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Pre-mRNA splicing factors play a fundamental role in regulating transcript diversity both temporally and spatially. Genetic defects in several spliceosome components have been linked to a set of non-overlapping spliceosomopathy phenotypes in humans, among which skeletal developmental defects and non-syndromic retinitis pigmentosa (RP) are frequent findings. Here we report that defects in spliceosome-associated protein CWC27 are associated with a spectrum of disease phenotypes ranging from isolated RP to severe syndromic forms. By whole-exome sequencing, recessive protein-truncating mutations in CWC27 were found in seven unrelated families that show a range of clinical phenotypes, including retinal degeneration, brachydactyly, craniofacial abnormalities, short stature, and neurological defects. Remarkably, variable expressivity of the human phenotype can be recapitulated in Cwc27 mutant mouse models, with significant embryonic lethality and severe phenotypes in the complete knockout mice while mice with a partial loss-of-function allele mimic the isolated retinal degeneration phenotype. Our study describes a retinal dystrophy-related phenotype spectrum as well as its genetic etiology and highlights the complexity of the spliceosomal gene network.

Original publication

DOI

10.1016/j.ajhg.2017.02.008

Type

Journal article

Journal

Am J Hum Genet

Publication Date

06/04/2017

Volume

100

Pages

592 - 604

Keywords

CRISPR-Cas9, CWC27, brachydachtyly, craniofacial defects, neurological defects, retinal degeneration, short stature, spliceosome, syndrome, Abnormalities, Multiple, Adolescent, Animals, Child, Child, Preschool, Cyclophilins, Female, Humans, Male, Mice, Mutation, Pedigree, Peptidylprolyl Isomerase, Retinal Degeneration, Young Adult