Recessive mutations in EPG5 cause Vici syndrome, a multisystem disorder with defective autophagy

Nat Genet. 2013 Jan;45(1):83-7. doi: 10.1038/ng.2497. Epub 2012 Dec 9.

Abstract

Vici syndrome is a recessively inherited multisystem disorder characterized by callosal agenesis, cataracts, cardiomyopathy, combined immunodeficiency and hypopigmentation. To investigate the molecular basis of Vici syndrome, we carried out exome and Sanger sequence analysis in a cohort of 18 affected individuals. We identified recessive mutations in EPG5 (previously KIAA1632), indicating a causative role in Vici syndrome. EPG5 is the human homolog of the metazoan-specific autophagy gene epg-5, encoding a key autophagy regulator (ectopic P-granules autophagy protein 5) implicated in the formation of autolysosomes. Further studies showed a severe block in autophagosomal clearance in muscle and fibroblasts from individuals with mutant EPG5, resulting in the accumulation of autophagic cargo in autophagosomes. These findings position Vici syndrome as a paradigm of human multisystem disorders associated with defective autophagy and suggest a fundamental role of the autophagy pathway in the immune system and the anatomical and functional formation of organs such as the brain and heart.

Publication types

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

MeSH terms

  • Agenesis of Corpus Callosum / genetics*
  • Antigens, Neoplasm / genetics*
  • Autophagy / genetics*
  • Autophagy-Related Proteins
  • Biopsy
  • Cataract / genetics*
  • Consanguinity
  • Exome
  • Family
  • Genes, Recessive*
  • Humans
  • Intracellular Signaling Peptides and Proteins
  • Lysosomal Membrane Proteins
  • Lysosomes / metabolism
  • Muscle, Skeletal / pathology
  • Muscle, Skeletal / ultrastructure
  • Mutation*
  • Proteins / metabolism
  • Vesicular Transport Proteins

Substances

  • Antigens, Neoplasm
  • Autophagy-Related Proteins
  • EPG5 protein, human
  • Intracellular Signaling Peptides and Proteins
  • Lysosomal Membrane Proteins
  • NBR1 protein, human
  • Proteins
  • Vesicular Transport Proteins

Supplementary concepts

  • Absent corpus callosum cataract immunodeficiency