4.3 Article

TREX1-Apex predator of cytosolic DNA metabolism

Journal

DNA REPAIR
Volume 94, Issue -, Pages -

Publisher

ELSEVIER
DOI: 10.1016/j.dnarep.2020.102894

Keywords

TREX1; Cytosolic DNA metabolism; DNA sensing; Autoimmunity; Genome stability

Funding

  1. National Institute of Health (NIH) [R01AI116725, T32AI007401, T32GM095440]
  2. Alliance for Lupus Research
  3. Artom memorial fellowship
  4. Comprehensive Cancer Center of Wake Forest University National Cancer Institute Cancer (Center Support Grant) [P30CA012197]
  5. Cowgill memorial fellowship

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The cytosolic Three prime Repair EXonuclease 1 (TREX1) is a powerful DNA-degrading enzyme required for clearing cytosolic DNA to prevent aberrant inflammation and autoimmunity. In the absence of TREX1 activity, cytosolic DNA pattern recognition receptors of the innate immune system are constitutively activated by undegraded TREX1 substrates. This triggers a chronic inflammatory response in humans expressing mutant TREX1 alleles, eliciting a spectrum of rare autoimmune diseases dependent on the nature of the mutation. The precise origins of cytosolic DNA targeted by TREX1 continue to emerge, but DNA emerging from the nucleus or taken up by the cell could represent potential sources. In this Review, we explore the biochemical and immunological data supporting the role of TREX1 in suppressing cytosolic DNA sensing, and discuss the possibility that TREX1 may contribute to maintenance of genome integrity.

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