BAF restricts cGAS on nuclear DNA to prevent innate immune activation

Science. 2020 Aug 14;369(6505):823-828. doi: 10.1126/science.aaw6421.

Abstract

The appearance of DNA in the cytosol is perceived as a danger signal that stimulates potent immune responses through cyclic guanosine monophosphate-adenosine monophosphate synthase (cGAS). How cells regulate the activity of cGAS toward self-DNA and guard against potentially damaging autoinflammatory responses is a fundamental biological question. Here, we identify barrier-to-autointegration factor 1 (BAF) as a natural opponent of cGAS activity on genomic self-DNA. We show that BAF dynamically outcompetes cGAS for DNA binding, hence prohibiting the formation of DNA-cGAS complexes that are essential for enzymatic activity. Upon acute loss of nuclear membrane integrity, BAF is necessary to restrict cGAS activity on exposed DNA. Our observations reveal a safeguard mechanism, distinct from physical separation, by which cells protect themselves against aberrant immune responses toward genomic DNA.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cell Nucleus / metabolism*
  • DNA / immunology*
  • DNA / metabolism
  • DNA-Binding Proteins / genetics
  • DNA-Binding Proteins / metabolism*
  • Gene Knockdown Techniques
  • HeLa Cells
  • Humans
  • Immunity, Innate*
  • Nuclear Envelope / metabolism
  • Nucleotidyltransferases / metabolism*

Substances

  • BANF1 protein, human
  • DNA-Binding Proteins
  • DNA
  • Nucleotidyltransferases
  • cGAS protein, human