Discovery and characterization of variance QTLs in human induced pluripotent stem cells.

Quantification of gene expression levels at the single cell level has revealed that gene expression can vary substantially even across a population of homogeneous cells. However, it is currently unclear what genomic features control variation in gene expression levels, and whether common genetic var...

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Main Authors: Abhishek K Sarkar, Po-Yuan Tung, John D Blischak, Jonathan E Burnett, Yang I Li, Matthew Stephens, Yoav Gilad
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2019-04-01
Series:PLoS Genetics
Online Access:https://doi.org/10.1371/journal.pgen.1008045
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spelling doaj-3ceae214409c455fb8382e3025a6c93b2021-04-21T13:51:54ZengPublic Library of Science (PLoS)PLoS Genetics1553-73901553-74042019-04-01154e100804510.1371/journal.pgen.1008045Discovery and characterization of variance QTLs in human induced pluripotent stem cells.Abhishek K SarkarPo-Yuan TungJohn D BlischakJonathan E BurnettYang I LiMatthew StephensYoav GiladQuantification of gene expression levels at the single cell level has revealed that gene expression can vary substantially even across a population of homogeneous cells. However, it is currently unclear what genomic features control variation in gene expression levels, and whether common genetic variants may impact gene expression variation. Here, we take a genome-wide approach to identify expression variance quantitative trait loci (vQTLs). To this end, we generated single cell RNA-seq (scRNA-seq) data from induced pluripotent stem cells (iPSCs) derived from 53 Yoruba individuals. We collected data for a median of 95 cells per individual and a total of 5,447 single cells, and identified 235 mean expression QTLs (eQTLs) at 10% FDR, of which 79% replicate in bulk RNA-seq data from the same individuals. We further identified 5 vQTLs at 10% FDR, but demonstrate that these can also be explained as effects on mean expression. Our study suggests that dispersion QTLs (dQTLs) which could alter the variance of expression independently of the mean can have larger fold changes, but explain less phenotypic variance than eQTLs. We estimate 4,015 individuals as a lower bound to achieve 80% power to detect the strongest dQTLs in iPSCs. These results will guide the design of future studies on understanding the genetic control of gene expression variance.https://doi.org/10.1371/journal.pgen.1008045
collection DOAJ
language English
format Article
sources DOAJ
author Abhishek K Sarkar
Po-Yuan Tung
John D Blischak
Jonathan E Burnett
Yang I Li
Matthew Stephens
Yoav Gilad
spellingShingle Abhishek K Sarkar
Po-Yuan Tung
John D Blischak
Jonathan E Burnett
Yang I Li
Matthew Stephens
Yoav Gilad
Discovery and characterization of variance QTLs in human induced pluripotent stem cells.
PLoS Genetics
author_facet Abhishek K Sarkar
Po-Yuan Tung
John D Blischak
Jonathan E Burnett
Yang I Li
Matthew Stephens
Yoav Gilad
author_sort Abhishek K Sarkar
title Discovery and characterization of variance QTLs in human induced pluripotent stem cells.
title_short Discovery and characterization of variance QTLs in human induced pluripotent stem cells.
title_full Discovery and characterization of variance QTLs in human induced pluripotent stem cells.
title_fullStr Discovery and characterization of variance QTLs in human induced pluripotent stem cells.
title_full_unstemmed Discovery and characterization of variance QTLs in human induced pluripotent stem cells.
title_sort discovery and characterization of variance qtls in human induced pluripotent stem cells.
publisher Public Library of Science (PLoS)
series PLoS Genetics
issn 1553-7390
1553-7404
publishDate 2019-04-01
description Quantification of gene expression levels at the single cell level has revealed that gene expression can vary substantially even across a population of homogeneous cells. However, it is currently unclear what genomic features control variation in gene expression levels, and whether common genetic variants may impact gene expression variation. Here, we take a genome-wide approach to identify expression variance quantitative trait loci (vQTLs). To this end, we generated single cell RNA-seq (scRNA-seq) data from induced pluripotent stem cells (iPSCs) derived from 53 Yoruba individuals. We collected data for a median of 95 cells per individual and a total of 5,447 single cells, and identified 235 mean expression QTLs (eQTLs) at 10% FDR, of which 79% replicate in bulk RNA-seq data from the same individuals. We further identified 5 vQTLs at 10% FDR, but demonstrate that these can also be explained as effects on mean expression. Our study suggests that dispersion QTLs (dQTLs) which could alter the variance of expression independently of the mean can have larger fold changes, but explain less phenotypic variance than eQTLs. We estimate 4,015 individuals as a lower bound to achieve 80% power to detect the strongest dQTLs in iPSCs. These results will guide the design of future studies on understanding the genetic control of gene expression variance.
url https://doi.org/10.1371/journal.pgen.1008045
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