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Stage- and sex-specific transcriptome analyses reveal distinctive sensory gene expression patterns in a butterfly
BACKGROUND: Animal behavior is largely driven by the information that animals are able to extract and process from their environment. However, the function and organization of sensory systems often change throughout ontogeny, particularly in animals that undergo indirect development. As an initial s...
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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/PMC8327453/ https://www.ncbi.nlm.nih.gov/pubmed/34340656 http://dx.doi.org/10.1186/s12864-021-07819-4 |
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author | Ernst, David A. Westerman, Erica L. |
author_facet | Ernst, David A. Westerman, Erica L. |
author_sort | Ernst, David A. |
collection | PubMed |
description | BACKGROUND: Animal behavior is largely driven by the information that animals are able to extract and process from their environment. However, the function and organization of sensory systems often change throughout ontogeny, particularly in animals that undergo indirect development. As an initial step toward investigating these ontogenetic changes at the molecular level, we characterized the sensory gene repertoire and examined the expression profiles of genes linked to vision and chemosensation in two life stages of an insect that goes through metamorphosis, the butterfly Bicyclus anynana. RESULTS: Using RNA-seq, we compared gene expression in the heads of late fifth instar larvae and newly eclosed adults that were reared under identical conditions. Over 50 % of all expressed genes were differentially expressed between the two developmental stages, with 4,036 genes upregulated in larval heads and 4,348 genes upregulated in adult heads. In larvae, upregulated vision-related genes were biased toward those involved with eye development, while phototransduction genes dominated the vision genes that were upregulated in adults. Moreover, the majority of the chemosensory genes we identified in the B. anynana genome were differentially expressed between larvae and adults, several of which share homology with genes linked to pheromone detection, host plant recognition, and foraging in other species of Lepidoptera. CONCLUSIONS: These results revealed promising candidates for furthering our understanding of sensory processing and behavior in the disparate developmental stages of butterflies and other animals that undergo metamorphosis. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12864-021-07819-4. |
format | Online Article Text |
id | pubmed-8327453 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-83274532021-08-03 Stage- and sex-specific transcriptome analyses reveal distinctive sensory gene expression patterns in a butterfly Ernst, David A. Westerman, Erica L. BMC Genomics Research BACKGROUND: Animal behavior is largely driven by the information that animals are able to extract and process from their environment. However, the function and organization of sensory systems often change throughout ontogeny, particularly in animals that undergo indirect development. As an initial step toward investigating these ontogenetic changes at the molecular level, we characterized the sensory gene repertoire and examined the expression profiles of genes linked to vision and chemosensation in two life stages of an insect that goes through metamorphosis, the butterfly Bicyclus anynana. RESULTS: Using RNA-seq, we compared gene expression in the heads of late fifth instar larvae and newly eclosed adults that were reared under identical conditions. Over 50 % of all expressed genes were differentially expressed between the two developmental stages, with 4,036 genes upregulated in larval heads and 4,348 genes upregulated in adult heads. In larvae, upregulated vision-related genes were biased toward those involved with eye development, while phototransduction genes dominated the vision genes that were upregulated in adults. Moreover, the majority of the chemosensory genes we identified in the B. anynana genome were differentially expressed between larvae and adults, several of which share homology with genes linked to pheromone detection, host plant recognition, and foraging in other species of Lepidoptera. CONCLUSIONS: These results revealed promising candidates for furthering our understanding of sensory processing and behavior in the disparate developmental stages of butterflies and other animals that undergo metamorphosis. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12864-021-07819-4. BioMed Central 2021-08-02 /pmc/articles/PMC8327453/ /pubmed/34340656 http://dx.doi.org/10.1186/s12864-021-07819-4 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 Ernst, David A. Westerman, Erica L. Stage- and sex-specific transcriptome analyses reveal distinctive sensory gene expression patterns in a butterfly |
title | Stage- and sex-specific transcriptome analyses reveal distinctive sensory gene expression patterns in a butterfly |
title_full | Stage- and sex-specific transcriptome analyses reveal distinctive sensory gene expression patterns in a butterfly |
title_fullStr | Stage- and sex-specific transcriptome analyses reveal distinctive sensory gene expression patterns in a butterfly |
title_full_unstemmed | Stage- and sex-specific transcriptome analyses reveal distinctive sensory gene expression patterns in a butterfly |
title_short | Stage- and sex-specific transcriptome analyses reveal distinctive sensory gene expression patterns in a butterfly |
title_sort | stage- and sex-specific transcriptome analyses reveal distinctive sensory gene expression patterns in a butterfly |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8327453/ https://www.ncbi.nlm.nih.gov/pubmed/34340656 http://dx.doi.org/10.1186/s12864-021-07819-4 |
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