The impact of reference gene selection in quantification of gene expression levels in guinea pig cervical tissues and cells
© Lindqvist et al.; licensee BioMed Central Ltd. 2013
Received: 12 July 2012
Accepted: 24 January 2013
Published: 30 January 2013
Accurate measurements of mRNA expression levels in tissues or cells are crucially dependent on the use of relevant reference genes for normalization of data. In this study we used quantitative real-time PCR and two Excel-based applets (geNorm and BestKeeper) to determine the best reference genes for quantification of target gene mRNA in a complex tissue organ such as the guinea pig cervix.
Gene expression studies were conducted in cervical epithelium and stroma during pregnancy and parturition and in cultures of primary cells from this tissue. Among 15 reference gene candidates examined, both geNorm and BestKeeper found CLF1 and CLTC to be the most stable in cervical stroma and cervical epithelium, ACTB and PPIB in primary stroma cells, and CLTC and PPIB in primary epithelial cells. The order of stability among the remaining candidate genes was not in such an agreement. Commonly used reference such as GAPDH and B2M demonstrated lower stability. Determination of pairwise variation values for reference gene combinations using geNorm revealed that the geometric mean of the two most stable genes provides sufficient normalization in most cases. However, for cervical stroma tissue in which many reference gene candidates displayed low stability, inclusion of three reference genes in the geometric mean may improve accuracy of target gene expression level analyses. Using the top ranked reference genes we examined the expression levels of target gene PTGS2 in cervical tissue and cultured cervical cells. We compared the results with PTGS2 expression normalized to the least stable gene and found significant differences in gene expression, up to 10-fold in some samples, emphasizing the importance of appropriately selecting reference genes.
We recommend using the geometric mean of CFL1 and CLTC for normalization of qPCR studies in guinea pig cervical tissue studies, ACTB and PPIB in primary stroma cells and CLTC and PPIB in primary epithelial cells from guinea pig.
KeywordsCervix Guinea pig qPCR Reference genes Parturition Progesterone Estradiol
Accurate measurement of relative mRNA expression levels in tissues or cells using quantitative real-time PCR (qPCR) is crucially dependent on normalization of the data. Due to overall differences in transcriptional activity between tissues and different cell types, normalization cannot be based simply on the amounts of starting material. Since all mRNA molecules in one sample are subject to the same efficiency of RNA purification, reverse transcription and polymerase amplification, quantification of a target gene in the sample is better normalized using the ratio of the target mRNA to an endogenous mRNA reference gene within the sample. It is imperative to use reference genes with minimal variability between samples that are not influenced by the study conditions. A multitude of reference genes have been utilized for this purpose, although none are universally applicable for all tissues or cell types [1, 2]. Thus, for every new experimental system, it is important to identify reference genes that fulfill these criteria. In addition, the widespread use of only one reference gene for normalization of qPCR data has been shown to be inadequate at times often resulting in values that are multiple-fold wrong . It has thus been suggested that using the geometric mean of two or more meticulously selected reference genes results in more accurate comparisons and quantification between study conditions.
In this study, we sought to identify reference genes suitable for determination of gene expression in guinea pig cervical tissues and cells. We also examined the impact of reference gene choice on the measured changes in expression of a gene that has been shown to be expressed and regulated in cervix at term pregnancy in women , i.e., PTGS2, the gene for cyclooxygenase 2. This gene product increases the levels of bioactive prostaglandins which are known to be of importance in cervical ripening. The temporal relationship between cervical ripening and increase in cervical prostaglandins is not known. In mice, rats, as well as other species that depend on progesterone withdrawal prior to parturition, a combination of loss of progesterone systemically  and locally  leads to increased prostaglandin biosynthesis in progesterone-responsive target tissues. In primates and guinea pigs, however, progesterone levels do not decline systemically prior to parturition. Studies of events involved in cervical ripening in humans are complicated by difficulties in obtaining cervical tissue from second and third trimesters of pregnancy. Indeed, most studies to date have been carried out on cervical biopsies taken either in connection with early termination of pregnancy [7, 8], at the time of vaginal delivery [7, 9–11], or Cesarean section at term [10, 12, 13], usually after cervical ripening. Thus, to study this process both in vivo and in vitro, we chose to use the pregnant guinea pig as a model system to dissect changes in gene expression in hormonal settings that mimic those of humans. Despite its historical popularity in research , few studies have been published in which guinea pig gene expression levels have been determined using qPCR. Further, to our knowledge, none have been conducted in cervical tissues or cells.
Several aspects of qPCR studies in the guinea pig cervix are worthy of consideration. First, the cervix is a complex tissue composed of several cell types. Specifically, the stromal compartment is comprised of highly specialized fibroblasts that orchestrate changes in the extracellular matrix and the biomechanical properties of the cervix [15, 16], but myofibroblasts and smooth muscle cells are also present. Endocervical epithelial cells line the cervical canal and are known to alter gene expression during cervical ripening and labor . Finally, a number of different immune cells infiltrate and are activated within the cervix and are believed to contribute to matrix remodeling and function of the cervix during pregnancy and parturition . Hence, to quantify changes in gene expression of the cervix as an organ, reference genes must be applicable to many cell types, all of which differ in transcriptional activity.
Here, we used Excel-based applets (geNorm and BestKeeper) to determine the most stable reference genes among 15 candidates for use in qPCR studies of gene expression levels in guinea pig cervical tissues and cell cultures. More specifically, cervical stroma and epithelial tissues from guinea pigs under various hormonal conditions (e.g., immature, mature nonpregnant and pregnant) were collected and analyzed. Likewise, gene expression levels were quantified in primary cervical stromal and epithelial cells in culture treated with or without estradiol and/or progesterone.
Guinea pig reference gene primer validation using liver cDNA
Amplification efficiency (%)
Expression stability according to geNorm and BestKeeper
Each DNase I-treated RNA sample was analyzed twice, and each qPCR was performed in triplicate. The intra-assay coefficient of variation (CV) ranged from 0.10-0.33 for cervical tissue samples, and from 0.10-0.39 for primary cervical cells. The inter-assay CV for tissues ranged from 0.54-3.06 and from 0.60-2.56 for primary cells. Expression level of the candidate reference genes in each tissue was examined before the geNorm or BestKeeper analyses were performed. Any reference gene for which the Cq was above 30 among in a category of samples was excluded from the study. Expression of TBP was found to be too low in all tissues and cell types. HMBS expression level was too low in stromal tissues and stromal cells, and TFRC expression was also too low in stromal tissues. The remaining candidates were included in the geNorm and Best Keeper analyses to determine expression stability.
Stability of various potential reference genes in guinea pig cervical tissues
Stability of reference gene candidates in guinea pig cervical primary cell cultures
M values (determined with geNorm) were lower in cultured primary cells relative to tissue samples, ranging from 0.1-0.35 in stroma cells and 0.1-0.25 in epithelial cells, suggesting that all tested gene candidates are expressed at rather stable levels in cultured cells. ACTB and PPIB were ranked as the two most stable genes in primary stroma cells whereas CLTC and PPIB were found to be the most stable in primary epithelial cells (Table 3). BestKeeper analysis also revealed the same two genes as top ranked (Table 3), with R values ranging from 0.981-0.999.
Pairwise variation to determine optimal number of reference genes
Target gene expression levels vary according to choice of reference gene set
Gene expression studies in tissue or cell samples depend on usage of appropriate reference genes. Many published qPCR studies normalize target gene expression with the same reference genes that were used for normalization of data obtained with Northern blotting (e.g. GAPDH, 18S, ACTB and HPRT). These genes have since been found to be regulated in certain situations, for example under the influence of steroid hormones [18–20]. In hormone-responsive tissues, such as the uterine cervix, expression levels of reference genes needs to be unaffected by hormonal change associated with the menstrual/estrous cycle or pregnancy, the effect of the presence of an embryo physical impact on the organ (pressure, stretching,) or growth hormones and prostaglandins released by the growing fetus or placenta. Different methods to find the most stable reference genes have been developed such as geNorm , BestKeeper , NormFinder , Principal Component Analysis , and methods based on restricted maximum likelihood with support of descriptive statistics . Kayis et al.  compared the ability of these different methods to rank reference gene stability in equine endometrium and found that, with the exception of NormFinder, all methods identified the same genes as the most stable. They also found that all methods gave similar results for the least stable genes in the same tissue. Here we chose to use geNorm and BestKeeper to identify the most stable reference genes of fifteen candidates in tissue and cell samples from the guinea pig cervix.
Although guinea pigs have been used historically and extensively for animal models in the laboratory, the guinea pig genome has not been completely sequenced. When deciding which reference gene candidates to include in this study, we chose to use only genes for which the guinea pig genomic/cDNA sequence was known and we only included mRNA reference genes. We based our exclusion of the commonly used 18S gene not only on the fact that it represents a different class of RNA but it is also present at a very high abundance in samples which makes dilution of the samples necessary conferring less precision and accuracy. Some reference genes included in the study (e.g. RPLP0) have been shown to be unregulated by estrogen in human breast cancer cells [25, 26]. Similarly, ACTB mRNA was reported to be unregulated in human endometrium during the course of the menstrual cycle . Thus, these two genes were of great interest as potential candidates for normalization of qPCR data in the guinea pig cervix. Our results indicate that ACTB is indeed a stable gene in guinea pig cervix, but only in stromal tissues and in cultured primary stroma cells. In epithelial tissues and cultured epithelia cells, ACTB ranked among the least stable. In addition, RPLP0 did not rank among the most stable in any of the samples, a finding that exemplifies the importance of evaluating reference for each new sample set and for each experimental set up.
It should be emphasized that cell populations and tissues used in this study are not pure. The collection technique allows us to dissect stroma- and epithelium-enriched tissue. No doubt, each tissue type may be contaminated by epithelial or stromal cells, respectively. Further, the extent of this contamination may vary according to pregnancy or hormonal state. The higher M values in tissue samples relative to those in cultured cervical cells are most likely due to heterogeneous cellular composition of tissues. Nonetheless, results from this study support the notion that even under these very variable conditions it is possible to identify reference genes that are expressed in a stable manner.
In summary, we used two different methods, geNorm and BestKeeper, to identify the most stable reference genes in guinea pig cervix among fifteen candidates. Both methods identified CFL1/CLTC as the most stable in cervical tissues, ACTB/PPIB for cultured stroma cells, and CLTC/PPIB for cultured epithelia cells. The minimum number of reference genes to be included in the geometric mean for normalization of qPCR data was found to be two in cervical epithelial tissue and cells, and in cultured stroma cells. In cervical stroma tissue, where the tested reference genes display a higher degree of instability, the mean of three, ACTB/CFL1/CLTC, improves the normalization according to geNorm. In our limited sample numbers there was no statistical difference demonstrated between two and three reference genes. Nevertheless, the importance of stable reference genes in quantification of mRNA levels in complex tissues cannot be overstated.
Guinea pig tissue collection
Hartley guinea pigs (Elm Hill Labs, Chelmsford, MA) were kept individually in the Animal Care Facility at UT Southwestern, housed at 21°C with 30-70% humidity under a 12 h light cycle, and fed Teklad Global Guinea Pig Diet 2040 pellets, water, and hay ad libitum. All animal procedures were approved by the UT Southwestern Institutional Animal Care and Use Committee. Twenty four female guinea pigs representing sexually immature (n=1), sexually mature non-pregnant (n=4), pregnant (n=15) and postpartum period (n=4) were sacrificed using i.p. Euthasol Euthanasia Solution (390 mg pentobarbital sodium and 50 mg phenytoin sodium/ml) injections according to IACUC approved protocol. The reproductive tract was immediately removed and the cervix excised and further micro dissected into cervical epithelium and stroma. Epithelium was obtained by scraping the lining of the endocervical canal with a scalpel whereas the remaining underlying connective tissue was considered stroma. Cervical and vaginal epithelium covering the external os were discarded. All tissues were snap frozen in liquid nitrogen and stored at −80°C.
Cervical tissues (5–50 mg) were thawed and homogenized in RNA STAT-60 (TelTest Inc., Friendswood, TX) using a tissue tearor (Biospec Products, Inc., Bartlesville, OK). Thereafter, total RNA was extracted according to the manufacturer’s protocol, using chloroform (C2432, Sigma, St. Louis, MO), isopropanol (I9516, Sigma, St. Louis, MO), and ethyl alcohol (E190, Pharmaco-Aaper, Brookfield, CT). Each RNA sample (~10 μg) was treated for 30 min @ 37°C with 2 U DNase I in 50 μl reactions (DNA-free, part no. AM1906, Ambion) for removal of contaminating genomic DNA, and subsequently stored at −80°C. Total RNA was isolated from cells in culture using an RNAqueous®-4PCR kit (cat. No. AM1914, Ambion, Austin, TX), and subsequently stored at −80°C.
Guinea pig cervical primary cell culture
Cervical tissues were obtained from a mature nonpregnant guinea pig. After mincing in 2–4 mm pieces, fresh tissues were incubated for 1 h at 37°C in solution containing collagenase B (1 mg/ml) (cat no. 11088823103, Roche, Indianapolis, IN) and DNase I (0.1 mg/ml) (cat no. 10104159001, Roche, Indianapolis, IN). The mixture was then strained through a 70 μm mesh (cat no. 352350, BD Biosciences, Bedford, MA) to achieve separation between stromal (flow through) and epithelial (retained) cells. The respective cells were collected, dispersed in DMEM without phenol red (cat no. 11054, Invitrogen, Carlsbad, CA) buffered with 10 mM HEPES (cat no. 15630, Invitrogen, Carlsbad, CA), and supplemented with 2 mM L-Glutamine (cat no. 25030, Invitrogen, Carlsbad, CA), 10% by volume fetal bovine serum (FBS) (cat no. S11150, Atlanta Biologicals, Lawrenceville, GA) and penicillin G (10 U/ml)-streptomycin sulfate (10 μg/ml)-amphotericin B (25 ng/ml) mix (cat no. 9350, Irvine Scientific, Santa Ana, CA). Cells were plated at 5 × 105 cells/cm2 and culture medium was changed every other day until near confluency (2–4 day). Preconfluent cells in passages 1–3 were used for experiments. Cells were serum-deprived for 3 day before treatment with 17β-estradiol (10 nM), progesterone (1 μM), a combination of 17β-estradiol and progesterone, or vehicle (ethanol) for 24 h.
Nucleic acid quantification and purity assessment were conducted spectrophotometrically using a SmartSpec™3000 (Bio-Rad, Hercules, CA), with expected 260/280 ratios above 1.8. A High Capacity cDNA Reverse Transcription Kit (part no. 4368813, Applied Biosystem, Carlsbad, CA) based on random primer priming with MultiScribe™ Reverse Transcriptase was used for cDNA synthesis from 2 μg total RNA in 20 μl reaction volumes, with the following reaction conditions; 25°C for 10 min, 37°C for 2 hrs, 85°C for 5 min, and 4°C for 1 min. The final product was diluted to correspond to 20 ng initial RNA input/μl, and was stored at −20°C.
Selection of reference and target genes, and primer design
Guinea pig reference and target gene information
Primer sequences 5’ to 3’
Amplicon size (bp)
Ensembl or GenBank accession no.
Sense and antisense
From ref. 
ATP synthase, F1 complex β subunit
5 and 6
Adenosine triphosphatase 6
Cell surface molecule component
3 and 4
1 and 2
Coated vesicle formation protein
C-terminal binding protein 1
4 and 5
Transcriptional repressor phosphoprotein
From ref. 
9 and 10
1 and 2
Protein folding catalyst
Ribosomal protein, large, P0
3 and 4
Succinate dehydrogenase, subunit A
4 and 5
Citric acid cycle enzyme
5 and 6
8 and 9
Tumor protein, translationally controlled 1
4 and 5
3 and 4
Quantitative real-time PCR (qPCR)
All qPCR was performed using 50% of iTaq SYBR green SUPERMIX with ROX (cat. no. 172–5851, Bio-Rad, Hercules, CA), 900 nM of each primer and 30 ng cDNA (assuming a 1:1 reversed transcription reaction efficiency) in 19 μl reactions in MicroAmp® Optical 384-Well Reaction Plates (part no. 4309849, Applied Biosystems, Carlsbad, CA) on a 7900HT Fast Real-Time PCR System (Applied Biosystems, Carlsbad, CA). The cycling program was: stage A 50°C for 2 min; stage B (denaturation) 95°C for 10 min; stage C (cycling) 95°C for 15 sec and then 60°C for 1 min repeated 40 times, and stage D (dissociation) 95°C for 15 sec then 60°C for 15 sec and a final 95°C for 15 sec. All samples were run in triplicate and each primer pair was validated using a 7 point 5-fold dilution series of guinea pig liver cDNA (50–0.0032 ng per reaction) and no template controls.
Analyses of qPCR results using geNorm and BestKeeper
Each RNA sample was analyzed twice from the reversed transcriptase step and on, and the threshold cycle (Cq) value for each sample was determined for all primer pairs. The mean Cq of triplicates for each sample run was then used for input in geNorm v3.5 and BestKeeper v1 applets, and the respective stability values were automatically calculated as described [3, 21].
Quantitative real-time PCR
No template control
ATP synthase F1 complex β subunit
C-terminal binding protein 1
Ribosomal protein large P0
Succinate dehydrogenase subunit A
Tumor protein translationally controlled 1
Fetal bovine serum.
The authors like to thank Dr. Matthew Riegel for providing expertise and advice regarding animal care and euthanasia. This work was supported by NIH grant HD011149.
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