AI Article Synopsis

  • Odorant degrading enzymes (ODEs) help terminate olfactory signals by quickly breaking down odorants near sensory receptors; this study investigates a specific enzyme called JHEdup in fruit flies.
  • The JHEdup gene is highly expressed in specific sensory structures that detect food esters, and mutant flies showed increased sensitivity to certain food odors compared to normal flies.
  • Phylogenetic analysis indicates that JHEdup evolved from a duplication of the juvenile hormone esterase gene in an ancestor of fruit flies and retains this function in multiple Drosophila species.

Article Abstract

Odorant degrading enzymes (ODEs) are thought to be responsible, at least in part, for olfactory signal termination in the chemosensory system by rapid degradation of odorants in the vicinity of the receptors. A carboxylesterase, specifically expressed in Drosophila antennae, called "juvenile hormone esterase duplication (JHEdup)" has been previously reported to hydrolyse different fruit esters in vitro. Here we functionally characterize JHEdup in vivo. We show that the jhedup gene is highly expressed in large basiconic sensilla that have been reported to detect several food esters. An electrophysiological analysis demonstrates that ab1A olfactory neurons of jhedup mutant flies exhibit an increased response to certain food acetates. Furthermore, mutant flies show a higher sensitivity towards the same odorants in behavioural assays. A phylogenetic analysis reveals that jhedup arose as a duplication of the juvenile hormone esterase gene during the evolution of Diptera, most likely in the ancestor of Schizophora, and has been conserved in all the 12 sequenced Drosophila species. Jhedup exhibits also an olfactory-predominant expression pattern in other Drosophila species. Our results support the implication of JHEdup in the degradation of food odorants in D. melanogaster and propose a neofunctionalization of this enzyme as a bona fide ODE in Drosophilids.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5626784PMC
http://dx.doi.org/10.1038/s41598-017-13015-wDOI Listing

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