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NEDD8 通过介导 YAP1 的泛素化增强 Hippo 信号通路。

NEDD8 enhances Hippo signaling by mediating YAP1 neddylation.

机构信息

College of Animal Science and Technology, Henan Agricultural University, Zhengzhou, P. R. China.

College of Animal Sciences and Veterinary Medicine, Henan Agricultural University, Zhengzhou, P. R. China.

出版信息

J Biol Chem. 2024 Aug;300(8):107512. doi: 10.1016/j.jbc.2024.107512. Epub 2024 Jul 1.

Abstract

The Hippo-YAP signaling pathway plays a central role in many biological processes such as regulating cell fate, organ size, and tissue growth, and its key components are spatiotemporally expressed and posttranslationally modified during these processes. Neddylation is a posttranslational modification that involves the covalent attachment of NEDD8 to target proteins by NEDD8-specific E1-E2-E3 enzymes. Whether neddylation is involved in Hippo-YAP signaling remains poorly understood. Here, we provide evidence supporting the critical role of NEDD8 in facilitating the Hippo-YAP signaling pathway by mediating neddylation of the transcriptional coactivator yes-associated protein 1 (YAP1). Overexpression of NEDD8 induces YAP1 neddylation and enhances YAP1 transactivity, but inhibition of neddylation suppresses YAP1 transactivity and attenuates YAP1 nuclear accumulation. Furthermore, inhibition of YAP1 signaling promotes MLN4924-induced ovarian granulosa cells apoptosis and disruption of nedd8 in zebrafish results in downregulation of yap1-activated genes and upregulation of yap1-repressed genes. Further assays show that the xiap ligase promotes nedd8 conjugates to yap1 and that yap1 neddylation. In addition, we identify lysine 159 as a major neddylation site on YAP1. These findings reveal a novel mechanism for neddylation in the regulation of Hippo-YAP signaling.

摘要

Hippo-YAP 信号通路在许多生物学过程中发挥着核心作用,如调节细胞命运、器官大小和组织生长,其关键组成部分在这些过程中时空表达并进行翻译后修饰。类泛素化是一种翻译后修饰,涉及 NEDD8 通过 NEDD8 特异性 E1-E2-E3 酶共价连接到靶蛋白上。类泛素化是否参与 Hippo-YAP 信号通路仍知之甚少。在这里,我们提供的证据表明,NEDD8 通过介导转录共激活因子 yes 相关蛋白 1(YAP1)的类泛素化,在促进 Hippo-YAP 信号通路中起着关键作用。NEDD8 的过表达诱导 YAP1 的类泛素化并增强 YAP1 的转录活性,但类泛素化的抑制抑制了 YAP1 的转录活性并减弱了 YAP1 的核积累。此外,抑制 YAP1 信号通路促进 MLN4924 诱导的卵巢颗粒细胞凋亡,并且在斑马鱼中 nedd8 的缺失导致 yap1 激活基因的下调和 yap1 抑制基因的上调。进一步的实验表明,xiap 连接酶促进了 nedd8 与 yap1 的缀合以及 yap1 的类泛素化。此外,我们确定赖氨酸 159 是 YAP1 上的主要类泛素化位点。这些发现揭示了类泛素化在调节 Hippo-YAP 信号通路中的新机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a0aa/11327456/707d3a63d633/gr1.jpg

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