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Article: DNA methylation in cell differentiation and reprogramming: An emerging systematic view

TitleDNA methylation in cell differentiation and reprogramming: An emerging systematic view
Authors
Keywords5-aza-cytidine
differentiation
DNA methylation
embryonic stem cell
ESC
induced pluripotent stem cells
iPS
pluripotency
reprogramming
Issue Date2010
Citation
Regenerative Medicine, 2010, v. 5, n. 4, p. 531-544 How to Cite?
AbstractEmbryonic stem cells have the unique ability to indefinitely self-renew and differentiate into any cell type found in the adult body. Differentiated cells can, in turn, be reprogrammed to embryonic stem-like induced pluripotent stem cells, providing exciting opportunities for achieving patient-specific stem cell therapy while circumventing immunological obstacles and ethical controversies. Since both differentiation and reprogramming are governed by major changes in the epigenome, current directions in the field aim to uncover the epigenetic signals that give pluripotent cells their unique properties. DNA methylation is one of the major epigenetic factors that regulates gene expression in mammals and is essential for establishing cellular identity. Recent analyses of pluripotent and somatic cell methylomes have provided important insights into the extensive role of DNA methylation during cell-fate commitment and reprogramming. In this article, the recent progress of differentiation and reprogramming research illuminated by high-throughput studies is discussed in the context of DNA methylation. © 2010 Future Medicine Ltd.
Persistent Identifierhttp://hdl.handle.net/10722/365687
ISSN
2023 Impact Factor: 2.4
2023 SCImago Journal Rankings: 0.517

 

DC FieldValueLanguage
dc.contributor.authorHuang, Kevin-
dc.contributor.authorFan, Guoping-
dc.date.accessioned2025-11-05T09:46:51Z-
dc.date.available2025-11-05T09:46:51Z-
dc.date.issued2010-
dc.identifier.citationRegenerative Medicine, 2010, v. 5, n. 4, p. 531-544-
dc.identifier.issn1746-0751-
dc.identifier.urihttp://hdl.handle.net/10722/365687-
dc.description.abstractEmbryonic stem cells have the unique ability to indefinitely self-renew and differentiate into any cell type found in the adult body. Differentiated cells can, in turn, be reprogrammed to embryonic stem-like induced pluripotent stem cells, providing exciting opportunities for achieving patient-specific stem cell therapy while circumventing immunological obstacles and ethical controversies. Since both differentiation and reprogramming are governed by major changes in the epigenome, current directions in the field aim to uncover the epigenetic signals that give pluripotent cells their unique properties. DNA methylation is one of the major epigenetic factors that regulates gene expression in mammals and is essential for establishing cellular identity. Recent analyses of pluripotent and somatic cell methylomes have provided important insights into the extensive role of DNA methylation during cell-fate commitment and reprogramming. In this article, the recent progress of differentiation and reprogramming research illuminated by high-throughput studies is discussed in the context of DNA methylation. © 2010 Future Medicine Ltd.-
dc.languageeng-
dc.relation.ispartofRegenerative Medicine-
dc.subject5-aza-cytidine-
dc.subjectdifferentiation-
dc.subjectDNA methylation-
dc.subjectembryonic stem cell-
dc.subjectESC-
dc.subjectinduced pluripotent stem cells-
dc.subjectiPS-
dc.subjectpluripotency-
dc.subjectreprogramming-
dc.titleDNA methylation in cell differentiation and reprogramming: An emerging systematic view-
dc.typeArticle-
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.2217/rme.10.35-
dc.identifier.pmid20632857-
dc.identifier.scopuseid_2-s2.0-77954811475-
dc.identifier.volume5-
dc.identifier.issue4-
dc.identifier.spage531-
dc.identifier.epage544-

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