Cargando…

Regulation of per and cry Genes Reveals a Central Role for the D-Box Enhancer in Light-Dependent Gene Expression

Light serves as a key environmental signal for synchronizing the circadian clock with the day night cycle. The zebrafish represents an attractive model for exploring how light influences the vertebrate clock mechanism. Direct illumination of most fish tissues and cell lines induces expression of a b...

Descripción completa

Detalles Bibliográficos
Autores principales: Mracek, Philipp, Santoriello, Cristina, Idda, M. Laura, Pagano, Cristina, Ben-Moshe, Zohar, Gothilf, Yoav, Vallone, Daniela, Foulkes, Nicholas S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3516543/
https://www.ncbi.nlm.nih.gov/pubmed/23236462
http://dx.doi.org/10.1371/journal.pone.0051278
_version_ 1782252322101919744
author Mracek, Philipp
Santoriello, Cristina
Idda, M. Laura
Pagano, Cristina
Ben-Moshe, Zohar
Gothilf, Yoav
Vallone, Daniela
Foulkes, Nicholas S.
author_facet Mracek, Philipp
Santoriello, Cristina
Idda, M. Laura
Pagano, Cristina
Ben-Moshe, Zohar
Gothilf, Yoav
Vallone, Daniela
Foulkes, Nicholas S.
author_sort Mracek, Philipp
collection PubMed
description Light serves as a key environmental signal for synchronizing the circadian clock with the day night cycle. The zebrafish represents an attractive model for exploring how light influences the vertebrate clock mechanism. Direct illumination of most fish tissues and cell lines induces expression of a broad range of genes including DNA repair, stress response and key clock genes. We have previously identified D- and E-box elements within the promoter of the zebrafish per2 gene that together direct light-induced gene expression. However, is the combined regulation by E- and D-boxes a general feature for all light-induced gene expression? We have tackled this question by examining the regulation of additional light-inducible genes. Our results demonstrate that with the exception of per2, all other genes tested are not induced by light upon blocking of de novo protein synthesis. We reveal that a single D-box serves as the principal light responsive element within the cry1a promoter. Furthermore, upon inhibition of protein synthesis D-box mediated gene expression is abolished while the E-box confers light driven activation as observed in the per2 gene. Given the existence of different photoreceptors in fish cells, our results implicate the D-box enhancer as a general convergence point for light driven signaling.
format Online
Article
Text
id pubmed-3516543
institution National Center for Biotechnology Information
language English
publishDate 2012
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-35165432012-12-12 Regulation of per and cry Genes Reveals a Central Role for the D-Box Enhancer in Light-Dependent Gene Expression Mracek, Philipp Santoriello, Cristina Idda, M. Laura Pagano, Cristina Ben-Moshe, Zohar Gothilf, Yoav Vallone, Daniela Foulkes, Nicholas S. PLoS One Research Article Light serves as a key environmental signal for synchronizing the circadian clock with the day night cycle. The zebrafish represents an attractive model for exploring how light influences the vertebrate clock mechanism. Direct illumination of most fish tissues and cell lines induces expression of a broad range of genes including DNA repair, stress response and key clock genes. We have previously identified D- and E-box elements within the promoter of the zebrafish per2 gene that together direct light-induced gene expression. However, is the combined regulation by E- and D-boxes a general feature for all light-induced gene expression? We have tackled this question by examining the regulation of additional light-inducible genes. Our results demonstrate that with the exception of per2, all other genes tested are not induced by light upon blocking of de novo protein synthesis. We reveal that a single D-box serves as the principal light responsive element within the cry1a promoter. Furthermore, upon inhibition of protein synthesis D-box mediated gene expression is abolished while the E-box confers light driven activation as observed in the per2 gene. Given the existence of different photoreceptors in fish cells, our results implicate the D-box enhancer as a general convergence point for light driven signaling. Public Library of Science 2012-12-06 /pmc/articles/PMC3516543/ /pubmed/23236462 http://dx.doi.org/10.1371/journal.pone.0051278 Text en © 2012 Mracek et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Mracek, Philipp
Santoriello, Cristina
Idda, M. Laura
Pagano, Cristina
Ben-Moshe, Zohar
Gothilf, Yoav
Vallone, Daniela
Foulkes, Nicholas S.
Regulation of per and cry Genes Reveals a Central Role for the D-Box Enhancer in Light-Dependent Gene Expression
title Regulation of per and cry Genes Reveals a Central Role for the D-Box Enhancer in Light-Dependent Gene Expression
title_full Regulation of per and cry Genes Reveals a Central Role for the D-Box Enhancer in Light-Dependent Gene Expression
title_fullStr Regulation of per and cry Genes Reveals a Central Role for the D-Box Enhancer in Light-Dependent Gene Expression
title_full_unstemmed Regulation of per and cry Genes Reveals a Central Role for the D-Box Enhancer in Light-Dependent Gene Expression
title_short Regulation of per and cry Genes Reveals a Central Role for the D-Box Enhancer in Light-Dependent Gene Expression
title_sort regulation of per and cry genes reveals a central role for the d-box enhancer in light-dependent gene expression
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3516543/
https://www.ncbi.nlm.nih.gov/pubmed/23236462
http://dx.doi.org/10.1371/journal.pone.0051278
work_keys_str_mv AT mracekphilipp regulationofperandcrygenesrevealsacentralroleforthedboxenhancerinlightdependentgeneexpression
AT santoriellocristina regulationofperandcrygenesrevealsacentralroleforthedboxenhancerinlightdependentgeneexpression
AT iddamlaura regulationofperandcrygenesrevealsacentralroleforthedboxenhancerinlightdependentgeneexpression
AT paganocristina regulationofperandcrygenesrevealsacentralroleforthedboxenhancerinlightdependentgeneexpression
AT benmoshezohar regulationofperandcrygenesrevealsacentralroleforthedboxenhancerinlightdependentgeneexpression
AT gothilfyoav regulationofperandcrygenesrevealsacentralroleforthedboxenhancerinlightdependentgeneexpression
AT vallonedaniela regulationofperandcrygenesrevealsacentralroleforthedboxenhancerinlightdependentgeneexpression
AT foulkesnicholass regulationofperandcrygenesrevealsacentralroleforthedboxenhancerinlightdependentgeneexpression