207172 |
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