Identification of a germline CSPG4 variation in a family with neurofibromatosis type 1-like phenotype

Cell Death Dis. 2021 Aug 3;12(8):765. doi: 10.1038/s41419-021-04056-1.

Abstract

Neurofibromatosis type 1 (NF1), an autosomal dominant and multisystem disorder, is generally considered to be caused by NF1 inactivation. However, there are also numerous studies showing that Neurofibromatosis type 1-like phenotype can be caused by the abnormalities in the other genes. Through targeted parallel sequencing, whole-exome sequencing, de novo genomic sequencing, and RNA isoform sequencing, we identified a germline V2097M variation in CSPG4 gene probably increased susceptibility to a NF1-like phenotype family. Besides, a series of in vitro functional studies revealed that this variant promoted cell proliferation by activating the MAPK/ERK signaling pathway via hindering ectodomain cleavage of CSPG4. Our data demonstrate that a germline variation in the CSPG4 gene might be a high risk to cause NF1-like phenotype. To our knowledge, this is the first report of mutations in the CSPG4 gene in human diseases.

Publication types

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

MeSH terms

  • Adult
  • Amino Acid Sequence
  • Cell Line, Tumor
  • Cell Proliferation / genetics
  • Child, Preschool
  • Chondroitin Sulfate Proteoglycans / chemistry
  • Chondroitin Sulfate Proteoglycans / genetics*
  • Family
  • Female
  • Genetic Predisposition to Disease
  • Germ Cells / metabolism*
  • Humans
  • Infant
  • MAP Kinase Signaling System
  • Male
  • Membrane Proteins / chemistry
  • Membrane Proteins / genetics*
  • Middle Aged
  • Models, Biological
  • Mutation / genetics*
  • Neurofibromatosis 1 / diagnostic imaging
  • Neurofibromatosis 1 / genetics*
  • Neurofibromatosis 1 / pathology*
  • Pedigree
  • Phenotype
  • Young Adult

Substances

  • CSPG4 protein, human
  • Chondroitin Sulfate Proteoglycans
  • Membrane Proteins