Abstract

The evolution of insect sociality has repeatedly involved changes in developmental events and their timing. Here, we propose the hypothesis that loss of a canonical regulator of moulting and metamorphosis, prothoracicotropic hormone (PTTH), and its receptor, Torso, is associated with the evolution of sociality in bees. Specifically, we posit that the increasing importance of social influences on early developmental timing in social bees has led to their decreased reliance on PTTH, which connects developmental timing with abiotic cues in solitary insects. At present, the evidence to support this hypothesis includes the absence of genes encoding PTTH and Torso from all fully-sequenced social bee genomes and its presence in all available genomes of solitary bees. Based on the bee phylogeny, the most parsimonious reconstruction of evolutionary events is that this hormone and its receptor have been lost multiple times, across independently social bee lineages. These gene losses shed light on possible molecular and cellular mechanisms that are associated with the evolution of social behavior in bees. We outline the available evidence for our hypothesis, and then contextualize it in light of what is known about developmental cues in social and solitary bees, and the multiple precedences of major developmental changes in social insects.

Highlights

  • Complex social lifestyles have evolved a limited number of times in animals, including more than 17 times in arthropods (Crozier and Pamilo, 1996)

  • We demonstrate that a number of social bee lineages have lost a canonical regulator of moulting and metamorphosis, prothoracicotropic hormone (PTTH), and its receptor, Torso, and propose that this loss might be connected to an increasing reliance on social rather than abiotic cues in the developmental timing of offspring in social bee nests

  • Our inferences about the loss of PTTH within bees, and our hypothesis that this is connected with social evolution, are based on currentlyavailable data and may change as more bee genomes are available for analysis

Read more

Summary

Introduction

Complex social lifestyles have evolved a limited number of times in animals, including more than 17 times in arthropods (Crozier and Pamilo, 1996). A genomic prediction of this hypothesis might be the loss of genes that hold important functions in the context of solitary lifestyles, occurring in concert with the transition to complex eusociality.

Results
Conclusion
Full Text
Published version (Free)

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