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Insect glycerol transporters evolved by functional co-option and gene replacement

Author

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  • Roderick Nigel Finn

    (Bergen High Technology Center, University of Bergen
    Institute of Marine Research)

  • François Chauvigné

    (Bergen High Technology Center, University of Bergen
    Institut de Recerca i Tecnologia Agroalimentàries (IRTA)-Institut de Ciències del Mar, Consejo Superior de Investigaciones Científicas (CSIC))

  • Jon Anders Stavang

    (Bergen High Technology Center, University of Bergen)

  • Xavier Belles

    (Institute of Evolutionary Biology (CSIC-Universitat Pompeu Fabra))

  • Joan Cerdà

    (Institut de Recerca i Tecnologia Agroalimentàries (IRTA)-Institut de Ciències del Mar, Consejo Superior de Investigaciones Científicas (CSIC))

Abstract

Transmembrane glycerol transport is typically facilitated by aquaglyceroporins in Prokaryota and Eukaryota. In holometabolan insects however, aquaglyceroporins are absent, yet several species possess polyol permeable aquaporins. It thus remains unknown how glycerol transport evolved in the Holometabola. By combining phylogenetic and functional studies, here we show that a more efficient form of glycerol transporter related to the water-selective channel AQP4 specifically evolved and multiplied in the insect lineage, resulting in the replacement of the ancestral branch of aquaglyceroporins in holometabolan insects. To recapitulate this evolutionary process, we generate specific mutants in distantly related insect aquaporins and human AQP4 and show that a single mutation in the selectivity filter converted a water-selective channel into a glycerol transporter at the root of the crown clade of hexapod insects. Integration of phanerozoic climate models suggests that these events were associated with the emergence of complete metamorphosis and the unparalleled radiation of insects.

Suggested Citation

  • Roderick Nigel Finn & François Chauvigné & Jon Anders Stavang & Xavier Belles & Joan Cerdà, 2015. "Insect glycerol transporters evolved by functional co-option and gene replacement," Nature Communications, Nature, vol. 6(1), pages 1-7, November.
  • Handle: RePEc:nat:natcom:v:6:y:2015:i:1:d:10.1038_ncomms8814
    DOI: 10.1038/ncomms8814
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