4.8 Article

ELAVL1 primarily couples mRNA stability with the 3′ UTRs of interferon-stimulated genes

期刊

CELL REPORTS
卷 35, 期 8, 页码 -

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CELL PRESS
DOI: 10.1016/j.celrep.2021.109178

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资金

  1. National Institutes of Health [1R35GM119569-01]
  2. Vanderbilt University Department Biochemistry start-up funds
  3. University of Colorado Anschutz Medical Campus RNA Bioscience Initiative
  4. Boettcher Foundation Webb-Waring Early Career Investigator Award [AWD-103075]
  5. Chemistry-Biology Interface training grant [5T32GM065086-14]
  6. Chemical Biology of Infectious Disease training grant [5T32AI11254-02]
  7. Cellular, Biochemical and Molecular Sciences Training Program [5T32GM008554]
  8. Clinical and Translation Science Award [UL1 TR002243]

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Research has shown that ELAVL1 transitions its binding sites upon cell immune stimulation and mediates RNA stability of genes regulating pathogen sensing and cytokine production pathways.
Upon pathogen detection, the innate immune system triggers signaling events leading to upregulation of proinflammatory and anti-microbial mRNA transcripts. RNA-binding proteins (RBPs) interact with these critical mRNAs and regulate their fates at the post-transcriptional level. One such RBP is ELAVL1 Although significant progress has been made in understanding how embryonic lethal vision-like protein 1 (ELAVL1) regulates mRNAs, its target repertoire and binding distribution within an immunological context remain poorly understood. We overlap four high-throughput approaches to define its context-dependent targets and determine its regulatory impact during immune activation. ELAVL1 transitions from binding overwhelmingly intronic sites to 3' UTR sites upon immune stimulation of cells, binding previously and newly expressed mRNAs. We find that ELAVL1 mediates the RNA stability of genes that regulate pathways essential to pathogen sensing and cytokine production. Our findings reveal the importance of examining RBP regulatory impact under dynamic transcriptomic events to understand their post-transcriptional regulatory roles within specific biological circuitries.

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