Interaction between the APOE ɛ4 allele and the APH-1b c+651T>G SNP in Alzheimer's disease

Abstract 

The γ-secretase complex is a multimeric aspartyl protease which plays a pivotal role in the production of amyloid β-peptide, the main component of senile plaques in Alzheimer's disease (AD). APH-1a and APH-1b have been recently identified as important subunits of the γ-secretase complex. We previously studied sequence variations in both genes and their association with AD in a small Italian population. The rare polymorphism c+651T>G in APH-1b showed a possible interaction with the Apolipoprotein E (APOE) ɛ4 allele in the AD population sample. We extended our genetic analysis to 449 AD patients and 435 controls and, in AD cases, we found a significant interaction (P=0.001) between the allelic variants in the two genes, resulting in a marked increase of the relative risk for AD (OR=28.6). Despite the amino acid substitution does not seem to modify either the intracellular localization or the half-life of APH-1b protein, these data suggest that a cooperative mechanism involving APOE and APH-1b plays a role in the susceptibility to develop AD.

Keywords: Alzheimer's disease, APH-1, APOE, Single nucleotide polymorphism, γ-Secretase, β-Amyloid