Abstract

BackgroundMating is a complex process, which is frequently associated with behavioural and physiological changes. However, understanding of the genetic underpinnings of these changes is limited. Honey bees are both a model system in behavioural genomics, and the dominant managed pollinator of human crops; consequently understanding the mating process has both pure and applied value. We used next-generation transcriptomics to probe changes in gene expression in the brains of honey bee queens, as they transition from virgin to mated reproductive status. In addition, we used CO2-narcosis, which induces oviposition without mating, to isolate the process of reproductive maturation.ResultsThe mating process produced significant changes in the expression of vision, chemo-reception, metabolic, and immune-related genes. Differential expression of these genes maps clearly onto known behavioural and physiological changes that occur during the transition from being a virgin queen to a newly-mated queen. A subset of these changes in gene expression were also detected in CO2-treated queens, as predicted from previous physiological studies. In addition, we compared our results to previous studies that used microarray techniques across a range of experimental time-points. Changes in expression of immune- and vision-related genes were common to all studies, supporting an involvement of these groups of genes in the mating process.ConclusionsOur study is an important step in understanding the molecular mechanisms regulating post-mating behavioural transitions in a natural system. The weak overlap in patterns of gene expression with previous studies demonstrates the high sensitivity of genome-wide approaches. Thus, while we build on previous microarray studies that explored post-mating changes in honey bees, the broader experimental design, use of RNA-sequencing, and focus on Australian honey bees, which remain free from the devastating parasite Varroa destructor, in the current study, provide unique insights into the biology of the mating process in honey bees.Electronic supplementary materialThe online version of this article (doi:10.1186/s12864-015-1750-7) contains supplementary material, which is available to authorized users.

Highlights

  • Mating is a complex process, which is frequently associated with behavioural and physiological changes

  • Genes that are associated with vision such as Rhodopsin 2 (Rh2), neither inactivation nor afterpotential A, Arrestin 2 (Arr2), G protein beta-subunit 76C (Gβ76C), chaoptin and Calhotin (Cpn) were all down-regulated in mated queens compared to virgins

  • Most of the genes in this group were the same genes found in the Gene Ontology (GO) terms “sensory perception” and “detection of stimulus” for the mated vs. virgin queen contrast; in addition we found neither inactivation nor afterpotential C and no receptor potential A

Read more

Summary

Introduction

Mating is a complex process, which is frequently associated with behavioural and physiological changes. Understanding of the genetic underpinnings of these changes is limited Honey bees are both a model system in behavioural genomics, and the dominant managed pollinator of human crops; understanding the mating process has both pure and applied value. We used next-generation transcriptomics to probe changes in gene expression in the brains of honey bee queens, as they transition from virgin to mated reproductive status. Complex social behaviour, which is central to reproductive success across the animal kingdom. Social insects are likely to play a key role in developing our understanding of the molecular underpinnings of mating behaviour and post-mating changes. Studies of social insects may provide unique insights into the molecular mechanisms at play during and after the mating process. Thanks to modern genomic tools, such insights are emerging for ants [15, 16], wasps [17, 18], termites [19, 20], and honey bees [21, 22]

Methods
Results
Discussion
Conclusion
Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.