Cortical β-catenin and APC regulate asymmetric nuclear β-catenin localization during asymmetric cell division in C. elegans

被引:78
|
作者
Mizumoto, Kota
Sawa, Hitoshi [1 ]
机构
[1] Ctr Dev Biol, Lab Cell Fate Decis, Kobe, Hyogo 6500047, Japan
[2] Kobe Univ, Grad Sch Sci & Technol, Dept Biosyst Sci, Div Bioinformat, Kobe, Hyogo 6578501, Japan
基金
日本学术振兴会;
关键词
D O I
10.1016/j.devcel.2007.01.004
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
In C. elegans, Wnt signaling regulates a number of asymmetric cell divisions. During telophase, WRM-1/beta-catenin localizes asymmetrically to the anterior cortex and the posterior daughter's nucleus. However, cortical WRM-1's functions are not known. Here, we use a membrane-targeted form of WRM-1 to show that cortical WRM-1 inhibits Wnt signaling and the nuclear localization of WRM-1. These functions are mediated by APR-1/APC, which regulates WRM-1 nuclear export. We also show that APR-1 as well as PRY-1/Axin and Dishevelled homologs localize asymmetrically to the cortex. Our results suggest a model in which cortical WRM-1 recruits APR-1 to the anterior cortex before and during division, and the cortical APR-1 stimulates WRM-1 export from the anterior nucleus at telophase. Because beta-catenin and APC are localized to the cortex in many cell types in different species, our results suggest that these cortical proteins may regulate asymmetric divisions or Wnt signaling in other organisms as well.
引用
收藏
页码:287 / 299
页数:13
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