AI Article Synopsis

  • Inferring positive selection in genomes is essential for understanding adaptation, but it's challenging due to the influence of various evolutionary processes.
  • The ABC-MK test is introduced as a new method to quantify long-term protein adaptation in specific lineages, demonstrating effectiveness through simulations.
  • When applied to the human proteome, results show that RNA virus-interacting proteins exhibit stronger signs of positive selection compared to DNA virus-interacting proteins, indicating RNA viruses may significantly impact human adaptation over evolutionary time.

Article Abstract

Inferring the effects of positive selection on genomes remains a critical step in characterizing the ultimate and proximate causes of adaptation across species, and quantifying positive selection remains a challenge due to the confounding effects of many other evolutionary processes. Robust and efficient approaches for adaptation inference could help characterize the rate and strength of adaptation in non-model species for which demographic history, mutational processes, and recombination patterns are not currently well-described. Here, we introduce an efficient and user-friendly extension of the McDonald-Kreitman test (ABC-MK) for quantifying long-term protein adaptation in specific lineages of interest. We characterize the performance of our approach with forward simulations and find that it is robust to many demographic perturbations and positive selection configurations, demonstrating its suitability for applications to non-model genomes. We apply ABC-MK to the human proteome and a set of known Virus Interacting Proteins (VIPs) to test the long-term adaptation in genes interacting with viruses. We find substantially stronger signatures of positive selection on RNA-VIPs than DNA-VIPs, suggesting that RNA viruses may be an important driver of human adaptation over deep evolutionary time scales.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10491248PMC
http://dx.doi.org/10.1101/2023.08.29.555322DOI Listing

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