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The genomic basis of circadian and circalunar timing adaptations in a midge

Organisms use endogenous clocks to anticipate regular environmental cycles, such as days and tides. Natural variants resulting in differently timed behaviour or physiology, known as chronotypes in humans, have not been well characterized at the molecular level. We sequenced the genome of Clunio mari...

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Autores principales: Kaiser, Tobias S., Poehn, Birgit, Szkiba, David, Preussner, Marco, Sedlazeck, Fritz J., Zrim, Alexander, Neumann, Tobias, Nguyen, Lam-Tung, Betancourt, Andrea J., Hummel, Thomas, Vogel, Heiko, Dorner, Silke, Heyd, Florian, von Haeseler, Arndt, Tessmar-Raible, Kristin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5133387/
https://www.ncbi.nlm.nih.gov/pubmed/27871090
http://dx.doi.org/10.1038/nature20151
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author Kaiser, Tobias S.
Poehn, Birgit
Szkiba, David
Preussner, Marco
Sedlazeck, Fritz J.
Zrim, Alexander
Neumann, Tobias
Nguyen, Lam-Tung
Betancourt, Andrea J.
Hummel, Thomas
Vogel, Heiko
Dorner, Silke
Heyd, Florian
von Haeseler, Arndt
Tessmar-Raible, Kristin
author_facet Kaiser, Tobias S.
Poehn, Birgit
Szkiba, David
Preussner, Marco
Sedlazeck, Fritz J.
Zrim, Alexander
Neumann, Tobias
Nguyen, Lam-Tung
Betancourt, Andrea J.
Hummel, Thomas
Vogel, Heiko
Dorner, Silke
Heyd, Florian
von Haeseler, Arndt
Tessmar-Raible, Kristin
author_sort Kaiser, Tobias S.
collection PubMed
description Organisms use endogenous clocks to anticipate regular environmental cycles, such as days and tides. Natural variants resulting in differently timed behaviour or physiology, known as chronotypes in humans, have not been well characterized at the molecular level. We sequenced the genome of Clunio marinus, a marine midge whose reproduction is timed by circadian and circalunar clocks. Midges from different locations show strain-specific genetic timing adaptations. We examined genetic variation in five C. marinus strains from different locations and mapped quantitative trait loci for circalunar and circadian chronotypes. The region most strongly associated with circadian chronotypes generates strain-specific differences in the abundance of calcium/calmodulin-dependent kinase II.1 (CaMKII.1) splice variants. As equivalent variants were shown to alter CaMKII activity in Drosophila melanogaster, and C. marinus (Cma)-CaMKII.1 increases the transcriptional activity of the dimer of the circadian proteins Cma-CLOCK and Cma-CYCLE, we suggest that modulation of alternative splicing is a mechanism for natural adaptation in circadian timing. SUPPLEMENTARY INFORMATION: The online version of this article (doi:10.1038/nature20151) contains supplementary material, which is available to authorized users.
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spelling pubmed-51333872017-05-21 The genomic basis of circadian and circalunar timing adaptations in a midge Kaiser, Tobias S. Poehn, Birgit Szkiba, David Preussner, Marco Sedlazeck, Fritz J. Zrim, Alexander Neumann, Tobias Nguyen, Lam-Tung Betancourt, Andrea J. Hummel, Thomas Vogel, Heiko Dorner, Silke Heyd, Florian von Haeseler, Arndt Tessmar-Raible, Kristin Nature Article Organisms use endogenous clocks to anticipate regular environmental cycles, such as days and tides. Natural variants resulting in differently timed behaviour or physiology, known as chronotypes in humans, have not been well characterized at the molecular level. We sequenced the genome of Clunio marinus, a marine midge whose reproduction is timed by circadian and circalunar clocks. Midges from different locations show strain-specific genetic timing adaptations. We examined genetic variation in five C. marinus strains from different locations and mapped quantitative trait loci for circalunar and circadian chronotypes. The region most strongly associated with circadian chronotypes generates strain-specific differences in the abundance of calcium/calmodulin-dependent kinase II.1 (CaMKII.1) splice variants. As equivalent variants were shown to alter CaMKII activity in Drosophila melanogaster, and C. marinus (Cma)-CaMKII.1 increases the transcriptional activity of the dimer of the circadian proteins Cma-CLOCK and Cma-CYCLE, we suggest that modulation of alternative splicing is a mechanism for natural adaptation in circadian timing. SUPPLEMENTARY INFORMATION: The online version of this article (doi:10.1038/nature20151) contains supplementary material, which is available to authorized users. Nature Publishing Group UK 2016-11-21 2016 /pmc/articles/PMC5133387/ /pubmed/27871090 http://dx.doi.org/10.1038/nature20151 Text en © The Author(s) 2016 https://creativecommons.org/licenses/by/4.0/This work is licensed under a Creative Commons Attribution 4.0 International (CC BY 4.0) licence. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons licence, users will need to obtain permission from the licence holder to reproduce the material. To view a copy of this licence, visit https://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Kaiser, Tobias S.
Poehn, Birgit
Szkiba, David
Preussner, Marco
Sedlazeck, Fritz J.
Zrim, Alexander
Neumann, Tobias
Nguyen, Lam-Tung
Betancourt, Andrea J.
Hummel, Thomas
Vogel, Heiko
Dorner, Silke
Heyd, Florian
von Haeseler, Arndt
Tessmar-Raible, Kristin
The genomic basis of circadian and circalunar timing adaptations in a midge
title The genomic basis of circadian and circalunar timing adaptations in a midge
title_full The genomic basis of circadian and circalunar timing adaptations in a midge
title_fullStr The genomic basis of circadian and circalunar timing adaptations in a midge
title_full_unstemmed The genomic basis of circadian and circalunar timing adaptations in a midge
title_short The genomic basis of circadian and circalunar timing adaptations in a midge
title_sort genomic basis of circadian and circalunar timing adaptations in a midge
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5133387/
https://www.ncbi.nlm.nih.gov/pubmed/27871090
http://dx.doi.org/10.1038/nature20151
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