The presenilin proteins, localized predominantly to the endoplasmic re
ticulum, are multi-transmembrane spanning proteins that are processed
to form an approximately 27kD N-terminal fragment and a corresponding
19kD C-terminal fragment. Mutations in the presenilin 1 and presenilin
2 genes have been identified that cause early onset familial Alzheime
r's disease Analysis of plasma and fibroblasts from patients revealed
that these mutations increase the concentration of A beta 42 Cells and
transgenic animals containing these mutations both give rise to incre
ases in the extracellular concentration of this peptide providing furt
her evidence for the role of A beta, particularly A beta 42, in Alzhei
mer's disease. These data provide strong evidence that alterations in
A beta concentration are an early and critical event in the pathology
of Alzheimer's disease.