The mechanism of γ-secretase activities through high molecular weight complex formation of presenilins is conserved in Drosophila melanogaster and mammals

Nobumasa Takasugi, Yasuko Takahashi, Yuichi Morohashi, Taisuke Tomita, Takeshi Iwatsubo

Research output: Contribution to journalArticle

39 Citations (Scopus)

Abstract

Mutations in presenilin 1 (PS1) and PS2 genes contribute to the pathogenesis of early onset familial Alzheimer's disease by increasing secretion of the pathologically relevant Aβ42 polypeptides. PS genes are also implicated in Notch signaling through proteolytic processing of the Notch receptor in Caenorhabditis elegans, Drosophila melanogaster, and mammals. Here we show that Drosophila PS (Psn) protein undergoes endoproteolytic cleavage and forms a stable high molecular weight (HMW) complex in Drosophila S2 or mouse neuro2a (N2a) cells in a similar manner to mammalian PS. The loss-of-function recessive point mutations located in the C-terminal region of Psn, that cause an early pupal-lethal phenotype resembling Notch mutant in vivo, disrupted the HMW complex formation, and abolished γ-secretase activities in cultured cells. The overexpression of Psn in mouse embryonic fibroblasts lacking PS1 and PS2 genes rescued the Notch processing. Moreover, disruption of the expression of Psn by double-stranded RNA-mediated interference completely abolished the γ-secretase activity in S2 cells. Surprisingly, γ-secretase activity dependent on wild-type Psn was associated with a drastic overproduction of Aβ1-42 from human βAPP in N2a cells, but not in S2 cells. Our data suggest that the mechanism of γ-secretase activities through formation of HMW PS complex, as well as its abolition by loss-of-function mutations located in the C terminus, are highly conserved features in Drosophila and mammals.

Original languageEnglish
Pages (from-to)50198-50205
Number of pages8
JournalJournal of Biological Chemistry
Volume277
Issue number51
DOIs
Publication statusPublished - Dec 20 2002
Externally publishedYes

ASJC Scopus subject areas

  • Biochemistry
  • Molecular Biology
  • Cell Biology

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