Cargando…

RT-qPCR Normalization Genes in the Red Alga Chondrus crispus

Chondrus crispus is a common red macroalga living on the rocky shores of the North Atlantic Ocean. It has a long research history, being a major source of carrageenan, a thickener widely used in the food industry, but also for physiological and ecological studies. To establish it as a model for red...

Descripción completa

Detalles Bibliográficos
Autores principales: Kowalczyk, Nathalie, Rousvoal, Sylvie, Hervé, Cécile, Boyen, Catherine, Collén, Jonas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3912222/
https://www.ncbi.nlm.nih.gov/pubmed/24498277
http://dx.doi.org/10.1371/journal.pone.0086574
_version_ 1782302059703304192
author Kowalczyk, Nathalie
Rousvoal, Sylvie
Hervé, Cécile
Boyen, Catherine
Collén, Jonas
author_facet Kowalczyk, Nathalie
Rousvoal, Sylvie
Hervé, Cécile
Boyen, Catherine
Collén, Jonas
author_sort Kowalczyk, Nathalie
collection PubMed
description Chondrus crispus is a common red macroalga living on the rocky shores of the North Atlantic Ocean. It has a long research history, being a major source of carrageenan, a thickener widely used in the food industry, but also for physiological and ecological studies. To establish it as a model for red algae, its genome has been sequenced, allowing the development of molecular tools such as quantification of gene expression, including RNAseq and RT-qPCR. To determine appropriate genes for RT-qPCR normalization, the expression of 14 genes was monitored in 18 conditions using two sets of algal samples: samples from the sequenced strain, cultured and stressed in laboratory conditions and C. crispus collected on the shore and stressed in situ. The expression stability of the genes between the samples was evaluated by comparing the Ct range and using the programs geNorm and NormFinder. The candidate genes encoded translation related proteins (initiation factors IF4A-1 and IF4A-2, elongation factor EF1α and eRF3, an eukaryotic polypeptide chain release factor), cytoskeleton proteins (two β-tubulins, α-tubulin and actin), enzymes involved in the pentose phosphate pathway (glucose 6-phosphate deshydrogenase), protein recycling process (ubiquitin and ubiquitin-conjugating enzyme) and glycolysis (isocitrate dehydrogenase). The two sets of samples showed different expression patterns. Most of the genes were stable in the algae cultivated in the laboratory, whereas environmental samples showed a more important variation in gene expression. When analyzing the two sets separately, the ranking of the most stables genes were different from one method to another. When considering all samples, the two statistical methods were concordant, revealing translation initiation factor 4A-2 and eukaryotic polypeptide chain release factor 3 as pertinent normalization genes. This study highlights thus the importance of testing reference genes according to the experiments as well as the genetic and physiological background of the organism.
format Online
Article
Text
id pubmed-3912222
institution National Center for Biotechnology Information
language English
publishDate 2014
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-39122222014-02-04 RT-qPCR Normalization Genes in the Red Alga Chondrus crispus Kowalczyk, Nathalie Rousvoal, Sylvie Hervé, Cécile Boyen, Catherine Collén, Jonas PLoS One Research Article Chondrus crispus is a common red macroalga living on the rocky shores of the North Atlantic Ocean. It has a long research history, being a major source of carrageenan, a thickener widely used in the food industry, but also for physiological and ecological studies. To establish it as a model for red algae, its genome has been sequenced, allowing the development of molecular tools such as quantification of gene expression, including RNAseq and RT-qPCR. To determine appropriate genes for RT-qPCR normalization, the expression of 14 genes was monitored in 18 conditions using two sets of algal samples: samples from the sequenced strain, cultured and stressed in laboratory conditions and C. crispus collected on the shore and stressed in situ. The expression stability of the genes between the samples was evaluated by comparing the Ct range and using the programs geNorm and NormFinder. The candidate genes encoded translation related proteins (initiation factors IF4A-1 and IF4A-2, elongation factor EF1α and eRF3, an eukaryotic polypeptide chain release factor), cytoskeleton proteins (two β-tubulins, α-tubulin and actin), enzymes involved in the pentose phosphate pathway (glucose 6-phosphate deshydrogenase), protein recycling process (ubiquitin and ubiquitin-conjugating enzyme) and glycolysis (isocitrate dehydrogenase). The two sets of samples showed different expression patterns. Most of the genes were stable in the algae cultivated in the laboratory, whereas environmental samples showed a more important variation in gene expression. When analyzing the two sets separately, the ranking of the most stables genes were different from one method to another. When considering all samples, the two statistical methods were concordant, revealing translation initiation factor 4A-2 and eukaryotic polypeptide chain release factor 3 as pertinent normalization genes. This study highlights thus the importance of testing reference genes according to the experiments as well as the genetic and physiological background of the organism. Public Library of Science 2014-02-03 /pmc/articles/PMC3912222/ /pubmed/24498277 http://dx.doi.org/10.1371/journal.pone.0086574 Text en © 2014 Kowalczyk 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
Kowalczyk, Nathalie
Rousvoal, Sylvie
Hervé, Cécile
Boyen, Catherine
Collén, Jonas
RT-qPCR Normalization Genes in the Red Alga Chondrus crispus
title RT-qPCR Normalization Genes in the Red Alga Chondrus crispus
title_full RT-qPCR Normalization Genes in the Red Alga Chondrus crispus
title_fullStr RT-qPCR Normalization Genes in the Red Alga Chondrus crispus
title_full_unstemmed RT-qPCR Normalization Genes in the Red Alga Chondrus crispus
title_short RT-qPCR Normalization Genes in the Red Alga Chondrus crispus
title_sort rt-qpcr normalization genes in the red alga chondrus crispus
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3912222/
https://www.ncbi.nlm.nih.gov/pubmed/24498277
http://dx.doi.org/10.1371/journal.pone.0086574
work_keys_str_mv AT kowalczyknathalie rtqpcrnormalizationgenesintheredalgachondruscrispus
AT rousvoalsylvie rtqpcrnormalizationgenesintheredalgachondruscrispus
AT hervececile rtqpcrnormalizationgenesintheredalgachondruscrispus
AT boyencatherine rtqpcrnormalizationgenesintheredalgachondruscrispus
AT collenjonas rtqpcrnormalizationgenesintheredalgachondruscrispus