A new functional screening system for identification of regulators for the generation of amyloid β-protein

被引:20
作者
Komano, H
Shiraishi, H
Kawamura, Y
Sai, X
Suzuki, R
Serneels, L
Kawaichi, M
Kitamura, T
Yanagisawa, K
机构
[1] Natl Inst Longev Sci, Dept Dementia Res, Obu, Aichi 4748522, Japan
[2] Japan Sci & Technol Corp, Kawaguchi, Saitama 3320012, Japan
[3] Katholieke Univ Leuven, Ctr Human Genet, B-3000 Louvain, Belgium
[4] Flanders Interuniv Inst Biotechnol, B-3000 Louvain, Belgium
[5] Nara Inst Sci & Technol, Div Gene Funct Anim, Nara 63001, Japan
[6] Univ Tokyo, Inst Med Sci, Div Cellular Therapy, Adv Clin Res Ctr, Tokyo 1088639, Japan
关键词
D O I
10.1074/jbc.M205255200
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Presenilin (PS) is essential for gamma-cleavage, which is required for the generation of amyloid beta-protein (Abeta) from the beta-amyloid precursor protein. However, it remains to be clarified how gamma-cleavage is regulated. To elucidate the regulation of PS-mediated gamma-cleavage, we developed a new functional screening method for identifying cDNA that enhances gamma-cleavage. This screening system utilizes our own developed cell line, where the expression of cDNA that enhances gamma-cleavage confers puromycin resistance. The cDNA library is retrovirally delivered to the above-mentioned cell line, allowing the identification of our target cDNAs by a combination of puromycin resistance selection and Abeta assay screening. With this screening method, we isolated several cDNAs enhancing gamma-cleavage, including the previously reported Herp. Here we also demonstrate that Rab1A, identified with this screening, can be a regulator of All generation. Thus, our established screening method is a powerful tool for identifying multiple regulators involved in gamma-cleavage in the All generation pathway, including modulators of gamma-secretase activity or the intracellular trafficking of factors necessary for gamma-cleavage.
引用
收藏
页码:39627 / 39633
页数:7
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