Mutation analysis of the seven in absentia homolog 1 (SIAH1) gene in Parkinson's disease

J Neural Transm (Vienna). 2006 Dec;113(12):1903-8. doi: 10.1007/s00702-006-0480-z. Epub 2006 Jun 6.

Abstract

Seven in absentia homolog 1 (SIAH-1) is a member of the RING-finger-containing E3 ubiquitin ligases. Two substrates of SIAH-1 are alpha-synuclein and synphilin-1, both of these proteins are involved in Parkinson's disease (PD). Recently, mutations in Parkin, another E3 ubiquitin ligase which ubiquinates synphilin-1 and glycosylated alpha-synuclein, have been defined as a major cause of autosomal recessive PD. The potential role of SIAH-1 in PD is further underlined as SIAH-1 protein is a component of the Lewy bodies and as it plays a role in apoptosis caused by nitric oxide (NO) induced oxidative stress. Thus, we performed a mutation screening of the SIAH-1 gene in PD patients. However, screening a large sample of 209 familial and sporadic PD patients we could not find any disease causing mutation. We therefore conclude that genetic alterations of SIAH-1 do not significantly contribute to the pathogenesis of PD.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aged
  • Chromatography, High Pressure Liquid
  • Cohort Studies
  • DNA / genetics*
  • DNA Mutational Analysis
  • Female
  • Gene Frequency
  • Humans
  • Male
  • Middle Aged
  • Nuclear Proteins / genetics*
  • Parkinson Disease / genetics*
  • Protein Denaturation
  • Reverse Transcriptase Polymerase Chain Reaction
  • Ubiquitin-Protein Ligases / genetics*

Substances

  • Nuclear Proteins
  • DNA
  • Ubiquitin-Protein Ligases
  • seven in absentia proteins