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Tribbles 假激酶 NIPI-3 通过调控 SKN-1/Nrf 活性来调节秀丽隐杆线虫的肠道免疫。

Tribbles pseudokinase NIPI-3 regulates intestinal immunity in Caenorhabditis elegans by controlling SKN-1/Nrf activity.

机构信息

Department of Microbiology and Molecular Genetics, The University of Texas Health Science Center at Houston, Houston, TX 77030, USA.

Department of Microbiology and Molecular Genetics, The University of Texas Health Science Center at Houston, Houston, TX 77030, USA.

出版信息

Cell Rep. 2021 Aug 17;36(7):109529. doi: 10.1016/j.celrep.2021.109529.

Abstract

In Caenorhabditis elegans, ROS generated in response to intestinal infection induces SKN-1, a protective transcription factor homologous to nuclear factor erythroid 2-related factor 1 or 2 (NRF1/2) in mammals. Many factors regulate SKN-1, including the p38 mitogen-activated protein kinase (MAPK) cascade that activates SKN-1 by phosphorylation. In this work, another positive regulator of SKN-1 is identified: NIPI-3, a Tribbles pseudokinase. NIPI-3 has been reported to protect against intestinal infection by negatively regulating the CCAT enhancer binding protein (C/EBP) bZIP transcription factor CEBP-1. Here we demonstrate that CEBP-1 positively regulates the vhp-1 transcript, which encodes a phosphatase that dephosphorylates the p38 MAPK called PMK-1. The increased levels of VHP-1 caused by CEBP-1 transcriptional enhancement result in less PMK-1 phosphorylation, affecting SKN-1 activity and intestinal resistance to the pathogen. The data support a model in which NIPI-3's negative regulation of CEBP-1 decreases VHP-1 phosphatase activity, allowing increased stimulation of SKN-1 activity by the p38 MAPK phosphorylation cascade in the intestine.

摘要

在秀丽隐杆线虫中,肠道感染引发的 ROS 会诱导 SKN-1,这是一种与哺乳动物中的核因子红细胞 2 相关因子 1 或 2(NRF1/2)同源的保护性转录因子。许多因素调节 SKN-1,包括激活 SKN-1 的 p38 丝裂原活化蛋白激酶(MAPK)级联,该级联通过磷酸化激活 SKN-1。在这项工作中,鉴定出 SKN-1 的另一个正调控因子:NIPI-3,一种 Tribbles 假激酶。据报道,NIPI-3 通过负调控 CCAT 增强子结合蛋白(C/EBP) bZIP 转录因子 CEBP-1 来保护免受肠道感染。在这里,我们证明 CEBP-1 正向调节编码一种称为 PMK-1 的磷酸酶的 vhp-1 转录本,该磷酸酶可使 p38 MAPK 去磷酸化。CEBP-1 转录增强导致 VHP-1 水平升高,从而导致 PMK-1 磷酸化减少,影响 SKN-1 活性和肠道对病原体的抵抗力。这些数据支持了一种模型,即 NIPI-3 对 CEBP-1 的负调控降低了 VHP-1 磷酸酶的活性,从而允许 p38 MAPK 磷酸化级联更有效地刺激肠道中的 SKN-1 活性。

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