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Comparative analysis of mite genomes reveals positive selection for diet adaptation. | LitMetric

Comparative analysis of mite genomes reveals positive selection for diet adaptation.

Commun Biol

State Key Laboratory of Ophthalmology, Zhongshan Ophthalmic Center, Sun Yat-sen University, Guangzhou, China.

Published: June 2021

AI Article Synopsis

  • Diet is a key factor influencing the evolution and adaptation of species, particularly in the diverse group Acari (mites and ticks) within Arachnida.
  • Through analysis of 15 Acari genomes, researchers found that herbivores face stronger evolutionary pressures, with specific genes related to olfactory functions and toxin metabolism showing significant adaptations.
  • Blood-feeding Acari have evolved unique genes for anticoagulation and digestion, while fat-feeding species have genes related to lipid metabolism that show high evolutionary rates, offering insights for developing new pesticides.

Article Abstract

Diet is a powerful evolutionary force for species adaptation and diversification. Acari is one of the most abundant clades of Arachnida, exhibiting diverse dietary types, while the underlying genetic adaptive mechanisms are not fully understood. Based on comparative analyses of 15 Acari genomes, we found genetic bases for three specialized diets. Herbivores experienced stronger selection pressure than other groups; the olfactory genes and gene families involving metabolizing toxins showed strong adaptive signals. Genes and gene families related to anticoagulation, detoxification, and haemoglobin digestion were found to be under strong selection pressure or significantly expanded in the blood-feeding species. Lipid metabolism genes have a faster evolutionary rate and been subjected to greater selection pressures in fat-feeding species; one positively selected site in the fatty-acid amide hydrolases 2 gene was identified. Our research provides a new perspective for the evolution of Acari and offers potential target loci for novel pesticide development.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8175442PMC
http://dx.doi.org/10.1038/s42003-021-02173-3DOI Listing

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