Presenilin I binds to amyloid precursor protein directly

被引:29
作者
Waragai, M
Imafuku, I
Takeuchi, S
Kanazawa, I
Oyama, F
Udagawa, Y
Kawabata, M
Okazawa, H
机构
[1] UNIV TOKYO,FAC MED,DEPT NEUROL,GRP MOL NEUROBIOL,BUNKYO KU,TOKYO 113,JAPAN
[2] UNIV TOKYO,FAC MED,DEPT NEUROPATHOL,BUNKYO KU,TOKYO 113,JAPAN
[3] JAPANESE FDN CANC RES,INST CANC,DEPT BIOCHEM,TOSHIMA KU,TOKYO 170,JAPAN
关键词
D O I
10.1006/bbrc.1997.7488
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
Mutations in the presenilin genres are associated with early onset familial Alzheimer's disease and lead to accumulation of beta-amyloid peptide in the brain of patients, suggesting that presenilin abnormalities induce pathological processing of amyloid precursor protein (APP) in Alzheimer's disease. Far the understanding of pathogenesis in this type of familiar Alzheimer disease, it is important to know whether presenilins are directly involved in the metabolism of beta-amyloid or not, To test whether presenilin 1 (PS1) directly binds to APP, we performed two-hybrid interaction assays between these proteins in yeast cells by using bait plasmids for normal and mutant PS1 and prey plasmids for APP fragments corresponding to the different molecular portions, Positive interaction was observed in any combination between PS1 bait plasmids and APP prey plasmids, Therefore, our results show that PS1 binds to APP directly and suggest that tame PS1 protein itself is involved in the metabolism of beta-amyloid peptide. (C) 1997 Academic Press.
引用
收藏
页码:480 / 482
页数:3
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