A β-catenin identified by functional rather than sequence criteria and its role in Wnt/MAPK signaling

被引:108
作者
Kidd, AR
Miskowski, JA
Siegfried, KR
Sawa, H
Kimble, J
机构
[1] Univ Wisconsin, Mol & Cellular Biol Program, Madison, WI 53706 USA
[2] Univ Wisconsin, Dept Biochem, Madison, WI 53706 USA
[3] Univ Wisconsin, Genet Lab, Madison, WI 53706 USA
[4] Univ Wisconsin, Howard Hughes Med Inst, Madison, WI 53706 USA
[5] RIKEN, Ctr Dev Biol, Lab Cell Fate Decis, Kobe, Hyogo 6500047, Japan
关键词
D O I
10.1016/j.cell.2005.03.029
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
Wnt/MAPK signaling is a common variant of Wnt signaling, in C. elegans and has been implicated in vertebrates. The sys-1 gene works with Wnt/MAPK signaling to control cell fates during C. elegans development. We report that the SYS-1 amino acid sequence is novel but that SYS-1 functions as P-catenin: SYS-1 rescues a bar-1/beta-catenin null mutant, binds the POP-1/TCF beta-catenin binding domain, and coactivates POP-1-dependent transcription. Moreover, we provide genetic and molecular evidence that SYS-1 levels are crucial to POP-1 activity. Our results suggest that Wnt/MAPK signaling promotes POP-1 export from the nucleus to accommodate the limiting availability of its SYS-1/beta-catenin transcriptional coactivator. Discovery of SYS-1/beta-catenin extends our definition of beta-catenins and brings together aspects of the canonical mechanism for Wnt signaling with the noncanonical Wnt/ MAPK mechanism. We discuss the idea that a similar pathway may be employed broadly in animal development.
引用
收藏
页码:761 / 772
页数:12
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