Analysis of Single-Cell Gene Pair Coexpression Landscapes by Stochastic Kinetic Modeling Reveals Gene-Pair Interactions in Development

Single-cell transcriptomics is advancing discovery of the molecular determinants of cell identity, while spurring development of novel data analysis methods. Stochastic mathematical models of gene regulatory networks help unravel the dynamic, molecular mechanisms underlying cell-to-cell heterogeneit...

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Main Authors: Cameron P. Gallivan, Honglei Ren, Elizabeth L. Read
Format: Article
Language:English
Published: Frontiers Media S.A. 2020-01-01
Series:Frontiers in Genetics
Subjects:
Online Access:https://www.frontiersin.org/article/10.3389/fgene.2019.01387/full
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spelling doaj-dfdf45cae83c47b69c85499b17dda3f52020-11-25T01:32:06ZengFrontiers Media S.A.Frontiers in Genetics1664-80212020-01-011010.3389/fgene.2019.01387505221Analysis of Single-Cell Gene Pair Coexpression Landscapes by Stochastic Kinetic Modeling Reveals Gene-Pair Interactions in DevelopmentCameron P. Gallivan0Honglei Ren1Honglei Ren2Elizabeth L. Read3Elizabeth L. Read4Department of Chemical & Biomolecular Engineering, University of California, Irvine, CA, United StatesNSF-Simons Center for Multiscale Cell Fate, University of California, Irvine, CA, United StatesMathematical and Computational Systems Biology Graduate Program, University of California, Irvine, CA, United StatesDepartment of Chemical & Biomolecular Engineering, University of California, Irvine, CA, United StatesNSF-Simons Center for Multiscale Cell Fate, University of California, Irvine, CA, United StatesSingle-cell transcriptomics is advancing discovery of the molecular determinants of cell identity, while spurring development of novel data analysis methods. Stochastic mathematical models of gene regulatory networks help unravel the dynamic, molecular mechanisms underlying cell-to-cell heterogeneity, and can thus aid interpretation of heterogeneous cell-states revealed by single-cell measurements. However, integrating stochastic gene network models with single cell data is challenging. Here, we present a method for analyzing single-cell gene-pair coexpression patterns, based on biophysical models of stochastic gene expression and interaction dynamics. We first developed a high-computational-throughput approach to stochastic modeling of gene-pair coexpression landscapes, based on numerical solution of gene network Master Equations. We then comprehensively catalogued coexpression patterns arising from tens of thousands of gene-gene interaction models with different biochemical kinetic parameters and regulatory interactions. From the computed landscapes, we obtain a low-dimensional “shape-space” describing distinct types of coexpression patterns. We applied the theoretical results to analysis of published single cell RNA sequencing data and uncovered complex dynamics of coexpression among gene pairs during embryonic development. Our approach provides a generalizable framework for inferring evolution of gene-gene interactions during critical cell-state transitions.https://www.frontiersin.org/article/10.3389/fgene.2019.01387/fullstochastic modellinggene expression noisegene regulatory networkssingle-cell datascRNA-seq
collection DOAJ
language English
format Article
sources DOAJ
author Cameron P. Gallivan
Honglei Ren
Honglei Ren
Elizabeth L. Read
Elizabeth L. Read
spellingShingle Cameron P. Gallivan
Honglei Ren
Honglei Ren
Elizabeth L. Read
Elizabeth L. Read
Analysis of Single-Cell Gene Pair Coexpression Landscapes by Stochastic Kinetic Modeling Reveals Gene-Pair Interactions in Development
Frontiers in Genetics
stochastic modelling
gene expression noise
gene regulatory networks
single-cell data
scRNA-seq
author_facet Cameron P. Gallivan
Honglei Ren
Honglei Ren
Elizabeth L. Read
Elizabeth L. Read
author_sort Cameron P. Gallivan
title Analysis of Single-Cell Gene Pair Coexpression Landscapes by Stochastic Kinetic Modeling Reveals Gene-Pair Interactions in Development
title_short Analysis of Single-Cell Gene Pair Coexpression Landscapes by Stochastic Kinetic Modeling Reveals Gene-Pair Interactions in Development
title_full Analysis of Single-Cell Gene Pair Coexpression Landscapes by Stochastic Kinetic Modeling Reveals Gene-Pair Interactions in Development
title_fullStr Analysis of Single-Cell Gene Pair Coexpression Landscapes by Stochastic Kinetic Modeling Reveals Gene-Pair Interactions in Development
title_full_unstemmed Analysis of Single-Cell Gene Pair Coexpression Landscapes by Stochastic Kinetic Modeling Reveals Gene-Pair Interactions in Development
title_sort analysis of single-cell gene pair coexpression landscapes by stochastic kinetic modeling reveals gene-pair interactions in development
publisher Frontiers Media S.A.
series Frontiers in Genetics
issn 1664-8021
publishDate 2020-01-01
description Single-cell transcriptomics is advancing discovery of the molecular determinants of cell identity, while spurring development of novel data analysis methods. Stochastic mathematical models of gene regulatory networks help unravel the dynamic, molecular mechanisms underlying cell-to-cell heterogeneity, and can thus aid interpretation of heterogeneous cell-states revealed by single-cell measurements. However, integrating stochastic gene network models with single cell data is challenging. Here, we present a method for analyzing single-cell gene-pair coexpression patterns, based on biophysical models of stochastic gene expression and interaction dynamics. We first developed a high-computational-throughput approach to stochastic modeling of gene-pair coexpression landscapes, based on numerical solution of gene network Master Equations. We then comprehensively catalogued coexpression patterns arising from tens of thousands of gene-gene interaction models with different biochemical kinetic parameters and regulatory interactions. From the computed landscapes, we obtain a low-dimensional “shape-space” describing distinct types of coexpression patterns. We applied the theoretical results to analysis of published single cell RNA sequencing data and uncovered complex dynamics of coexpression among gene pairs during embryonic development. Our approach provides a generalizable framework for inferring evolution of gene-gene interactions during critical cell-state transitions.
topic stochastic modelling
gene expression noise
gene regulatory networks
single-cell data
scRNA-seq
url https://www.frontiersin.org/article/10.3389/fgene.2019.01387/full
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