Journal
JOURNAL OF BIOLOGICAL CHEMISTRY
Volume 275, Issue 5, Pages 3173-3178Publisher
AMER SOC BIOCHEMISTRY MOLECULAR BIOLOGY INC
DOI: 10.1074/jbc.275.5.3173
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- NIA NIH HHS [AG06173, AG15379] Funding Source: Medline
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The discovery that a deficiency of presenilin 1 (PS1) decreases the production of amyloid beta-protein (A beta) identified the presenilins as important mediators of the gamma-secretase cleavage of beta-amyloid precursor protein (APP). Recently, we found that two conserved transmembrane (TM) aspartates in PS1 are critical for AP production, providing evidence that PS1 either functions as a required diaspartyl cofactor for gamma-secretase or is itself gamma-secretase. Presenilin 2 (PS2) shares substantial sequence and possibly functional homology with PS1. Here, we show that the two TM aspartates in PS2 are also critical for gamma-secretase activity, providing further evidence that PS2 is functionally homologous to PS1. Cells stably co-expressing TM Asp -> Ala mutations in both PS1 and PS2 show further accumulation of the APP-derived gamma-secretase substrates, C83 and C99. The production of A beta is reduced to undetectable levels in the conditioned media of these cells. Furthermore, endoproteolysis of the exogenous Asp mutant PS2 is absent, and endogenous PS1 C-terminal fragments are diminished to undetectable levels. Therefore, the co-expression of PS1 and PS2 TM Asp -> Ala mutants suppresses the formation of any detectable PS1 or PS2 heterodimeric fragments and essentially abolishes the production of A beta. These results explain the residual A beta production seen in PS1-deficient cells and demonstrate the absolute requirement of functional presenilins for A beta generation. We conclude that presenilins, and their TM aspartates in particular, are attractive targets for lowering A beta therapeutically to prevent Alzheimer's disease.
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