Noncoding RNA MaIL1 is an integral component of the TLR4-TRIF pathway

Proc Natl Acad Sci U S A. 2020 Apr 21;117(16):9042-9053. doi: 10.1073/pnas.1920393117. Epub 2020 Apr 2.

Abstract

RNA has been proposed as an important scaffolding factor in the nucleus, aiding protein complex assembly in the dense intracellular milieu. Architectural contributions of RNA to cytosolic signaling pathways, however, remain largely unknown. Here, we devised a multidimensional gradient approach, which systematically locates RNA components within cellular protein networks. Among a subset of noncoding RNAs (ncRNAs) cosedimenting with the ubiquitin-proteasome system, our approach unveiled ncRNA MaIL1 as a critical structural component of the Toll-like receptor 4 (TLR4) immune signal transduction pathway. RNA affinity antisense purification-mass spectrometry (RAP-MS) revealed MaIL1 binding to optineurin (OPTN), a ubiquitin-adapter platforming TBK1 kinase. MaIL1 binding stabilized OPTN, and consequently, loss of MaIL1 blunted OPTN aggregation, TBK1-dependent IRF3 phosphorylation, and type I interferon (IFN) gene transcription downstream of TLR4. MaIL1 expression was elevated in patients with active pulmonary infection and was highly correlated with IFN levels in bronchoalveolar lavage fluid. Our study uncovers MaIL1 as an integral RNA component of the TLR4-TRIF pathway and predicts further RNAs to be required for assembly and progression of cytosolic signaling networks in mammalian cells.

Keywords: glycerol gradient; immunity; interferon; lncRNA; macrophage.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adaptor Proteins, Vesicular Transport / metabolism
  • Adult
  • Aged
  • Blood Buffy Coat / cytology
  • Bronchoalveolar Lavage Fluid / immunology
  • Cell Cycle Proteins / metabolism*
  • Female
  • Gene Expression Regulation / immunology
  • Gene Knockdown Techniques
  • Humans
  • Interferon Regulatory Factor-3 / metabolism
  • Interferon Type I / blood
  • Interferon Type I / genetics*
  • Interferon Type I / immunology
  • Macrophages
  • Male
  • Membrane Transport Proteins / metabolism*
  • Middle Aged
  • Phosphorylation / genetics
  • Primary Cell Culture
  • Protein Serine-Threonine Kinases / metabolism
  • Protein Stability
  • RNA, Untranslated / blood
  • RNA, Untranslated / genetics
  • RNA, Untranslated / metabolism*
  • RNA-Seq
  • Respiratory Tract Infections / blood
  • Respiratory Tract Infections / immunology*
  • Respiratory Tract Infections / microbiology
  • Signal Transduction / genetics
  • Signal Transduction / immunology
  • Toll-Like Receptor 4 / metabolism*
  • Young Adult

Substances

  • Adaptor Proteins, Vesicular Transport
  • Cell Cycle Proteins
  • IRF3 protein, human
  • Interferon Regulatory Factor-3
  • Interferon Type I
  • Membrane Transport Proteins
  • OPTN protein, human
  • RNA, Untranslated
  • TICAM1 protein, human
  • TLR4 protein, human
  • Toll-Like Receptor 4
  • Protein Serine-Threonine Kinases
  • TBK1 protein, human