- Research article
- Open Access
Development of a new set of reference genes for normalization of real-time RT-PCR data of porcine backfat and longissimus dorsi muscle, and evaluation with PPARGC1A
© Erkens et al; licensee BioMed Central Ltd. 2006
Received: 09 June 2006
Accepted: 09 October 2006
Published: 09 October 2006
An essential part of using real-time RT-PCR is that expression results have to be normalized before any conclusions can be drawn. This can be done by using one or multiple, validated reference genes, depending on the desired accuracy of the results. In the pig however, very little information is available on the expression stability of reference genes. The aim of this study was therefore to develop a new set of reference genes which can be used for normalization of mRNA expression data of genes expressed in porcine backfat and longissimus dorsi muscle, both representing an economically important part of a pig's carcass. Because of its multiple functions in fat metabolism and muscle fibre type composition, peroxisome proliferative activated receptor γ coactivator 1α (PPARGC1A) is a very interesting candidate gene for meat quality, and was an ideal gene to evaluate our developed set of reference genes for normalization of mRNA expression data of both tissue types.
The mRNA expression stability of 10 reference genes was determined. The expression of RPL13A and SDHA appeared to be highly unstable. After normalization to the geometric mean of the three most stably expressed reference genes (ACTB, TBP and TOP2B), the results not only showed that the mRNA expression of PPARGC1A was significantly higher in each of the longissimus dorsi muscle samples than in backfat (P < 0.05), but also that the expression was significantly higher in the most cranial of the three muscle samples (P < 0.05).
This study provides a new set of reference genes (ACTB, TBP and TOP2B) suitable for normalization of real-time RT-PCR data of backfat and longissimus dorsi muscle in the pig. The obtained PPARGC1A expression results, after application of this set of reference genes, are a first step in unravelling the PPARGC1A expression pattern in the pig and provide a basis for possible selection towards improved meat quality while maintaining a lean carcass.
Because of consumers' demands, the emphasis of modern day porcine breeding programmes and selection criteria is gradually shifting towards a higher meat quality, instead of the more classical focus of just selecting for a lean carcass and high growth rate . Two strongly genetically determined factors influencing meat quality are the amount of intramuscular fat (IMF) and muscle fibre type composition . The first factor has a large impact on the taste of the meat and its deposition is strongly influenced by the surrounding muscle . Peri- and post-mortem biochemical processes in muscle and meat are strongly influenced by muscle fibre type composition and in their turn influence meat tenderness . The fibre type composition depends on the location and use of a muscle. Muscles used for posture are more oxidative, while more active muscles contain more glycolytic fibres . In general, meat quality increases if more oxidative fibres and less glycolytic fibres are present, but the influence of fat distribution and fibre type composition on meat quality also varies between different breeds [1, 5, 6].
Unfortunately the selection of leaner pigs was often accompanied by a decrease in IMF and a lower percentage of oxidative fibres, resulting in a decrease of meat quality [7, 8]. To understand the complex relationship between all the traits affecting meat quality, it is important to trace the responsible genes. One particularly interesting gene in this regard is the peroxisome proliferative activated receptor γ coactivator 1α (PPARGC1A), a coactivator that influences the expression of many genes through a whole range of nuclear hormone receptors and other transcription factors, like the peroxisome proliferative activated receptors (PPAR α, β, γ), nuclear respiratory factors and the thyroid hormone receptor [9, 10]. PPARGC1A plays an important role in adipogenesis and adipocyte differentiation , mitochondrial biogenesis and respiration [9, 12], and hepatic gluconeogenesis . This means that the gene is involved in adaptive thermogenesis, fat metabolism and energy homeostasis. PPARGC1A can be induced by cold and exercise, it has been proven to function as a natural protection against obesity in brown fat of mice by producing heat and it is especially expressed in tissues with a high energy demand, like muscle and brown fat [9, 10, 14]. The expression is higher in muscles that contain more oxidative fibres and it has been shown that PPARGC1A is an important factor in determining fibre type in that it enhances the number of oxidative muscle fibres [15, 16]. Also, other candidate genes for meat quality like glucose transporter 4 (GLUT4) are regulated by PPARGC1A, making it an even more interesting gene . All these functions and the fact that already a quantitative trait locus for leaf fat weight in the pig has been located in the chromosomal region to which PPARGC1A was mapped , illustrate that PPARGC1A is a very promising candidate gene with regard to meat quality.
In humans, PPARGC1A has been thoroughly investigated because of its presumed role in the obesity pandemic and correlated diseases like type II diabetes mellitus and cardiovascular complications, especially in search of possible future therapies [19–21]. In the pig however, very little is known about PPARGC1A although it has a great economic potential and, because of the strong genetical resemblance between pig and man, the information could be useful in human research as well [22, 23]. Jacobs et al.  already described the porcine PPARGC1A coding sequence and discovered several polymorphisms, of which at least one was significantly associated with backfat.
To study mRNA expression levels, one needs a set of carefully selected and validated reference genes (also called housekeeping genes) for normalization purposes. In the pig however, virtually no information is available on reference genes. In this study, we therefore designed assays to measure the mRNA expression levels of several candidate reference genes, followed by determination of their expression stability and suitability for normalization purposes in the tissues of interest. The first aim of this study was to develop a set of reference genes that can be used for normalizing real-time RT-PCR mRNA expression data from backfat and longissimus dorsi muscle of the pig. These two tissues comprise an important part of the carcass and have quite opposite demands regarding fat content, as explained above. If the regulation of PPARGC1A expression proves to be different in these tissues, unravelling the mechanism can possibly enable future selection towards one feature without influencing the other. Therefore the second aim of our study was to assess whether PPARGC1A mRNA expression differs between backfat and several longissimus dorsi muscle locations.
Reference gene expression and selection
The same analysis was performed on the data obtained from the larger independent group of 30 pigs and showed exactly the same significant differences in PPARGC1A expression (See additional file 1: AddFileRelativeExpression30pigs.doc).
Real-time RT-PCR is a sensitive and accurate technique for measuring gene expression , but to be able to compare mRNA expression across samples, it is essential to correct for variables such as differences in the amount of starting material in the reaction and enzyme efficiency. This normalization can be performed by using internal reference genes. Contrary to original expectations, it has been proven that their expression level can vary extensively with tissue type and (experimental) conditions, and that their use needs to be validated for each type of tissue and every experimental setup [26–28]. Furthermore Vandesompele et al.  showed that more than one reference gene should be used for accurate normalization of expression data.
In the pig however, very little is known about the expression of reference genes, certainly in combination with real-time RT-PCR. Analysis of the expression stability of the 10 chosen reference genes showed that RPL13A and SDHA cannot be used for normalization of longissimus dorsi and backfat data. The expression of RPL13A, a component of the 60S ribosomal subunit, varied per animal. As far as we know, this is the first time such an expression pattern is described for this reference gene, and could reflect a large difference in basic transcriptional activity depending on the animal and/or tissue used. Because of the importance of a correct protein synthesis mechanism, it is likely that for the samples in which no RPL13A was detected, its function was (partly) taken over by another ribosomal protein [29–31], or that an alternative splice product exists to which the used primer(s) could not anneal [32, 33]. Another possible explanation for this variability is technical variation, because the assay could have been at the limit of its sensitivity. SDHA, an enzyme involved in energy production (Krebs cycle and respiratory chain) , could not be detected in backfat samples, except for a very weak signal in a few pigs. This could indicate SDHA is present in much lower concentrations in backfat compared to longissimus dorsimuscle, which agrees with one of the main functions of white adipose tissue, storing energy. But from the data presented here no definitive conclusions can be drawn regarding the cause of this variability.
As mentioned before, expression results are considerably more reliable if they are normalized using the geometric mean of multiple reference genes . GeNorm analysis indicated that addition of the 3rd reference gene to the normalization factor had the largest impact on reducing variability. Though variability further decreased by including a 4th and 5th gene, the decrease is minimal and does not outweigh the practical considerations accompanying the inclusion of more genes. Therefore, the use of the geometric mean of the 3 most stably expressed reference genes (ACTB, TOP2B and TBP; Figure 2) provides reliable results for backfat and longissimus dorsi mRNA expression comparison in the pig.
Although it has been investigated which tissues express PPARGC1A and what the effects of sequence polymorphisms are [16, 18, 35], little is known in the pig about its relative mRNA expression when comparing tissues to one another. Because this knowledge is essential in researching differences in PPARGC1A regulation in view of selection for improved meat quality, we compared its mRNA expression in 2 economically important tissue types. Our results not only clearly indicate that the PPARGC1A mRNA expression is significantly higher in longissimus dorsi muscle than in backfat (P < 0.05), but also that its expression is significantly higher in the most cranial of the 3 muscle samples (P < 0.05; Figure 3). The PCR efficiencies of the standard curves indicated that the lower mRNA expression of PPARGC1A in backfat was not due to inhibition. Nevertheless, if there would be any inhibition present, this should be corrected for by normalization. These results correspond with findings in humans where PPARGC1A mRNA expression in vastus lateralis muscle was clearly higher than in subcutaneous fat , and are similar to studies in the pig on the mRNA expression of PPARγ (one of the transcription factors coactivated by PPARGC1A) which showed variation between visceral and subcutaneous fat . In a study on the effect of exercise on PPARGC1A protein expression in rats, differences were not only found between various skeletal muscles, but also basal protein expression in a control group differed between the more oxidative and the more glycolytic part of the gastrocnemius muscle . Keeping this in mind, a possible explanation for the higher mRNA expression in the most cranial longissimus dorsi sample could be that because of its location, it has other energy demands and fibre type composition compared to more caudal parts of the muscle. Our findings could indicate a tissue and location specific regulation of PPARGC1A expression correlating with the functions of PPARGC1A in longissimus dorsi muscle and backfat . But on the other hand mRNA expression differences do not necessarily translate into protein expression differences .
The data from this study not only present a newly developed set of reference genes for normalization of mRNA expression data from porcine backfat and longissimus dorsi muscle, but also prove that significant differences exist in PPARGC1A mRNA expression between and within (for muscle) these economically important tissues, providing a basis for possible selection towards improved meat quality while maintaining a lean carcass.
Sample collection and cDNA synthesis
Information on the primers used for real-time PCR
Primer sequence (5'→3')
GenBank accession number or reference
Full reference gene names
Full gene name
hypoxanthine phosphoribosyltransferase 1
ribosomal protein L13a
succinate dehydrogenase complex, subunit A
TATA box binding protein
topoisomerase II beta
tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, zeta polypeptide
Real-time PCR assays
Real-time PCR was conducted on the iCycler iQ Real-Time PCR Detection System (Bio-Rad), each reaction consisting of 7.5 μl Platinum SYBR Green qPCR SuperMix UDG (uracil-N-glycosylase; Invitrogen) spiked with 0.15 pmole fluorescein calibration dye (Bio-Rad), 2.5 μl cDNA, the optimized amount of primer and supplemented with water (Molecular Biology Grade, Eppendorf) to a total volume of 15 μl. The real-time PCR program started with a 2 minute UDG incubation step at 50°C, followed by a 3 minute denaturation at 95°C, during which the hot start platinum Taq DNA polymerase was fully activated. This was followed by 40 cycles of 15 seconds of denaturation at 95°C and 30 seconds of annealing/elongation at the optimal annealing temperature (Ta) for each specific primer (Table 1), during which fluorescence was measured. Next a melting curve was constructed by increasing the temperature from 70 to 95°C in sequential steps of 0.5°C for 10 seconds, at which fluorescence was measured. This allowed the verification of the presence of one gene-specific peak and the absence of primer dimer peaks, which also give a fluorescent signal and influence PCR efficiency. During optimization all PCR products were loaded onto a 2% agarose gel (Gentaur) for verification. A 10-fold dilution series of cDNA was included in each run to determine PCR efficiency by constructing a relative standard curve. PCR efficiencies were consistently > 92% and were used to convert the Ct-values into raw data (not yet normalized, relative quantities). All experiments contained a negative control and samples were analyzed in 2 independent runs.
Reference gene selection
To determine the mRNA expression stability of the 10 reference genes, their expression in the 4 tissue samples (biological replicates) of 20 randomly selected animals was measured using real-time PCR, as described above. This means that for each reference gene 80 reactions were performed in duplicate (technical replicates), in 2 separate runs. To correct for technical inter-run variation between replicated reactions of the same sample measured in different runs, the data from these 2 runs were calibrated by calculating the average Ct-value over all the samples in each run and subtracting the difference between these 2 averages from each individual sample in the run with the highest average Ct-value. After this calibration step, the average Ct-value of each duplicate reaction was converted to relative quantities and these were analyzed using the geNorm algorithm, which is based on the principle that the expression ratio of 2 ideal reference genes should be identical in all samples . Using this algorithm, the most stably expressed reference genes and their optimal number for normalization were determined.
The same procedure of real-time PCR, calibration and conversion to relative quantities was repeated for the 4 tissue samples of the remaining 30 animals, performed with only the 3 most stably expressed reference genes as determined by geNorm.
PPARGC1A mRNA expression and data processing
Real-time PCR was conducted with the primers for PPARGC1A on the 4 samples of all 50 animals, after which the mRNA expression data were calibrated and converted into raw data in the same manner as described above for the reference genes. Then for each animal the geometric mean of the raw expression data of the 3 most stably expressed reference genes (i.e. normalization factor, NF) was calculated and used for subsequent normalization, dividing the raw PPARGC1A mRNA expression data by the NF. These normalized expression levels of PPARGC1A were then converted into logarithmic values, the average per sample type and the 95% confidence interval was calculated, these in their turn were converted into linear rescaled values and eventually plotted in a graph (Figure 3).
The authors like to thank Marc Mattheeuws and Ruben Van Gansbeke for their help in collecting samples, and Lies Bogaert for assisting in graphical design. This work was supported by Ghent University BOF-grant no 01104005.
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