Differential contribution of the three Aph1 genes to -secretase activity in vivo

-Secretase is the protease responsible for amyloid peptide release and is needed for Notch, N-Cadherin, and possibly other signaling pathways. The protease complex consists of at least four subunits, i.e., Presenilin, Aph1, Pen2, and Nicastrin. Two different genes encode Aph1A and Aph1B in man. A duplication of Aph1B in rodents has given rise to a third gene, Aph1C. Different mixes of -secretase subunits assemble in at least four human and six rodent complexes but it is not known whether they have different activities in vivo. We report here the inactivation of the three Aph1 genes in mice. Aph1A / embryos show a lethal phenotype characterized by angiogenesis defects in the yolk sac, neuronal tube malformations, and mild somitogenesis defects. Aph1B / or C / or the combined Aph1BC / mice (which can be considered as a model for total Aph1B loss in human) survive into adulthood. However, Aph1BC / deficiency causes a mild but significant reduction in amyloid percursor protein processing in selective regions of the adult brain. We conclude that the biochemical and physiological repercussions of genetically reducing -secretase activity via the different Aph1 components are quite divergent and tissue specific. Our work provides in vivo evidence for the concept that different -secretase complexes may exert different biological functions. In the context of Alzheimer’s disease therapy, this implies the theoretical possibility that targeting specific -secretase subunit combinations could yield less toxic drugs than the currently available general inhibitors of -secretase activity.