Mutations in the Spliceosome Component CWC27 Cause Retinal Degeneration with or without Additional Developmental Anomalies

Am J Hum Genet. 2017 Apr 6;100(4):592-604. doi: 10.1016/j.ajhg.2017.02.008. Epub 2017 Mar 9.

Abstract

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.

Keywords: CRISPR-Cas9; CWC27; brachydachtyly; craniofacial defects; neurological defects; retinal degeneration; short stature; spliceosome; syndrome.

MeSH terms

  • Abnormalities, Multiple / genetics*
  • Adolescent
  • Animals
  • Child
  • Child, Preschool
  • Cyclophilins / genetics*
  • Cyclophilins / metabolism
  • Female
  • Humans
  • Male
  • Mice
  • Mutation*
  • Pedigree
  • Peptidylprolyl Isomerase / genetics*
  • Peptidylprolyl Isomerase / metabolism
  • Retinal Degeneration / genetics*
  • Young Adult

Substances

  • Cwc27 protein, human
  • Cyclophilins
  • CWC27 spliceosome-associated protein, mouse
  • Peptidylprolyl Isomerase