Dimerization of presenilin-1 in vivo:: suggestion of novel regulatory mechanisms leading to higher order complexes

被引:31
作者
Hébert, SS
Godin, C
Tomiyama, T
Mori, H
Lévesque, G
机构
[1] CHUQ, Mol & Human Genet Unit, Quebec City, PQ G1L 3L5, Canada
[2] Osaka City Univ, Sch Med, Dept Neurosci, Abeno Ku, Osaka 5458585, Japan
[3] Univ Laval, Dept Med Biol, Quebec City, PQ, Canada
基金
加拿大健康研究院;
关键词
presenilin; gamma-secretase; oligomerization; protein dimerization; yeast two-hybrid; western blotting;
D O I
10.1016/S0006-291X(02)02984-4
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
A growing body of evidence indicates that presenilins could exist and be active as oligomeric complexes. Using yeast two-hybrid and cell culture analysis, we provide evidence that presenilin-1 (PSI) may self-oligomerize giving rise to specific full-length/full-length homodimers. When expressed in N2A and HEK239T cultured cells, full-length PS1-wt and 5'myc-PS1-wt form specific homodimers corresponding to twice their molecular weight. The Alzheimer's disease-associated PSI mutations Y115H, M146L, L392V, DeltaE10(PS1(1-289/320-467)), the gamma-secretase dominant negative mutant D257A, and the PS1 polymorphism mutant E318G do not affect their ability to self-oligomerize. Under non-denaturing conditions, endogenous PS1 forms specific homo-oligomers in human cultured cells. The results obtained herein suggest that PS1 associates intramolecularly to form higher order complexes, which may be needed for endoproteolytic cleavage and/or gamma-secretase-associated activity. (C) 2002 Elsevier Science (USA). All rights reserved.
引用
收藏
页码:119 / 126
页数:8
相关论文
共 38 条
[1]   Missense mutation E318G of the presenilin-1 gene appears to be a nonpathogenic polymorphism [J].
Aldudo, J ;
Bullido, MJ ;
Frank, A ;
Valdivieso, F .
ANNALS OF NEUROLOGY, 1998, 44 (06) :985-986
[2]   Detection of the presenilin 1 COOH-terminal fragment in the extracellular compartment: A release enhanced by apoptosis [J].
Benussi, L ;
Alberici, A ;
Mayhaus, M ;
Langer, U ;
Ghidoni, R ;
Mazzoli, F ;
Nicosia, F ;
Barbiero, L ;
Frisoni, G ;
Zanetti, O ;
Gasparini, L ;
Nitsch, RM ;
Binetti, G .
EXPERIMENTAL CELL RESEARCH, 2001, 269 (02) :256-265
[3]   The proteolytic fragments of the Alzheimer's disease-associated presenilin-1 form heterodimers and occur as a 100-150-kDa molecular mass complex [J].
Capell, A ;
Grünberg, J ;
Pesold, B ;
Diehlmann, A ;
Citron, M ;
Nixon, R ;
Beyreuther, K ;
Selkoe, DJ ;
Haass, C .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (06) :3205-3211
[4]   Homodimerization of presenilin N-terminal fragments is affected by mutations linked to Alzheimer's disease [J].
Cervantes, S ;
González-Duarte, R ;
Marfany, G .
FEBS LETTERS, 2001, 505 (01) :81-86
[5]   The presenilin genes: A new gene family involved in Alzheimer disease pathology [J].
Cruts, M ;
Hendriks, L ;
Van Broeckhoven, C .
HUMAN MOLECULAR GENETICS, 1996, 5 :1449-1455
[6]   Presenilins and Alzheimer's disease: biological functions and pathogenic mechanisms [J].
Czech, C ;
Tremp, G ;
Pradier, L .
PROGRESS IN NEUROBIOLOGY, 2000, 60 (04) :363-384
[7]   An Alzheimer's disease-linked PS1 variant rescues the developmental abnormalities of PS1-deficient embryos [J].
Davis, JA ;
Naruse, S ;
Chen, H ;
Eckman, C ;
Younkin, S ;
Price, DL ;
Borchelt, DR ;
Sisodia, SS ;
Wong, PC .
NEURON, 1998, 20 (03) :603-609
[8]   Phosphorylation, subcellular localization, and membrane orientation of the Alzheimer's disease-associated presenilins [J].
DeStrooper, B ;
Beullens, M ;
Contreras, B ;
Levesque, L ;
Craessaerts, K ;
Cordell, B ;
Moechars, D ;
Bollen, M ;
Fraser, P ;
StGeorgeHyslop, P ;
VanLeuven, F .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (06) :3590-3598
[9]   Cell surface expression of the Alzheimer disease-related presenilin proteins [J].
Dewji, NN ;
Singer, SJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (18) :9926-9931
[10]   Mice lacking both presenilin genes exhibit early embryonic patterning defects [J].
Donoviel, DB ;
Hadjantonakis, AK ;
Ikeda, M ;
Zheng, H ;
Hyslop, PS ;
Bernstein, A .
GENES & DEVELOPMENT, 1999, 13 (21) :2801-2810