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Dynamic transcriptomic profiles of zebrafish gills in response to zinc supplementation

BACKGROUND: Dietary zinc supplementation may help to promote growth, boost the immune system, protect against diabetes, and aid recovery from diarrhoea. We exploited the zebrafish (Danio rerio) gill as a unique vertebrate ion transporting epithelium model to study the time-dependent regulatory netwo...

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Autores principales: Zheng, Dongling, Kille, Peter, Feeney, Graham P, Cunningham, Phil, Handy, Richard D, Hogstrand, Christer
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3091702/
https://www.ncbi.nlm.nih.gov/pubmed/20937081
http://dx.doi.org/10.1186/1471-2164-11-553
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author Zheng, Dongling
Kille, Peter
Feeney, Graham P
Cunningham, Phil
Handy, Richard D
Hogstrand, Christer
author_facet Zheng, Dongling
Kille, Peter
Feeney, Graham P
Cunningham, Phil
Handy, Richard D
Hogstrand, Christer
author_sort Zheng, Dongling
collection PubMed
description BACKGROUND: Dietary zinc supplementation may help to promote growth, boost the immune system, protect against diabetes, and aid recovery from diarrhoea. We exploited the zebrafish (Danio rerio) gill as a unique vertebrate ion transporting epithelium model to study the time-dependent regulatory networks of gene-expression leading to homeostatic control during zinc supplementation. This organ forms a conduit for zinc uptake whilst exhibiting conservation of zinc trafficking components. RESULTS: Fish were maintained with either zinc supplemented water (4.0 μM) and diet (2023 mg zinc kg(-1)) or water and diet containing Zn(2+ )at 0.25 μM and 233 mg zinc kg(-1), respectively. Gill tissues were harvested at five time points (8 hours to 14 days) and transcriptome changes analysed in quintuplicate using a 16 K microarray with results anchored to gill Zn(2+ )influx and whole body nutrient composition (protein, carbohydrate, lipid, elements). The number of regulated genes increased up to day 7 but declined as the fish acclimated. In total 525 genes were regulated (having a fold-change more than 1.8 fold change and an adjusted P-value less than 0.1 which is controlling a 10% False discovery rate, FDR) by zinc supplementation, but little overlap was observed between genes regulated at successive time-points. Many genes displayed cyclic expression, typical for homeostatic control mechanisms. Annotation enrichment analysis revealed strong overrepresentation of "transcription factors", with specific association evident with "steroid hormone receptors". A suite of genes linked to "development" were also statistically overrepresented. More specifically, early regulation of genes was linked to a few key transcription factors (e.g. Mtf1, Jun, Stat1, Ppara, Gata3) and was followed by hedgehog and bone morphogenic protein signalling. CONCLUSIONS: The results suggest that zinc supplementation reactivated developmental pathways in the gill and stimulated stem cell differentiation, a response likely reflecting gill remodelling in response to its altered environment. This provides insight to the role of zinc during cell differentiation and illustrates the critical nature of maintaining zinc status. The study also highlights the importance of temporal transcriptomics analysis in order resolve the discrete elements of biological processes, such as zinc acclimation.
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spelling pubmed-30917022011-05-11 Dynamic transcriptomic profiles of zebrafish gills in response to zinc supplementation Zheng, Dongling Kille, Peter Feeney, Graham P Cunningham, Phil Handy, Richard D Hogstrand, Christer BMC Genomics Research Article BACKGROUND: Dietary zinc supplementation may help to promote growth, boost the immune system, protect against diabetes, and aid recovery from diarrhoea. We exploited the zebrafish (Danio rerio) gill as a unique vertebrate ion transporting epithelium model to study the time-dependent regulatory networks of gene-expression leading to homeostatic control during zinc supplementation. This organ forms a conduit for zinc uptake whilst exhibiting conservation of zinc trafficking components. RESULTS: Fish were maintained with either zinc supplemented water (4.0 μM) and diet (2023 mg zinc kg(-1)) or water and diet containing Zn(2+ )at 0.25 μM and 233 mg zinc kg(-1), respectively. Gill tissues were harvested at five time points (8 hours to 14 days) and transcriptome changes analysed in quintuplicate using a 16 K microarray with results anchored to gill Zn(2+ )influx and whole body nutrient composition (protein, carbohydrate, lipid, elements). The number of regulated genes increased up to day 7 but declined as the fish acclimated. In total 525 genes were regulated (having a fold-change more than 1.8 fold change and an adjusted P-value less than 0.1 which is controlling a 10% False discovery rate, FDR) by zinc supplementation, but little overlap was observed between genes regulated at successive time-points. Many genes displayed cyclic expression, typical for homeostatic control mechanisms. Annotation enrichment analysis revealed strong overrepresentation of "transcription factors", with specific association evident with "steroid hormone receptors". A suite of genes linked to "development" were also statistically overrepresented. More specifically, early regulation of genes was linked to a few key transcription factors (e.g. Mtf1, Jun, Stat1, Ppara, Gata3) and was followed by hedgehog and bone morphogenic protein signalling. CONCLUSIONS: The results suggest that zinc supplementation reactivated developmental pathways in the gill and stimulated stem cell differentiation, a response likely reflecting gill remodelling in response to its altered environment. This provides insight to the role of zinc during cell differentiation and illustrates the critical nature of maintaining zinc status. The study also highlights the importance of temporal transcriptomics analysis in order resolve the discrete elements of biological processes, such as zinc acclimation. BioMed Central 2010-10-11 /pmc/articles/PMC3091702/ /pubmed/20937081 http://dx.doi.org/10.1186/1471-2164-11-553 Text en Copyright ©2010 Zheng 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
Zheng, Dongling
Kille, Peter
Feeney, Graham P
Cunningham, Phil
Handy, Richard D
Hogstrand, Christer
Dynamic transcriptomic profiles of zebrafish gills in response to zinc supplementation
title Dynamic transcriptomic profiles of zebrafish gills in response to zinc supplementation
title_full Dynamic transcriptomic profiles of zebrafish gills in response to zinc supplementation
title_fullStr Dynamic transcriptomic profiles of zebrafish gills in response to zinc supplementation
title_full_unstemmed Dynamic transcriptomic profiles of zebrafish gills in response to zinc supplementation
title_short Dynamic transcriptomic profiles of zebrafish gills in response to zinc supplementation
title_sort dynamic transcriptomic profiles of zebrafish gills in response to zinc supplementation
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3091702/
https://www.ncbi.nlm.nih.gov/pubmed/20937081
http://dx.doi.org/10.1186/1471-2164-11-553
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