Selection of ovine housekeeping genes for normalisation by real-time RT-PCR; analysis of PrPgene expression and genetic susceptibility to scrapie
© Garcia-Crespo et al; licensee BioMed Central Ltd. 2005
Received: 15 June 2005
Accepted: 28 September 2005
Published: 28 September 2005
Cellular prion protein expression is essential for the development of transmissible spongiform encephalopathies (TSEs), and in sheep, genetic susceptibility to scrapie has been associated to PrP gene polymorphisms. To test the hypothetical linkage between PrP gene expression and genetic susceptibility, PrP mRNA levels were measured by real-time RT-PCR in six ovine tissues of animals with different genotypes.
Previous to the PrP gene expression analysis the stability of several housekeeping (HK) genes was assessed in order to select the best ones for relative quantification. The normalisation of gene expression was carried out using a minimum of three HK genes in order to detect small expression differences more accurately than using a single control gene. The expression stability analysis of six HK genes showed a large tissue-associated variation reflecting the existence of tissue-specific factors. Thereby, a specific set of HK genes was required for an accurate normalisation of the PrP gene expression within each tissue. Statistical differences in the normalised PrP mRNA levels were found among the tissues, obtaining the highest expression level in obex, followed by ileum, lymph node, spleen, cerebellum and cerebrum. A tendency towards increased PrP mRNA levels and genetic susceptibility was observed in central nervous system. However, the results did not support the hypothesis that PrP mRNA levels vary between genotypes.
The results on PrP gene expression presented here provide valuable baseline data for future studies on scrapie pathogenesis. On the other hand, the results on stability data of several HK genes reported in this study could prove very useful in other gene expression studies carried out in these relevant ovine tissues.
Scrapie is a neurodegenerative disease of the group of transmissible spongiform encephalopathies (TSEs) that affects sheep and goats [1, 2]. The lesions appear mainly in the nervous system in the form of vacuoles triggered by the conversion of the cellular prion protein (PrPc) into the abnormal isoform (PrPSc) followed by its pathological accumulation . Although the exact origin of the disease remains unknown, the "protein only" hypothesis supports the concept that PrPSc is the transmissible agent causing the disease . Therefore, the presence of PrPc is essential to develop scrapie [3, 4]. However, little is known about the physiological role of PrPc and basic PrPc regulating mechanisms.
The development of clinical signs of scrapie has been linked to some PrP gene polymorphisms [5, 6]. According to this genetic profile, animals have been classified into risk groups from Type 1 to Type 5 in increasing order of susceptibility to scrapie according to the UK National Scrapie Plan (NSP) . The reasons for the different genetic susceptibility have been assessed in vitro revealing low conversion efficiencies of PrPc into PrPSc in resistant genotypes [8, 9]. However, individual factors, and unknown genes or proteins might be involved in this genetic susceptibility.
The oral route is the main pathway of transmission of prions in nature. Once the agent has entered into the host, an early amplification occurs in the lymphoreticular system followed by the subsequent spread to several tissues through lymphatic routes, blood or peripheral nervous system. This precedes replication in the central nervous system (CNS) [10, 11]. Taking into account that the presence of PrPc is essential to develop scrapie [3, 4], knowing the distribution of PrPc in lymphoid and nervous tissues is relevant to understanding the pathogenesis of the disease. Likewise, PrP transcript levels and subsequent translation product abundance might play an important role in the transmission and development of the disease. In this sense, absolute quantification studies on bovine and golden hamster PrP gene expression revealed high levels of PrP mRNA in CNS and lymphoid tissues [12, 13], however, these results must be considered with caution due to possible artefacts of the quantification method used. Several methods and techniques can be used to measure mRNA levels. Northern blot analysis has traditionally been used, but more recently, real-time RT-PCR technology provides higher sensitivity and more accurate expression profiles [14, 15]. In contrast to absolute quantification, relative quantification is not influenced by artefacts during sample preparation and it provides the means to detect small expression differences. However, this technique is more demanding than absolute quantification in the sense that it requires the selection of highly stable housekeeping (HK) genes to normalise the expression of the target gene. Although several studies on ovine gene expression have been reported using a single HK gene, the use of at least three stable HK genes is more suitable .
The aim of this work was to select and evaluate the stability of several ovine HK genes for relative expression analyses, and use them to test the hypothetical linkage between PrP gene expression and genetic susceptibility to scrapie.
Primer optimisation and amplification specificity
Primers sequences and real-time PCR amplification parameters
Forward & reverse primers 5' → 3'
Amplicon size (bp)
Tm b (°C)
Selection of the optimal HK genes and normalisation of gene expression
Expression stability values (M) of the six candidate HK genes
Mesenteric lymph node
HK genes stability series for each tissue
Mesenteric lymph node
Normalised PrP gene expression analysis
Relative mRNA expression levels of PrP gene (arbitrary units)
Mesenteric lymph node
nPrP b (SDc)
When the expression values were considered within each tissue, several specific significant (p < 0.05) or marginally significant (p < 0.10) differences were found between pairwise comparisons. In cerebral samples, animals from Type 1 showed the lowest PrP gene expression value, followed by animals from Type 5, Type 3 and Type 2, but only the lower expression level in Type 1 than in Type 2 animals was marginally significant (p = 0.0700). In cerebellum samples, Type 1 showed the lowest expression value followed by Type 2, Type 5 and Type 3. Expression level in Type 1 was marginally lower than in Type 3 (p = 0.0668). In obex samples, Type 1 showed the lowest expression value followed by Type 5, Type 2 and Type 3. Again, expression level in Type 1 was marginally lower than in Type 3 (p = 0.0633). In spleen samples, Type 1 showed the highest expression value followed by Type 3, Type 5, and Type 2. Expression in Type 1 was significantly higher than in Type 2 (p = 0.0281) and in Type 5 (p = 0.0671), and in Type 2 lower than in Type 3 (p = 0.0937). In ileum samples Type 1 showed the highest expression value followed by Type 3, Type 5, and Type 2. In mesenteric lymph node samples Type 1 showed the lowest expression value followed by Type 2, Type 5, and Type 3. When data were grouped in nervous tissues (cerebrum, cerebellum and obex) versus lymphoid tissues (spleen, ileum and lymph node), the models showed a relationship between the PrP mRNA levels and the effect of tissue type (p = 0.0160). A statistical association was found for the interaction between tissue type and risk group (p = 0.0623). PrP mRNA level in lymphoid tissues was significantly higher than in nervous tissues (p = 0.0160). In nervous tissues, Type 3 showed the highest expression value followed by Type 2, Type 5, and Type 1. The expression found in Type 1 was lower than in Type 2 (p = 0.0496), Type 3 (p = 0.0174), and Type 5 (p = 0.0863). Regarding lymphoid tissues samples, Type 1 showed the highest expression value followed by Type 3, Type 5, and Type 2. Expression in Type 1 was higher than in Type 2 (p = 0.0840).
Real-time RT-PCR was chosen among several techniques available to measure the mRNA levels of PrP gene in six important tissues for the transmission and the development of scrapie. Real-time RT-PCR technology provides high sensitivity and accurate expression profiles [14, 15] and in that approach, two basic protocols can be followed: absolute quantification and relative quantification. For gene expression studies, relative quantification is more suitable because the influence of unavoidable artefacts during sample preparation is taken into account. Several works on ovine gene expression have been carried out using the common practice of normalising with a single control gene like 18S rRNA, GAPDH or ACTB [17–19]. However, inter-individual variation of traditionally considered stable HK genes can be high enough to bias gene expression profiles when calculated using only one HK gene for normalisation. Therefore, the use of more than a single HK gene is recommended particularly to detect small expression differences more accurately. Thereby, the sensitivity of this approach depends on how well the HK genes are selected. Thus, in this study a robust method described by Vandesompele et al.  has been followed where the use of a minimum of three stable HK genes is required for an accurate normalisation of the target gene expression after assessing the stability of a given set of HK genes.
The expression stability observed in the six HK genes analysed in the present work varied with the tissue, and therefore, different sets of HK genes were necessary to normalise the PrP gene expression within each tissue. This variability of the HK genes stability among samples from a variety of sources is consistent with the literature [15, 20–22] and reflects the existence of a tissue-specific metabolism and/or unknown tissue-specific factors. These findings clearly demonstrate that there is no single universal control gene for all tissues or cell types. Thereby, these inherent variations have to be taken into consideration and the stability of the HK genes needs to be studied in each scenario prior to any relative quantification study in order to obtain results as accurate as possible. GAPDH and ACTB have been traditionally considered invariable (equally expressed) genes and consequently, they have been widely used as single control genes for gene expression in many studies. However, the expression of these genes can vary from 7 to 23-fold depending on the cell type or tissue . In our study, GAPDH gene showed the lowest variation among the panel of six tissues, whereas ACTB showed the penultimate worst score in variability. This is in agreement with the reported invalidity of ACTB gene for gene expression in ovine interstitial cells from heart valves . Consistent with this variation and in order to improve the accuracy of our results, we normalised the PrP gene expression using the most stable sets of HK genes in each of the six tissues analysed.
In order to test the hypothesis of the linkage between PrP gene expression and PrP genotype-associated susceptibility, 22 Latxa sheep with different genotypes were analysed. Special care was taken with the statistical analysis because the number of samples available for our study was not too large. In this sense, a general linear model was used to control all the effects for which information was available in order to reduce risks of errors linked to repeated separate comparisons and to guarantee that no type α errors were committed. The results revealed statistically significant differences in the PrP gene expression among the panel of six tissues. The highest PrP mRNA expression level in CNS samples was found in obex followed by cerebellum and cerebrum. This circumstance might be translated into high levels of PrPc and perhaps into high levels of PrPSc aggregates considering PrPc as the substrate for conversion into the pathologic isoform. The different PrPc content in the three tissues of the CNS would be in accordance with the spatiotemporal appearance of PrPSc aggregates and would also support the idea that the obex is the best source of material for the detection of PrPSc in TSE rapid tests analyses.
Factors inherent in the nature of the different tissues like transcripts stability or postranscriptional regulation of the PrP gene have also to be considered. In this context, some studies focused on PrP mRNA have shown that there are two PrP mRNA transcripts (2.1 and 4.6 kb mRNA) with a tissue-specific distribution, different stability rates and different efficiency of translation [24–26]. Moreover, a previous work revealed that the isoform profile and the abundance of the PrPc in sheep were tissue-specific, showing lower PrPc abundance in lymphoid tissues (three orders of magnitude) than in CNS tissues . However, our results showed higher PrP transcripts in lymphoid tissues suggesting that a postranscriptional regulation of the PrP gene occurs in these tissues. Therefore, the comparison of PrP gene expression among tissues might be a very complex issue. When expression values from nervous tissues were grouped, a tendency towards increased mRNA expression levels of PrP gene and genetic susceptibility to scrapie was observed in CNS tissues. In these tissues, Type 1 animals showed the lowest expression levels and a gradual increase of PrP gene expression was found towards Type 3. Curiously, Type 3 animals showed more PrP mRNA levels than Type 5, however, no statistical differences were found. On the other hand, in spleen and ileum, Type 1 showed the highest expression levels. Inherent artefacts such as PCR inhibitors in spleen samples or the heterogeneous distribution of the immune system in ileum of different animals might have contributed to the high variability found in these samples.
In general, most of the differences found in this study were only marginally significant, and therefore, the results presented here cannot support the existence of a relationship between PrP mRNA levels and risk group. Interestingly, recent studies using a smaller number of samples have revealed PrP genotype-specific differences in PrPc levels in mononuclear cells of peripheral ovine blood  and in the amount of PrPSc (but no PrPc) in experimentally infected sheep brain . Therefore, if PrPc synthesis were PrP genotype-dependent, this study would show that this association does not occur at the transcriptional level. However, an association at later stages, i.e. at the postranscriptional regulation level (including mRNA transport out of the nucleus, transcripts stability and regulation at the level of translation) cannot be excluded. Thus, since expression of genes is controlled at several steps, further studies applying different approaches are needed. In addition, the complexity of scrapie pathogenesis might also be influenced by other still unknown genes or strain-specific factors.
The global overview of scrapie pathogenesis is quite complex, but being PrPc the substrate for the conversion of the pathogenic form, PrP mRNA transcripts play an important role, and in this sense, the results on PrP gene expression presented here provide valuable baseline data for future studies. In any case, whatever the mechanism for susceptibility, this study showed that it is not related to the regulation of the PrP gene transcripts. On the other hand, the results on stability data of several HK genes reported in this study could prove very useful in other gene expression studies carried out in these ovine tissues. Future gene expression studies including a larger and more diverse (i.e. different breeds) set of samples would benefit from these data.
Twenty-two healthy sheep from Latxa breed were selected according to their susceptibility to scrapie  and the distribution of genotypes within the Latxa sheep population . Hence, all the highly susceptible genotypes (Type 5) described in Latxa breed were included, along with those other genotypes present in more than 1.5% of the population. In any case, only the most prevalent genotypes were represented by more than one individual. Thus, three animals with ARR/ARR genotype, five ARQ/ARQ, one VRQ/VRQ, one ARH/ARH, five ARR/ARQ, five ARQ/VRQ, one ARQ/ARH and one animal with ARH/VRQ genotype were selected. PrP genotyping was performed by real-time PCR as previously described . The age of the animals ranged from 3 to 12 years old. All the animals were negative to TSE by the PrPSc detection kit Platelia®BSE (Bio-Rad, Hercules, CA, USA) on an obex sample. Animals were sacrificed under controlled conditions and a sample from the same region of cerebrum (neocortex), cerebellum, obex, spleen, terminal ileum and mesenteric lymph node was aseptically taken from each animal. All tissues were frozen immediately at -80°C until RNA extraction was performed.
RNA extraction and cDNA synthesis
Tissue samples were homogenised with a Ribolyzer (Hybaid, Ashford, UK) and total RNA was isolated using the RNeasy Protect Mini kit (Qiagen, Hilden, Germany). Total RNA was treated with DNase I (Ambion, Austin, TX, USA) to avoid genomic DNA amplification and first strand cDNA was synthesised using random hexamers and MultiScribe™ reverse transcriptase (Applied Biosystems, Foster City, CA, USA) according to manufacturer's instructions. In addition, the effectiveness of the DNase treatment was assessed in RT-negative samples. After reverse transcription, the same batch of diluted cDNA was subjected to real-time PCR to amplify six HK genes and the PrP gene.
Primers design and optimisation
Six commonly used HK genes were selected to normalise the expression of the target gene PrP: β-actin (ACTB), tyrosine 3-monooxygenase (YWHAZ), ribosomal protein L19 (RPL19), glyceraldehyde-3-phosphate dehydrogenase (GAPDH), glucose-6-phosphate dehydrogenase (G6PDH) and succinate dehydrogenase (SDHA). Primers were designed to span one intron using Primer Express software (Applied Biosystems, Foster City, CA, USA) (Table 1). Primers for the ACTB, GAPDH, RPL19, G6PDH and PrP genes were designed from ovine sequences obtained from GenBank. For the SDHA and YWHAZ genes, ovine sequences were not available and therefore, multiple sequence alignments of these genes obtained from different animal species (Bos taurus, Mus musculus, Rattus norvegicus and Homo sapiens) were carried out using the program AlingX (Vector NTI 8.0 suite, Informax Inc., North Bethesda, MD, USA) to identify conserved regions for primer design. Four concentrations of primers (50 nM, 100 nM, 200 nM and 300 nM) were evaluated, and formation of primer-dimers was assessed by melting curve analysis. Thus, only those concentrations of primers which showed dimer-free reactions were used for the final analysis.
The same number of samples (22) for each tissue were analysed to prevent bias in the results. PCR reactions were set up with the automatic workstation Biomek 2000 (Beckman-Coulter, Fullerton, CA, USA) to minimise pippetting errors. Each sample was analysed in triplicate in a total reaction volume of 10 μl consisting of 10 ng of cDNA, 2xSYBRGreen buffer (Applied Biosystems, Foster City, CA, USA) and the required amount of forward and reverse primers (Table 1). Reactions were run on an ABI PRISM 7000 thermocycler (Applied Biosystems, Foster City, CA, USA) using the following cycling conditions: 95°C for 10 min and 40 cycles at 95°C for 15 s and 60°C for 1 min. For each experiment, a non-template reaction was included as negative control. The specificity of the PCR reactions was confirmed by melting curves analysis of the products as well as by size verification of the amplicons in a conventional agarose gel. In addition, PCR products from the HK genes and PrP gene were cloned into pCR®4-TOPO vector using TOPO TA Cloning® kit (Invitrogen, CA, USA) and submitted to a commercial subcontractor for automatic dye-terminator cycle sequencing. The sequences of SDHA and YWHAZ genes were deposited in GenBank under accession nos. AY970969 and AY970970, respectively.
The threshold cycle values (Ct) were determined at the same fluorescence threshold line for each gene and the Ct value for each sample was obtained by calculating the arithmetic mean of the triplicate values when the standard deviation was lower than 0.16. Ct values were transformed into raw quantity values (Q) according to the following equation, Q = E (Min Ct-Sample Ct) (geNorm user manual, http://medgen.ugent.be/~jvdesomp/genorm/geNorm_manual.pdf), where "E" is the efficiency of the real-time PCR for each gene and "Min Ct" is the minimum Ct value for the samples analysed. E values were calculated for each gene from the given slope after running serial dilutions of cDNA and the following formula E= [10(-1/slope)] .
Selection of the optimal HK genes and normalisation of PrP gene expression
The method described by Vandesompele et al.  was followed to assess the stability of the expression of the HK genes under study using the MS Excel application (geNorm 3.3). Briefly, this application calculates the expression stability measure (M) for the set of HK genes and selects the minimum number of HK genes needed for the normalisation. Thus, genes with the lowest M values have the most stable expression and following the stepwise exclusion of the less stable HK gene M values are re-calculated and the stability series is obtained. Once ranked, the minimum number of HK genes needed was calculated using a cut-off value of 0.15 for Vn/n+1 . The normalisation factor (NF) was then calculated as the geometric mean of their Q values.
Finally, the normalised expression level of the PrP gene (nPrP) was calculated as the ratio between the Q values of PrP gene amplification and the NF calculated for each sample.
In order to compare among tissues, analysis of variance of the reference values (NF) was carried out with the GLM procedure of the SAS statistical package version 8 (SAS institute, Cary, NC, USA). Once the results of this model showed no significant differences among tissues, the PrP/NF ratios (nPrP) were transformed according to the formula arc sin √ (nPrPx100-1) as recommended for use of parametric tests on relative data. Then nPrP values along with all available independent variables (sex, age, tissue and genetic susceptibility) and their interactions were submitted to the GLM procedure of SAS statistical package version 8 (SAS institute, Cary, NC, USA). This analysis showed that sex and age had no significant effects and therefore, only tissue and genetic susceptibility and their interactions as independent variables for effects on nPrP were included in the final model. Genetic susceptibility was considered as risk levels . Comparison of means was carried out using a Student's t test with the SAS statistical package version 8 (SAS institute, Cary, NC, USA).
Financial support was provided by the Basque Government (Projects PI-00-20 and EC2001-3). D. Garcia-Crespo was the recipient of a Predoctoral Fellowship from the Dpto. de Educación, Universidades e Investigación of the Basque Government. We thank A. L. García-Pérez and J. Barandika for their collaboration in the selection of the animals and the TSE laboratory staff for their contribution in rapid test analyses. We thank N. Gomez for helpful comments on the manuscript.
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