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Identification of reference genes for RT-qPCR data normalization in Gammarus fossarum (Crustacea Amphipoda)

Gene expression profiling via RT-qPCR is a robust technique increasingly used in ecotoxicology. Determination and validation of optimal reference genes is a requirement for initiating RT-qPCR experiments. To our best knowledge, this study is the first attempt of identifying a set of reference genes...

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Autores principales: Mehennaoui, Kahina, Legay, Sylvain, Serchi, Tommaso, Guérold, François, Giamberini, Laure, Gutleb, Arno C., Cambier, Sébastien
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6189083/
https://www.ncbi.nlm.nih.gov/pubmed/30323236
http://dx.doi.org/10.1038/s41598-018-33561-1
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author Mehennaoui, Kahina
Legay, Sylvain
Serchi, Tommaso
Guérold, François
Giamberini, Laure
Gutleb, Arno C.
Cambier, Sébastien
author_facet Mehennaoui, Kahina
Legay, Sylvain
Serchi, Tommaso
Guérold, François
Giamberini, Laure
Gutleb, Arno C.
Cambier, Sébastien
author_sort Mehennaoui, Kahina
collection PubMed
description Gene expression profiling via RT-qPCR is a robust technique increasingly used in ecotoxicology. Determination and validation of optimal reference genes is a requirement for initiating RT-qPCR experiments. To our best knowledge, this study is the first attempt of identifying a set of reference genes for the freshwater crustacean Gammarus fossarum. Six candidate genes (Actin, TUB, UB, SDH, Clathrin and GAPDH) were tested in order to determine the most stable ones in different stress conditions and to increase the robustness of RT-qPCR data. SDH and Clathrin appeared as the most stable ones. A validation was performed using G. fossarum samples exposed for 15 days to AgNO(3), silver nanoparticles (AgNPs) 40 nm and gold nanoparticles (AuNPs) 40 nm. Effects on HSP90 were evaluated and data normalized using Clathrin and SDH. A down-regulation of HSP90 was observed when G. fossarum were exposed to AuNPs 40 nm whereas no effects were observed when G. fossarum were exposed to AgNPs 40 nm. This study highlights the importance of the preliminary determination of suitable reference genes for RT-qPCR experiments. Additionally, this study allowed, for the first time, the determination of a set of valuable genes that can be used in other RT-qPCR studies using G. fossarum as model organism.
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spelling pubmed-61890832018-10-22 Identification of reference genes for RT-qPCR data normalization in Gammarus fossarum (Crustacea Amphipoda) Mehennaoui, Kahina Legay, Sylvain Serchi, Tommaso Guérold, François Giamberini, Laure Gutleb, Arno C. Cambier, Sébastien Sci Rep Article Gene expression profiling via RT-qPCR is a robust technique increasingly used in ecotoxicology. Determination and validation of optimal reference genes is a requirement for initiating RT-qPCR experiments. To our best knowledge, this study is the first attempt of identifying a set of reference genes for the freshwater crustacean Gammarus fossarum. Six candidate genes (Actin, TUB, UB, SDH, Clathrin and GAPDH) were tested in order to determine the most stable ones in different stress conditions and to increase the robustness of RT-qPCR data. SDH and Clathrin appeared as the most stable ones. A validation was performed using G. fossarum samples exposed for 15 days to AgNO(3), silver nanoparticles (AgNPs) 40 nm and gold nanoparticles (AuNPs) 40 nm. Effects on HSP90 were evaluated and data normalized using Clathrin and SDH. A down-regulation of HSP90 was observed when G. fossarum were exposed to AuNPs 40 nm whereas no effects were observed when G. fossarum were exposed to AgNPs 40 nm. This study highlights the importance of the preliminary determination of suitable reference genes for RT-qPCR experiments. Additionally, this study allowed, for the first time, the determination of a set of valuable genes that can be used in other RT-qPCR studies using G. fossarum as model organism. Nature Publishing Group UK 2018-10-15 /pmc/articles/PMC6189083/ /pubmed/30323236 http://dx.doi.org/10.1038/s41598-018-33561-1 Text en © The Author(s) 2018 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
Mehennaoui, Kahina
Legay, Sylvain
Serchi, Tommaso
Guérold, François
Giamberini, Laure
Gutleb, Arno C.
Cambier, Sébastien
Identification of reference genes for RT-qPCR data normalization in Gammarus fossarum (Crustacea Amphipoda)
title Identification of reference genes for RT-qPCR data normalization in Gammarus fossarum (Crustacea Amphipoda)
title_full Identification of reference genes for RT-qPCR data normalization in Gammarus fossarum (Crustacea Amphipoda)
title_fullStr Identification of reference genes for RT-qPCR data normalization in Gammarus fossarum (Crustacea Amphipoda)
title_full_unstemmed Identification of reference genes for RT-qPCR data normalization in Gammarus fossarum (Crustacea Amphipoda)
title_short Identification of reference genes for RT-qPCR data normalization in Gammarus fossarum (Crustacea Amphipoda)
title_sort identification of reference genes for rt-qpcr data normalization in gammarus fossarum (crustacea amphipoda)
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6189083/
https://www.ncbi.nlm.nih.gov/pubmed/30323236
http://dx.doi.org/10.1038/s41598-018-33561-1
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