Wnt3A plays a major role in the segmentation clock controlling somitogenesis

被引:468
作者
Aulehla, A
Wehrle, C
Brand-Saberi, B
Kemler, R
Gossler, A
Kanzler, B
Herrmann, BG
机构
[1] Max Planck Inst Immunbiol, Abt Entwicklungsbiol, D-79108 Freiburg, Germany
[2] Max Planck Inst Immunbiol, Abt Mol Embryol, D-79108 Freiburg, Germany
[3] Univ Freiburg, Anat Inst 2, D-79104 Freiburg, Germany
[4] Hannover Med Sch, Inst Mol Biol, D-30625 Hannover, Germany
关键词
D O I
10.1016/S1534-5807(03)00055-8
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The vertebral column derives from somites generated by segmentation of presomitic mesoderm (PSM). Somitogenesis involves a molecular oscillator, the segmentation clock, controlling periodic Notch signaling in the PSM. Here, we establish a novel link between Wnt/beta-catenin signaling and the segmentation clock. Axin2, a negative regulator of the Writ pathway, is directly controlled by Wnt/beta-catenin and shows oscillating expression in the PSM, even when Notch signaling is impaired, alternating with Lfng expression. Moreover, Wnt3a is required for oscillating Notch signaling activity in the PSM. We propose that the segmentation clock is established by Wnt/beta-catenin signaling via a negative-feedback mechanism and that Wnt3a controls the segmentation process in vertebrates.
引用
收藏
页码:395 / 406
页数:12
相关论文
共 43 条
[1]   Brachyury is a target gene of the Wnt/β-catenin signaling pathway [J].
Arnold, SJ ;
Stappert, J ;
Bauer, A ;
Kispert, A ;
Herrmann, BG ;
Kemler, R .
MECHANISMS OF DEVELOPMENT, 2000, 91 (1-2) :249-258
[2]   Dynamic expression of lunatic fringe suggests a link between notch signaling and an autonomous cellular oscillator driving somite segmentation [J].
Aulehla, A ;
Johnson, RL .
DEVELOPMENTAL BIOLOGY, 1999, 207 (01) :49-61
[3]   Interaction between wingless and notch signaling pathways mediated by dishevelled [J].
Axelrod, JD ;
Matsuno, K ;
ArtavanisTsakonas, S ;
Perrimon, N .
SCIENCE, 1996, 271 (5257) :1826-1832
[4]   Interaction between Notch signalling and Lunatic fringe during somite boundary formation in the mouse [J].
Barrantes, ID ;
Elia, AJ ;
Wünsch, K ;
De Angelis, MH ;
Mak, TW ;
Rossant, J ;
Conlon, RA ;
Gossler, A ;
de la Pompa, JL .
CURRENT BIOLOGY, 1999, 9 (09) :470-480
[5]   Distinct regulatory elements direct Delta 1 expression in the nervous system and paraxial mesoderm of transgenic mice [J].
Beckers, J ;
Caron, A ;
de Angelis, MH ;
Hans, S ;
Campos-Ortega, JA ;
Gossler, A .
MECHANISMS OF DEVELOPMENT, 2000, 95 (1-2) :23-34
[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]   EARLY STAGES OF CHICK SOMITE DEVELOPMENT [J].
CHRIST, B ;
ORDAHL, CP .
ANATOMY AND EMBRYOLOGY, 1995, 191 (05) :381-396
[8]   Clock regulatory elements control cyclic expression of Lunatic fringe during somitogenesis [J].
Cole, SE ;
Levorse, JM ;
Tilghman, SM ;
Vogt, TF .
DEVELOPMENTAL CELL, 2002, 3 (01) :75-84
[9]  
CONLON RA, 1995, DEVELOPMENT, V121, P1533
[10]   CLOCK AND WAVEFRONT MODEL FOR CONTROL OF NUMBER OF REPEATED STRUCTURES DURING ANIMAL MORPHOGENESIS [J].
COOKE, J ;
ZEEMAN, EC .
JOURNAL OF THEORETICAL BIOLOGY, 1976, 58 (02) :455-476