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A natural timeless polymorphism allowing circadian clock synchronization in “white nights”
Daily temporal organisation offers a fitness advantage and is determined by an interplay between environmental rhythms and circadian clocks. While light:dark cycles robustly synchronise circadian clocks, it is not clear how animals experiencing only weak environmental cues deal with this problem. Li...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8971440/ https://www.ncbi.nlm.nih.gov/pubmed/35361756 http://dx.doi.org/10.1038/s41467-022-29293-6 |
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author | Lamaze, Angelique Chen, Chenghao Leleux, Solene Xu, Min George, Rebekah Stanewsky, Ralf |
author_facet | Lamaze, Angelique Chen, Chenghao Leleux, Solene Xu, Min George, Rebekah Stanewsky, Ralf |
author_sort | Lamaze, Angelique |
collection | PubMed |
description | Daily temporal organisation offers a fitness advantage and is determined by an interplay between environmental rhythms and circadian clocks. While light:dark cycles robustly synchronise circadian clocks, it is not clear how animals experiencing only weak environmental cues deal with this problem. Like humans, Drosophila originate in sub-Saharan Africa and spread North up to the polar circle, experiencing long summer days or even constant light (LL). LL disrupts clock function, due to constant activation of CRYPTOCHROME, which induces degradation of the clock protein TIMELESS (TIM), but temperature cycles are able to overcome these deleterious effects of LL. We show here that for this to occur a recently evolved natural timeless allele (ls-tim) is required, encoding the less light-sensitive L-TIM in addition to S-TIM, the only form encoded by the ancient s-tim allele. We show that only ls-tim flies can synchronise their behaviour to semi-natural conditions typical for Northern European summers, suggesting that this functional gain is driving the Northward ls-tim spread. |
format | Online Article Text |
id | pubmed-8971440 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-89714402022-04-20 A natural timeless polymorphism allowing circadian clock synchronization in “white nights” Lamaze, Angelique Chen, Chenghao Leleux, Solene Xu, Min George, Rebekah Stanewsky, Ralf Nat Commun Article Daily temporal organisation offers a fitness advantage and is determined by an interplay between environmental rhythms and circadian clocks. While light:dark cycles robustly synchronise circadian clocks, it is not clear how animals experiencing only weak environmental cues deal with this problem. Like humans, Drosophila originate in sub-Saharan Africa and spread North up to the polar circle, experiencing long summer days or even constant light (LL). LL disrupts clock function, due to constant activation of CRYPTOCHROME, which induces degradation of the clock protein TIMELESS (TIM), but temperature cycles are able to overcome these deleterious effects of LL. We show here that for this to occur a recently evolved natural timeless allele (ls-tim) is required, encoding the less light-sensitive L-TIM in addition to S-TIM, the only form encoded by the ancient s-tim allele. We show that only ls-tim flies can synchronise their behaviour to semi-natural conditions typical for Northern European summers, suggesting that this functional gain is driving the Northward ls-tim spread. Nature Publishing Group UK 2022-03-31 /pmc/articles/PMC8971440/ /pubmed/35361756 http://dx.doi.org/10.1038/s41467-022-29293-6 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Lamaze, Angelique Chen, Chenghao Leleux, Solene Xu, Min George, Rebekah Stanewsky, Ralf A natural timeless polymorphism allowing circadian clock synchronization in “white nights” |
title | A natural timeless polymorphism allowing circadian clock synchronization in “white nights” |
title_full | A natural timeless polymorphism allowing circadian clock synchronization in “white nights” |
title_fullStr | A natural timeless polymorphism allowing circadian clock synchronization in “white nights” |
title_full_unstemmed | A natural timeless polymorphism allowing circadian clock synchronization in “white nights” |
title_short | A natural timeless polymorphism allowing circadian clock synchronization in “white nights” |
title_sort | natural timeless polymorphism allowing circadian clock synchronization in “white nights” |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8971440/ https://www.ncbi.nlm.nih.gov/pubmed/35361756 http://dx.doi.org/10.1038/s41467-022-29293-6 |
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