Probable novel PSEN2 Val214Leu mutation in Alzheimer's disease supported by structural prediction

BMC Neurol. 2014 May 15:14:105. doi: 10.1186/1471-2377-14-105.

Abstract

Background: PSEN2 mutations are rare variants, and fewer than 30 different PSEN2 mutations have been found. So far, it has not been reported in Asia.

Case presentation: PSEN2 mutation at codon 214 for predicting a valine to leucine substitution was found in a 70-year-old woman, who showed a dementia of the Alzheimer type. We did not find the mutation in 614 control chromosomes. We also predicted the structures of presenilin 2 protein with native Val 214 residue and Leu 214 mutation, which revealed significant structural changes in the region.

Conclusion: It could be a novel mutation verified with structural prediction in a patient with Alzheimer's disease.

Publication types

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

MeSH terms

  • Aged
  • Alzheimer Disease / genetics*
  • Amino Acid Substitution
  • DNA Mutational Analysis
  • Exons / genetics
  • Female
  • Humans
  • Leucine / genetics
  • Models, Molecular
  • Mutation / physiology
  • Presenilin-2 / genetics*
  • Protein Structure, Tertiary
  • Valine / genetics

Substances

  • PSEN2 protein, human
  • Presenilin-2
  • Leucine
  • Valine