β-Catenin regulates Cripto- and Wnt3-dependent gene expression programs in mouse axis and mesoderm formation

被引:140
作者
Morkel, M
Huelsken, J
Wakamiya, M
Ding, JX
van de Wetering, M
Clevers, H
Taketo, MM
Behringer, RR
Shen, MM
Birchmeier, W
机构
[1] Max Delbruck Ctr Mol Med, D-13125 Berlin, Germany
[2] Univ Texas, MD Anderson Canc Ctr, Dept Mol Genet, Houston, TX 77030 USA
[3] Univ Med & Dent New Jersey, Robert Wood Johnson Med Sch, Ctr Adv Biotechnol & Med, Piscataway, NJ 08854 USA
[4] Univ Med & Dent New Jersey, Robert Wood Johnson Med Sch, Dept Pediat, Piscataway, NJ 08854 USA
[5] Univ Utrecht Hosp, Dept Immunol, NL-3584 CX Utrecht, Netherlands
[6] Kyoto Univ, Grad Sch Med, Dept Pharmacol, Kyoto 6068501, Japan
来源
DEVELOPMENT | 2003年 / 130卷 / 25期
关键词
microarray; anteroposterior axis; gastrulation; signalling pathways; Tdgf1; nanog;
D O I
10.1242/dev.00859
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Gene expression profiling of beta-catenin, Cripto and Wnt3 mutant mouse embryos has been used to characterise the genetic networks that regulate early embryonic development. We have defined genes whose expression is regulated by beta-catenin during formation of the anteroposterior axis and the mesoderm, and have identified Cripto, which encodes a Nodal co-receptor, as a primary target of beta-catenin signals both in embryogenesis as well as in colon carcinoma cell lines and tissues. We have also defined groups of genes regulated by Wnt3/beta-catenin signalling during primitive streak and mesoderm formation. Our data assign a key role to beta-catenin upstream of two distinct gene expression programs during anteroposterior axis and mesoderm formation.
引用
收藏
页码:6283 / 6294
页数:12
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