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Methylation and gene expression differences between reproductive and sterile bumblebee workers

Phenotypic plasticity is the production of multiple phenotypes from a single genome and is notably observed in social insects. Multiple epigenetic mechanisms have been associated with social insect plasticity, with DNA methylation being explored to the greatest extent. DNA methylation is thought to...

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Autores principales: Marshall, Hollie, Lonsdale, Zoë N., Mallon, Eamonn B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6791180/
https://www.ncbi.nlm.nih.gov/pubmed/31636941
http://dx.doi.org/10.1002/evl3.129
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author Marshall, Hollie
Lonsdale, Zoë N.
Mallon, Eamonn B.
author_facet Marshall, Hollie
Lonsdale, Zoë N.
Mallon, Eamonn B.
author_sort Marshall, Hollie
collection PubMed
description Phenotypic plasticity is the production of multiple phenotypes from a single genome and is notably observed in social insects. Multiple epigenetic mechanisms have been associated with social insect plasticity, with DNA methylation being explored to the greatest extent. DNA methylation is thought to play a role in caste determination in Apis mellifera, and other social insects, but there is limited knowledge on its role in other bee species. In this study, we analyzed whole genome bisulfite sequencing and RNA‐seq data sets from head tissue of reproductive and sterile castes of the eusocial bumblebee Bombus terrestris. We found that genome‐wide methylation in B. terrestris is similar to other holometabolous insects and does not differ between reproductive castes. We did, however, find differentially methylated genes between castes, which are enriched for multiple biological processes including reproduction. However, we found no relationship between differential methylation and differential gene expression or differential exon usage between castes. Our results also indicate high intercolony variation in methylation. These findings suggest that methylation is associated with caste differences but may serve an alternate function, other than direct caste determination in this species. This study provides the first insights into the nature of a bumblebee caste‐specific methylome as well as its interaction with gene expression and caste‐specific alternative splicing, providing greater understanding of the role of methylation in phenotypic plasticity within social bee species. Future experimental work is needed to determine the function of methylation and other epigenetic mechanisms in insects.
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spelling pubmed-67911802019-10-21 Methylation and gene expression differences between reproductive and sterile bumblebee workers Marshall, Hollie Lonsdale, Zoë N. Mallon, Eamonn B. Evol Lett Letters Phenotypic plasticity is the production of multiple phenotypes from a single genome and is notably observed in social insects. Multiple epigenetic mechanisms have been associated with social insect plasticity, with DNA methylation being explored to the greatest extent. DNA methylation is thought to play a role in caste determination in Apis mellifera, and other social insects, but there is limited knowledge on its role in other bee species. In this study, we analyzed whole genome bisulfite sequencing and RNA‐seq data sets from head tissue of reproductive and sterile castes of the eusocial bumblebee Bombus terrestris. We found that genome‐wide methylation in B. terrestris is similar to other holometabolous insects and does not differ between reproductive castes. We did, however, find differentially methylated genes between castes, which are enriched for multiple biological processes including reproduction. However, we found no relationship between differential methylation and differential gene expression or differential exon usage between castes. Our results also indicate high intercolony variation in methylation. These findings suggest that methylation is associated with caste differences but may serve an alternate function, other than direct caste determination in this species. This study provides the first insights into the nature of a bumblebee caste‐specific methylome as well as its interaction with gene expression and caste‐specific alternative splicing, providing greater understanding of the role of methylation in phenotypic plasticity within social bee species. Future experimental work is needed to determine the function of methylation and other epigenetic mechanisms in insects. John Wiley and Sons Inc. 2019-08-05 /pmc/articles/PMC6791180/ /pubmed/31636941 http://dx.doi.org/10.1002/evl3.129 Text en © 2019 The Author(s). Evolution Letters published by Wiley Periodicals, Inc. on behalf of Society for the Study of Evolution (SSE) and European Society for Evolutionary Biology (ESEB). This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Letters
Marshall, Hollie
Lonsdale, Zoë N.
Mallon, Eamonn B.
Methylation and gene expression differences between reproductive and sterile bumblebee workers
title Methylation and gene expression differences between reproductive and sterile bumblebee workers
title_full Methylation and gene expression differences between reproductive and sterile bumblebee workers
title_fullStr Methylation and gene expression differences between reproductive and sterile bumblebee workers
title_full_unstemmed Methylation and gene expression differences between reproductive and sterile bumblebee workers
title_short Methylation and gene expression differences between reproductive and sterile bumblebee workers
title_sort methylation and gene expression differences between reproductive and sterile bumblebee workers
topic Letters
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6791180/
https://www.ncbi.nlm.nih.gov/pubmed/31636941
http://dx.doi.org/10.1002/evl3.129
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