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Exit from Naive Pluripotency Induces a Transient X Chromosome Inactivation-like State in Males

A hallmark of naive pluripotency is the presence of two active X chromosomes in females. It is not clear whether prevention of X chromosome inactivation (XCI) is mediated by gene networks that preserve the naive state. Here, we show that robust naive pluripotent stem cell (nPSC) self-renewal repress...

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Autores principales: Sousa, Elsa J., Stuart, Hannah T., Bates, Lawrence E., Ghorbani, Mohammadmersad, Nichols, Jennifer, Dietmann, Sabine, Silva, José C.R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cell Press 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5989057/
https://www.ncbi.nlm.nih.gov/pubmed/29804891
http://dx.doi.org/10.1016/j.stem.2018.05.001
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author Sousa, Elsa J.
Stuart, Hannah T.
Bates, Lawrence E.
Ghorbani, Mohammadmersad
Nichols, Jennifer
Dietmann, Sabine
Silva, José C.R.
author_facet Sousa, Elsa J.
Stuart, Hannah T.
Bates, Lawrence E.
Ghorbani, Mohammadmersad
Nichols, Jennifer
Dietmann, Sabine
Silva, José C.R.
author_sort Sousa, Elsa J.
collection PubMed
description A hallmark of naive pluripotency is the presence of two active X chromosomes in females. It is not clear whether prevention of X chromosome inactivation (XCI) is mediated by gene networks that preserve the naive state. Here, we show that robust naive pluripotent stem cell (nPSC) self-renewal represses expression of Xist, the master regulator of XCI. We found that nPSCs accumulate Xist on the male X chromosome and on both female X chromosomes as they become NANOG negative at the onset of differentiation. This is accompanied by the appearance of a repressive chromatin signature and partial X-linked gene silencing, suggesting a transient and rapid XCI-like state in male nPSCs. In the embryo, Xist is transiently expressed in males and in females from both X chromosomes at the onset of naive epiblast differentiation. In conclusion, we propose that XCI initiation is gender independent and triggered by destabilization of naive identity, suggesting that gender-specific mechanisms follow, rather than precede, XCI initiation.
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spelling pubmed-59890572018-06-06 Exit from Naive Pluripotency Induces a Transient X Chromosome Inactivation-like State in Males Sousa, Elsa J. Stuart, Hannah T. Bates, Lawrence E. Ghorbani, Mohammadmersad Nichols, Jennifer Dietmann, Sabine Silva, José C.R. Cell Stem Cell Article A hallmark of naive pluripotency is the presence of two active X chromosomes in females. It is not clear whether prevention of X chromosome inactivation (XCI) is mediated by gene networks that preserve the naive state. Here, we show that robust naive pluripotent stem cell (nPSC) self-renewal represses expression of Xist, the master regulator of XCI. We found that nPSCs accumulate Xist on the male X chromosome and on both female X chromosomes as they become NANOG negative at the onset of differentiation. This is accompanied by the appearance of a repressive chromatin signature and partial X-linked gene silencing, suggesting a transient and rapid XCI-like state in male nPSCs. In the embryo, Xist is transiently expressed in males and in females from both X chromosomes at the onset of naive epiblast differentiation. In conclusion, we propose that XCI initiation is gender independent and triggered by destabilization of naive identity, suggesting that gender-specific mechanisms follow, rather than precede, XCI initiation. Cell Press 2018-06-01 /pmc/articles/PMC5989057/ /pubmed/29804891 http://dx.doi.org/10.1016/j.stem.2018.05.001 Text en Crown Copyright © 2018 Published by Elsevier Inc. All rights reserved. http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Sousa, Elsa J.
Stuart, Hannah T.
Bates, Lawrence E.
Ghorbani, Mohammadmersad
Nichols, Jennifer
Dietmann, Sabine
Silva, José C.R.
Exit from Naive Pluripotency Induces a Transient X Chromosome Inactivation-like State in Males
title Exit from Naive Pluripotency Induces a Transient X Chromosome Inactivation-like State in Males
title_full Exit from Naive Pluripotency Induces a Transient X Chromosome Inactivation-like State in Males
title_fullStr Exit from Naive Pluripotency Induces a Transient X Chromosome Inactivation-like State in Males
title_full_unstemmed Exit from Naive Pluripotency Induces a Transient X Chromosome Inactivation-like State in Males
title_short Exit from Naive Pluripotency Induces a Transient X Chromosome Inactivation-like State in Males
title_sort exit from naive pluripotency induces a transient x chromosome inactivation-like state in males
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5989057/
https://www.ncbi.nlm.nih.gov/pubmed/29804891
http://dx.doi.org/10.1016/j.stem.2018.05.001
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