| Literature DB >> 34407394 |
Chenggang Wu1, Ozgur Karakuzu1, Danielle A Garsin2.
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.Entities:
Keywords: C. elegans; NIPI-3; Nrf; ROS; SKN-1; Tribbles pseudokinase; bZIP; bacterial pathogenesis; innate immunity; p38 MAPK
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Year: 2021 PMID: 34407394 PMCID: PMC8393239 DOI: 10.1016/j.celrep.2021.109529
Source DB: PubMed Journal: Cell Rep Impact factor: 9.423