Functional interaction between β-catenin and FOXO in oxidative stress signaling

被引:609
作者
Essers, MAG
de Vries-Smits, LMM
Barker, N
Polderman, PE
Burgering, BMT
Korswagen, HC
机构
[1] Netherlands Inst Dev Biol, Hubrecht Lab, NL-3584 CT Utrecht, Netherlands
[2] Ctr Biomed Genet, NL-3584 CT Utrecht, Netherlands
[3] Univ Med Ctr, Dept Physiol Chem, NL-3584 CG Utrecht, Netherlands
[4] Univ Med Ctr, Ctr Biomed Genet, NL-3584 CG Utrecht, Netherlands
关键词
D O I
10.1126/science.1109083
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
beta-Catenin is a multifunctional protein that mediates Writ signaling by binding to members of the T cell factor (TCF) family of transcription factors. Here, we report an evolutionarily conserved interaction of beta-catenin with FOXO transcription factors, which are regulated by insulin and oxidative stress signaling. beta-Catenin binds directly to FOXO and enhances FOXO transcriptional activity in mammalian cells. In Caenorhabditis elegans, loss of the beta-catenin BAR-1 reduces the activity of the FOXO ortholog DAF-16 in dauer formation and life span. Association of beta-catenin with FOXO was enhanced in cells exposed to oxidative stress. Furthermore, BAR-1 was required for the oxidative stress-induced expression of the DAF-16 target gene sod-3 and for resistance to oxidative damage. These results demonstrate a role for beta-catenin in regulating FOXO function that is particularly important under conditions of oxidative stress.
引用
收藏
页码:1181 / 1184
页数:4
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