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Photoperiodic diapause under the control of circadian clock genes in an insect

BACKGROUND: Most organisms have evolved a circadian clock in order to anticipate daily environmental changes and many of these organisms are also capable of sophisticated measurement of daylength (photoperiodism) that is used to regulate seasonal events such as diapause, migration and polymorphism....

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Autores principales: Ikeno, Tomoko, Tanaka, Shinichi I, Numata, Hideharu, Goto, Shin G
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2942818/
https://www.ncbi.nlm.nih.gov/pubmed/20815865
http://dx.doi.org/10.1186/1741-7007-8-116
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author Ikeno, Tomoko
Tanaka, Shinichi I
Numata, Hideharu
Goto, Shin G
author_facet Ikeno, Tomoko
Tanaka, Shinichi I
Numata, Hideharu
Goto, Shin G
author_sort Ikeno, Tomoko
collection PubMed
description BACKGROUND: Most organisms have evolved a circadian clock in order to anticipate daily environmental changes and many of these organisms are also capable of sophisticated measurement of daylength (photoperiodism) that is used to regulate seasonal events such as diapause, migration and polymorphism. It has been generally accepted that the same elements are involved in both circadian (daily) and seasonal (annual) rhythms because both rely upon daily light-dark cycles. However, as reasonable as this sounds, there remains no conclusive evidence of such a molecular machinery in insects. We have approached this issue by using RNA interference (RNAi) in Riptortus pedestris. RESULTS: The cuticle deposition rhythm exhibited the major properties of circadian rhythms, indicating that the rhythm is regulated by a circadian clock. RNAi directed against the circadian clock genes of period and cycle, which are negative and positive regulators in the circadian clock, respectively, disrupted the cuticle deposition rhythm and distinct cuticle layers were produced by these RNAi. Simultaneously, period RNAi caused the insect to avert diapause under a diapause-inducing photoperiod whereas cycle RNAi induced diapause under a diapause-averting photoperiod. The expression patterns of juvenile hormone-regulated genes and the application of juvenile hormone analogue suggested that neither ovarian development itself nor a downstream cascade of juvenile hormone secretion, were disturbed by period and cycle RNAi. CONCLUSIONS: This study revealed that the circadian clock genes are crucial not only for daily rhythms but also for photoperiodic diapause. RNAi directed against period and cycle had opposite effects not only in the circadian cuticle deposition rhythm but also in the photoperiodic diapause. These RNAi also had opposite effects on juvenile hormone-regulated gene expression. It is still possible that the circadian clock genes pleiotropically affect ovarian development but, based on these results, we suggest that the circadian clock operated by the circadian clock genes, period and cycle, governs seasonal timing as well as the daily rhythms. See Commentary: http://www.biomedcentral.com/1741-7007/8/115
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spelling pubmed-29428182010-09-21 Photoperiodic diapause under the control of circadian clock genes in an insect Ikeno, Tomoko Tanaka, Shinichi I Numata, Hideharu Goto, Shin G BMC Biol Research Article BACKGROUND: Most organisms have evolved a circadian clock in order to anticipate daily environmental changes and many of these organisms are also capable of sophisticated measurement of daylength (photoperiodism) that is used to regulate seasonal events such as diapause, migration and polymorphism. It has been generally accepted that the same elements are involved in both circadian (daily) and seasonal (annual) rhythms because both rely upon daily light-dark cycles. However, as reasonable as this sounds, there remains no conclusive evidence of such a molecular machinery in insects. We have approached this issue by using RNA interference (RNAi) in Riptortus pedestris. RESULTS: The cuticle deposition rhythm exhibited the major properties of circadian rhythms, indicating that the rhythm is regulated by a circadian clock. RNAi directed against the circadian clock genes of period and cycle, which are negative and positive regulators in the circadian clock, respectively, disrupted the cuticle deposition rhythm and distinct cuticle layers were produced by these RNAi. Simultaneously, period RNAi caused the insect to avert diapause under a diapause-inducing photoperiod whereas cycle RNAi induced diapause under a diapause-averting photoperiod. The expression patterns of juvenile hormone-regulated genes and the application of juvenile hormone analogue suggested that neither ovarian development itself nor a downstream cascade of juvenile hormone secretion, were disturbed by period and cycle RNAi. CONCLUSIONS: This study revealed that the circadian clock genes are crucial not only for daily rhythms but also for photoperiodic diapause. RNAi directed against period and cycle had opposite effects not only in the circadian cuticle deposition rhythm but also in the photoperiodic diapause. These RNAi also had opposite effects on juvenile hormone-regulated gene expression. It is still possible that the circadian clock genes pleiotropically affect ovarian development but, based on these results, we suggest that the circadian clock operated by the circadian clock genes, period and cycle, governs seasonal timing as well as the daily rhythms. See Commentary: http://www.biomedcentral.com/1741-7007/8/115 BioMed Central 2010-09-03 /pmc/articles/PMC2942818/ /pubmed/20815865 http://dx.doi.org/10.1186/1741-7007-8-116 Text en Copyright ©2010 Ikeno et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Ikeno, Tomoko
Tanaka, Shinichi I
Numata, Hideharu
Goto, Shin G
Photoperiodic diapause under the control of circadian clock genes in an insect
title Photoperiodic diapause under the control of circadian clock genes in an insect
title_full Photoperiodic diapause under the control of circadian clock genes in an insect
title_fullStr Photoperiodic diapause under the control of circadian clock genes in an insect
title_full_unstemmed Photoperiodic diapause under the control of circadian clock genes in an insect
title_short Photoperiodic diapause under the control of circadian clock genes in an insect
title_sort photoperiodic diapause under the control of circadian clock genes in an insect
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2942818/
https://www.ncbi.nlm.nih.gov/pubmed/20815865
http://dx.doi.org/10.1186/1741-7007-8-116
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