van de Hoef Diana L, Hughes James, Livne-Bar Izhar, Garza Dan, Konsolaki Mary, Boulianne Gabrielle L
Department of Molecular Genetics, University of Toronto, Toronto, Ontario, Canada.
Genesis. 2009 Apr;47(4):246-60. doi: 10.1002/dvg.20485.
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.
γ-分泌酶复合物参与切割跨膜蛋白,如Notch以及阿尔茨海默病的一个靶向基因——淀粉样前体蛋白(APP)。早老素在γ-分泌酶的催化核心内发挥作用,早老素的突变形式被确定为家族性阿尔茨海默病的致病因素。最近的研究表明,除了Notch和APP外,早老素还调节许多信号转导途径,包括细胞内钙信号传导。因此,早老素似乎具有多种作用。为了进一步了解早老素的功能,我们通过对依赖早老素的Notch相关表型的增强子和抑制子进行遗传修饰筛选,在果蝇中寻找与早老素相互作用的基因。我们鉴定出177个修饰因子,包括Notch途径的已知成员和参与细胞内钙稳态的基因。我们进一步证明,这些修饰因子中有53个与APP发生遗传相互作用。对这些基因的表征可能为早老素在发育和疾病中的功能提供有价值的见解。