Phenotypic spectrum of alpha-synuclein mutations: New insights from patients and cellular models

Parkinsonism Relat Disord. 2016 Jan;22 Suppl 1:S16-20. doi: 10.1016/j.parkreldis.2015.08.015. Epub 2015 Aug 18.


The identification of the p.A53T mutation in the SNCA gene encoding alpha-synuclein (alpha-syn), as causative of autosomal dominant Parkinson disease (PD) represented a fundamental milestone, which paved the way to the extremely prolific field of PD genetics. Despite being the oldest player in this field and only a rare cause of inherited PD, research on alpha-syn has remained incredibly active over nearly twenty decades, leading to identify alpha-syn aggregation as a key mechanism in PD pathogenesis. The past two years have witnessed new exciting findings, with the discovery of at least three novel pathogenic mutations (p.H50Q, p.G51D and p.A53E) causative of complex parkinsonian phenotypes, and the identification of additional patients carrying "old" SNCA mutations (p.A53T, p.A30P, p.E46K and whole gene multiplications), which has allowed to further expand their phenotypic spectrum. This review aims at providing a clinical and functional update on the most recent findings in alpha-syn genetics, at the same time discussing novel avenues of SNCA research such as those on somatic mutations and epigenetic mechanisms.

Keywords: Alpha-synuclein; Genotype-phenotype correlates; Mutations; SNCA.

Publication types

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

MeSH terms

  • Animals
  • Humans
  • Mutation / genetics*
  • Parkinsonian Disorders / diagnosis
  • Parkinsonian Disorders / genetics*
  • Phenotype*
  • alpha-Synuclein / genetics*


  • SNCA protein, human
  • alpha-Synuclein