Dynamic status of REST in the mouse ESC pluripotency network.

REST is abundantly expressed in mouse embryonic stem cells (ESCs). Many genome-wide analyses have found REST to be an integral part of the ESC pluripotency network. However, experimental systems have produced contradictory findings: (1) REST is required for the maintenance of ESC pluripotency and lo...

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Main Authors: Sanjay K Singh, Bethany L Veo, Mohamedi N Kagalwala, Weiwei Shi, Shoudan Liang, Sadhan Majumder
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2012-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3429488?pdf=render
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author Sanjay K Singh
Bethany L Veo
Mohamedi N Kagalwala
Weiwei Shi
Shoudan Liang
Sadhan Majumder
author_facet Sanjay K Singh
Bethany L Veo
Mohamedi N Kagalwala
Weiwei Shi
Shoudan Liang
Sadhan Majumder
author_sort Sanjay K Singh
collection DOAJ
description REST is abundantly expressed in mouse embryonic stem cells (ESCs). Many genome-wide analyses have found REST to be an integral part of the ESC pluripotency network. However, experimental systems have produced contradictory findings: (1) REST is required for the maintenance of ESC pluripotency and loss of REST causes increased expression of differentiation markers, (2) REST is not required for the maintenance of ESC pluripotency and loss of REST does not change expression of differentiation markers, and (3) REST is not required for the maintenance of ESC pluripotency but loss of REST causes decreased expression of differentiation markers. These reports highlight gaps in our knowledge of the ESC network.Employing biochemical and genome-wide analyses of various culture conditions and ESC lines, we have attempted to resolve some of the discrepancies in the literature.We show that Rest+/- and Rest-/- AB-1 mutant ESCs, which did not exhibit a role of REST in ESC pluripotency when cultured in the presence of feeder cells, did show impaired self-renewal when compared with the parental cells under feeder-free culture conditions, but only in early passage cells. In late passage cells, both Rest+/- and Rest-/- AB-1 ESCs restored pluripotency, suggesting a passage and culture condition-dependent response. Genome-wide analysis followed by biochemical validation supported this response and further indicated that the restoration of pluripotency was associated by increased expression of the ESC pluripotency factors. E14Tg2a.4 ESCs with REST-knockdown, which earlier showed a REST-dependent pluripotency when cultured under feeder-free conditions, as well as Rest-/- AB-1 ESCs, showed no REST-dependent pluripotency when cultured in the presence of either feeder cells or laminin, indicating that extracellular matrix components can rescue REST's role in ESC pluripotency.REST regulates ESC pluripotency in culture condition- and ESC line-dependent fashion and ESC pluripotency needs to be evaluated in a context dependent manner.
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spelling doaj.art-52bb67fb69f84a2a8a70fc78948b5e5c2022-12-22T03:45:51ZengPublic Library of Science (PLoS)PLoS ONE1932-62032012-01-0178e4365910.1371/journal.pone.0043659Dynamic status of REST in the mouse ESC pluripotency network.Sanjay K SinghBethany L VeoMohamedi N KagalwalaWeiwei ShiShoudan LiangSadhan MajumderREST is abundantly expressed in mouse embryonic stem cells (ESCs). Many genome-wide analyses have found REST to be an integral part of the ESC pluripotency network. However, experimental systems have produced contradictory findings: (1) REST is required for the maintenance of ESC pluripotency and loss of REST causes increased expression of differentiation markers, (2) REST is not required for the maintenance of ESC pluripotency and loss of REST does not change expression of differentiation markers, and (3) REST is not required for the maintenance of ESC pluripotency but loss of REST causes decreased expression of differentiation markers. These reports highlight gaps in our knowledge of the ESC network.Employing biochemical and genome-wide analyses of various culture conditions and ESC lines, we have attempted to resolve some of the discrepancies in the literature.We show that Rest+/- and Rest-/- AB-1 mutant ESCs, which did not exhibit a role of REST in ESC pluripotency when cultured in the presence of feeder cells, did show impaired self-renewal when compared with the parental cells under feeder-free culture conditions, but only in early passage cells. In late passage cells, both Rest+/- and Rest-/- AB-1 ESCs restored pluripotency, suggesting a passage and culture condition-dependent response. Genome-wide analysis followed by biochemical validation supported this response and further indicated that the restoration of pluripotency was associated by increased expression of the ESC pluripotency factors. E14Tg2a.4 ESCs with REST-knockdown, which earlier showed a REST-dependent pluripotency when cultured under feeder-free conditions, as well as Rest-/- AB-1 ESCs, showed no REST-dependent pluripotency when cultured in the presence of either feeder cells or laminin, indicating that extracellular matrix components can rescue REST's role in ESC pluripotency.REST regulates ESC pluripotency in culture condition- and ESC line-dependent fashion and ESC pluripotency needs to be evaluated in a context dependent manner.http://europepmc.org/articles/PMC3429488?pdf=render
spellingShingle Sanjay K Singh
Bethany L Veo
Mohamedi N Kagalwala
Weiwei Shi
Shoudan Liang
Sadhan Majumder
Dynamic status of REST in the mouse ESC pluripotency network.
PLoS ONE
title Dynamic status of REST in the mouse ESC pluripotency network.
title_full Dynamic status of REST in the mouse ESC pluripotency network.
title_fullStr Dynamic status of REST in the mouse ESC pluripotency network.
title_full_unstemmed Dynamic status of REST in the mouse ESC pluripotency network.
title_short Dynamic status of REST in the mouse ESC pluripotency network.
title_sort dynamic status of rest in the mouse esc pluripotency network
url http://europepmc.org/articles/PMC3429488?pdf=render
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