Department of Molecular Genetics and Cell Biology, The University of Chicago, Chicago, IL 60637, USA.
Dev Cell. 2011 Nov 15;21(5):888-95. doi: 10.1016/j.devcel.2011.08.028.
Recent studies have shown that the Hippo-Salvador-Warts (HSW) pathway restrains tissue growth by phosphorylating and inactivating the oncoprotein Yorkie. How growth-suppressive signals are transduced upstream of Hippo remains unclear. We show that the Sterile 20 family kinase, Tao-1, directly phosphorylates T195 in the Hippo activation loop and that, like other HSW pathway genes, Tao-1 functions to restrict cell proliferation in developing imaginal epithelia. This relationship appears to be evolutionarily conserved, because mammalian Tao-1 similarly affects MST kinases. In S2 cells, Tao-1 mediates the effects of the upstream HSW components Merlin and Expanded, consistent with the idea that Tao-1 functions in tissues to regulate Hippo phosphorylation. These results demonstrate that one family of Ste20 kinases can activate another and identify Tao-1 as a component of the regulatory network controlling HSW pathway signaling, and therefore tissue growth, during development.
最近的研究表明,Hippo-Salvador-Warts (HSW) 途径通过磷酸化和失活癌蛋白 Yorkie 来抑制组织生长。Hippo 上游的生长抑制信号如何传递仍不清楚。我们表明,Sterile 20 家族激酶 Tao-1 直接磷酸化 Hippo 激活环中的 T195,并且像其他 HSW 途径基因一样,Tao-1 作用于限制发育中的 imaginal 上皮细胞的增殖。这种关系似乎在进化上是保守的,因为哺乳动物 Tao-1 同样影响 MST 激酶。在 S2 细胞中,Tao-1 介导上游 HSW 成分 Merlin 和 Expanded 的作用,这与 Tao-1 在组织中发挥作用以调节 Hippo 磷酸化的观点一致。这些结果表明,一组 Ste20 激酶可以激活另一种激酶,并将 Tao-1 鉴定为调控网络的组成部分,该网络控制 HSW 途径信号传导,从而控制发育过程中的组织生长。