Mapping dynamic regulation of gene expression using single-cell transcriptomics and application to complex disease genetics

Summary: Single-cell transcriptome data can provide insights into how genetic variation influences biological processes involved in human physiology and disease. However, the identification of gene-level associations in distinct cell types faces several challenges, including the limited reference re...

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Main Authors: Hanna Abe, Phillip Lin, Dan Zhou, Douglas M. Ruderfer, Eric R. Gamazon
Format: Article
Language:English
Published: Elsevier 2025-04-01
Series:HGG Advances
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Online Access:http://www.sciencedirect.com/science/article/pii/S2666247724001374
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author Hanna Abe
Phillip Lin
Dan Zhou
Douglas M. Ruderfer
Eric R. Gamazon
author_facet Hanna Abe
Phillip Lin
Dan Zhou
Douglas M. Ruderfer
Eric R. Gamazon
author_sort Hanna Abe
collection DOAJ
description Summary: Single-cell transcriptome data can provide insights into how genetic variation influences biological processes involved in human physiology and disease. However, the identification of gene-level associations in distinct cell types faces several challenges, including the limited reference resources from population-scale studies, data sparsity in single-cell RNA sequencing, and the complex cell state pattern of expression within individual cell types. Here, we develop genetic models of cell-type-specific and cell-state-adjusted gene expression in mid-brain neurons undergoing differentiation from induced pluripotent stem cells. The resulting framework quantifies the dynamics of the genetic regulation of gene expression and estimates its cell-type specificity. As an application, we show that the approach detects known and new genes associated with schizophrenia and enables insights into context-dependent disease mechanisms. We provide a genomic resource from a phenome-wide application of our models to more than 1,500 phenotypes from the UK Biobank. Using longitudinal, genetically determined expression, we implement a predictive causality framework, evaluating the prediction of future values of a target gene expression using prior values of a putative regulatory gene. Collectively, the results of this work demonstrate the insights that can be gained into the molecular underpinnings of disease by quantifying the genetic control of gene expression at single-cell resolution.
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spelling doaj-art-f39896bd548e4276961fe66ab46c635a2025-01-31T05:12:27ZengElsevierHGG Advances2666-24772025-04-0162100397Mapping dynamic regulation of gene expression using single-cell transcriptomics and application to complex disease geneticsHanna Abe0Phillip Lin1Dan Zhou2Douglas M. Ruderfer3Eric R. Gamazon4Vanderbilt University, Nashville, TN, USA; Corresponding authorDivision of Genetic Medicine, Department of Medicine, Vanderbilt University Medical Center, Nashville, TN, USADivision of Genetic Medicine, Department of Medicine, Vanderbilt University Medical Center, Nashville, TN, USADivision of Genetic Medicine, Department of Medicine, Vanderbilt University Medical Center, Nashville, TN, USA; Department of Biomedical Informatics and Psychiatry and Behavioral Sciences, Vanderbilt University Medical Center, Nashville, TN, USADivision of Genetic Medicine, Department of Medicine, Vanderbilt University Medical Center, Nashville, TN, USA; Clare Hall, University of Cambridge, Cambridge, UK; Corresponding authorSummary: Single-cell transcriptome data can provide insights into how genetic variation influences biological processes involved in human physiology and disease. However, the identification of gene-level associations in distinct cell types faces several challenges, including the limited reference resources from population-scale studies, data sparsity in single-cell RNA sequencing, and the complex cell state pattern of expression within individual cell types. Here, we develop genetic models of cell-type-specific and cell-state-adjusted gene expression in mid-brain neurons undergoing differentiation from induced pluripotent stem cells. The resulting framework quantifies the dynamics of the genetic regulation of gene expression and estimates its cell-type specificity. As an application, we show that the approach detects known and new genes associated with schizophrenia and enables insights into context-dependent disease mechanisms. We provide a genomic resource from a phenome-wide application of our models to more than 1,500 phenotypes from the UK Biobank. Using longitudinal, genetically determined expression, we implement a predictive causality framework, evaluating the prediction of future values of a target gene expression using prior values of a putative regulatory gene. Collectively, the results of this work demonstrate the insights that can be gained into the molecular underpinnings of disease by quantifying the genetic control of gene expression at single-cell resolution.http://www.sciencedirect.com/science/article/pii/S2666247724001374TWASsingle-cellPheWAScell-stateGranger-causalityschizophrenia
spellingShingle Hanna Abe
Phillip Lin
Dan Zhou
Douglas M. Ruderfer
Eric R. Gamazon
Mapping dynamic regulation of gene expression using single-cell transcriptomics and application to complex disease genetics
HGG Advances
TWAS
single-cell
PheWAS
cell-state
Granger-causality
schizophrenia
title Mapping dynamic regulation of gene expression using single-cell transcriptomics and application to complex disease genetics
title_full Mapping dynamic regulation of gene expression using single-cell transcriptomics and application to complex disease genetics
title_fullStr Mapping dynamic regulation of gene expression using single-cell transcriptomics and application to complex disease genetics
title_full_unstemmed Mapping dynamic regulation of gene expression using single-cell transcriptomics and application to complex disease genetics
title_short Mapping dynamic regulation of gene expression using single-cell transcriptomics and application to complex disease genetics
title_sort mapping dynamic regulation of gene expression using single cell transcriptomics and application to complex disease genetics
topic TWAS
single-cell
PheWAS
cell-state
Granger-causality
schizophrenia
url http://www.sciencedirect.com/science/article/pii/S2666247724001374
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AT philliplin mappingdynamicregulationofgeneexpressionusingsinglecelltranscriptomicsandapplicationtocomplexdiseasegenetics
AT danzhou mappingdynamicregulationofgeneexpressionusingsinglecelltranscriptomicsandapplicationtocomplexdiseasegenetics
AT douglasmruderfer mappingdynamicregulationofgeneexpressionusingsinglecelltranscriptomicsandapplicationtocomplexdiseasegenetics
AT ericrgamazon mappingdynamicregulationofgeneexpressionusingsinglecelltranscriptomicsandapplicationtocomplexdiseasegenetics