Cargando…
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...
Autores principales: | , , , , , , |
---|---|
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 |
_version_ | 1783329386132406272 |
---|---|
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. |
format | Online Article Text |
id | pubmed-5989057 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Cell Press |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT sousaelsaj exitfromnaivepluripotencyinducesatransientxchromosomeinactivationlikestateinmales AT stuarthannaht exitfromnaivepluripotencyinducesatransientxchromosomeinactivationlikestateinmales AT bateslawrencee exitfromnaivepluripotencyinducesatransientxchromosomeinactivationlikestateinmales AT ghorbanimohammadmersad exitfromnaivepluripotencyinducesatransientxchromosomeinactivationlikestateinmales AT nicholsjennifer exitfromnaivepluripotencyinducesatransientxchromosomeinactivationlikestateinmales AT dietmannsabine exitfromnaivepluripotencyinducesatransientxchromosomeinactivationlikestateinmales AT silvajosecr exitfromnaivepluripotencyinducesatransientxchromosomeinactivationlikestateinmales |