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Diapause vs. reproductive programs: transcriptional phenotypes in a keystone copepod

Many arthropods undergo a seasonal dormancy termed “diapause” to optimize timing of reproduction in highly seasonal environments. In the North Atlantic, the copepod Calanus finmarchicus completes one to three generations annually with some individuals maturing into adults, while others interrupt the...

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Autores principales: Lenz, Petra H., Roncalli, Vittoria, Cieslak, Matthew C., Tarrant, Ann M., Castelfranco, Ann M., Hartline, Daniel K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8007741/
https://www.ncbi.nlm.nih.gov/pubmed/33782539
http://dx.doi.org/10.1038/s42003-021-01946-0
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author Lenz, Petra H.
Roncalli, Vittoria
Cieslak, Matthew C.
Tarrant, Ann M.
Castelfranco, Ann M.
Hartline, Daniel K.
author_facet Lenz, Petra H.
Roncalli, Vittoria
Cieslak, Matthew C.
Tarrant, Ann M.
Castelfranco, Ann M.
Hartline, Daniel K.
author_sort Lenz, Petra H.
collection PubMed
description Many arthropods undergo a seasonal dormancy termed “diapause” to optimize timing of reproduction in highly seasonal environments. In the North Atlantic, the copepod Calanus finmarchicus completes one to three generations annually with some individuals maturing into adults, while others interrupt their development to enter diapause. It is unknown which, why and when individuals enter the diapause program. Transcriptomic data from copepods on known programs were analyzed using dimensionality reduction of gene expression and functional analyses to identify program-specific genes and biological processes. These analyses elucidated physiological differences and established protocols that distinguish between programs. Differences in gene expression were associated with maturation of individuals on the reproductive program, while those on the diapause program showed little change over time. Only two of six filters effectively separated copepods by developmental program. The first one included all genes annotated to RNA metabolism and this was confirmed using differential gene expression analysis. The second filter identified 54 differentially expressed genes that were consistently up-regulated in individuals on the diapause program in comparison with those on the reproductive program. Annotated to oogenesis, RNA metabolism and fatty acid biosynthesis, these genes are both indicators for diapause preparation and good candidates for functional studies.
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spelling pubmed-80077412021-04-16 Diapause vs. reproductive programs: transcriptional phenotypes in a keystone copepod Lenz, Petra H. Roncalli, Vittoria Cieslak, Matthew C. Tarrant, Ann M. Castelfranco, Ann M. Hartline, Daniel K. Commun Biol Article Many arthropods undergo a seasonal dormancy termed “diapause” to optimize timing of reproduction in highly seasonal environments. In the North Atlantic, the copepod Calanus finmarchicus completes one to three generations annually with some individuals maturing into adults, while others interrupt their development to enter diapause. It is unknown which, why and when individuals enter the diapause program. Transcriptomic data from copepods on known programs were analyzed using dimensionality reduction of gene expression and functional analyses to identify program-specific genes and biological processes. These analyses elucidated physiological differences and established protocols that distinguish between programs. Differences in gene expression were associated with maturation of individuals on the reproductive program, while those on the diapause program showed little change over time. Only two of six filters effectively separated copepods by developmental program. The first one included all genes annotated to RNA metabolism and this was confirmed using differential gene expression analysis. The second filter identified 54 differentially expressed genes that were consistently up-regulated in individuals on the diapause program in comparison with those on the reproductive program. Annotated to oogenesis, RNA metabolism and fatty acid biosynthesis, these genes are both indicators for diapause preparation and good candidates for functional studies. Nature Publishing Group UK 2021-03-29 /pmc/articles/PMC8007741/ /pubmed/33782539 http://dx.doi.org/10.1038/s42003-021-01946-0 Text en © The Author(s) 2021 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
Lenz, Petra H.
Roncalli, Vittoria
Cieslak, Matthew C.
Tarrant, Ann M.
Castelfranco, Ann M.
Hartline, Daniel K.
Diapause vs. reproductive programs: transcriptional phenotypes in a keystone copepod
title Diapause vs. reproductive programs: transcriptional phenotypes in a keystone copepod
title_full Diapause vs. reproductive programs: transcriptional phenotypes in a keystone copepod
title_fullStr Diapause vs. reproductive programs: transcriptional phenotypes in a keystone copepod
title_full_unstemmed Diapause vs. reproductive programs: transcriptional phenotypes in a keystone copepod
title_short Diapause vs. reproductive programs: transcriptional phenotypes in a keystone copepod
title_sort diapause vs. reproductive programs: transcriptional phenotypes in a keystone copepod
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8007741/
https://www.ncbi.nlm.nih.gov/pubmed/33782539
http://dx.doi.org/10.1038/s42003-021-01946-0
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