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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...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2017
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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 |
format | Online Article Text |
id | pubmed-5352225 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
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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