A novel TRAPPC11 mutation in two Turkish families associated with cerebral atrophy, global retardation, scoliosis, achalasia and alacrima

J Med Genet. 2017 Mar;54(3):176-185. doi: 10.1136/jmedgenet-2016-104108. Epub 2016 Oct 5.

Abstract

Background: Triple A syndrome (MIM #231550) is associated with mutations in the AAAS gene. However, about 30% of patients with triple A syndrome symptoms but an unresolved diagnosis do not harbour mutations in AAAS.

Objective: Search for novel genetic defects in families with a triple A-like phenotype in whom AAAS mutations are not detected.

Methods: Genome-wide linkage analysis, whole-exome sequencing and functional analyses were used to discover and verify a novel genetic defect in two families with achalasia, alacrima, myopathy and further symptoms. Effect and pathogenicity of the mutation were verified by cell biological studies.

Results: We identified a homozygous splice mutation in TRAPPC11 (c.1893+3A>G, [NM_021942.5], g.4:184,607,904A>G [hg19]) in four patients from two unrelated families leading to incomplete exon skipping and reduction in full-length mRNA levels. TRAPPC11 encodes for trafficking protein particle complex subunit 11 (TRAPPC11), a protein of the transport protein particle (TRAPP) complex. Western blot analysis revealed a dramatic decrease in full-length TRAPPC11 protein levels and hypoglycosylation of LAMP1. Trafficking experiments in patient fibroblasts revealed a delayed arrival of marker proteins in the Golgi and a delay in their release from the Golgi to the plasma membrane. Mutations in TRAPPC11 have previously been described to cause limb-girdle muscular dystrophy type 2S (MIM #615356). Indeed, muscle histology of our patients also revealed mild dystrophic changes. Immunohistochemically, β-sarcoglycan was absent from focal patches.

Conclusions: The identified novel TRAPPC11 mutation represents an expansion of the myopathy phenotype described before and is characterised particularly by achalasia, alacrima, neurological and muscular phenotypes.

Keywords: Achalasia; Alacrimia; Scoliosis; Transport protein particle complex; Triple A syndrome.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Adrenal Insufficiency / epidemiology
  • Adrenal Insufficiency / genetics*
  • Adrenal Insufficiency / physiopathology
  • Child
  • Consanguinity
  • Esophageal Achalasia / epidemiology
  • Esophageal Achalasia / genetics*
  • Esophageal Achalasia / physiopathology
  • Exons / genetics
  • Female
  • Homozygote
  • Humans
  • Male
  • Mutation / genetics*
  • Pedigree
  • RNA Splice Sites / genetics
  • Turkey / epidemiology
  • Vesicular Transport Proteins / genetics*

Substances

  • RNA Splice Sites
  • TRAPPC11 protein, human
  • Vesicular Transport Proteins

Supplementary concepts

  • Achalasia Addisonianism Alacrimia syndrome

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