Coding and non-coding roles of MOCCI (C15ORF48) coordinate to regulate host inflammation and immunity

Nat Commun. 2021 Apr 9;12(1):2130. doi: 10.1038/s41467-021-22397-5.

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.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

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

Substances

  • MIRN147 microRNA, human
  • MicroRNAs
  • Neoplasm Proteins
  • Nuclear Proteins
  • Reactive Oxygen Species
  • c15orf48 protein, human
  • Electron Transport Complex IV
  • NDUFA4 protein, human