Functional characterization supports multiple evolutionary origins of pheromone receptors in bark beetles.

Ips typographus Xenopus laevis oocytes cis-verbenol HEK293 cells homology modeling ligand docking odorant receptor (OR)

Journal

Molecular biology and evolution
ISSN: 1537-1719
Titre abrégé: Mol Biol Evol
Pays: United States
ID NLM: 8501455

Informations de publication

Date de publication:
17 Sep 2024
Historique:
received: 23 02 2024
revised: 21 08 2024
accepted: 13 09 2024
medline: 17 9 2024
pubmed: 17 9 2024
entrez: 17 9 2024
Statut: aheadofprint

Résumé

Chemical communication using pheromones is thought to have contributed to the diversification and speciation of insects. The species-specific pheromones are detected by specialized pheromone receptors. Whereas the evolution and function of pheromone receptors have been extensively studied in Lepidoptera, only a few pheromone receptors have been identified in beetles, which limits our understanding of their evolutionary histories and physiological functions. To shed light on these questions, we aimed to functionally characterize potential pheromone receptors in the spruce bark beetle Ips typographus ('Ityp') and explore their evolutionary origins and molecular interactions with ligands. Males of this species release an aggregation pheromone comprising 2-methyl-3-buten-2-ol and (4S)-cis-verbenol, which attracts both sexes to attacked trees. Using two systems for functional characterization, we show that the highly expressed odorant receptor (OR) ItypOR41 responds specifically to (4S)-cis-verbenol, with structurally similar compounds eliciting minor responses. We next targeted the closely related ItypOR40 and ItypOR45. Whereas ItypOR40 was unresponsive, ItypOR45 showed an overlapping response profile with ItypOR41, but a broader tuning. Our phylogenetic analysis shows that these ORs are present in a different OR clade as compared to all other known beetle pheromone receptors, suggesting multiple evolutionary origins of pheromone receptors in bark beetles. Next, using computational analyses and experimental validation, we reveal two amino acid residues (Gln179 and Trp310) that are important for ligand binding and pheromone specificity of ItypOR41 for (4S)-cis-verbenol, possibly via hydrogen bonding to Gln179. Collectively, our results shed new light on the origins, specificity, and ligand binding mechanisms of pheromone receptors in beetles.

Identifiants

pubmed: 39288326
pii: 7759652
doi: 10.1093/molbev/msae196
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

© The Author(s) 2024. Published by Oxford University Press on behalf of Society for Molecular Biology and Evolution.

Auteurs

Twinkle Biswas (T)

Department of Biology, Lund University, Lund, Sweden.
Max Planck center next Generation Insect Chemical Ecology (nGICE), Department of Biology, Lund University, Lund, Sweden.

Cassie Sims (C)

Department of Biology, Lund University, Lund, Sweden.
Max Planck center next Generation Insect Chemical Ecology (nGICE), Department of Biology, Lund University, Lund, Sweden.

Jothi Kumar Yuvaraj (JK)

Department of Biology, Lund University, Lund, Sweden.

Rebecca E Roberts (RE)

Department of Biology, Lund University, Lund, Sweden.

Christer Löfstedt (C)

Department of Biology, Lund University, Lund, Sweden.
Max Planck center next Generation Insect Chemical Ecology (nGICE), Department of Biology, Lund University, Lund, Sweden.

Martin N Andersson (MN)

Department of Biology, Lund University, Lund, Sweden.
Max Planck center next Generation Insect Chemical Ecology (nGICE), Department of Biology, Lund University, Lund, Sweden.

Classifications MeSH