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The bimodally expressed microRNA miR‐142 gates exit from pluripotency

A stem cell's decision to self‐renew or differentiate is thought to critically depend on signaling cues provided by its environment. It is unclear whether stem cells have the intrinsic capacity to control their responsiveness to environmental signals that can be fluctuating and noisy. Using a n...

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Detalles Bibliográficos
Autores principales: Sladitschek, Hanna L, Neveu, Pierre A
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4704488/
https://www.ncbi.nlm.nih.gov/pubmed/26690966
http://dx.doi.org/10.15252/msb.20156525
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author Sladitschek, Hanna L
Neveu, Pierre A
author_facet Sladitschek, Hanna L
Neveu, Pierre A
author_sort Sladitschek, Hanna L
collection PubMed
description A stem cell's decision to self‐renew or differentiate is thought to critically depend on signaling cues provided by its environment. It is unclear whether stem cells have the intrinsic capacity to control their responsiveness to environmental signals that can be fluctuating and noisy. Using a novel single‐cell microRNA activity reporter, we show that miR‐142 is bimodally expressed in embryonic stem cells, creating two states indistinguishable by pluripotency markers. A combination of modeling and quantitative experimental data revealed that mESCs switch stochastically between the two miR‐142 states. We find that cells with high miR‐142 expression are irresponsive to differentiation signals while cells with low miR‐142 expression can respond to differentiation cues. We elucidate the molecular mechanism underpinning the bimodal regulation of miR‐142 as a double‐negative feedback loop between miR‐142 and KRAS/ERK signaling and derive a quantitative description of this bistable system. miR‐142 switches the activation status of key intracellular signaling pathways thereby locking cells in an undifferentiated state. This reveals a novel mechanism to maintain a stem cell reservoir buffered against fluctuating signaling environments.
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spelling pubmed-47044882016-01-18 The bimodally expressed microRNA miR‐142 gates exit from pluripotency Sladitschek, Hanna L Neveu, Pierre A Mol Syst Biol Articles A stem cell's decision to self‐renew or differentiate is thought to critically depend on signaling cues provided by its environment. It is unclear whether stem cells have the intrinsic capacity to control their responsiveness to environmental signals that can be fluctuating and noisy. Using a novel single‐cell microRNA activity reporter, we show that miR‐142 is bimodally expressed in embryonic stem cells, creating two states indistinguishable by pluripotency markers. A combination of modeling and quantitative experimental data revealed that mESCs switch stochastically between the two miR‐142 states. We find that cells with high miR‐142 expression are irresponsive to differentiation signals while cells with low miR‐142 expression can respond to differentiation cues. We elucidate the molecular mechanism underpinning the bimodal regulation of miR‐142 as a double‐negative feedback loop between miR‐142 and KRAS/ERK signaling and derive a quantitative description of this bistable system. miR‐142 switches the activation status of key intracellular signaling pathways thereby locking cells in an undifferentiated state. This reveals a novel mechanism to maintain a stem cell reservoir buffered against fluctuating signaling environments. John Wiley and Sons Inc. 2015-12-21 /pmc/articles/PMC4704488/ /pubmed/26690966 http://dx.doi.org/10.15252/msb.20156525 Text en © 2015 The Authors. Published under the terms of the CC BY 4.0 license This is an open access article under the terms of the Creative Commons Attribution 4.0 (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Articles
Sladitschek, Hanna L
Neveu, Pierre A
The bimodally expressed microRNA miR‐142 gates exit from pluripotency
title The bimodally expressed microRNA miR‐142 gates exit from pluripotency
title_full The bimodally expressed microRNA miR‐142 gates exit from pluripotency
title_fullStr The bimodally expressed microRNA miR‐142 gates exit from pluripotency
title_full_unstemmed The bimodally expressed microRNA miR‐142 gates exit from pluripotency
title_short The bimodally expressed microRNA miR‐142 gates exit from pluripotency
title_sort bimodally expressed microrna mir‐142 gates exit from pluripotency
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4704488/
https://www.ncbi.nlm.nih.gov/pubmed/26690966
http://dx.doi.org/10.15252/msb.20156525
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