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Transcriptome analysis of chicken ES, blastodermal and germ cells reveals that chick ES cells are equivalent to mouse ES cells rather than EpiSC

Pluripotent Embryonic Stem cell (ESC) lines can be derived from a variety of sources. Mouse lines derived from the early blastocyst and from primordial germ cells (PGCs) can contribute to all somatic lineages and to the germ line, whereas cells from slightly later embryos (EpiSC) no longer contribut...

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Autores principales: Jean, Christian, Oliveira, Nidia M.M., Intarapat, Sittipon, Fuet, Aurélie, Mazoyer, Clément, De Almeida, Irene, Trevers, Katherine, Boast, Sharon, Aubel, Pauline, Bertocchini, Federica, Stern, Claudio D., Pain, Bertrand
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4305369/
https://www.ncbi.nlm.nih.gov/pubmed/25514344
http://dx.doi.org/10.1016/j.scr.2014.11.005
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author Jean, Christian
Oliveira, Nidia M.M.
Intarapat, Sittipon
Fuet, Aurélie
Mazoyer, Clément
De Almeida, Irene
Trevers, Katherine
Boast, Sharon
Aubel, Pauline
Bertocchini, Federica
Stern, Claudio D.
Pain, Bertrand
author_facet Jean, Christian
Oliveira, Nidia M.M.
Intarapat, Sittipon
Fuet, Aurélie
Mazoyer, Clément
De Almeida, Irene
Trevers, Katherine
Boast, Sharon
Aubel, Pauline
Bertocchini, Federica
Stern, Claudio D.
Pain, Bertrand
author_sort Jean, Christian
collection PubMed
description Pluripotent Embryonic Stem cell (ESC) lines can be derived from a variety of sources. Mouse lines derived from the early blastocyst and from primordial germ cells (PGCs) can contribute to all somatic lineages and to the germ line, whereas cells from slightly later embryos (EpiSC) no longer contribute to the germ line. In chick, pluripotent ESCs can be obtained from PGCs and from early blastoderms. Established PGC lines and freshly isolated blastodermal cells (cBC) can contribute to both germinal and somatic lineages but established lines from the former (cESC) can only produce somatic cell types. For this reason, cESCs are often considered to be equivalent to mouse EpiSC. To define these cell types more rigorously, we have performed comparative microarray analysis to describe a transcriptomic profile specific for each cell type. This is validated by real time RT-PCR and in situ hybridisation. We find that both cES and cBC cells express classic pluripotency-related genes (including cPOUV/OCT4, NANOG, SOX2/3, KLF2 and SALL4), whereas expression of DAZL, DND1, DDX4 and PIWIL1 defines a molecular signature for germ cells. Surprisingly, contrary to the prevailing view, our results also suggest that cES cells resemble mouse ES cells more closely than mouse EpiSC.
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spelling pubmed-43053692015-01-27 Transcriptome analysis of chicken ES, blastodermal and germ cells reveals that chick ES cells are equivalent to mouse ES cells rather than EpiSC Jean, Christian Oliveira, Nidia M.M. Intarapat, Sittipon Fuet, Aurélie Mazoyer, Clément De Almeida, Irene Trevers, Katherine Boast, Sharon Aubel, Pauline Bertocchini, Federica Stern, Claudio D. Pain, Bertrand Stem Cell Res Article Pluripotent Embryonic Stem cell (ESC) lines can be derived from a variety of sources. Mouse lines derived from the early blastocyst and from primordial germ cells (PGCs) can contribute to all somatic lineages and to the germ line, whereas cells from slightly later embryos (EpiSC) no longer contribute to the germ line. In chick, pluripotent ESCs can be obtained from PGCs and from early blastoderms. Established PGC lines and freshly isolated blastodermal cells (cBC) can contribute to both germinal and somatic lineages but established lines from the former (cESC) can only produce somatic cell types. For this reason, cESCs are often considered to be equivalent to mouse EpiSC. To define these cell types more rigorously, we have performed comparative microarray analysis to describe a transcriptomic profile specific for each cell type. This is validated by real time RT-PCR and in situ hybridisation. We find that both cES and cBC cells express classic pluripotency-related genes (including cPOUV/OCT4, NANOG, SOX2/3, KLF2 and SALL4), whereas expression of DAZL, DND1, DDX4 and PIWIL1 defines a molecular signature for germ cells. Surprisingly, contrary to the prevailing view, our results also suggest that cES cells resemble mouse ES cells more closely than mouse EpiSC. Elsevier 2015-01 /pmc/articles/PMC4305369/ /pubmed/25514344 http://dx.doi.org/10.1016/j.scr.2014.11.005 Text en © 2014 The Authors. Published by Elsevier B.V. http://creativecommons.org/licenses/by/3.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/3.0/).
spellingShingle Article
Jean, Christian
Oliveira, Nidia M.M.
Intarapat, Sittipon
Fuet, Aurélie
Mazoyer, Clément
De Almeida, Irene
Trevers, Katherine
Boast, Sharon
Aubel, Pauline
Bertocchini, Federica
Stern, Claudio D.
Pain, Bertrand
Transcriptome analysis of chicken ES, blastodermal and germ cells reveals that chick ES cells are equivalent to mouse ES cells rather than EpiSC
title Transcriptome analysis of chicken ES, blastodermal and germ cells reveals that chick ES cells are equivalent to mouse ES cells rather than EpiSC
title_full Transcriptome analysis of chicken ES, blastodermal and germ cells reveals that chick ES cells are equivalent to mouse ES cells rather than EpiSC
title_fullStr Transcriptome analysis of chicken ES, blastodermal and germ cells reveals that chick ES cells are equivalent to mouse ES cells rather than EpiSC
title_full_unstemmed Transcriptome analysis of chicken ES, blastodermal and germ cells reveals that chick ES cells are equivalent to mouse ES cells rather than EpiSC
title_short Transcriptome analysis of chicken ES, blastodermal and germ cells reveals that chick ES cells are equivalent to mouse ES cells rather than EpiSC
title_sort transcriptome analysis of chicken es, blastodermal and germ cells reveals that chick es cells are equivalent to mouse es cells rather than episc
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4305369/
https://www.ncbi.nlm.nih.gov/pubmed/25514344
http://dx.doi.org/10.1016/j.scr.2014.11.005
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