A new pathogenic mutation in the APP gene (1716V) increases the relative proportion of A beta 42(43)

被引:173
作者
Eckman, CB
Mehta, ND
Crook, R
Pereztur, J
Prihar, G
Pfeiffer, E
GraffRadford, N
Hinder, P
Yager, D
Zenk, B
Refolo, LM
Prada, CM
Younkin, SG
Hutton, M
Hardy, J
机构
[1] MAYO CLIN JACKSONVILLE,JACKSONVILLE,FL 32224
[2] CASE WESTERN RESERVE UNIV,DEPT NEUROSCI,CLEVELAND,OH 44106
[3] UNIV S FLORIDA,SUNCOAST GERONTOL CTR & LAB,DEPT PSYCHIAT,TAMPA,FL 33613
[4] UNIV S FLORIDA,SUNCOAST GERONTOL CTR & LAB,DEPT PHARMACOL,TAMPA,FL 33613
[5] UNIV S FLORIDA,SUNCOAST GERONTOL CTR & LAB,DEPT NEUROL,TAMPA,FL 33613
[6] UNIV S FLORIDA,SUNCOAST GERONTOL CTR & LAB,DEPT BIOCHEM,TAMPA,FL 33613
关键词
D O I
10.1093/hmg/6.12.2087
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
We report a novel mutation in the amyloid precursor protein gene (APR I716V) which probably leads to familial early onset Alzheimer's disease with an onset age in the mid 50s. Cells transfected with cDNAs bearing this mutation produce more A beta 1-42(43) than those transfected with wild-type APP and this effect is additive with that of the previously reported APP V717I mutation thus providing a novel approach for further increasing A beta 1-42(43) in model systems.
引用
收藏
页码:2087 / 2089
页数:3
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