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Transcriptional regulation underlying the temperature response of embryonic development rate in the winter moth
Climate change will strongly affect the developmental timing of insects, as their development rate depends largely on ambient temperature. However, we know little about the genetic mechanisms underlying the temperature sensitivity of embryonic development in insects. We investigated embryonic develo...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9828122/ https://www.ncbi.nlm.nih.gov/pubmed/36161402 http://dx.doi.org/10.1111/mec.16705 |
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author | van Dis, Natalie E. Risse, Judith E. Pijl, Agata S. Hut, Roelof A. Visser, Marcel E. Wertheim, Bregje |
author_facet | van Dis, Natalie E. Risse, Judith E. Pijl, Agata S. Hut, Roelof A. Visser, Marcel E. Wertheim, Bregje |
author_sort | van Dis, Natalie E. |
collection | PubMed |
description | Climate change will strongly affect the developmental timing of insects, as their development rate depends largely on ambient temperature. However, we know little about the genetic mechanisms underlying the temperature sensitivity of embryonic development in insects. We investigated embryonic development rate in the winter moth (Operophtera brumata), a species with egg dormancy which has been under selection due to climate change. We used RNA sequencing to investigate which genes are involved in the regulation of winter moth embryonic development rate in response to temperature. Over the course of development, we sampled eggs before and after an experimental change in ambient temperature, including two early development weeks when the temperature sensitivity of eggs is low and two late development weeks when temperature sensitivity is high. We found temperature‐responsive genes that responded in a similar way across development, as well as genes with a temperature response specific to a particular development week. Moreover, we identified genes whose temperature effect size changed around the switch in temperature sensitivity of development rate. Interesting candidate genes for regulating the temperature sensitivity of egg development rate included genes involved in histone modification, hormonal signalling, nervous system development and circadian clock genes. The diverse sets of temperature‐responsive genes we found here indicate that there are many potential targets of selection to change the temperature sensitivity of embryonic development rate. Identifying for which of these genes there is genetic variation in wild insect populations will give insight into their adaptive potential in the face of climate change. |
format | Online Article Text |
id | pubmed-9828122 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-98281222023-01-10 Transcriptional regulation underlying the temperature response of embryonic development rate in the winter moth van Dis, Natalie E. Risse, Judith E. Pijl, Agata S. Hut, Roelof A. Visser, Marcel E. Wertheim, Bregje Mol Ecol ORIGINAL ARTICLES Climate change will strongly affect the developmental timing of insects, as their development rate depends largely on ambient temperature. However, we know little about the genetic mechanisms underlying the temperature sensitivity of embryonic development in insects. We investigated embryonic development rate in the winter moth (Operophtera brumata), a species with egg dormancy which has been under selection due to climate change. We used RNA sequencing to investigate which genes are involved in the regulation of winter moth embryonic development rate in response to temperature. Over the course of development, we sampled eggs before and after an experimental change in ambient temperature, including two early development weeks when the temperature sensitivity of eggs is low and two late development weeks when temperature sensitivity is high. We found temperature‐responsive genes that responded in a similar way across development, as well as genes with a temperature response specific to a particular development week. Moreover, we identified genes whose temperature effect size changed around the switch in temperature sensitivity of development rate. Interesting candidate genes for regulating the temperature sensitivity of egg development rate included genes involved in histone modification, hormonal signalling, nervous system development and circadian clock genes. The diverse sets of temperature‐responsive genes we found here indicate that there are many potential targets of selection to change the temperature sensitivity of embryonic development rate. Identifying for which of these genes there is genetic variation in wild insect populations will give insight into their adaptive potential in the face of climate change. John Wiley and Sons Inc. 2022-10-06 2022-11 /pmc/articles/PMC9828122/ /pubmed/36161402 http://dx.doi.org/10.1111/mec.16705 Text en © 2022 The Authors. Molecular Ecology published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes. |
spellingShingle | ORIGINAL ARTICLES van Dis, Natalie E. Risse, Judith E. Pijl, Agata S. Hut, Roelof A. Visser, Marcel E. Wertheim, Bregje Transcriptional regulation underlying the temperature response of embryonic development rate in the winter moth |
title | Transcriptional regulation underlying the temperature response of embryonic development rate in the winter moth |
title_full | Transcriptional regulation underlying the temperature response of embryonic development rate in the winter moth |
title_fullStr | Transcriptional regulation underlying the temperature response of embryonic development rate in the winter moth |
title_full_unstemmed | Transcriptional regulation underlying the temperature response of embryonic development rate in the winter moth |
title_short | Transcriptional regulation underlying the temperature response of embryonic development rate in the winter moth |
title_sort | transcriptional regulation underlying the temperature response of embryonic development rate in the winter moth |
topic | ORIGINAL ARTICLES |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9828122/ https://www.ncbi.nlm.nih.gov/pubmed/36161402 http://dx.doi.org/10.1111/mec.16705 |
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