4.5 Article

A single-cell transcriptomic atlas tracking the neural basis of division of labour in an ant superorganism

Journal

NATURE ECOLOGY & EVOLUTION
Volume 6, Issue 8, Pages 1191-+

Publisher

NATURE PORTFOLIO
DOI: 10.1038/s41559-022-01784-1

Keywords

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Funding

  1. National Natural Science Foundation of China [31970573, 31900399]
  2. Shenzhen Key Laboratory of Single-Cell Omics [ZDSYS20190902093613831]
  3. Villum Foundation [25900]

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Using single-cell transcriptomics, this study characterized the brain cell repertoire of the pharaoh ant and identified changes in cell composition that underlie division of labour and reproductive specialization. The study found that male and worker ant brains have opposite trends in cell composition, while the composition of gyne and queen brains remained generalized. Role differentiation from virgin gynes to inseminated queens induced abundance changes in roughly 35% of cell types.
Using single-cell transcriptomics, the authors generate a brain cell atlas for the pharaoh ant including individuals of different sexes and castes and show changes in cell composition underlying division of labour and reproductive specialization. Ant colonies with permanent division of labour between castes and highly distinct roles of the sexes have been conceptualized to be superorganisms, but the cellular and molecular mechanisms that mediate caste/sex-specific behavioural specialization have remained obscure. Here we characterized the brain cell repertoire of queens, gynes (virgin queens), workers and males of Monomorium pharaonis by obtaining 206,367 single-nucleus transcriptomes. In contrast to Drosophila, the mushroom body Kenyon cells are abundant in ants and display a high diversity with most subtypes being enriched in worker brains, the evolutionarily derived caste. Male brains are as specialized as worker brains but with opposite trends in cell composition with higher abundances of all optic lobe neuronal subtypes, while the composition of gyne and queen brains remained generalized, reminiscent of solitary ancestors. Role differentiation from virgin gynes to inseminated queens induces abundance changes in roughly 35% of cell types, indicating active neurogenesis and/or programmed cell death during this transition. We also identified insemination-induced cell changes probably associated with the longevity and fecundity of the reproductive caste, including increases of ensheathing glia and a population of dopamine-regulated Dh31-expressing neurons. We conclude that permanent caste differentiation and extreme sex-differentiation induced major changes in the neural circuitry of ants.

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