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Identification and functional analysis of early gene expression induced by circadian light-resetting in Drosophila

BACKGROUND: The environmental light–dark cycle is the dominant cue that maintains 24-h biological rhythms in multicellular organisms. In Drosophila, light entrainment is mediated by the photosensitive protein CRYPTOCHROME, but the role and extent of transcription regulation in light resetting of the...

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Autores principales: Adewoye, Adeolu B., Kyriacou, Charalambos P., Tauber, Eran
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4521455/
https://www.ncbi.nlm.nih.gov/pubmed/26231660
http://dx.doi.org/10.1186/s12864-015-1787-7
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author Adewoye, Adeolu B.
Kyriacou, Charalambos P.
Tauber, Eran
author_facet Adewoye, Adeolu B.
Kyriacou, Charalambos P.
Tauber, Eran
author_sort Adewoye, Adeolu B.
collection PubMed
description BACKGROUND: The environmental light–dark cycle is the dominant cue that maintains 24-h biological rhythms in multicellular organisms. In Drosophila, light entrainment is mediated by the photosensitive protein CRYPTOCHROME, but the role and extent of transcription regulation in light resetting of the dipteran clock is yet unknown. Given the broad transcriptional changes in response to light previously identified in mammals, we have sought to analyse light-induced global transcriptional changes in the fly’s head by using Affymetrix microarrays. Flies were subjected to a 30-min light pulse during the early night (3 h after lights-off), a stimulus which causes a substantial phase delay of the circadian rhythm. We then analysed changes in gene expression 1 h after the light stimulus. RESULTS: We identified 200 genes whose transcripts were significantly altered in response to the light pulse at a false discovery rate cut-off of 10 %. Analysis of these genes and their biological functions suggests the involvement of at least six biological processes in light-induced delay phase shifts of rhythmic activities. These processes include signalling, ion channel transport, receptor activity, synaptic organisation, signal transduction, and chromatin remodelling. Using RNAi, the expression of 22 genes was downregulated in the clock neurons, leading to significant effects on circadian output. For example, while continuous light normally causes arrhythmicity in wild-type flies, the knockdown of Kr-h1, Nipped-A, Thor, nrv1, Nf1, CG11155 (ionotropic glutamate receptor), and Fmr1 resulted in flies that were rhythmic, suggesting a disruption in the light input pathway to the clock. CONCLUSIONS: Our analysis provides a first insight into the early responsive genes that are activated by light and their contribution to light resetting of the Drosophila clock. The analysis suggests multiple domains and pathways that might be associated with light entrainment, including a mechanism that was represented by a light-activated set of chromatin remodelling genes. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12864-015-1787-7) contains supplementary material, which is available to authorized users.
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spelling pubmed-45214552015-08-01 Identification and functional analysis of early gene expression induced by circadian light-resetting in Drosophila Adewoye, Adeolu B. Kyriacou, Charalambos P. Tauber, Eran BMC Genomics Research Article BACKGROUND: The environmental light–dark cycle is the dominant cue that maintains 24-h biological rhythms in multicellular organisms. In Drosophila, light entrainment is mediated by the photosensitive protein CRYPTOCHROME, but the role and extent of transcription regulation in light resetting of the dipteran clock is yet unknown. Given the broad transcriptional changes in response to light previously identified in mammals, we have sought to analyse light-induced global transcriptional changes in the fly’s head by using Affymetrix microarrays. Flies were subjected to a 30-min light pulse during the early night (3 h after lights-off), a stimulus which causes a substantial phase delay of the circadian rhythm. We then analysed changes in gene expression 1 h after the light stimulus. RESULTS: We identified 200 genes whose transcripts were significantly altered in response to the light pulse at a false discovery rate cut-off of 10 %. Analysis of these genes and their biological functions suggests the involvement of at least six biological processes in light-induced delay phase shifts of rhythmic activities. These processes include signalling, ion channel transport, receptor activity, synaptic organisation, signal transduction, and chromatin remodelling. Using RNAi, the expression of 22 genes was downregulated in the clock neurons, leading to significant effects on circadian output. For example, while continuous light normally causes arrhythmicity in wild-type flies, the knockdown of Kr-h1, Nipped-A, Thor, nrv1, Nf1, CG11155 (ionotropic glutamate receptor), and Fmr1 resulted in flies that were rhythmic, suggesting a disruption in the light input pathway to the clock. CONCLUSIONS: Our analysis provides a first insight into the early responsive genes that are activated by light and their contribution to light resetting of the Drosophila clock. The analysis suggests multiple domains and pathways that might be associated with light entrainment, including a mechanism that was represented by a light-activated set of chromatin remodelling genes. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12864-015-1787-7) contains supplementary material, which is available to authorized users. BioMed Central 2015-08-01 /pmc/articles/PMC4521455/ /pubmed/26231660 http://dx.doi.org/10.1186/s12864-015-1787-7 Text en © Adewoye et al. 2015 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Adewoye, Adeolu B.
Kyriacou, Charalambos P.
Tauber, Eran
Identification and functional analysis of early gene expression induced by circadian light-resetting in Drosophila
title Identification and functional analysis of early gene expression induced by circadian light-resetting in Drosophila
title_full Identification and functional analysis of early gene expression induced by circadian light-resetting in Drosophila
title_fullStr Identification and functional analysis of early gene expression induced by circadian light-resetting in Drosophila
title_full_unstemmed Identification and functional analysis of early gene expression induced by circadian light-resetting in Drosophila
title_short Identification and functional analysis of early gene expression induced by circadian light-resetting in Drosophila
title_sort identification and functional analysis of early gene expression induced by circadian light-resetting in drosophila
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4521455/
https://www.ncbi.nlm.nih.gov/pubmed/26231660
http://dx.doi.org/10.1186/s12864-015-1787-7
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