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Neural activity mapping of bumble bee (Bombus ignitus) brains during foraging flight using immediate early genes
Honey bees and bumble bees belong to the same family (Apidae) and their workers exhibit a division of labor, but the style of division of labor differs between species. The molecular and neural bases of the species-specific social behaviors of Apidae workers have not been analyzed. Here, we focused...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7217898/ https://www.ncbi.nlm.nih.gov/pubmed/32398802 http://dx.doi.org/10.1038/s41598-020-64701-1 |
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author | Iino, Shiori Shiota, Yurika Nishimura, Masakazu Asada, Shinichi Ono, Masato Kubo, Takeo |
author_facet | Iino, Shiori Shiota, Yurika Nishimura, Masakazu Asada, Shinichi Ono, Masato Kubo, Takeo |
author_sort | Iino, Shiori |
collection | PubMed |
description | Honey bees and bumble bees belong to the same family (Apidae) and their workers exhibit a division of labor, but the style of division of labor differs between species. The molecular and neural bases of the species-specific social behaviors of Apidae workers have not been analyzed. Here, we focused on two immediate early genes, hormone receptor 38 (HR38) and early growth response gene-1 (Egr1), and late-upregulated ecdysone receptor (EcR), all of which are upregulated by foraging flight and expressed preferentially in the small-type Kenyon cells of the mushroom bodies (MBs) in the honey bee brain. Gene expression analyses in Bombus ignitus revealed that HR38 and Egr1, but not EcR, exhibited an immediate early response during awakening from CO(2) anesthesia. Both premature mRNA for HR38 and mature mRNA for Egr1 were induced during foraging flight, and mRNAs for HR38 and Egr1 were sparsely detected inside the whole MB calyces. In contrast, EcR expression was higher in forager brains than in nurse bees and was expressed preferentially in the small-type Kenyon cells inside the MBs. Our findings suggest that Kenyon cells are active during foraging flight and that the function of late-upregulated EcR in the brain is conserved among these Apidae species. |
format | Online Article Text |
id | pubmed-7217898 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-72178982020-05-19 Neural activity mapping of bumble bee (Bombus ignitus) brains during foraging flight using immediate early genes Iino, Shiori Shiota, Yurika Nishimura, Masakazu Asada, Shinichi Ono, Masato Kubo, Takeo Sci Rep Article Honey bees and bumble bees belong to the same family (Apidae) and their workers exhibit a division of labor, but the style of division of labor differs between species. The molecular and neural bases of the species-specific social behaviors of Apidae workers have not been analyzed. Here, we focused on two immediate early genes, hormone receptor 38 (HR38) and early growth response gene-1 (Egr1), and late-upregulated ecdysone receptor (EcR), all of which are upregulated by foraging flight and expressed preferentially in the small-type Kenyon cells of the mushroom bodies (MBs) in the honey bee brain. Gene expression analyses in Bombus ignitus revealed that HR38 and Egr1, but not EcR, exhibited an immediate early response during awakening from CO(2) anesthesia. Both premature mRNA for HR38 and mature mRNA for Egr1 were induced during foraging flight, and mRNAs for HR38 and Egr1 were sparsely detected inside the whole MB calyces. In contrast, EcR expression was higher in forager brains than in nurse bees and was expressed preferentially in the small-type Kenyon cells inside the MBs. Our findings suggest that Kenyon cells are active during foraging flight and that the function of late-upregulated EcR in the brain is conserved among these Apidae species. Nature Publishing Group UK 2020-05-12 /pmc/articles/PMC7217898/ /pubmed/32398802 http://dx.doi.org/10.1038/s41598-020-64701-1 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Iino, Shiori Shiota, Yurika Nishimura, Masakazu Asada, Shinichi Ono, Masato Kubo, Takeo Neural activity mapping of bumble bee (Bombus ignitus) brains during foraging flight using immediate early genes |
title | Neural activity mapping of bumble bee (Bombus ignitus) brains during foraging flight using immediate early genes |
title_full | Neural activity mapping of bumble bee (Bombus ignitus) brains during foraging flight using immediate early genes |
title_fullStr | Neural activity mapping of bumble bee (Bombus ignitus) brains during foraging flight using immediate early genes |
title_full_unstemmed | Neural activity mapping of bumble bee (Bombus ignitus) brains during foraging flight using immediate early genes |
title_short | Neural activity mapping of bumble bee (Bombus ignitus) brains during foraging flight using immediate early genes |
title_sort | neural activity mapping of bumble bee (bombus ignitus) brains during foraging flight using immediate early genes |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7217898/ https://www.ncbi.nlm.nih.gov/pubmed/32398802 http://dx.doi.org/10.1038/s41598-020-64701-1 |
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