Axin: A master scaffold for multiple signaling pathways

被引:132
作者
Luo, W
Lin, SC
机构
[1] Hong Kong Univ Sci & Technol, Dept Biochem, Kowloon, Hong Kong, Peoples R China
[2] Xiamen Univ, Dept Biol, Xiamen, Peoples R China
关键词
Axin; biological function; Axin identification; Axin/JNK signaling pathway; Wnt pathway;
D O I
10.1159/000076563
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
Axin was originally identified from the characterization of the Fused locus, the disruption of which leads to duplication of axis and embryonic lethality. It is a multidomain protein that interacts with multiple proteins and functions as a negative regulator of Wnt signaling by down-regulating the beta-catenin levels. Recently, it was demonstrated that Axin also plays an important role in a JNK signaling pathway. Axin utilizes discriminatory domains for its distinct roles in the Wnt pathway and in the Axin/JNK pathway. Here we review the data that show how Axin regulates multiple signaling pathways by serving as a scaffold protein, controlling diverse cellular functions in proliferation, fate determination, and suppression of tumorigenesis. Copyright (C) 2004 S. Karger AG, Basel.
引用
收藏
页码:99 / 113
页数:15
相关论文
共 133 条
[1]   beta-catenin is a target for the ubiquitin-proteasome pathway [J].
Aberle, H ;
Bauer, A ;
Stappert, J ;
Kispert, A ;
Kemler, R .
EMBO JOURNAL, 1997, 16 (13) :3797-3804
[2]   Regulation of armadillo by a Drosophila APC inhibits neuronal apoptosis during retinal development [J].
Ahmed, Y ;
Hayashi, S ;
Levine, A ;
Wieschaus, E .
CELL, 1998, 93 (07) :1171-1182
[3]   Axin-mediated CKI phosphorylation of β-catenin at Ser 45:: a molecular switch for the Wnt pathway [J].
Amit, S ;
Hatzubai, A ;
Birman, Y ;
Andersen, JS ;
Ben-Shushan, E ;
Mann, M ;
Ben-Neriah, Y ;
Alkalay, I .
GENES & DEVELOPMENT, 2002, 16 (09) :1066-1076
[4]   AXIN1 mutations but not deletions in cerebellar medulloblastomas [J].
Baeza, N ;
Masuoka, J ;
Kleihues, P ;
Ohgaki, H .
ONCOGENE, 2003, 22 (04) :632-636
[5]   CAP defines a second signalling pathway required for insulin-stimulated glucose transport [J].
Baumann, CA ;
Ribon, V ;
Kanzaki, M ;
Thurmond, DC ;
Mora, S ;
Shigematsu, S ;
Bickel, PE ;
Pessin, JE ;
Saltiel, AR .
NATURE, 2000, 407 (6801) :202-207
[6]   Functional interaction of an axin homolog, conductin, with β-catenin, APC, and GSK3β [J].
Behrens, J ;
Jerchow, BA ;
Würtele, M ;
Grimm, J ;
Asbrand, C ;
Wirtz, R ;
Kühl, M ;
Wedlich, D ;
Birchmeier, W .
SCIENCE, 1998, 280 (5363) :596-599
[7]   Functional interaction of beta-catenin with the transcription factor LEF-1 [J].
Behrens, J ;
vonKries, JP ;
Kuhl, M ;
Bruhn, L ;
Wedlich, D ;
Grosschedl, R ;
Birchmeier, W .
NATURE, 1996, 382 (6592) :638-642
[8]  
Birgbauer E, 2000, DEVELOPMENT, V127, P1231
[9]   A beta-catenin/XTcf-3 complex binds to the siamois promoter to regulate dorsal axis specification in Xenopus [J].
Brannon, M ;
Gomperts, M ;
Sumoy, L ;
Moon, RT ;
Kimelman, D .
GENES & DEVELOPMENT, 1997, 11 (18) :2359-2370
[10]   Regulators of G protein signaling: A bestiary of modular protein binding domains [J].
Burchett, SA .
JOURNAL OF NEUROCHEMISTRY, 2000, 75 (04) :1335-1351