X11α and x11β interact with presenilin-1 via their PDZ domains

被引:88
作者
Lau, KF
McLoughlin, DM
Standen, C
Miller, CCJ
机构
[1] Inst Psychiat, Dept Neurosci, London SE5 8AF, England
[2] Inst Psychiat, Old Age Psychiat Sect, London SE5 8AF, England
基金
英国惠康基金;
关键词
D O I
10.1006/mcne.2000.0898
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
X11 alpha and X11 beta are two neuronal adaptor proteins that interact with the Alzheimer's disease amyloid precursor protein (APP). X11 alpha and X11 beta stabilise APP and inhibit production of proteolytic APP fragments including the AP peptide that is deposited in the brains of Alzheimer's disease patients. The mechanisms by which X11 alpha and X11 beta modulate APP processing are not clear but one possibility is that they influence the activity of the secretases that cleave APP to give rise to A beta. Presenilin-1 is required for gamma -secretase activity and here we demonstrate that both X11 alpha and X11 beta interact with presenilin-1. X11/presenilin-1 binding is via two X11 PDZ domains and sequences within the carboxy-terminus of presenilin-1. We also demonstrate that both X11 alpha and X11 beta mediate the formation of complexes between APP and presenilin-1. These results suggest that the X11 regulation of APP processing is controlled, at least in part, via their interactions with APP and presenilin-1.
引用
收藏
页码:557 / 565
页数:9
相关论文
共 47 条
[1]   Mapping of the human and murine X11-like genes (APBA2 and Apba2), the murine Fe65 gene (Apbb1), and the human Fe65-like gene (APBB2):: genes encoding phosphotyrosine-binding domain proteins that interact with the Alzheimer's disease amyloid precursor protein [J].
Blanco, G ;
Irving, NG ;
Brown, SDM ;
Miller, CCJ ;
McLoughlin, DM .
MAMMALIAN GENOME, 1998, 9 (06) :473-475
[2]  
Borg JP, 1996, MOL CELL BIOL, V16, P6229
[3]  
Borg JP, 1999, J NEUROSCI, V19, P1307
[4]   Identification of an evolutionarily conserved heterotrimeric protein complex involved in protein targeting [J].
Borg, JP ;
Straight, SW ;
Kaech, SM ;
de Taddeo-Borg, M ;
Kroon, DE ;
Karnak, D ;
Turner, RS ;
Kim, SK ;
Margolis, B .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (48) :31633-31636
[5]   The X11α protein slows cellular amyloid precursor protein processing and reduces Aβ40 and Aβ42 secretion [J].
Borg, JP ;
Yang, YN ;
De Taddéo-Borg, M ;
Margolis, B ;
Turner, RS .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (24) :14761-14766
[6]  
Brownlees J, 2000, J CELL SCI, V113, P401
[7]   A tripartite protein complex with the potential to couple synaptic vesicle exocytosis to cell adhesion in brain [J].
Butz, S ;
Okamoto, M ;
Südhof, TC .
CELL, 1998, 94 (06) :773-782
[8]   Deficiency of presenilin-1 inhibits the normal cleavage of amyloid precursor protein [J].
De Strooper, B ;
Saftig, P ;
Craessaerts, K ;
Vanderstichele, H ;
Guhde, G ;
Annaert, W ;
Von Figura, K ;
Van Leuven, F .
NATURE, 1998, 391 (6665) :387-390
[9]   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
[10]  
DONG H, 1997, NATURE, V386