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A photoperiodic time measurement served by the biphasic expression of Cryptochrome1ab in the zebrafish eye

The zebrafish (Danio rerio) is a model species that is used to study the circadian clock. It possesses light-entrainable circadian clocks in both central and peripheral tissues, and its core circadian factor cryptochromes (CRYs) have diverged significantly during evolution. In order to elucidate the...

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Autores principales: Okano, Keiko, Saratani, Yuya, Tamasawa, Ayumi, Shoji, Yosuke, Toda, Riko, Okano, Toshiyuki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7081220/
https://www.ncbi.nlm.nih.gov/pubmed/32193419
http://dx.doi.org/10.1038/s41598-020-61877-4
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author Okano, Keiko
Saratani, Yuya
Tamasawa, Ayumi
Shoji, Yosuke
Toda, Riko
Okano, Toshiyuki
author_facet Okano, Keiko
Saratani, Yuya
Tamasawa, Ayumi
Shoji, Yosuke
Toda, Riko
Okano, Toshiyuki
author_sort Okano, Keiko
collection PubMed
description The zebrafish (Danio rerio) is a model species that is used to study the circadian clock. It possesses light-entrainable circadian clocks in both central and peripheral tissues, and its core circadian factor cryptochromes (CRYs) have diverged significantly during evolution. In order to elucidate the functional diversity and involvement of CRYs in photoperiodic mechanisms, we investigated the daily expression profiles of six Cry transcripts in central (brain and eye) and peripheral (fin, skin and muscle) tissues. The zCry genes exhibited gene-specific diurnal conserved variations, and were divided into morning and evening groups. Notably, zCry1ab exhibited biphasic expression profiles in the eye, with peaks in the morning and evening. Comparing ocular zCry1ab expression in different photoperiods (18L:6D, 14L:10D, 10L:14D and 6L:18D) revealed that zCry1ab expression duration changed depending on the photoperiod: it increased at midnight and peaked before lights off. zCry1ab expression in constant light or dark after entrainment under long- or short-day conditions suggested that the evening clock and photic input pathway are involved in photoperiod-dependent zCry1ab expression. Laser microdissection followed by qRT-PCR analysis showed that the evening peak of zCry1ab was likely ascribed to visual photoreceptors. These results suggest the presence of an eye-specific photoperiodic time measurement served by zCry1ab.
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spelling pubmed-70812202020-03-23 A photoperiodic time measurement served by the biphasic expression of Cryptochrome1ab in the zebrafish eye Okano, Keiko Saratani, Yuya Tamasawa, Ayumi Shoji, Yosuke Toda, Riko Okano, Toshiyuki Sci Rep Article The zebrafish (Danio rerio) is a model species that is used to study the circadian clock. It possesses light-entrainable circadian clocks in both central and peripheral tissues, and its core circadian factor cryptochromes (CRYs) have diverged significantly during evolution. In order to elucidate the functional diversity and involvement of CRYs in photoperiodic mechanisms, we investigated the daily expression profiles of six Cry transcripts in central (brain and eye) and peripheral (fin, skin and muscle) tissues. The zCry genes exhibited gene-specific diurnal conserved variations, and were divided into morning and evening groups. Notably, zCry1ab exhibited biphasic expression profiles in the eye, with peaks in the morning and evening. Comparing ocular zCry1ab expression in different photoperiods (18L:6D, 14L:10D, 10L:14D and 6L:18D) revealed that zCry1ab expression duration changed depending on the photoperiod: it increased at midnight and peaked before lights off. zCry1ab expression in constant light or dark after entrainment under long- or short-day conditions suggested that the evening clock and photic input pathway are involved in photoperiod-dependent zCry1ab expression. Laser microdissection followed by qRT-PCR analysis showed that the evening peak of zCry1ab was likely ascribed to visual photoreceptors. These results suggest the presence of an eye-specific photoperiodic time measurement served by zCry1ab. Nature Publishing Group UK 2020-03-19 /pmc/articles/PMC7081220/ /pubmed/32193419 http://dx.doi.org/10.1038/s41598-020-61877-4 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
Okano, Keiko
Saratani, Yuya
Tamasawa, Ayumi
Shoji, Yosuke
Toda, Riko
Okano, Toshiyuki
A photoperiodic time measurement served by the biphasic expression of Cryptochrome1ab in the zebrafish eye
title A photoperiodic time measurement served by the biphasic expression of Cryptochrome1ab in the zebrafish eye
title_full A photoperiodic time measurement served by the biphasic expression of Cryptochrome1ab in the zebrafish eye
title_fullStr A photoperiodic time measurement served by the biphasic expression of Cryptochrome1ab in the zebrafish eye
title_full_unstemmed A photoperiodic time measurement served by the biphasic expression of Cryptochrome1ab in the zebrafish eye
title_short A photoperiodic time measurement served by the biphasic expression of Cryptochrome1ab in the zebrafish eye
title_sort photoperiodic time measurement served by the biphasic expression of cryptochrome1ab in the zebrafish eye
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7081220/
https://www.ncbi.nlm.nih.gov/pubmed/32193419
http://dx.doi.org/10.1038/s41598-020-61877-4
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