Identifying Genes That Interact With Drosophila Presenilin and Amyloid Precursor Protein

被引:30
作者
de Hoef, Diana L. van [2 ]
Hughes, James [2 ]
Livne-Bar, Izhar [2 ]
Garza, Dan [3 ]
Konsolaki, Mary [4 ]
Boulianne, Gabrielle L. [1 ,2 ]
机构
[1] Univ Toronto, Hosp Sick Children, Program Dev & Stem Cell Biol, MARS Ctr, Toronto, ON M5G 1L7, Canada
[2] Univ Toronto, Dept Mol Genet, Toronto, ON M5G 1L7, Canada
[3] Novartis Inst Biomed Res, Cambridge, MA USA
[4] Rutgers State Univ, Dept Genet, Nelson Biol Labs, Piscataway, NJ USA
关键词
Alzheimer's disease; APP; Drosophila; presenilin; genetic modifier; GAMMA-SECRETASE COMPLEX; MESSENGER-RNA LOCALIZATION; ALZHEIMERS-DISEASE; RYANODINE RECEPTOR; CONVERTING-ENZYME; ENDOPLASMIC-RETICULUM; CALCIUM-RELEASE; FK506-BINDING PROTEIN; CELL-PROLIFERATION; REMODELING COMPLEX;
D O I
10.1002/dvg.20485
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
The gamma-secretase complex is involved in cleaving transmembrane proteins such as Notch and one of the genes targeted in Alzheimer's disease known as amyloid precursor protein (APP). Presenilins function within the catalytic core of gamma-secretase, and mutated forms of presenilins were identified as causative factors in familial Alzheimer's disease. Recent studies show that in addition to Notch and APP, numerous signal transduction pathways are modulated by presenilins, including intracellular calcium signaling. Thus, presenilins appear to have diverse roles. To further understand presenilin function, we searched for Presenilin-interacting genes in Drosophila by performing a genetic modifier screen for enhancers and suppressors of Presenilin-dependent Notch-related phenotypes. We identified 177 modifiers, including known members of the Notch pathway and genes involved in intracellular calcium homeostasis. We further demonstrate that 53 of these modifiers genetically interacted with APP. Characterization of these genes may provide valuable insights into Presenilin function in development and disease. genesis 47:246-260, 2009. (C) 2009 Wiley-Liss, Inc.
引用
收藏
页码:246 / 260
页数:15
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