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Evolutionary analyses reveal immune cell receptor GPR84 as a conserved receptor for bacteria-derived molecules

Amadeus Samuel Schulze, Gunnar Kleinau, Rosanna Krakowsky and 6 more

iScience · 2022

doi:10.1016/j.isci.2022.105087 (opens in a new tab)

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Abstract

The G protein-coupled receptor 84 (GPR84) is found in immune cells and its expression is increased under inflammatory conditions. Activation of GPR84 by medium-chain fatty acids results in pro-inflammatory responses. Here, we screened available vertebrate genome data and found that GPR84 is present in vertebrates for more than 500 million years but absent in birds and a pseudogene in bats. Cloning and functional characterization of several mammalian GPR84 orthologs in combination with evolutionary and model-based structural analyses revealed evidence for positive selection of bear GPR84 orthologs. Naturally occurring human GPR84 variants are most frequent in Asian populations causing a loss of function. Further, we identified cis - and trans -2-decenoic acid, both known to mediate bacterial communication, as evolutionary highly conserved ligands. Our integrated set of approaches contributes to a comprehensive understanding of GPR84 in terms of evolutionary and structural aspects, highlighting GPR84 as a conserved immune cell receptor for bacteria-derived molecules.

Abstract licence: CC BY-NC

References121

  1. 2.
  2. 33.
  3. 68.
  4. 77.
  5. 81.
  6. 83.
  7. 86.
  8. 91.
  9. 95.
  10. 98.
  11. 100.

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