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Female developmental environment delays development of male honeybee (Apis mellifera)
BACKGROUND: Nutrition and cell size play an important role in the determination of caste differentiation in queen and worker of honeybees (Apis mellifera), whereas the haploid genome dominates the differentiation of drones. However, the effects of female developmental environment on the development...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8477528/ https://www.ncbi.nlm.nih.gov/pubmed/34579651 http://dx.doi.org/10.1186/s12864-021-08014-1 |
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author | Liu, Yi Bo Yi, Yao Abdelmawla, Amal Zheng, Yun Lin Zeng, Zhi Jiang He, Xu Jiang |
author_facet | Liu, Yi Bo Yi, Yao Abdelmawla, Amal Zheng, Yun Lin Zeng, Zhi Jiang He, Xu Jiang |
author_sort | Liu, Yi Bo |
collection | PubMed |
description | BACKGROUND: Nutrition and cell size play an important role in the determination of caste differentiation in queen and worker of honeybees (Apis mellifera), whereas the haploid genome dominates the differentiation of drones. However, the effects of female developmental environment on the development of males remain unclear. In this study, young drone larvae were transferred into worker cells (WCs) or remained in drone cells (DCs) to rear drones. The drone larvae were also grafted into queen cells (QCs) for 48 h and then transplanted into drone cells until emerging. Morphological indexes and reproductive organs of these three types of newly emerged drones were measured. Newly emerged drones and third instar drone larvae from WCs, DCs and QCs were sequenced by RNA sequencing (RNA-Seq). RESULTS: The amount of food remaining in cells of the QC and WC groups was significantly different to that in the DC group at the early larval stage. Morphological results showed that newly emerged DC drones had bigger body sizes and more well-developed reproductive tissues than WC and QC drones, whereas the reproductive tissues of QC drones were larger than those of WC drones. Additionally, whole body gene expression results showed a clear difference among three groups. At larval stage there were 889, 1761 and 1927 significantly differentially expressed genes (DEGs) in WC/DC, QC/DC and WC/QC comparisons, respectively. The number of DEGs decreased in adult drones of these three comparisons [678 (WC/DC), 338 (QC/DC) and 518 (WC/QC)]. A high number of DEGs were involved in sex differentiation, growth, olfaction, vision, mammalian target of rapamycin (mTOR), Wnt signaling pathways, and other processes. CONCLUSIONS: This study demonstrated that the developmental environment of honeybee females can delay male development, which may serve as a model for understanding the regulation of sex differentiation and male development in social insects by environmental factors. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12864-021-08014-1. |
format | Online Article Text |
id | pubmed-8477528 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-84775282021-09-28 Female developmental environment delays development of male honeybee (Apis mellifera) Liu, Yi Bo Yi, Yao Abdelmawla, Amal Zheng, Yun Lin Zeng, Zhi Jiang He, Xu Jiang BMC Genomics Research Article BACKGROUND: Nutrition and cell size play an important role in the determination of caste differentiation in queen and worker of honeybees (Apis mellifera), whereas the haploid genome dominates the differentiation of drones. However, the effects of female developmental environment on the development of males remain unclear. In this study, young drone larvae were transferred into worker cells (WCs) or remained in drone cells (DCs) to rear drones. The drone larvae were also grafted into queen cells (QCs) for 48 h and then transplanted into drone cells until emerging. Morphological indexes and reproductive organs of these three types of newly emerged drones were measured. Newly emerged drones and third instar drone larvae from WCs, DCs and QCs were sequenced by RNA sequencing (RNA-Seq). RESULTS: The amount of food remaining in cells of the QC and WC groups was significantly different to that in the DC group at the early larval stage. Morphological results showed that newly emerged DC drones had bigger body sizes and more well-developed reproductive tissues than WC and QC drones, whereas the reproductive tissues of QC drones were larger than those of WC drones. Additionally, whole body gene expression results showed a clear difference among three groups. At larval stage there were 889, 1761 and 1927 significantly differentially expressed genes (DEGs) in WC/DC, QC/DC and WC/QC comparisons, respectively. The number of DEGs decreased in adult drones of these three comparisons [678 (WC/DC), 338 (QC/DC) and 518 (WC/QC)]. A high number of DEGs were involved in sex differentiation, growth, olfaction, vision, mammalian target of rapamycin (mTOR), Wnt signaling pathways, and other processes. CONCLUSIONS: This study demonstrated that the developmental environment of honeybee females can delay male development, which may serve as a model for understanding the regulation of sex differentiation and male development in social insects by environmental factors. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12864-021-08014-1. BioMed Central 2021-09-27 /pmc/articles/PMC8477528/ /pubmed/34579651 http://dx.doi.org/10.1186/s12864-021-08014-1 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Article Liu, Yi Bo Yi, Yao Abdelmawla, Amal Zheng, Yun Lin Zeng, Zhi Jiang He, Xu Jiang Female developmental environment delays development of male honeybee (Apis mellifera) |
title | Female developmental environment delays development of male honeybee (Apis mellifera) |
title_full | Female developmental environment delays development of male honeybee (Apis mellifera) |
title_fullStr | Female developmental environment delays development of male honeybee (Apis mellifera) |
title_full_unstemmed | Female developmental environment delays development of male honeybee (Apis mellifera) |
title_short | Female developmental environment delays development of male honeybee (Apis mellifera) |
title_sort | female developmental environment delays development of male honeybee (apis mellifera) |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8477528/ https://www.ncbi.nlm.nih.gov/pubmed/34579651 http://dx.doi.org/10.1186/s12864-021-08014-1 |
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