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柠檬酸盐激酶与 LATS2 相互作用,并通过封闭其疏水性磷酸化基序来抑制其活性。

Citron kinase interacts with LATS2 and inhibits its activity by occluding its hydrophobic phosphorylation motif.

机构信息

Department of Biological Sciences, KAIST 291 Daehak-ro, Yuseong-gu, Daejeon 34141, Republic of Korea.

Department of Molecular Biotechnology and Health Sciences, University of Turin, 10126 Turin, Italy.

出版信息

J Mol Cell Biol. 2019 Dec 23;11(11):1006-1017. doi: 10.1093/jmcb/mjz013.

Abstract

The inhibitory effect of large tumor suppressor kinase (LATS1/2) on the activity of the oncoprotein yes-associated protein (YAP) is crucial to maintain tissue homeostasis. Proteomic studies have identified several new regulators of this process. Recently, citron kinase (CIT) was listed as a potential binding candidate of Hippo-related components, suggesting a new connection between CIT and the Hippo pathway. Aside from CIT's role in cytokinesis, the molecular crosstalk between CIT and the Hippo pathway is largely unknown. Here, we demonstrate a role for CIT as a scaffold protein linking LATS2 and YAP. More importantly, CIT interacts with LATS2 to directly suppress LATS2 phosphorylation at the hydrophobic motif-targeted by MST1, leading to LATS2 inactivation and YAP activation. By studying their genetic interactions, we found that Sticky, the CIT homolog in Drosophila melanogaster, functions with Warts to control Drosophila eye development. Together, our study confirms citron kinase as a novel regulator of the Hippo pathway.

摘要

大肿瘤抑制激酶 (LATS1/2) 对癌蛋白 yes 相关蛋白 (YAP) 活性的抑制作用对于维持组织内稳态至关重要。蛋白质组学研究已经确定了这一过程的几个新的调节因子。最近,柠檬激酶 (CIT) 被列为 Hippo 相关成分的潜在结合候选物,这表明 CIT 与 Hippo 通路之间存在新的联系。除了 CIT 在细胞分裂中的作用外,CIT 和 Hippo 通路之间的分子相互作用在很大程度上尚不清楚。在这里,我们证明了 CIT 作为一种支架蛋白,将 LATS2 和 YAP 连接起来。更重要的是,CIT 与 LATS2 相互作用,直接抑制 MST1 靶向的疏水性基序上的 LATS2 磷酸化,导致 LATS2 失活和 YAP 激活。通过研究它们的遗传相互作用,我们发现果蝇中的 CIT 同源物 Sticky 与 Warts 一起控制果蝇眼睛的发育。总之,我们的研究证实了柠檬激酶是 Hippo 通路的一个新的调节因子。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ea5f/6927243/0ed6fa13817e/mjz013f01.jpg

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