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Towards reconstructing the ancestral brain gene-network regulating caste differentiation in ants

Specialized queens and life-time unmated workers evolved once in the common ancestor of all ants, but whether caste development across ants continues to be at least partly regulated by a single core set of genes remains obscure. We analysed brain transcriptomes from five ant species (three subfamili...

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Detalles Bibliográficos
Autores principales: Qiu, Bitao, Larsen, Rasmus Stenbak, Chang, Ni-Chen, Wang, John, Boomsma, Jacobus J., Zhang, Guojie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6217981/
https://www.ncbi.nlm.nih.gov/pubmed/30349091
http://dx.doi.org/10.1038/s41559-018-0689-x
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author Qiu, Bitao
Larsen, Rasmus Stenbak
Chang, Ni-Chen
Wang, John
Boomsma, Jacobus J.
Zhang, Guojie
author_facet Qiu, Bitao
Larsen, Rasmus Stenbak
Chang, Ni-Chen
Wang, John
Boomsma, Jacobus J.
Zhang, Guojie
author_sort Qiu, Bitao
collection PubMed
description Specialized queens and life-time unmated workers evolved once in the common ancestor of all ants, but whether caste development across ants continues to be at least partly regulated by a single core set of genes remains obscure. We analysed brain transcriptomes from five ant species (three subfamilies) and reconstructed the origins of genes with caste-biased expression. Ancient genes predating the Neoptera were more likely to regulate gyne (virgin queen) phenotypes, while caste differentiation roles of younger, ant-lineage-specific genes varied. Transcriptome profiling showed that the ancestral network for caste-specific gene-regulation has been maintained, but that signatures of common ancestry are obscured by later modifications. Adjusting for such differences, we identified a core gene-set that: 1. consistently displayed similar directions and degrees of caste-differentiated expression, and 2. have mostly not been reported as being involved in caste differentiation. These core regulatory genes exist in the genomes of ant species that secondarily lost the queen caste, but expression differences for reproductive and sterile workers are minor and similar to social paper wasps that lack differentiated castes. Many caste-biased ant genes have caste-differentiated expression in honeybees, but directions of caste bias were uncorrelated, as expected when permanent castes evolved independently in both lineages.
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spelling pubmed-62179812019-04-22 Towards reconstructing the ancestral brain gene-network regulating caste differentiation in ants Qiu, Bitao Larsen, Rasmus Stenbak Chang, Ni-Chen Wang, John Boomsma, Jacobus J. Zhang, Guojie Nat Ecol Evol Article Specialized queens and life-time unmated workers evolved once in the common ancestor of all ants, but whether caste development across ants continues to be at least partly regulated by a single core set of genes remains obscure. We analysed brain transcriptomes from five ant species (three subfamilies) and reconstructed the origins of genes with caste-biased expression. Ancient genes predating the Neoptera were more likely to regulate gyne (virgin queen) phenotypes, while caste differentiation roles of younger, ant-lineage-specific genes varied. Transcriptome profiling showed that the ancestral network for caste-specific gene-regulation has been maintained, but that signatures of common ancestry are obscured by later modifications. Adjusting for such differences, we identified a core gene-set that: 1. consistently displayed similar directions and degrees of caste-differentiated expression, and 2. have mostly not been reported as being involved in caste differentiation. These core regulatory genes exist in the genomes of ant species that secondarily lost the queen caste, but expression differences for reproductive and sterile workers are minor and similar to social paper wasps that lack differentiated castes. Many caste-biased ant genes have caste-differentiated expression in honeybees, but directions of caste bias were uncorrelated, as expected when permanent castes evolved independently in both lineages. 2018-10-22 2018-11 /pmc/articles/PMC6217981/ /pubmed/30349091 http://dx.doi.org/10.1038/s41559-018-0689-x Text en Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use:http://www.nature.com/authors/editorial_policies/license.html#terms
spellingShingle Article
Qiu, Bitao
Larsen, Rasmus Stenbak
Chang, Ni-Chen
Wang, John
Boomsma, Jacobus J.
Zhang, Guojie
Towards reconstructing the ancestral brain gene-network regulating caste differentiation in ants
title Towards reconstructing the ancestral brain gene-network regulating caste differentiation in ants
title_full Towards reconstructing the ancestral brain gene-network regulating caste differentiation in ants
title_fullStr Towards reconstructing the ancestral brain gene-network regulating caste differentiation in ants
title_full_unstemmed Towards reconstructing the ancestral brain gene-network regulating caste differentiation in ants
title_short Towards reconstructing the ancestral brain gene-network regulating caste differentiation in ants
title_sort towards reconstructing the ancestral brain gene-network regulating caste differentiation in ants
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6217981/
https://www.ncbi.nlm.nih.gov/pubmed/30349091
http://dx.doi.org/10.1038/s41559-018-0689-x
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