Comparison of Olfactory Genes in Two Species: Emphasis on Candidates Involved in the Detection of Type-II Sex Pheromones.

Front Physiol

Key Laboratory of Tea Biology and Resource Utilization, Ministry of Agriculture, Tea Research Institute, Chinese Academy of Agricultural Sciences, Hangzhou, China.

Published: November 2018

AI Article Synopsis

  • Two sibling species are significant pests of chewing tea in China, and their sexual reproduction is influenced by differences in sex pheromone detection.
  • Researchers sequenced the transcriptomes of the antennae from male and female individuals to analyze the olfactory genes that identify these pheromones, finding 36 odorant-binding proteins and 52 olfactory receptors.
  • While many genes were highly similar between the two species, differences in gene abundance suggest they use distinct levels of pheromone receptors for recognizing sex pheromones, which may be vital for managing these pest species.

Article Abstract

The sibling species and are the major chewing tea pests in China. A difference in sex pheromone components plays a central role in premating isolation in these two species. To investigate the mechanism of premating isolation in these two species, we sequenced the transcriptomes of the antennae of female and male individuals and performed phylogenetic analyses, abundance analyses, and tissue expression profile analyses to compare the olfactory genes involved in the detection of sex pheromones. A total of 36 odorant-binding proteins (OBPs) and 52 olfactory receptors (ORs) were identified in . Phylogenetic analyses showed that EoblOBP2, 3, and 25 were grouped in the pheromone-binding protein clade with EgriOBP2, 3, 25, and another lepidopteran PBP. EoblOR25 and 28 were grouped with EgriOR25, 28, and pheromone receptors for the detection of Type-I sex pheromone components. EoblOR24, 31, 37, and 44 were grouped with EgriOR24, 31, 37, and 44. All of these 4 EoblORs and 4 showed higher abundance in male antennae than in female ones. Therefore, OBP2, 3, 25 and OR24, 31, 37, 44 of and might be responsible for sex pheromone component detection. However, the sequences of these genes in and were more than 90% identical. This indicates that these orthologous genes might play similar roles in the detection of sex pheromones. In contrast, the observed and differed in abundance between the antennae of the two species. Therefore, we speculate that these two species use the different transcript levels of PRs to differentiate sex pheromone components. The results of the present study might contribute in deciphering the mechanism for premating isolation in these species and may be of use in devising strategies for their management.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6247094PMC
http://dx.doi.org/10.3389/fphys.2018.01602DOI Listing

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