Antagonistic regulation of convergent extension movements in Xenopus by Wnt/β-catenin and Wnt/Ca2+ signaling

被引:181
作者
Kühl, M
Geis, K
Sheldahl, LC
Pukrop, T
Moon, RT
Wedlich, D
机构
[1] Univ Gottingen, Abt Entwicklungsbiochem, Jr Grp SFB 271, D-37073 Gottingen, Germany
[2] Univ Ulm, Biochem Abt, D-89081 Ulm, Germany
[3] Univ Washington, Sch Med, Howard Hughes Med Inst, Dept Pharmacol, Seattle, WA 98195 USA
[4] Univ Washington, Sch Med, Ctr Dev Biol, Seattle, WA 98195 USA
[5] Univ Karlsruhe, Inst Zool 2, D-76131 Karlsruhe, Germany
关键词
D O I
10.1016/S0925-4773(01)00416-6
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Convergent extension movements are the main driving force of Xenopus gastrulation. A fine-tuned regulation of cadherin-mediated cell-cell adhesion is thought to be required for this process. Members of the Wnt family of extracellular glycoproteins have been shown to modulate cadherin-mediated cell-cell adhesion, convergent extension movements, and cell differentiation. Here we show that endogenous Wnt/beta -catenin signaling activity is essential for convergent extension movements due to its effect on gene expression rather than on cadherins. Our data also suggest that XLEF-1 rather than XTCF-3 is required for convergent extension movements and that XLEF-1 functions in this context in the Wnt/beta -catenin pathway to regulate Xnr-3. In contrast, activation of the Wnt/Ca2+, pathway blocks convergent extension movements, with potential regulation of the Wnt/beta -catenin pathway at two different levels. PKC, activated by the Wnt/Ca2+ pathway, blocks the Wnt/beta -catenin pathway upstream of beta -catenin and phosphorylates Dishevelled. CamKII, also activated by the Wnt/Ca2+ pathway, inhibits the Wnt/beta -catenin signaling cascade downstream of beta -catenin. Thus, an opposing cross-talk of two distinct Wnt signaling cascades regulates convergent extension movements in Xenopus. (C) 2001 Elsevier Science Ireland Ltd. All rights reserved.
引用
收藏
页码:61 / 76
页数:16
相关论文
共 54 条
[1]   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
[2]   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
[3]   Dishevelled activates JNK and discriminates between JNK pathways in planar polarity and wingless signaling [J].
Boutros, M ;
Paricio, N ;
Strutt, DI ;
Mlodzik, M .
CELL, 1998, 94 (01) :109-118
[4]   EXPRESSION OF WNT-1 IN PC12 CELLS RESULTS IN MODULATION OF PLAKOGLOBIN AND E-CADHERIN AND INCREASED CELLULAR ADHESION [J].
BRADLEY, RS ;
COWIN, P ;
BROWN, AMC .
JOURNAL OF CELL BIOLOGY, 1993, 123 (06) :1857-1865
[5]   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
[6]   Contribution of cadherins to directional cell migration and histogenesis in Xenopus embryos [J].
Broders, F ;
Thiery, JP .
CELL ADHESION AND COMMUNICATION, 1995, 3 (05) :419-+
[7]  
CUI YZ, 1995, DEVELOPMENT, V121, P2177
[8]  
Deardorff' MA, 1998, DEVELOPMENT, V125, P2687
[9]  
Djiane A, 2000, DEVELOPMENT, V127, P3091
[10]  
DU SJ, 1995, MOL CELL BIOL, V15, P2625