Abstract

Collective behaviour forms the basis for many anti-predator strategies. Within Lepidoptera, larval gregariousness has evolved convergently across many phylogenetically disparate lineages. While the selection pressures shaping variation in larval social behaviours are well investigated, much less is known about the mechanisms that control social attraction and behavioural coordination. Similarly, little is known about how secondary selection pressures associated with social living shape genome evolution. Here, using genomic data for over 60 species from an adaptive radiation of Neotropical butterflies, the Heliconiini, in which gregarious behaviour has evolved repeatedly, we explore the molecular basis of repeated convergent shifts towards gregarious larvae. We focus on three main areas of genomic evolution: differential selection on homologous genes, accelerated rates of evolution on non-coding regions of key genes, and differential gene expression in the brains of solitary and gregarious larvae. We identify strong signatures of convergent molecular evolution, on both coding and non-coding loci, in Heliconiini lineages which evolved gregarious behaviour. Molecular convergence is also detected at the transcriptomic level in larval brains, suggesting convergent shifts in gene regulation in neural tissue. Among loci showing strong signals of convergent evolution in gregarious lineages, we identify several strong candidates linked to neural activity, feeding behaviour, and immune pathways. Our results suggest sociality profoundly changes the selection pressures acting on multiple physiological, immunological and behavioural traits.

Competing Interest Statement

The authors have declared no competing interest.

Footnotes

* Minor changes to correct errors in text.

* https://github.com/francicco/-ConvergentMolEvolutionGregLarvalBehaviour

Details

Title
Convergent molecular evolution associated with repeated transitions to gregarious larval behaviour in Heliconiini
Author
Cicconardi, Francesco; Mclellan, Callum F; Seguret, Alice; W Owen Mcmillan; Montgomery, Stephen H
University/institution
Cold Spring Harbor Laboratory Press
Section
New Results
Publication year
2025
Publication date
Jan 23, 2025
Publisher
Cold Spring Harbor Laboratory Press
ISSN
2692-8205
Source type
Working Paper
Language of publication
English
ProQuest document ID
3156258963
Copyright
© 2025. This article is published under http://creativecommons.org/licenses/by/4.0/ (“the License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.