A hypomorphic allele of SLC35D1 results in Schneckenbecken-like dysplasia

Hum Mol Genet. 2019 Nov 1;28(21):3543-3551. doi: 10.1093/hmg/ddz200.

Abstract

We report the case of a consanguineous couple who lost four pregnancies associated with skeletal dysplasia. Radiological examination of one fetus was inconclusive. Parental exome sequencing showed that both parents were heterozygous for a novel missense variant, p.(Pro133Leu), in the SLC35D1 gene encoding a nucleotide sugar transporter. The affected fetus was homozygous for the variant. The radiological features were reviewed, and being similar, but atypical, the phenotype was classified as a 'Schneckenbecken-like dysplasia.' The effect of the missense change was assessed using protein modelling techniques and indicated alterations in the mouth of the solute channel. A detailed biochemical investigation of SLC35D1 transport function and that of the missense variant p.(Pro133Leu) revealed that SLC35D1 acts as a general UDP-sugar transporter and that the p.(Pro133Leu) mutation resulted in a significant decrease in transport activity. The reduced transport activity observed for p.(Pro133Leu) was contrasted with in vitro activity for SLC35D1 p.(Thr65Pro), the loss-of-function mutation was associated with Schneckenbecken dysplasia. The functional classification of SLC35D1 as a general nucleotide sugar transporter of the endoplasmic reticulum suggests an expanded role for this transporter beyond chondroitin sulfate biosynthesis to a variety of important glycosylation reactions occurring in the endoplasmic reticulum.

Keywords: SLC35D1; Schneckenbecken dysplasia; genetics; nucleotide sugar transporters; radiology.

Publication types

  • Case Reports
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alleles
  • Animals
  • Endoplasmic Reticulum / genetics
  • Endoplasmic Reticulum / metabolism
  • Female
  • Fetal Diseases / genetics*
  • Fetal Diseases / metabolism
  • Fetal Diseases / pathology
  • Heterozygote
  • Humans
  • Loss of Function Mutation
  • Male
  • Mice
  • Monosaccharide Transport Proteins / genetics*
  • Monosaccharide Transport Proteins / metabolism
  • Mutation, Missense
  • Osteochondrodysplasias / embryology
  • Osteochondrodysplasias / genetics*
  • Osteochondrodysplasias / metabolism

Substances

  • Monosaccharide Transport Proteins
  • SLC35D1 protein, human

Supplementary concepts

  • Schneckenbecken dysplasia