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Nat Commun ; 12(1): 2130, 2021 04 09.
Article in English | MEDLINE | ID: mdl-33837217

ABSTRACT

Mito-SEPs are small open reading frame-encoded peptides that localize to the mitochondria to regulate metabolism. Motivated by an intriguing negative association between mito-SEPs and inflammation, here we screen for mito-SEPs that modify inflammatory outcomes and report a mito-SEP named "Modulator of cytochrome C oxidase during Inflammation" (MOCCI) that is upregulated during inflammation and infection to promote host-protective resolution. MOCCI, a paralog of the NDUFA4 subunit of cytochrome C oxidase (Complex IV), replaces NDUFA4 in Complex IV during inflammation to lower mitochondrial membrane potential and reduce ROS production, leading to cyto-protection and dampened immune response. The MOCCI transcript also generates miR-147b, which targets the NDUFA4 mRNA with similar immune dampening effects as MOCCI, but simultaneously enhances RIG-I/MDA-5-mediated viral immunity. Our work uncovers a dual-component pleiotropic regulation of host inflammation and immunity by MOCCI (C15ORF48) for safeguarding the host during infection and inflammation.


Subject(s)
Electron Transport Complex IV/genetics , Genetic Pleiotropy/immunology , Inflammation/immunology , MicroRNAs/metabolism , Neoplasm Proteins/genetics , Neoplasm Proteins/metabolism , Nuclear Proteins/genetics , Nuclear Proteins/metabolism , Cell Line , Electron Transport Complex IV/metabolism , Gene Knockout Techniques , Humans , Inflammation/genetics , Inflammation/pathology , Membrane Potential, Mitochondrial/immunology , MicroRNAs/genetics , Mitochondria/immunology , Mitochondria/pathology , Primary Cell Culture , Reactive Oxygen Species/metabolism , Up-Regulation/immunology
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