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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...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2015
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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. |
format | Online Article Text |
id | pubmed-4704488 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
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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