Analysis of genome-wide knockout mouse database identifies candidate ciliopathy genes

Author:

Higgins Kendall,Moore Bret A.,Berberovic Zorana,Adissu Hibret A.,Eskandarian Mohammad,Flenniken Ann M.,Shao Andy,Imai Denise M.,Clary Dave,Lanoue Louise,Newbigging Susan,Nutter Lauryl M. J.,Adams David J.,Bosch Fatima,Braun Robert E.,Brown Steve D. M.,Dickinson Mary E.,Dobbie Michael,Flicek Paul,Gao Xiang,Galande Sanjeev,Grobler Anne,Heaney Jason D.,Herault Yann,de Angelis Martin Hrabe,Chin Hsian-Jean Genie,Mammano Fabio,Qin Chuan,Shiroishi Toshihiko,Sedlacek Radislav,Seong J.-K.,Xu Ying,Beaudet Arthur L.,Braun Bob,Karp Natasha,Mallon Ann-Marie,Meehan Terrence,Obata Yuichi,Parkinson Helen,Smedley Damian,Tocchini-Valentini Glauco,Wells Sara,Lloyd K. C. Kent,McKerlie Colin,Moshiri Ala,

Abstract

AbstractWe searched a database of single-gene knockout (KO) mice produced by the International Mouse Phenotyping Consortium (IMPC) to identify candidate ciliopathy genes. We first screened for phenotypes in mouse lines with both ocular and renal or reproductive trait abnormalities. The STRING protein interaction tool was used to identify interactions between known cilia gene products and those encoded by the genes in individual knockout mouse strains in order to generate a list of “candidate ciliopathy genes.” From this list, 32 genes encoded proteins predicted to interact with known ciliopathy proteins. Of these, 25 had no previously described roles in ciliary pathobiology. Histological and morphological evidence of phenotypes found in ciliopathies in knockout mouse lines are presented as examples (genes Abi2, Wdr62, Ap4e1, Dync1li1, and Prkab1). Phenotyping data and descriptions generated on IMPC mouse line are useful for mechanistic studies, target discovery, rare disease diagnosis, and preclinical therapeutic development trials. Here we demonstrate the effective use of the IMPC phenotype data to uncover genes with no previous role in ciliary biology, which may be clinically relevant for identification of novel disease genes implicated in ciliopathies.

Funder

National Institutes of Health

Government of Canada through Genome Canada/Ontario Genomics

Publisher

Springer Science and Business Media LLC

Subject

Multidisciplinary

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