The topology, structure and PE interaction of LITAF underpin a Charcot-Marie-Tooth disease type 1C

BMC Biol. 2016 Dec 7;14(1):109. doi: 10.1186/s12915-016-0332-8.

Abstract

Background: Mutations in Lipopolysaccharide-induced tumour necrosis factor-α factor (LITAF) cause the autosomal dominant inherited peripheral neuropathy, Charcot-Marie-Tooth disease type 1C (CMT1C). LITAF encodes a 17 kDa protein containing an N-terminal proline-rich region followed by an evolutionarily-conserved C-terminal 'LITAF domain', which contains all reported CMT1C-associated pathogenic mutations.

Results: Here, we report the first structural characterisation of LITAF using biochemical, cell biological, biophysical and NMR spectroscopic approaches. Our structural model demonstrates that LITAF is a monotopic zinc-binding membrane protein that embeds into intracellular membranes via a predicted hydrophobic, in-plane, helical anchor located within the LITAF domain. We show that specific residues within the LITAF domain interact with phosphoethanolamine (PE) head groups, and that the introduction of the V144M CMT1C-associated pathogenic mutation leads to protein aggregation in the presence of PE.

Conclusions: In addition to the structural characterisation of LITAF, these data lead us to propose that an aberrant LITAF-PE interaction on the surface of intracellular membranes contributes to the molecular pathogenesis that underlies this currently incurable disease.

Keywords: Charcot-Marie-Tooth disease; Endosomes; Lipopolysaccharide-induced tumour necrosis factor-α factor; Neuropathy.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Carrier Proteins / chemistry
  • Carrier Proteins / genetics
  • Cell Line
  • Charcot-Marie-Tooth Disease / diagnosis
  • Charcot-Marie-Tooth Disease / genetics*
  • Ethanolamines / chemistry*
  • HeLa Cells
  • Humans
  • Membrane Proteins / chemistry
  • Membrane Proteins / genetics
  • Mutation*
  • Nuclear Proteins / chemistry
  • Nuclear Proteins / genetics*
  • Protein Aggregation, Pathological
  • Protein Conformation
  • Transcription Factors / chemistry
  • Transcription Factors / genetics*

Substances

  • Carrier Proteins
  • Ethanolamines
  • LITAF protein, human
  • Membrane Proteins
  • Nuclear Proteins
  • Transcription Factors
  • zinc-binding protein
  • phosphorylethanolamine

Supplementary concepts

  • Charcot-Marie-Tooth disease, Type 1C