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FoxA2 hunting research identifies the early trail of mesenchymal differentiation
Epigenetic regulation offers a flexible means to instruct cell functions and fate. In human embryonic stem cells (hESCs), thousands of genes are targets for histone modifications leading to activation or suppression of transcription. Novel research now indicates that, in hESCs, the transcription sta...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2013
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3706786/ https://www.ncbi.nlm.nih.gov/pubmed/23672958 http://dx.doi.org/10.1186/scrt188 |
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author | Madeddu, Paolo |
author_facet | Madeddu, Paolo |
author_sort | Madeddu, Paolo |
collection | PubMed |
description | Epigenetic regulation offers a flexible means to instruct cell functions and fate. In human embryonic stem cells (hESCs), thousands of genes are targets for histone modifications leading to activation or suppression of transcription. Novel research now indicates that, in hESCs, the transcription start site of FOXA2, encoding a member of the forkhead family of transcription factors, is bivalently marked with histone modifications for both gene activation and repression. Moreover, FOXA2 is remarkably upregulated at an early stage of endothelial differentiation. These discoveries provide better understanding of the natural program of differentiation and also open up new opportunities for large scale production of endothelial progenitors. |
format | Online Article Text |
id | pubmed-3706786 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-37067862013-07-15 FoxA2 hunting research identifies the early trail of mesenchymal differentiation Madeddu, Paolo Stem Cell Res Ther Commentary Epigenetic regulation offers a flexible means to instruct cell functions and fate. In human embryonic stem cells (hESCs), thousands of genes are targets for histone modifications leading to activation or suppression of transcription. Novel research now indicates that, in hESCs, the transcription start site of FOXA2, encoding a member of the forkhead family of transcription factors, is bivalently marked with histone modifications for both gene activation and repression. Moreover, FOXA2 is remarkably upregulated at an early stage of endothelial differentiation. These discoveries provide better understanding of the natural program of differentiation and also open up new opportunities for large scale production of endothelial progenitors. BioMed Central 2013-04-24 /pmc/articles/PMC3706786/ /pubmed/23672958 http://dx.doi.org/10.1186/scrt188 Text en Copyright © 2013 BioMed Central Ltd. |
spellingShingle | Commentary Madeddu, Paolo FoxA2 hunting research identifies the early trail of mesenchymal differentiation |
title | FoxA2 hunting research identifies the early trail of mesenchymal differentiation |
title_full | FoxA2 hunting research identifies the early trail of mesenchymal differentiation |
title_fullStr | FoxA2 hunting research identifies the early trail of mesenchymal differentiation |
title_full_unstemmed | FoxA2 hunting research identifies the early trail of mesenchymal differentiation |
title_short | FoxA2 hunting research identifies the early trail of mesenchymal differentiation |
title_sort | foxa2 hunting research identifies the early trail of mesenchymal differentiation |
topic | Commentary |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3706786/ https://www.ncbi.nlm.nih.gov/pubmed/23672958 http://dx.doi.org/10.1186/scrt188 |
work_keys_str_mv | AT madeddupaolo foxa2huntingresearchidentifiestheearlytrailofmesenchymaldifferentiation |