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

被引:53
|
作者
Chen, Jenny [1 ,2 ]
Swofford, Ross [1 ]
Johnson, Jeremy [1 ]
Cummings, Beryl B. [1 ,3 ]
Rogel, Noga [4 ]
Lindblad-Toh, Kerstin [1 ,5 ]
Haerty, Wilfried [6 ]
di Palma, Federica [6 ,7 ]
Regev, Aviv [4 ,8 ,9 ,10 ]
机构
[1] Broad Inst MIT & Harvard, Cambridge, MA 02142 USA
[2] MIT, Div Hlth Sci & Technol, Cambridge, MA 02139 USA
[3] Harvard Med Sch, Program Biol & Biomed Sci, Boston, MA 02115 USA
[4] Broad Inst MIT & Harvard, Klarman Cell Observ, Cambridge, MA 02142 USA
[5] Uppsala Univ, Dept Med Biochem & Microbiol, Sci Life Lab, S-75236 Uppsala, Sweden
[6] Earlham Inst, Norwich NR4 7UZ, Norfolk, England
[7] Univ East Anglia, Dept Biol & Med Sci, Norwich NR4 7TJ, Norfolk, England
[8] MIT, Dept Biol, Cambridge, MA 02142 USA
[9] MIT, Koch Inst, Cambridge, MA 02142 USA
[10] Howard Hughes Med Inst, Chevy Chase, MD 20815 USA
基金
英国生物技术与生命科学研究理事会; 瑞典研究理事会;
关键词
ADAPTIVE EVOLUTION; COMPARATIVE GENOMICS; SELECTION; MOUSE; MODEL; MUTATIONS; PROTEINS; RESOURCE; ELEMENTS; DATABASE;
D O I
10.1101/gr.237636.118
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The evolutionary history of a gene helps predict its function and relationship to phenotypic traits. Although sequence conservation is commonly used to decipher gene function and assess medical relevance, methods for functional inference from comparative expression data are lacking. Here, we use RNA-seq across seven tissues from 17 mammalian species to show that expression evolution across mammals is accurately modeled by the Ornstein-Uhlenbeck process, a commonly proposed model of continuous trait evolution. We apply this model to identify expression pathways under neutral, stabilizing, and directional selection. We further demonstrate novel applications of this model to quantify the extent of stabilizing selection on a gene's expression, parameterize the distribution of each gene's optimal expression level, and detect deleterious expression levels in expression data from individual patients. Our work provides a statistical framework for interpreting expression data across species and in disease.
引用
收藏
页码:53 / 63
页数:11
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