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Selection of reference genes for qRT-PCR examination of wild populations of Atlantic cod Gadus morhua
BMC Research Notes volume 1, Article number: 47 (2008)
Extensive sequencing efforts have been taking place for the Atlantic cod (Gadus morhua) in recent years, the number of ESTs in the Genbank has reached more than 140.000. Despite its importance in North Atlantic fisheries and potential use in aquaculture, relatively few gene expression examination exists for this species, and systematic evaluations of reference gene stability in quantitative real-time RT-PCR (qRT-PCR) studies are lacking.
The stability of 10 potential reference genes was examined in six tissues of Atlantic cod obtained from four populations, to determine the most suitable genes to be used in qRT-PCR analyses. Relative transcription levels of genes encoding β-actin (ACTB), elongation factor 1A (EF1A), actin-related protein-2 (ARP-2), glyceraldehyde-3P-dehydrogenase (GAPDH), ubiquitin (Ubi), acidic ribosomal protein (ARP), ribosomal protein S9 (S9), ribosomal protein L4 (RPL4), RPL22 and RPL37 were quantified in gills, brain, liver, head kidney, muscle and middle intestine in six juvenile fish from three wild populations and from farmed Atlantic cod. Reference gene stability was investigated using the geNorm and NormFinder tools. Based on calculations performed with the geNorm, which determines the most stable genes from a set of tested genes in a given cDNA sample, ARP, Ubi, S9 and RPL37 were among the most stable genes in all tissues. When the same calculations were done with NormFinder, the same genes plus RPL4 and EF1A were ranked as the preferable genes.
Overall, this work suggests that the Ubi and ARP can be useful as reference genes in qRT-PCR examination of gene expression studying wild populations of Atlantic cod.
The specificity and ease-of-use of quantitative reverse transcription real-time PCR (qRT-PCR) has made this method the dominant technique for quantification of relative mRNA levels in cells. In qRT-PCR, the expression levels of the target genes of interest are normally estimated on the basis of endogenous controls, also called reference genes. The purpose of these controls is to remove or reduce differences due to biological and technical variability, i.e. differences in RNA quantity and quality. The ideal endogenous control should be expressed at a constant level at all stages of development or between treatment groups. It should also be expressed at roughly the same level as the mRNA under study. Hence, data normalization is a prerequisite of the qRT-PCR analytical process, and is essential for accurate comparison of mRNA measurements between different samples [1, 2]. However, no golden standard exists for normalization of qRT-PCR data, and data normalization remains a real problem in qRT-PCR. Numerous studies have shown that no single universal gene has a constant expression level under all developmental or experimental conditions. The best choice of reference genes to be used as endogenous control varies, depending on the cells or tissues studied, and has to be validated in each experiment. Many different genes have therefore been selected for normalization of mRNA expression data [3–7]. If the selected reference genes fluctuate randomly between treatment groups, differences in expression between the genes of interest will be missed.
The Atlantic cod (Gadus morhua) has a wide distribution across the North Atlantic . Several important cod stocks are of great economic and social importance. As a consequence, Canadian and Norwegian groups have sequenced more than 140.000 ESTs in this species. For the time being, there are no reports on suitable reference genes for qRT-PCR examinations of wild-caught Atlantic cod available. The aim of this work was therefore to evaluate the usefulness of 10 potential reference genes for qRT-PCR in the Atlantic cod. Our hypothesis was that reference genes are stable in tissues within and between populations of cod living in contaminated habitats. Genes encoding 5 commonly used housekeeping proteins plus 5 ribosomal proteins were selected for examination. To evaluate their usefulness as reference genes, RNA from six tissues (gill, brain, liver, head kidney, muscle and intestine) of six adult male cod from four populations were subjected to qRT-PCR analysis [see Additional file 1 for methods]. Two of the populations were sampled from heavily contaminated recipients, one control from an unpolluted fjord locality and one from an aquaculture facility. We used the geNorm and NormFinder tools to evaluate the individual stability of the reference genes, ranking the genes according to their usefulness as reference genes in qRT-PCR examinations.
Results and Discussion
Even if alternatives exist it is becoming more evident today that in order to obtain trustworthy gene expression data using real-time RT-PCR it is necessary to normalize the data with internal control genes, based on their mRNA levels. Every examination therefore requires that one quantify one or even better two or more reference genes and evaluate their expression stability in order to normalize the expression data. In the current examination the stability of 10 potential reference genes (Table 1, Table 2) were screened in six tissues of Atlantic cod sampled from four different populations in Western Norway, two of them from locations contaminated with xenobiotics. This experiment represents the first attempt to characterize and evaluate potential reference genes in qRT-PCR studies of Atlantic cod. Fish from three different wild populations as well as farmed fish were studied. Sediments in Store Lungegårdsvann in Bergen town and in Sørfjorden close to Odda are contaminated with POPs and heavy metals that might affect fish inhabiting these locations. Biota from these locations are affected by the pollutants [9, 10]. Farmed cod will of course have a steady supply of food, and will in general be in a better condition than wild cod. For future qRT-PCR examinations of wild cod, it is a prerequisite to have candidate reference genes that exhibit stable expression across different populations.
Ranking of the most stable reference genes in gills, brain, liver, head kidney, muscle and intestine analyzed by geNorm is presented in Fig. 1. The geNorm software ranks the selected reference genes according to the determined gene-stability measure (M-value), representing the average pair-wise variation of a particular gene with all other reference genes, from the most stable (lowest M values) to the least stable (highest M values) . The best two genes are ranked without distinguishing between them. In gills, Ubi and RPL37 ranked best with S9 ranking number three (Fig. 1A). The two worst genes were GAPDH and ACTB. ARP and Ubi followed by S9 were the most stably expressed genes in brain tissue according to geNorm, whereas GAPDH and ACTB ranked worst (Fig. 1B). In liver ARP and RPL37 were ranked as the two best genes, with Ubi ranking number three (Fig. 1C). ACTB and ARP-2, two genes encoding structural proteins, were ranked as the most unsuitable reference genes in liver. Two ribosomal protein genes ranked best in head kidney tissue, S9 and RPL37, followed by Ubi, whereas GAPDH and ACTB again were classified as the most unstable genes (Fig. 1D). In muscle ARP and Ubi were the best genes, followed by RPL22 (Fig. 1E). ARP and Ubi were also ranked as the best genes in brain tissue. Again GAPDH and ACTB were estimated to be the least stable genes. ARP and RPL37 were the most stable reference genes in intestinal tissue, with Ubi ranking number third (Fig. 1F). Also in this tissue ACTB and GAPDH were the worst genes. Overall, according to the geNorm algorithm genes encoding ribosomal proteins plus Ubi should be used for normalization of qRT-PCR data in the six examined tissues of Atlantic cod.
Since geNorm uses a pair-wise comparison approach, co-regulated genes belonging to the same pathway or system with a similar expression profile tend to get too good score [6, 11]. The NormFinder software, on the other hand, ranks the genes on a model-based approach. If the expression profiles suggest that several candidate genes are co-regulated, a model-based evaluation method should be considered. Analyzed with NormFinder, RPL4 was the most stable gene in gill tissue, followed by Ubi and S9 (Fig. 2A). RPL37, suggested as one of the top-ranking genes with geNorm, was ranked number 4 with NormFinder. Both geNorm and NormFinder rank GAPDH and ACTB as the least suitable reference genes in gills. In brain tissue, Ubi, ARP and RPL37 are ranked as the most suitable normalization genes, whereas GAPDH and ACTB again have the least stable expression profiles (Fig. 2B). S9, RPL4 and RPL22 are also considered to be suitable normalization genes in brain tissue according to the NormFinder tool. Ubi ranks best in liver tissue, followed by EF1A, ARP, RPL4, RPL37 and S9, all with almost the same expression profile stability (Fig. 2C). In liver the two structural proteins ARP-2 and ACTB were the least stable genes. RPL4, Ubi and ARP-2 were the most stable reference genes in head kidney tissue (Fig. 2D). The expression of GAPDH in head kidney varied a lot between the examined individuals, again putting a question mark on the use of this gene as a reference gene in qRT-PCR studies. In muscle tissue Ubi, RPL4 and ARP were the most stable reference genes according to NormFinder, with GAPDH and ACTB ranking worst (Fig. 2E). ARP, Ubi and RPL4 were the best reference genes in intestinal tissue evaluated using NormFinder, and ACTB and GAPDH ranking worst (Fig. 2F). The NormFinder software also suggest the optimal number of genes that should be included in order to calculate the normalization factor, to be used for normalization of target genes. These numbers are presented for each tissue in Fig. 2.
In all six examined tissues, both geNorm and NormFinder rank genes encoding ribosomal proteins and Ubi as the best candidate reference genes for normalization of qRT-PCR data. There are discrepancies between the two algorithms, but Ubi and ARP are among the best ranking genes analyzed with both methods in all tissues. In order to check if the selected genes encoding ribosomal proteins have equal expression profiles and are co-regulated, distribution patterns were investigated with principal component analysis (PCA). The geNorm algorithm is highly dependent on the assumption that none of the genes being analyzed are co-regulated . Only in liver tissue did the genes encoding ribosomal proteins group tight together in the PCA plot (Fig. 3). In liver tissue Ubi, EF1A and GAPDH are grouping together with these genes, whereas the genes encoding the structural proteins ACTB and ARP-2 clearly deviates from the other genes.
Many fish studies has shown that GAPDH expression varies a lot between individuals and under various physiological conditions [12–15], so it was not surprising to find that this gene ranked among the least stable genes in all six examined tissues. Still, GAPDH should be considered included as a reference gene under certain experimental conditions or in specific tissues . It was more surprising to find that ACTB also was ranked as one of the two least stable genes in all tissues. Genes encoding structural proteins like actins have in many ways replaced GAPDH as the golden standard in gene expression analysis . Apparently, in Atlantic cod tissues ACTB should be used with caution as a reference gene. Especially in liver tissue, were the ACTB and ARP-2 genes encoding structural proteins were ranked as the two least stable genes.
In order to compare the geNorm and NormFinder results with an independent ranking method, the data were also analyzed with the Bestkeeper tool . Bestkeeper uses a pair-wise correlation analysis of all pairs of candidate genes, and calculate the geometric mean of the best suited ones. The Bestkeeper ranking is shown in Table 3. Overall, the Bestkeeper results are in line with the geNorm and NormFinder data, with minor deviations. For example, in muscle tissue EF1A is ranked as the most stable gene. GAPDH and ACTB are again ranked as the least stable genes in all tissues. Analyzing reference genes in virus infected cells, Radonic et al.  concluded that the Bestkeeper tool gave results that slightly deviated from, but nevertheless corresponded to, those obtained using geNorm. Thus, under most experimental conditions it is appropriate to evaluate reference gene stability with only one of these tools.
One of the aims of this investigation was to evaluate if potential reference genes are stable in a certain tissues across different populations inhabiting contaminated areas. The expression of candidate genes might be differentially regulated in fish living in strongly contaminated location, for example under conditions were they are experiencing physiological stress that might affect the metabolism. Using PCA, Atlantic cod from the two contaminated locations did not group together (data not shown). Instead, in intestinal tissue individuals from the farmed population grouped together (Fig. 4). Farmed fish are fed on a daily basis with a standard diet, so it is not surprising that the expression of the selected 10 genes group together in a PCA plot in intestinal tissue. Our results therefore suggest that the studied candidate reference genes can be used for normalization of qRT-PCR data across different wild populations of Atlantic cod. Our data, based on geNorm and NormFinder calculations, suggest that the Atlantic cod Ubi and ARP genes that have been tested in the present study may be good candidate reference genes in brain, liver, muscle and intestinal tissues. The study also suggest that ACTB gene should be applied with caution in qRT-PCR examinations of Atlantic cod, as this gene was ranked as on of the least stable in all examined tissues, and also showed considerable variation from sample to sample (Fig. 5).
In conclusion, this study suggests that Ubi and ARP are potential candidate reference genes in qRT-PCR examinations of relative gene expression in gill, brain, liver, head kidney, muscle and intestine tissues of wild populations of Atlantic cod.
Bustin SA, Nolan T: Analysis of mRNA expression by real-time PCR. Real-time PCR. An essential guide. Edited by: Edwards K, Logan J, Saunders N. 2004, Norfolk, UK: Horizon Bioscience, 125-184.
Huggett J, Dheda K, Bustin S, Zumla A: Real-time RT-PCR normalisation; strategies and considerations. Genes Immun. 2005, 6 (4): 279-284. 10.1038/sj.gene.6364190.
Radonic A, Thulke S, Mackay IM, Landt O, Siegert W, Nitsche A: Guideline to reference gene selection for quantitative real-time PCR. Biochem Biophys Res Comm. 2004, 313 (4): 856-862. 10.1016/j.bbrc.2003.11.177.
Dheda K, Huggett JF, Bustin SA, Johnson MA, Rook G, Zumla A: Validation of housekeeping genes for normalizing RNA expression in real-time PCR. Biotechniques. 2004, 37 (1): 112-119.
Vandesompele J, Preter KD, Pattyn F, Poppe B, Roy NV, Paepe AD, Speleman F: Accurate normalization of real-time quantitative RT-PCR data by geometric averaging of multiple internal control genes. Genome Biol. 2002, 3 (7): research0034.1-0034.11. 10.1186/gb-2002-3-7-research0034.
Andersen CL, Jensen JL, Orntoft TF: Normalization of real-time quantitative reverse transcription-PCR data: A model-based variance estimation approach to identify genes suited for normalization, applied to bladder and colon cancer data sets. Cancer Research. 2004, 64 (15): 5245-5250. 10.1158/0008-5472.CAN-04-0496.
Pfaffl MW, Tichopad A, Prgomet C, Neuvians TP: Determination of stable housekeeping genes, differently regulated target genes and sample integrity: BestKeeper – Excel-based tool using pair-wise correlations. Biotechnol Letters. 2004, 26: 509-515. 10.1023/B:BILE.0000019559.84305.47.
Hanneson R: Fisheries management: The case of the North Atlantic cod. 1996, Oxford: Blackwell Scientific
Johnsen TM, Bjerkeng B, Molvær J, Nygaard E: Miljøvurdering av utfylling av sprengstein i Store Lungegårdsvann. NIVA Report 3927-98, Oslo, Norway. 1998, 1-46. (In Norwegian)
Skei J, Tellefsen T: Monitoring the environmental conditions in the Sørfjord 2005. Part 3. Environmental Toxins in Organisms. Report no.959/2006. TA-No. 2190, (In Norwegian), /2006. Norwegian State Pollution Monitoring Programme
Bustin SA, Benes V, Nolan T, Pfaffl MW: Quantitative real-time RT-PCR – a perspective. J Mol Endocrin. 2005, 34: 597-601. 10.1677/jme.1.01755.
Olsvik PA, Lie KK, Jordal AE, Nilsen TO, Hordvik I: Evaluation of potential reference genes in real-time RT-PCR studies of Atlantic salmon. BMC Mol Biol. 2005, 6: 21-10.1186/1471-2199-6-21.
Zhang ZB, Hu JY: Development and validation of endogenous reference genes for expression profiling of medaka (Oryzias latipes) exposed to endocrine disrupting chemicals by quantitative real-time RT-PCR. Toxicol Sci. 2007, 95 (2): 356-368. 10.1093/toxsci/kfl161.
Tang RY, Dodd A, Lai D, McNabb WC, Love DR: Validation of zebrafish (Danio rerio) reference genes for quantitative real-time RT-PCR normalization. Acta Biochim Biophys Sin. 2007, 39 (5): 384-390. 10.1111/j.1745-7270.2007.00283.x.
Infante C, Matsuoka MP, Asensio E, Canavate JP, Reith M, Manchado M: Selection of housekeeping genes for gene expression studies in larvae from flatfish using real-time PCR. BMC Mol Biol. 2008, 9: 28-10.1186/1471-2199-9-28.
Spinsanti G, Panti C, Lazzeri E, Marsili L, Casini S, Frati F, Fossi CM: Selection of reference genes for quantitative RT-PCR studies in striped dolphin (Stenella coeruleoalba) skin biopsies. BMC Mol Biol. 2006, 7: 32-10.1186/1471-2199-7-32.
Radonic A, Thulke S, Bae HG, Muller MA, Siegert W, Nitsche A: Reference gene selection for quantitative real-time PCR analysis in virus infected cells: SARS corona virus, Yellow fever virus, Human Herpesvirus-6, Camelpox virus and Cytomegalovirus infections. Virol J. 2005, 2 (7):
We gratefully acknowledge Eva Mykkeltvedt and Hui-Shan Tung, NIFES, for analytical help. This work was financed by the National Institute of Nutrition and Seafood Research, Bergen, Norway.
PAO was responsible for the experiment, data analysis and wrote the manuscript. KKL participated in planning, sampling, and contributed throughout the experimental process. LS contributed in the statistical analysis of the data. All authors read and approved the final manuscript.
An erratum to this article is available at http://dx.doi.org/10.1186/1756-0500-4-456.
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Olsvik, P.A., Søfteland, L. & Lie, K.K. Selection of reference genes for qRT-PCR examination of wild populations of Atlantic cod Gadus morhua. BMC Res Notes 1, 47 (2008). https://doi.org/10.1186/1756-0500-1-47
- Reference Gene
- Head Kidney
- Candidate Reference Gene
- Stable Reference Gene
- Principal Component Analysis Plot
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