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Article: Adaptive radiation and social evolution of the ants

TitleAdaptive radiation and social evolution of the ants
Authors
Keywordscaste differentiation
formicidae
gene-regulatory networks
genome evolution
MAPK/insulin/JH pathways
phylogenomics
reproductive division of labor
selection signatures
superorganismal colonies
synteny
Issue Date1-Jan-2025
PublisherElsevier
Citation
Cell, 2025 How to Cite?
Abstract

Ants originated over 150 million years ago through an irreversible transition to superorganismal colony life. Comparative analyses of 163 ant genomes, including newly generated whole-genome sequences of 145 ant species, reveal extensive genome rearrangements correlated with speciation rates. Meanwhile, conserved syntenic blocks are enriched with co-expressed genes involved in basal metabolism and caste differentiation. Gene families related to digestion, endocrine signaling, cuticular hydrocarbon synthesis, and chemoreception expanded in the ant ancestor, while many caste-associated genes underwent positive selection in the formicoid ancestor. Elaborations and reductions of queen-worker dimorphism and other social traits left convergent signatures of intensified or relaxed selection in conserved signaling and metabolic pathways, suggesting that a core gene set was used to diversify organizational complexity. Previously uncharacterized genetic regulators of caste development were confirmed by functional experiments. This study reconstructs the genetic underpinning of social traits and their integration within gene-regulatory networks shaping caste phenotypes.


Persistent Identifierhttp://hdl.handle.net/10722/359317
ISSN
2023 Impact Factor: 45.5
2023 SCImago Journal Rankings: 24.342

 

DC FieldValueLanguage
dc.contributor.authorVizueta, Joel-
dc.contributor.authorXiong, Zijun-
dc.contributor.authorDing, Guo-
dc.contributor.authorLarsen, Rasmus S.-
dc.contributor.authorRan, Hao-
dc.contributor.authorGao, Qionghua-
dc.contributor.authorStiller, Josefin-
dc.contributor.authorDai, Wei-
dc.contributor.authorJiang, Wei-
dc.contributor.authorZhao, Jie-
dc.contributor.authorGuo, Chunxue-
dc.contributor.authorZhang, Xiafang-
dc.contributor.authorZuo, Dashuang-
dc.contributor.authorZhong, Wenjiang-
dc.contributor.authorSchiøtt, Morten-
dc.contributor.authorLiu, Chengyuan-
dc.contributor.authorZhang, Hailin-
dc.contributor.authorDai, Xueqin-
dc.contributor.authorAndreu, Ignasi-
dc.contributor.authorShi, Yue-
dc.contributor.authorTretter, Sandra-
dc.contributor.authorHe, Ding-
dc.contributor.authorGautam, Shubham-
dc.contributor.authorLi, Zelin-
dc.contributor.authorHickey, Glenn-
dc.contributor.authorIvens, Aniek B.F.-
dc.contributor.authorMeurville, Marie Pierre-
dc.contributor.authorHita-Garcia, Francisco-
dc.contributor.authorKass, Jamie M.-
dc.contributor.authorGuénard, Benoit-
dc.contributor.authorMoreau, Corrie-
dc.contributor.authorPaten, Benedict-
dc.contributor.authorLeBoeuf, Adria C.-
dc.contributor.authorEconomo, Evan P.-
dc.contributor.authorChapuisat, Michel-
dc.contributor.authorShik, Jonathan Z.-
dc.contributor.authorWard, Philip S.-
dc.contributor.authorHeinze, Jürgen-
dc.contributor.authorSchultz, Ted R.-
dc.contributor.authorLi, Qiye-
dc.contributor.authorDunn, Robert R.-
dc.contributor.authorSanders, Nathan J.-
dc.contributor.authorLiu, Weiwei-
dc.contributor.authorSchrader, Lukas-
dc.contributor.authorBoomsma, Jacobus J.-
dc.contributor.authorZhang, Guojie-
dc.date.accessioned2025-08-30T00:30:10Z-
dc.date.available2025-08-30T00:30:10Z-
dc.date.issued2025-01-01-
dc.identifier.citationCell, 2025-
dc.identifier.issn0092-8674-
dc.identifier.urihttp://hdl.handle.net/10722/359317-
dc.description.abstract<p>Ants originated over 150 million years ago through an irreversible transition to superorganismal colony life. Comparative analyses of 163 ant genomes, including newly generated whole-genome sequences of 145 ant species, reveal extensive genome rearrangements correlated with speciation rates. Meanwhile, conserved syntenic blocks are enriched with co-expressed genes involved in basal metabolism and caste differentiation. Gene families related to digestion, endocrine signaling, cuticular hydrocarbon synthesis, and chemoreception expanded in the ant ancestor, while many caste-associated genes underwent positive selection in the formicoid ancestor. Elaborations and reductions of queen-worker dimorphism and other social traits left convergent signatures of intensified or relaxed selection in conserved signaling and metabolic pathways, suggesting that a core gene set was used to diversify organizational complexity. Previously uncharacterized genetic regulators of caste development were confirmed by functional experiments. This study reconstructs the genetic underpinning of social traits and their integration within gene-regulatory networks shaping caste phenotypes.</p>-
dc.languageeng-
dc.publisherElsevier-
dc.relation.ispartofCell-
dc.rightsThis work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.-
dc.subjectcaste differentiation-
dc.subjectformicidae-
dc.subjectgene-regulatory networks-
dc.subjectgenome evolution-
dc.subjectMAPK/insulin/JH pathways-
dc.subjectphylogenomics-
dc.subjectreproductive division of labor-
dc.subjectselection signatures-
dc.subjectsuperorganismal colonies-
dc.subjectsynteny-
dc.titleAdaptive radiation and social evolution of the ants-
dc.typeArticle-
dc.identifier.doi10.1016/j.cell.2025.05.030-
dc.identifier.scopuseid_2-s2.0-105008570750-
dc.identifier.eissn1097-4172-
dc.identifier.issnl0092-8674-

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