A new and simple approach for genotyping Alzheimer's disease presenilin-1 mutant knock-in mice

Vanessa Gautheron, Alexandra Auffret, Mark P. Mattson, Jean Mariani, Béatrice Vernet der Garabedian

Research output: Contribution to journalArticlepeer-review

6 Scopus citations


The use of transgenic mice expressing point mutations demands that the detection of the different alleles is efficient and reliable. In addition, the multiplication of transgenes included in mouse models of human disease underlines the importance of correct controls and the fact that investigators need an accurate and rapid genotyping of the littermates generated. In this study, we demonstrate a powerful alternative for genotyping using presenilin-1 mutant knock-in (PS1M146KI) mice as an example. Mutations in the presenilin-1 (PS1) gene are causally linked to many cases of early-onset inherited Alzheimer's disease (AD). PS1M146VKI mice that express the PS1M146V targeted allele at normal physiological levels and triple-transgenic model (3×Tg-AD) derived from homozygous PS1M146VKI mice were generated to study the pathogenesis of AD. Genotyping PS1M146VKI line requires many steps and thus a large quantity of DNA. In PS1M146VKI mice, only three nucleotides are modified in the gene. Here we show that this small mutated DNA sequence can affect its secondary structure resulting in altered mobility that can be easily detected on a polyacrylamide gel, by the single-strand conformation polymorphism (SSCP) technique. Our results demonstrate that SSCP is a simple, accurate, repeatable and efficient method for the routine genotyping of this current AD model. This method could be easily applied to other transgenic mice.

Original languageEnglish (US)
Pages (from-to)235-240
Number of pages6
JournalJournal of Neuroscience Methods
Issue number2
StatePublished - Jul 30 2009
Externally publishedYes


  • Alzheimer's disease
  • Genotyping
  • Knock-in
  • Presenilin-1
  • SSCP

ASJC Scopus subject areas

  • Neuroscience(all)


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