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The role of pluripotency gene regulatory network components in mediating transitions between pluripotent cell states()

Pluripotency is a property that early embryonic cells possess over a considerable developmental time span. Accordingly, pluripotent cell lines can be established from the pre-implantation or post-implantation mouse embryo as embryonic stem (ES) or epiblast stem (EpiSC) cell lines, respectively. Main...

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Detalles Bibliográficos
Autores principales: Festuccia, Nicola, Osorno, Rodrigo, Wilson, Valerie, Chambers, Ian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3790975/
https://www.ncbi.nlm.nih.gov/pubmed/23932125
http://dx.doi.org/10.1016/j.gde.2013.06.003
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author Festuccia, Nicola
Osorno, Rodrigo
Wilson, Valerie
Chambers, Ian
author_facet Festuccia, Nicola
Osorno, Rodrigo
Wilson, Valerie
Chambers, Ian
author_sort Festuccia, Nicola
collection PubMed
description Pluripotency is a property that early embryonic cells possess over a considerable developmental time span. Accordingly, pluripotent cell lines can be established from the pre-implantation or post-implantation mouse embryo as embryonic stem (ES) or epiblast stem (EpiSC) cell lines, respectively. Maintenance of the pluripotent phenotype depends on the function of specific transcription factors (TFs) operating within a pluripotency gene regulatory network (PGRN). As cells move from an ES cell to an EpiSC state, the PGRN changes with expression of some TFs reduced (e.g. Nanog) or eliminated (e.g. Esrrb). Re-expressing such TFs can move cells back to an earlier developmental identity and is being applied to attempt establishment of human cell lines with the properties of mouse ES cells.
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spelling pubmed-37909752013-10-07 The role of pluripotency gene regulatory network components in mediating transitions between pluripotent cell states() Festuccia, Nicola Osorno, Rodrigo Wilson, Valerie Chambers, Ian Curr Opin Genet Dev Article Pluripotency is a property that early embryonic cells possess over a considerable developmental time span. Accordingly, pluripotent cell lines can be established from the pre-implantation or post-implantation mouse embryo as embryonic stem (ES) or epiblast stem (EpiSC) cell lines, respectively. Maintenance of the pluripotent phenotype depends on the function of specific transcription factors (TFs) operating within a pluripotency gene regulatory network (PGRN). As cells move from an ES cell to an EpiSC state, the PGRN changes with expression of some TFs reduced (e.g. Nanog) or eliminated (e.g. Esrrb). Re-expressing such TFs can move cells back to an earlier developmental identity and is being applied to attempt establishment of human cell lines with the properties of mouse ES cells. Elsevier 2013-10 /pmc/articles/PMC3790975/ /pubmed/23932125 http://dx.doi.org/10.1016/j.gde.2013.06.003 Text en © 2013 The Authors https://creativecommons.org/licenses/by-nc-nd/3.0/ Open Access under CC BY-NC-ND 3.0 (https://creativecommons.org/licenses/by-nc-nd/3.0/) license
spellingShingle Article
Festuccia, Nicola
Osorno, Rodrigo
Wilson, Valerie
Chambers, Ian
The role of pluripotency gene regulatory network components in mediating transitions between pluripotent cell states()
title The role of pluripotency gene regulatory network components in mediating transitions between pluripotent cell states()
title_full The role of pluripotency gene regulatory network components in mediating transitions between pluripotent cell states()
title_fullStr The role of pluripotency gene regulatory network components in mediating transitions between pluripotent cell states()
title_full_unstemmed The role of pluripotency gene regulatory network components in mediating transitions between pluripotent cell states()
title_short The role of pluripotency gene regulatory network components in mediating transitions between pluripotent cell states()
title_sort role of pluripotency gene regulatory network components in mediating transitions between pluripotent cell states()
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3790975/
https://www.ncbi.nlm.nih.gov/pubmed/23932125
http://dx.doi.org/10.1016/j.gde.2013.06.003
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