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A quantitative model for characterizing the evolutionary history of mammalian gene expression

Jenny Chen, Ross Swofford, Jeremy Johnson, Beryl B. Cummings, Noga Rogel, Kerstin Lindblad-Toh, Wilfried Haerty, Federica di Palma, Aviv Regev
doi: https://doi.org/10.1101/229096
Jenny Chen
1Broad Institute of MIT and Harvard, Cambridge, MA.
2Division of Health Science and Technology, MIT, Cambridge, MA.
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Ross Swofford
1Broad Institute of MIT and Harvard, Cambridge, MA.
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Jeremy Johnson
1Broad Institute of MIT and Harvard, Cambridge, MA.
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Beryl B. Cummings
1Broad Institute of MIT and Harvard, Cambridge, MA.
3Program in Biological and Biomedical Sciences, Harvard Medical School, Boston, MA.
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Noga Rogel
1Broad Institute of MIT and Harvard, Cambridge, MA.
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Kerstin Lindblad-Toh
1Broad Institute of MIT and Harvard, Cambridge, MA.
4Science for Life Laboratory, Department of Medical Biochemistry and Microbiology, Uppsala University, Uppsala, Sweden.
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Wilfried Haerty
5Earlham Institute, Norwich, United Kingdom.
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Federica di Palma
5Earlham Institute, Norwich, United Kingdom.
6Department of Biological and Medical Sciences University of East Anglia, Norwich UK.
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Aviv Regev
1Broad Institute of MIT and Harvard, Cambridge, MA.
7Department of Biology and Koch Institute, MIT, Boston, MA 02142, USA.
8Howard Hughes Medical Institute, Chevy Chase, MD 20815, USA.
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Abstract

Characterizing the evolutionary history of a gene’s expression profile is a critical component for understanding the relationship between genotype, expression, and phenotype. However, it is not well-established how best to distinguish the different evolutionary forces acting on gene expression. Here, we use RNA-seq across 7 tissues from 17 mammalian species to show that expression evolution across mammals is accurately modeled by the Ornstein-Uhlenbeck (OU) process. This stochastic process models expression trajectories across time as Gaussian distributions whose variance is parameterized by the rate of genetic drift and strength of stabilizing selection. We use these mathematical properties to identify expression pathways under neutral, stabilizing, and directional selection, and quantify the extent of selective pressure on a gene’s expression. We further detect deleterious expression levels outside expected evolutionary distributions in expression data from individual patients. Our work provides a statistical framework for interpreting expression data across species and in disease.

One Sentence Summary We demonstrate the power of a stochastic model for quantifying selective pressure on expression and estimating evolutionary distributions of optimal gene expression.

Copyright 
The copyright holder for this preprint is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under a CC-BY 4.0 International license.
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Posted December 04, 2017.
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A quantitative model for characterizing the evolutionary history of mammalian gene expression
Jenny Chen, Ross Swofford, Jeremy Johnson, Beryl B. Cummings, Noga Rogel, Kerstin Lindblad-Toh, Wilfried Haerty, Federica di Palma, Aviv Regev
bioRxiv 229096; doi: https://doi.org/10.1101/229096
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A quantitative model for characterizing the evolutionary history of mammalian gene expression
Jenny Chen, Ross Swofford, Jeremy Johnson, Beryl B. Cummings, Noga Rogel, Kerstin Lindblad-Toh, Wilfried Haerty, Federica di Palma, Aviv Regev
bioRxiv 229096; doi: https://doi.org/10.1101/229096

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