In vivo regulation of Yorkie phosphorylation and localization

被引:334
作者
Oh, Hyangyee
Irvine, Kenneth D. [1 ]
机构
[1] Rutgers State Univ, Howard Hughes Med Inst, Waksman Inst, Piscataway, NJ 08854 USA
[2] Rutgers State Univ, Dept Mol Biol & Biochem, Piscataway, NJ 08854 USA
来源
DEVELOPMENT | 2008年 / 135卷 / 06期
关键词
fat; growth; hippo; transcription; Drosophila;
D O I
10.1242/dev.015255
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Yorkie (Yki), a transcription factor of the Fat and Hippo signaling pathways, is negatively regulated by the Warts kinase. Here, we use Phos-tag gels to characterize Warts-dependent phosphorylation of Yki in vivo, and show that Warts promotes phosphorylation of Yki at multiple sites. We also show that Warts inhibits Yki nuclear localization in vivo, and can promote binding of Yki to 14-3-3 proteins in cultured cells. In vivo assessment of the influence of individual upstream regulators of Warts reveals that some mutants (e. g. fat) have only partial effects on Yki phosphorylation, and weak effects on Yki localization, whereas other genotypes (e. g. ex fat double mutants) have stronger effects on both Yki phosphorylation and localization. We also identify serine 168 as a critical site through which negative regulation of Yki by Warts-mediated phosphorylation occurs, but find that this site is not sufficient to explain effects of Hippo signaling on Yki in vivo. These results identify modulation of subcellular localization as a mechanism of Yki regulation, and establish that this regulation occurs in vivo through multiple sites of Warts-dependent phosphorylation on Yki.
引用
收藏
页码:1081 / 1088
页数:8
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