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

Authors :
Higgins K
Moore BA
Berberovic Z
Adissu HA
Eskandarian M
Flenniken AM
Shao A
Imai DM
Clary D
Lanoue L
Newbigging S
Nutter LMJ
Adams DJ
Bosch F
Braun RE
Brown SDM
Dickinson ME
Dobbie M
Flicek P
Gao X
Galande S
Grobler A
Heaney JD
Herault Y
de Angelis MH
Chin HG
Mammano F
Qin C
Shiroishi T
Sedlacek R
Seong JK
Xu Y
Lloyd KCK
McKerlie C
Moshiri A
Source :
Scientific reports [Sci Rep] 2022 Dec 01; Vol. 12 (1), pp. 20791. Date of Electronic Publication: 2022 Dec 01.
Publication Year :
2022

Abstract

We 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.<br /> (© 2022. The Author(s).)

Details

Language :
English
ISSN :
2045-2322
Volume :
12
Issue :
1
Database :
MEDLINE
Journal :
Scientific reports
Publication Type :
Academic Journal
Accession number :
36456625
Full Text :
https://doi.org/10.1038/s41598-022-19710-7