Deletion of P2 promoter of GJB1 gene a cause of Charcot-Marie-Tooth disease

Neuromuscul Disord. 2017 Aug;27(8):766-770. doi: 10.1016/j.nmd.2017.05.001. Epub 2017 May 4.

Abstract

X-linked Charcot-Marie-Tooth disease (CMT) is the second most common cause of CMT, and is usually caused by mutations in the gap junction protein beta 1 (GJB1) gene. This gene has nerve specific P2 promoter that work synergistically with SOX10 and EGR2 genes to initiate transcription. Mutation in this region is known to cause Schwann cell dysfunction. A single large family of X linked peripheral neuropathy was identified in our practice. Next generation sequencing for targeted panel assay identified an upstream exon-splicing deletion identified extending from nucleotide c.-5413 to approximately - c.-49. This matches the sequence of 32 nucleotides at positions c.*218-*249 in the 3'UTR downstream of the GJB1 gene. The deleted fragment included the entire P2 promoter region. The deletion segregated with the disease. To our knowledge a deletion of the P2 promoter alone as a cause of CMT has not been reported previously.

Keywords: Charcot-Marie-Tooth disease; Connexin 32; Deletion; GJB1; P2 promoter; Schwann cell dysfunction; X-linked.

MeSH terms

  • Adolescent
  • Adult
  • Aged
  • Charcot-Marie-Tooth Disease / genetics*
  • Charcot-Marie-Tooth Disease / pathology
  • Charcot-Marie-Tooth Disease / physiopathology
  • Child
  • Child, Preschool
  • Connexins / genetics*
  • Family
  • Female
  • Gap Junction beta-1 Protein
  • Humans
  • Male
  • Middle Aged
  • Phenotype
  • Promoter Regions, Genetic*
  • Sequence Deletion*
  • Sural Nerve / pathology
  • Sural Nerve / physiopathology
  • Young Adult

Substances

  • Connexins