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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...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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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. |
format | Online Article Text |
id | pubmed-7010688 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
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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