Relating multivariate shapes to genescapes using phenotype-biological process associations for craniofacial shape

Author:

Aponte Jose D1ORCID,Katz David C1,Roth Daniela M2ORCID,Vidal-García Marta1ORCID,Liu Wei1,Andrade Fernando3,Roseman Charles C3,Murray Steven A4,Cheverud James3,Graf Daniel25,Marcucio Ralph S6ORCID,Hallgrímsson Benedikt17ORCID

Affiliation:

1. Department of Cell Biology & Anatomy, Alberta Children’s Hospital Research Institute and McCaig Bone and Joint Institute, Cumming School of Medicine, University of Calgary

2. School of Dentistry, Faculty of Medicine and Dentistry, University of Alberta

3. Department of Biology, Loyola University Chicago

4. The Jackson Laboratory

5. Department of Medical Genetics, Faculty of Medicine and Dentistry, University of Alberta

6. Department of Orthopaedic Surgery, School of Medicine, University of California, San Francisco

7. Department of Animal Biology, University of Illinois Urbana Champaign

Abstract

Realistic mappings of genes to morphology are inherently multivariate on both sides of the equation. The importance of coordinated gene effects on morphological phenotypes is clear from the intertwining of gene actions in signaling pathways, gene regulatory networks, and developmental processes underlying the development of shape and size. Yet, current approaches tend to focus on identifying and localizing the effects of individual genes and rarely leverage the information content of high-dimensional phenotypes. Here, we explicitly model the joint effects of biologically coherent collections of genes on a multivariate trait – craniofacial shape – in a sample of n = 1145 mice from the Diversity Outbred (DO) experimental line. We use biological process Gene Ontology (GO) annotations to select skeletal and facial development gene sets and solve for the axis of shape variation that maximally covaries with gene set marker variation. We use our process-centered, multivariate genotype-phenotype (process MGP) approach to determine the overall contributions to craniofacial variation of genes involved in relevant processes and how variation in different processes corresponds to multivariate axes of shape variation. Further, we compare the directions of effect in phenotype space of mutations to the primary axis of shape variation associated with broader pathways within which they are thought to function. Finally, we leverage the relationship between mutational and pathway-level effects to predict phenotypic effects beyond craniofacial shape in specific mutants. We also introduce an online application that provides users the means to customize their own process-centered craniofacial shape analyses in the DO. The process-centered approach is generally applicable to any continuously varying phenotype and thus has wide-reaching implications for complex trait genetics.

Funder

National Institutes of Health

Natural Sciences and Engineering Research Council of Canada

Canadian Institutes of Health Research

Publisher

eLife Sciences Publications, Ltd

Subject

General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,General Medicine,General Neuroscience

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