Peter MacCallum Cancer Centre, 305 Grattan St, Melbourne, VIC 3000, Australia; Sir Peter MacCallum Department of Oncology, University of Melbourne, Parkville, VIC 3010, Australia.
Department of Pathology and Cell Biology, Columbia University College of Physicians and Surgeons, 630 West 168th Street, New York, NY 10032, USA.
Dev Cell. 2018 Dec 3;47(5):564-575.e5. doi: 10.1016/j.devcel.2018.09.024. Epub 2018 Oct 25.
Hippo-like pathways are ancient signaling modules first identified in yeasts. The best-defined metazoan module forms the core of the Hippo pathway, which regulates organ size and cell fate. Hippo-like kinase modules consist of a Sterile 20-like kinase, an NDR kinase, and non-catalytic protein scaffolds. In the Hippo pathway, the upstream kinase Hippo can be activated by another kinase, Tao-1. Here, we delineate a related Hippo-like signaling module that Tao-1 regulates to control tracheal morphogenesis in Drosophila melanogaster. Tao-1 activates the Sterile 20-like kinase GckIII by phosphorylating its activation loop, a mode of regulation that is conserved in humans. Tao-1 and GckIII act upstream of the NDR kinase Tricornered to ensure proper tube formation in trachea. Our study reveals that Tao-1 activates two related kinase modules to control both growth and morphogenesis. The Hippo-like signaling pathway we have delineated has a potential role in the human vascular disease cerebral cavernous malformation.
Hippo 样途径是最早在酵母中鉴定的古老信号模块。定义最明确的后生动物模块构成 Hippo 途径的核心,该途径调节器官大小和细胞命运。Hippo 样激酶模块由一个 Sterile 20 样激酶、一个 NDR 激酶和非催化蛋白支架组成。在 Hippo 途径中,上游激酶 Hippo 可以被另一种激酶 Tao-1 激活。在这里,我们描述了 Tao-1 调节的一个相关的 Hippo 样信号模块,以控制果蝇的气管形态发生。Tao-1 通过磷酸化其激活环来激活 Sterile 20 样激酶 GckIII,这种调节模式在人类中是保守的。Tao-1 和 GckIII 在前 NDR 激酶 Tricornered 的上游发挥作用,以确保气管中管的正确形成。我们的研究表明,Tao-1 激活两个相关的激酶模块来控制生长和形态发生。我们所描述的 Hippo 样信号通路可能在人类血管疾病脑动静脉畸形中发挥作用。