Resumen
The evolution of sociality involves shifts in physiology and behavior, most notably the emergence of a reproductive division of labor. Within social colonies, these distinct behavioral phenotypes arise from differential regulation of a shared genome. Changes in transcription factor (TF) binding motifs are one potential mechanism underpinning this plasticity, with prior studies suggesting that social species exhibit expansions in TF binding sites. However, it remains unclear whether motif expansions are reversed when sociality is lost. Here we analyze predicted TF motif occurrences across gene promoters in 42 bee species spanning millions of years of evolutionary divergence and multiple independent gains and losses of sociality. We compare motif presence across species to test whether motif expansions are a convergent feature of social evolution and whether their presence secondarily decreases when social behavior is lost. Our findings are consistent with previous research, demonstrating an expansion of TF motifs in lineages which have gained sociality. However, contrary to expectation, we do not observe genome-wide motif contractions in lineages which have secondarily lost social behavior. Despite this overall pattern, we still identify several motifs, promoter regions, and specific motif-promoter pairs which exhibit complementary changes with both gains and losses of sociality. These regulatory targets are enriched for similar organismal functions, providing strong candidates for further study. Our results lend additional support to the hypothesis that novel phenotypes may arise through modification of existing gene regulatory networks.
| Idioma original | English |
|---|---|
| Número de artículo | evag003 |
| Número de páginas | 17 |
| Publicación | Genome Biology and Evolution |
| Volumen | 18 |
| N.º | 2 |
| DOI | |
| Estado | Published - feb 1 2026 |
Nota bibliográfica
Publisher Copyright:© The Author(s) 2026. Published by Oxford University Press on behalf of Society for Molecular Biology and Evolution.
Financiación
This work was supported by a grant from the National Institutes of Health NIGMS (grant no. R35GM156952) to B.M.J. We thank members of the Jones Lab at the University ofKentucky, Dr. Clare Rittschof, and Dr. Julian Dupuis forproviding feedback and comments on initial drafts ofthis manuscript. We are grateful to the NationalCenter for Biotechnology Information (NCBI) and theDarwin Tree of Life project for maintaining genome resources, as well as Dr. Priscila Santos for providing accessto the Tetrapedia diversipes genome. We also thankthe University of Kentucky Center for ComputationalSciences and Information Technology Services ResearchComputing for their support and use of the MorganCompute Cluster and associated research computingresources.
| Financiadores | Número del financiador |
|---|---|
| NationalCenter for Biotechnology Information | |
| National Institutes of Health (NIH) | R35GM156952 |
ASJC Scopus subject areas
- Ecology, Evolution, Behavior and Systematics
- Genetics
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