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Dynamics of embryonic stem cell differentiation inferred from single-cell transcriptomics show a series of transitions through discrete cell states

The complexity of gene regulatory networks that lead multipotent cells to acquire different cell fates makes a quantitative understanding of differentiation challenging. Using a statistical framework to analyze single-cell transcriptomics data, we infer the gene expression dynamics of early mouse em...

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Autores principales: Jang, Sumin, Choubey, Sandeep, Furchtgott, Leon, Zou, Ling-Nan, Doyle, Adele, Menon, Vilas, Loew, Ethan B, Krostag, Anne-Rachel, Martinez, Refugio A, Madisen, Linda, Levi, Boaz P, Ramanathan, Sharad
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5352225/
https://www.ncbi.nlm.nih.gov/pubmed/28296635
http://dx.doi.org/10.7554/eLife.20487
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author Jang, Sumin
Choubey, Sandeep
Furchtgott, Leon
Zou, Ling-Nan
Doyle, Adele
Menon, Vilas
Loew, Ethan B
Krostag, Anne-Rachel
Martinez, Refugio A
Madisen, Linda
Levi, Boaz P
Ramanathan, Sharad
author_facet Jang, Sumin
Choubey, Sandeep
Furchtgott, Leon
Zou, Ling-Nan
Doyle, Adele
Menon, Vilas
Loew, Ethan B
Krostag, Anne-Rachel
Martinez, Refugio A
Madisen, Linda
Levi, Boaz P
Ramanathan, Sharad
author_sort Jang, Sumin
collection PubMed
description The complexity of gene regulatory networks that lead multipotent cells to acquire different cell fates makes a quantitative understanding of differentiation challenging. Using a statistical framework to analyze single-cell transcriptomics data, we infer the gene expression dynamics of early mouse embryonic stem (mES) cell differentiation, uncovering discrete transitions across nine cell states. We validate the predicted transitions across discrete states using flow cytometry. Moreover, using live-cell microscopy, we show that individual cells undergo abrupt transitions from a naïve to primed pluripotent state. Using the inferred discrete cell states to build a probabilistic model for the underlying gene regulatory network, we further predict and experimentally verify that these states have unique response to perturbations, thus defining them functionally. Our study provides a framework to infer the dynamics of differentiation from single cell transcriptomics data and to build predictive models of the gene regulatory networks that drive the sequence of cell fate decisions during development. DOI: http://dx.doi.org/10.7554/eLife.20487.001
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spelling pubmed-53522252017-03-17 Dynamics of embryonic stem cell differentiation inferred from single-cell transcriptomics show a series of transitions through discrete cell states Jang, Sumin Choubey, Sandeep Furchtgott, Leon Zou, Ling-Nan Doyle, Adele Menon, Vilas Loew, Ethan B Krostag, Anne-Rachel Martinez, Refugio A Madisen, Linda Levi, Boaz P Ramanathan, Sharad eLife Computational and Systems Biology The complexity of gene regulatory networks that lead multipotent cells to acquire different cell fates makes a quantitative understanding of differentiation challenging. Using a statistical framework to analyze single-cell transcriptomics data, we infer the gene expression dynamics of early mouse embryonic stem (mES) cell differentiation, uncovering discrete transitions across nine cell states. We validate the predicted transitions across discrete states using flow cytometry. Moreover, using live-cell microscopy, we show that individual cells undergo abrupt transitions from a naïve to primed pluripotent state. Using the inferred discrete cell states to build a probabilistic model for the underlying gene regulatory network, we further predict and experimentally verify that these states have unique response to perturbations, thus defining them functionally. Our study provides a framework to infer the dynamics of differentiation from single cell transcriptomics data and to build predictive models of the gene regulatory networks that drive the sequence of cell fate decisions during development. DOI: http://dx.doi.org/10.7554/eLife.20487.001 eLife Sciences Publications, Ltd 2017-03-15 /pmc/articles/PMC5352225/ /pubmed/28296635 http://dx.doi.org/10.7554/eLife.20487 Text en © 2017, Jang et al http://creativecommons.org/licenses/by/4.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Computational and Systems Biology
Jang, Sumin
Choubey, Sandeep
Furchtgott, Leon
Zou, Ling-Nan
Doyle, Adele
Menon, Vilas
Loew, Ethan B
Krostag, Anne-Rachel
Martinez, Refugio A
Madisen, Linda
Levi, Boaz P
Ramanathan, Sharad
Dynamics of embryonic stem cell differentiation inferred from single-cell transcriptomics show a series of transitions through discrete cell states
title Dynamics of embryonic stem cell differentiation inferred from single-cell transcriptomics show a series of transitions through discrete cell states
title_full Dynamics of embryonic stem cell differentiation inferred from single-cell transcriptomics show a series of transitions through discrete cell states
title_fullStr Dynamics of embryonic stem cell differentiation inferred from single-cell transcriptomics show a series of transitions through discrete cell states
title_full_unstemmed Dynamics of embryonic stem cell differentiation inferred from single-cell transcriptomics show a series of transitions through discrete cell states
title_short Dynamics of embryonic stem cell differentiation inferred from single-cell transcriptomics show a series of transitions through discrete cell states
title_sort dynamics of embryonic stem cell differentiation inferred from single-cell transcriptomics show a series of transitions through discrete cell states
topic Computational and Systems Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5352225/
https://www.ncbi.nlm.nih.gov/pubmed/28296635
http://dx.doi.org/10.7554/eLife.20487
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