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Single-cell RNA-sequencing of differentiating iPS cells reveals dynamic genetic effects on gene expression

Recent developments in stem cell biology have enabled the study of cell fate decisions in early human development that are impossible to study in vivo. However, understanding how development varies across individuals and, in particular, the influence of common genetic variants during this process ha...

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Autores principales: Cuomo, Anna S. E., Seaton, Daniel D., McCarthy, Davis J., Martinez, Iker, Bonder, Marc Jan, Garcia-Bernardo, Jose, Amatya, Shradha, Madrigal, Pedro, Isaacson, Abigail, Buettner, Florian, Knights, Andrew, Natarajan, Kedar Nath, Vallier, Ludovic, Marioni, John C., Chhatriwala, Mariya, Stegle, Oliver
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7010688/
https://www.ncbi.nlm.nih.gov/pubmed/32041960
http://dx.doi.org/10.1038/s41467-020-14457-z
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author Cuomo, Anna S. E.
Seaton, Daniel D.
McCarthy, Davis J.
Martinez, Iker
Bonder, Marc Jan
Garcia-Bernardo, Jose
Amatya, Shradha
Madrigal, Pedro
Isaacson, Abigail
Buettner, Florian
Knights, Andrew
Natarajan, Kedar Nath
Vallier, Ludovic
Marioni, John C.
Chhatriwala, Mariya
Stegle, Oliver
author_facet Cuomo, Anna S. E.
Seaton, Daniel D.
McCarthy, Davis J.
Martinez, Iker
Bonder, Marc Jan
Garcia-Bernardo, Jose
Amatya, Shradha
Madrigal, Pedro
Isaacson, Abigail
Buettner, Florian
Knights, Andrew
Natarajan, Kedar Nath
Vallier, Ludovic
Marioni, John C.
Chhatriwala, Mariya
Stegle, Oliver
author_sort Cuomo, Anna S. E.
collection PubMed
description Recent developments in stem cell biology have enabled the study of cell fate decisions in early human development that are impossible to study in vivo. However, understanding how development varies across individuals and, in particular, the influence of common genetic variants during this process has not been characterised. Here, we exploit human iPS cell lines from 125 donors, a pooled experimental design, and single-cell RNA-sequencing to study population variation of endoderm differentiation. We identify molecular markers that are predictive of differentiation efficiency of individual lines, and utilise heterogeneity in the genetic background across individuals to map hundreds of expression quantitative trait loci that influence expression dynamically during differentiation and across cellular contexts.
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spelling pubmed-70106882020-02-12 Single-cell RNA-sequencing of differentiating iPS cells reveals dynamic genetic effects on gene expression Cuomo, Anna S. E. Seaton, Daniel D. McCarthy, Davis J. Martinez, Iker Bonder, Marc Jan Garcia-Bernardo, Jose Amatya, Shradha Madrigal, Pedro Isaacson, Abigail Buettner, Florian Knights, Andrew Natarajan, Kedar Nath Vallier, Ludovic Marioni, John C. Chhatriwala, Mariya Stegle, Oliver Nat Commun Article Recent developments in stem cell biology have enabled the study of cell fate decisions in early human development that are impossible to study in vivo. However, understanding how development varies across individuals and, in particular, the influence of common genetic variants during this process has not been characterised. Here, we exploit human iPS cell lines from 125 donors, a pooled experimental design, and single-cell RNA-sequencing to study population variation of endoderm differentiation. We identify molecular markers that are predictive of differentiation efficiency of individual lines, and utilise heterogeneity in the genetic background across individuals to map hundreds of expression quantitative trait loci that influence expression dynamically during differentiation and across cellular contexts. Nature Publishing Group UK 2020-02-10 /pmc/articles/PMC7010688/ /pubmed/32041960 http://dx.doi.org/10.1038/s41467-020-14457-z Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Cuomo, Anna S. E.
Seaton, Daniel D.
McCarthy, Davis J.
Martinez, Iker
Bonder, Marc Jan
Garcia-Bernardo, Jose
Amatya, Shradha
Madrigal, Pedro
Isaacson, Abigail
Buettner, Florian
Knights, Andrew
Natarajan, Kedar Nath
Vallier, Ludovic
Marioni, John C.
Chhatriwala, Mariya
Stegle, Oliver
Single-cell RNA-sequencing of differentiating iPS cells reveals dynamic genetic effects on gene expression
title Single-cell RNA-sequencing of differentiating iPS cells reveals dynamic genetic effects on gene expression
title_full Single-cell RNA-sequencing of differentiating iPS cells reveals dynamic genetic effects on gene expression
title_fullStr Single-cell RNA-sequencing of differentiating iPS cells reveals dynamic genetic effects on gene expression
title_full_unstemmed Single-cell RNA-sequencing of differentiating iPS cells reveals dynamic genetic effects on gene expression
title_short Single-cell RNA-sequencing of differentiating iPS cells reveals dynamic genetic effects on gene expression
title_sort single-cell rna-sequencing of differentiating ips cells reveals dynamic genetic effects on gene expression
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7010688/
https://www.ncbi.nlm.nih.gov/pubmed/32041960
http://dx.doi.org/10.1038/s41467-020-14457-z
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