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Circadian clock mechanism driving mammalian photoperiodism
The annual photoperiod cycle provides the critical environmental cue synchronizing rhythms of life in seasonal habitats. In 1936, Bünning proposed a circadian-based coincidence timer for photoperiodic synchronization in plants. Formal studies support the universality of this so-called coincidence ti...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7453030/ https://www.ncbi.nlm.nih.gov/pubmed/32855407 http://dx.doi.org/10.1038/s41467-020-18061-z |
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author | Wood, S. H. Hindle, M. M. Mizoro, Y. Cheng, Y. Saer, B. R. C. Miedzinska, K. Christian, H. C. Begley, N. McNeilly, J. McNeilly, A. S. Meddle, S. L. Burt, D. W. Loudon, A. S. I. |
author_facet | Wood, S. H. Hindle, M. M. Mizoro, Y. Cheng, Y. Saer, B. R. C. Miedzinska, K. Christian, H. C. Begley, N. McNeilly, J. McNeilly, A. S. Meddle, S. L. Burt, D. W. Loudon, A. S. I. |
author_sort | Wood, S. H. |
collection | PubMed |
description | The annual photoperiod cycle provides the critical environmental cue synchronizing rhythms of life in seasonal habitats. In 1936, Bünning proposed a circadian-based coincidence timer for photoperiodic synchronization in plants. Formal studies support the universality of this so-called coincidence timer, but we lack understanding of the mechanisms involved. Here we show in mammals that long photoperiods induce the circadian transcription factor BMAL2, in the pars tuberalis of the pituitary, and triggers summer biology through the eyes absent/thyrotrophin (EYA3/TSH) pathway. Conversely, long-duration melatonin signals on short photoperiods induce circadian repressors including DEC1, suppressing BMAL2 and the EYA3/TSH pathway, triggering winter biology. These actions are associated with progressive genome-wide changes in chromatin state, elaborating the effect of the circadian coincidence timer. Hence, circadian clock-pituitary epigenetic pathway interactions form the basis of the mammalian coincidence timer mechanism. Our results constitute a blueprint for circadian-based seasonal timekeeping in vertebrates. |
format | Online Article Text |
id | pubmed-7453030 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-74530302020-09-04 Circadian clock mechanism driving mammalian photoperiodism Wood, S. H. Hindle, M. M. Mizoro, Y. Cheng, Y. Saer, B. R. C. Miedzinska, K. Christian, H. C. Begley, N. McNeilly, J. McNeilly, A. S. Meddle, S. L. Burt, D. W. Loudon, A. S. I. Nat Commun Article The annual photoperiod cycle provides the critical environmental cue synchronizing rhythms of life in seasonal habitats. In 1936, Bünning proposed a circadian-based coincidence timer for photoperiodic synchronization in plants. Formal studies support the universality of this so-called coincidence timer, but we lack understanding of the mechanisms involved. Here we show in mammals that long photoperiods induce the circadian transcription factor BMAL2, in the pars tuberalis of the pituitary, and triggers summer biology through the eyes absent/thyrotrophin (EYA3/TSH) pathway. Conversely, long-duration melatonin signals on short photoperiods induce circadian repressors including DEC1, suppressing BMAL2 and the EYA3/TSH pathway, triggering winter biology. These actions are associated with progressive genome-wide changes in chromatin state, elaborating the effect of the circadian coincidence timer. Hence, circadian clock-pituitary epigenetic pathway interactions form the basis of the mammalian coincidence timer mechanism. Our results constitute a blueprint for circadian-based seasonal timekeeping in vertebrates. Nature Publishing Group UK 2020-08-27 /pmc/articles/PMC7453030/ /pubmed/32855407 http://dx.doi.org/10.1038/s41467-020-18061-z Text en © The Author(s) 2020 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 Wood, S. H. Hindle, M. M. Mizoro, Y. Cheng, Y. Saer, B. R. C. Miedzinska, K. Christian, H. C. Begley, N. McNeilly, J. McNeilly, A. S. Meddle, S. L. Burt, D. W. Loudon, A. S. I. Circadian clock mechanism driving mammalian photoperiodism |
title | Circadian clock mechanism driving mammalian photoperiodism |
title_full | Circadian clock mechanism driving mammalian photoperiodism |
title_fullStr | Circadian clock mechanism driving mammalian photoperiodism |
title_full_unstemmed | Circadian clock mechanism driving mammalian photoperiodism |
title_short | Circadian clock mechanism driving mammalian photoperiodism |
title_sort | circadian clock mechanism driving mammalian photoperiodism |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7453030/ https://www.ncbi.nlm.nih.gov/pubmed/32855407 http://dx.doi.org/10.1038/s41467-020-18061-z |
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