Identification of stable endogenous control genes for transcriptional profiling of photon, proton and carbon-ion irradiated cells
© Sharungbam et al.; licensee BioMed Central Ltd. 2012
Received: 1 December 2011
Accepted: 17 May 2012
Published: 17 May 2012
Quantitative analysis of transcriptional regulation of genes is a prerequisite for a better understanding of the molecular mechanisms of action of different radiation qualities such as photon, proton or carbon ion irradiation. Microarrays and real-time quantitative RT-PCR (qRT-PCR) are considered the two cornerstones of gene expression analysis. In interpreting these results it is critical to normalize the expression levels of the target genes by that of appropriately selected endogenous control genes (ECGs) or housekeeping genes. We sought to systematically investigate common ECG candidates for their stability after different radiation modalities in different human cell lines by qRT-PCR. We aimed to identify the most robust set of ECGs or housekeeping genes for transcriptional analysis in irradiation studies.
We tested the expression stability of 32 ECGs in three human cancer cell lines. The epidermoid carcinoma cells (A431), the non small cell lung carcinoma cells (A549) and the pancreatic adenocarincoma cells (BxPC3) were irradiated with photon, proton and carbon ions. Expression Heat maps, clustering and statistic algorithms were employed using SUMO software package. The expression stability was evaluated by computing: mean, standard deviation, ANOVA, coefficient of variation and the stability measure (M) given by the geNorm algorithm.
Expression analysis revealed significant cell type specific regulation of 18 out of 32 ECGs (p < 0.05). A549 and A431 cells shared a similar pattern of ECG expression as the function of different radiation qualities as compared to BxPC3. Of note, the ribosomal protein 18S, one of the most frequently used ECG, was differentially regulated as the function of different radiation qualities (p ≤ 0.01). A comprehensive search for the most stable ECGs using the geNorm algorithm identified 3 ECGs for A431 and BxPC3 to be sufficient for normalization. In contrast, 6 ECGs were required to properly normalize expression data in the more variable A549 cells. Considering both variables tested, i.e. cell type and radiation qualities, 5 genes-- RPLP0, UBC, PPIA, TBP and PSMC4-- were identified as the consensus set of stable ECGs.
Caution is warranted when selecting the internal control gene for the qRT-PCR gene expression studies. Here, we provide a template of stable ECGs for investigation of radiation induced gene expression.
KeywordsEndogenous control genes Internal control genes qRT-PCR Photon Proton Carbon-ion Tumour cells A431 A549 and BxPC3
In addition to direct, e.g. DNA damaging effect, system level cellular responses to ionizing radiation are attributed to the initiation of intracellular signals and subsequent differential regulation of genes/pathways governing various cellular processes . Therefore, detecting differential regulation of genes is critical for a better understanding of radiation-induced molecular effects. Transcriptional perturbation after cell exposure to different radiation qualities is investigated to unravel the systems biology of cellular response underlying, normal tissue toxicity, carcinogenesis, or anti-cancer effects of irradiation [1–3]. Therefore, these studies have ramification for a broad spectrum of basic and applied sciences ranging from effects of space radiation to carcinogenesis to cancer therapy.
In contrast to conventional photon irradiation the molecular effects of proton or heavier ions (e.g. carbon ions) are less explored yet. However, emerging data indicate molecular differences in transcriptional response of cells to particles as compared to photon irradiation [4, 5].
One reliable and highly sensitive tool that allows rapid and accurate results in gene expression analysis is the qRT-PCR [6, 7]. As in any gene expression analysis, selection of a valid normalization or endogenous control to correct for differences in RNA sampling is critical to avoid misinterpretation of results. Inter-sample variation due to sample collection, RNA preparation and quality, inherent sample differences, pipetting errors, different efficacies of the radiation qualities and reverse transcription efficiency are common sources of variability. The ideal endogenous control should have a constant expression level under different experimental conditions and be sufficiently abundant across different samples and cell lines. Although any gene that is stably expressed under a defined experimental condition can be used for normalization, the selection is most commonly made from the constitutively expressed ECGs.
However, the expression levels of the commonly used ECGs may not only vary in different cell lines but also under different experimental treatments or pathological states [8–25]. This necessitates the selection of ECGs which are appropriate for each experimental system. Although, there has been systematic selection of ECGs for various experimental systems, such selection has not been conducted so far for studying the effects of different radiation qualities.
Here, we investigate the expression stability of 32 commonly used ECGs in three human cancer cell lines irradiated with photon, proton and carbon ions. Differential regulation of ECGs was found as the function of both variables, radiation quality and cell type, respectively. Reliable internal control genes for individual cell lines were identified such as PGK1, RPL37A and PSMC4 for A431; RPLPO, UBC, GAPDH, MT-ATP6, CASC3 and PES1 for A549; and RPL37A, RPLPO and CASC3 for BxPC3. A systematic analysis further revealed 5 stable genes among the 32 candidate ECGs tested to normalize gene expression data generated in different cells and after various radiation qualities.
Expression of the 32 ECGs
In this study, 32 ECGs (Additional file 1) were evaluated to identify the most suitable reference genes for gene expression profiling of irradiated cell lines. This collection of genes constitutes frequently used ECGs which were selected based on their relative high abundance and constitutive expression determined by literature search and/or whole genome microarray data. The three prototypic tumour cell lines-- A431, A549 and BxPC3 used in this study are among most commonly investigated model cell lines for each tumor entity. They were irradiated with photon, proton and carbon ions. After total-RNA isolation and quality control using lab-on-chip bioanalyzer, qRT-PCR was performed using Taqman primer and probes.
CT-values and ECG regulation
Cycle threshold (CT) values and coefficient of variation (CV) of 32 endogenous control genes across the samples of the cell lines
Mean CT ± SEM
18.44 ± 0.29
24.61 ± 0.41
23.45 ± 0.42
17.83 ± 0.34
21.90 ± 0.46
23.71 ± 0.51
19.81 ± 0.43
16.53 ± 0.37
24.19 ± 0.56
15.66 ± 0.38
22.12 ± 0.55
24.47 ± 0.64
23.30 ± 0.63
24.11 ± 0.70
18.14 ± 0.53
18.05 ± 0.53
23.64 ± 0.72
18.08 ± 0.55
23.10 ± 0.71
22.08 ± 0.68
23.98 ± 0.81
19.35 ± 0.69
24.01 ± 0.95
22.98 ± 0.95
17.80 ± 0.75
22.76 ± 1.00
24.80 ± 1.13
26.29 ± 1.37
23.96 ± 1.26
22.13 ± 1.18
19.33 ± 1.21
10.78 ± 1.02
ECG regulation using heat map
The results in this section corroborated the findings of many other previous studies that the ECGs might be differentially regulated depending upon the experimental set-up and the cell type [8–25]. More importantly, this analysis seems to suggest that the ECGs are differentially regulated by the different cell types and radiation qualities. We attempted to confirm this observation employing a systematic analysis of the expression levels.
Identification of appropriate ECGs
Gene expression levels obtained using PCR should be appropriately normalized by one or more carefully selected stable internal control genes. The geNorm algorithm developed by Vandesompele et al.  can determine the expression stability of control genes on the basis of non-normalized expression levels. This measure relies on the principle that the expression ratio of two internal control genes is constant in all samples regardless of the experimental condition or cell type. This algorithm computes a gene expression stability measure (M) for each gene based on the average pairwise expression ratio and then performs a stepwise exclusion of the least stable gene. Then the M values are computed again and stepwise exclusion performed until two genes are left. The genes with the lowest M values are considered to be the most stable across all the samples for each cell line.
Ranking of the 32 ECGs
Control genes ranked in order of their expression stability*
Calculation of normalization factor
Figure 6 shows that the value of V3/ 4 was low for A431, implying that the first 3 ECGs (PGK1, RPL37A, PSMC4) were sufficient to be used for normalization. For A549, the low value of V 6/7 indicated that the first 6 ECGs (RPLPO, UBC, GAPDH, MT-ATP6, CASC3, PES1) were sufficient for normalization. In BxPC3, the three most stable ECGs (RPL37A, RPLPO, CASC3) were sufficient for normalization purposes.
Validation of the gene-stability measure M
Radiation-specific expression of the ECGs within the cell lines
Identifying the consensus set of ECGs for comparative studies across all cell types
The emergence of a growing number of particle therapy facilities worldwide will stimulate comparative studies aiming to decipher the molecular mechanisms underlying differential biological effects of these novel radiation qualities. Comparative investigation of gene regulation on transcriptional level as the function of radiation treatment constitutes a cornerstone of these studies. Quantitative real time PCR (qRT-PCR) is considered the most sensitive method for detection of gene expression level. One limitation of this method is the need for proper endogenous control gene. To generate relative expression levels, the expression of the reference gene/s needs minimally alter among different types of cells or treatments. The goal of this study was to identify such ECGs.
We analysed the expression levels of 32 ECGs using the clustering, statistical methods such as ANOVA and the geNorm algorithm. Global analysis lead to the finding that gene expression profile in pancreatic cancer cells (BxPC3) is different as compared to the two other epithelial cancer cells tested i.e. epidermoid and lung carcinoma cells (A431 and A549). The ECGs in BxPC3 showed least variation in expression whereas A549 showed maximum variation in expression as the function of radiation qualities. Among the three cell lines, the ECGs were more stable in BxPC3. From the point of view of selecting appropriate ECGs this feature might be advantageous. On the other hand, it means that the ECGs in BxPC3 are less regulated by different radiation qualities.
ANOVA analysis of non normalized data revealed that 18 out of the 32 ECGs showed cell type specific differential regulation as shown by the differences in the expression profile between A431, A549 and BxPC3. In addition, significant radiation quality specific regulation was shown by one gene the ribosomal protein 18S. Of note, this gene is one of the most commonly used internal control genes. Therefore, our data suggest validation of this gene prior to its use as internal control in radiation biology studies.
Although the clustering and ANOVA analysis of the raw data provided an overall overview and information about ECGs regulation, they do not allow the selection of appropriate stable ECGs for normalization of the qRT-PCR data. Next, the geNorm algorithm was employed to test for the stability of the 32 candidate ECGs as reference genes as well as selection of the optimal number of genes for normalization of gene expression.
Using the geNorm algorithm the two most stable ECGs for each cell line were determined- PGK1-RPL37A in A431, RPLPO-UBC in A549, and RPL37A-RPLPO in BxPC3. Further the optimal number of ECGs for the normalization of gene expression in each cell line was determined and validated: three ECGs each for A431 (PGK1, RPL37A, and PSMC4) and BxPC3 (RPL37A, RPLPO and CASC3) were recommended. In contrast, six ECGs for A549 data (RPLPO, UBC, GAPDH, MTATP6, CASC3 and PES1) were required.
The normalized gene expression for each cell line in Figure 8 showed that 18S and B2M are unstable genes under different radiation qualities. This is in contrast to earlier studies using 18S and B2M as reference genes for proton therapy . Besides, PPIA ACTB and UBC for particle therapy using 0.5 Gy 4He ions in normal human lung fibroblasts  and ACTB for A549  were reported as reference genes. However, Table 2 showed that these genes have intermediate stability within the cell line examined here.
Figure 8 demonstrates the regulation of particular genes treated with different radiation qualities. For instance, Figure 8B showed that in A549, CDKN1A-- a gene downstream of p53 pathway which is also implicated in regulation of cell growth and cell response to DNA damage-- is up regulated under all the radiation qualities, with maximum up regulation under photon. The gene YWHAZ-- involved in signal transduction by binding to phosphorylated serine residues on a variety of signaling molecule-- is up regulated in A431- photon while minimally regulated in A549-photon. GADD45A-- which binds to proliferating cell nuclear antigen, stimulates DNA excision repair in vitro and inhibits entry of cells into S phase-- was down regulated in A431 but up regulated in BxPC3. 18S-- a component of the ribosome, the protein manufacturing machinery of all living cells-- is seen to be up regulated in carbon ion while its regulation varies for proton and photon in different cell lines.
In addition, five most stable ECGs (RPLPO UBC TBP PPIA and PSMC4) in three cell lines were selected as internal control genes for the normalisation of the gene expression independent of radiation qualities and cell type. This selection was based on the guideline of Vandesompele et al. .
The gene expression in each cell lines normalized by the selected five stable ECGs was shown in Figure 9. The expression of ACTB showed 2.8-fold difference between the highest and lowest expression levels, whereas YWHAZ, 18S, GADD45A showed 5.8, 3.14 and 4-fold difference between the highest and lowest expression levels. The expression Heat map (Figure 3) also illustrate the regulation of YWHAZ, GADD45A and 18S.
List of ECGs qualified as internal control genes across the cell and radiation qualities
Ribosomal protein, large, P0
Protease 26S subunit, ATPase, 4
Peptidylprolyl isomerase A
TATA box binding protein
Careful selection and validation of ECGs prior to conducting radiation biology experiment is warranted. We report that different radiation qualities induced differential regulation of a number of ECGs among the candidate 32 “housekeeping genes”. Additional cell type specific gene expression was observed. Identification of the best internal control gene is a prerequisite for a successful quantitative measure of gene expression via RT-PCR. In this paper we provide a template for the identification of appropriate ECGs for the radiation induced gene expression studies. We identified reliable genes for individual expression profiling of the cell lines, the normalization of A431 may be done by PGK1, RPL37A and PSMC4; A549 by RPLPO, UBC, GAPDH, MT-ATP6, CASC3 and PES1; and BxPC3 by RPL37A, RPLPO and CASC3. However, the 5 ECGs-- TBP, UBC, RPLPO, PPIA, PSMC4-- can be taken as the most suitable candidate reference genes for radiation response expression profiling in the tumor models studied. Moreover, this robust set of the most suitable candidate ECGs for radiation experiment may be applied and validated for the clinicopathological analysis of cancer specimens of epithelial tumors, non-small cell lung cancer and pancreatic adenocarcinoma.
The three different human tumour cell lines, i.e., the lung carcinoma cells (A549), the epidermoid carcinoma cells (A431) and pancreatic cancer cells (BxPC3) were used for the study. A549 and A431 cell lines were obtained from Deutsche Sammlung von Mikroorganismen und Zellkulturen GmbH (DSMZ) and BxPC3 from the American Type Culture Collection. The A549 and A431 cell lines were grown in 5 ml Dulbeccos Modified Eagle's Medium (DMEM) (Biochrom), BxPC3 was grown in 5 ml RPMI 1640 medium (GIBCO Invitrogen) supplemented with 10.0% FCS in T25 flasks (Becton Dickinson). Cells were cultured under standard conditions in a fully humidified incubator with 5.0% CO2 at 37.0°C.
Cells were irradiated in T25 flasks with 2Gy of photon, 2Gy of proton and 1Gy of carbon ion. Photon was delivered by a linear accelerator at 6 Mev (Mevatron, Siemens, Erlangen, Germany). Particle irradiation with proton and carbon ion was done using a pencil beam in a spread out Bragg peak with 1.5 cm width equivalent to a depth of 14.0 cm in water, at the Heidelberg Ion Therapy Center (HIT) . After irradiation, the cells were incubated for 12 h at 37.0°C. Control cells were treated identically but without irradiation. Cells were scrapped using the cell scraper after adding 300.0 μl TRIzol (Invitrogen) and collected in 1.5 ml Eppendorf tubes and subsequently stored at −20.0°C.
RNA isolation and cDNA synthesis
RNA was isolated in phase lock tubes using TRIzol (Invitrogen) according to the manufacturer’s protocol. To avoid genomic DNA contamination RNA was treated with Dnase I (Ambion). Purified RNA was eluted in 20.0μL of nuclease-free water and stored at −20.0°C. RNA concentration and purity was assessed using a Nanodrop ND-1000 spectrophotometer (Peqlab). Integrity and concentration of RNA samples were determined by using RNA 6000 Nano Lab Chip kits and a 2100 Bioanalyzer (Agilent). RNA (2.0 μg) was subjected to reverse transcription reaction using the high-capacity cDNA reverse transcription kit (Applied Biosystems) according to the manufacturer’s protocol.
To assess the expression of Human Endogenous Control gene set, real-time quantitative reverse transcription PCR (qRT-PCR) was performed on 32 candidate genes using TaqMan® chemistry (Applied Biosystems). Experiments were performed at least in triplicates for the three cell lines-- A431, A549 and BxPC3. Plates were run on a 7900HT Fast Real-Time PCR Systems (Applied Biosystems) using Fast 96-well blocks, Standard Fast PCR cycling protocol with 10.0μL reaction volumes. Cycling conditions used were-- 1 cycle initiation at 50.0°C for 2 min and 1 cycle at 95.0°C for 10 min, followed by amplification for 40 cycles at 95.0°C for 15 s and 60.0°C for 1 min. Amplification data were collected via Sequence Detection Systems 2.3 software (Applied Biosystems). The CT-values were computed with RQ Manager 2.xx (Applied Biosystems).
Statistical analysis of data was performed using SUMO software package (http://www.oncoexpress.de/software/sumo). ANOVA was used to detect variation in the expression of the ECGs across the samples according to the radiation qualities and cell lines respectively. The average expression stability measure values (M) were computed using the geNorm algorithm suggested by Vandesompele et al.  (also incorporated in the SUMO program package).
We thank Claudia Rittmüller, Christiane Rutenberg and Barbara Schwager for the excellent technical assistance. This work was supported in part by the German Krebshilfe (Deutsche Krebshilfe, Max-Eder 108876), DFG National Priority Research Program: the Tumour-Vessel Interface “SPP1190”, NASA Specialized Center of Research NNJ04HJ12G, and the German Federal Ministry of Research and Technology (Bundesministerium für Bildung und Forschung – BMBF 03NUK004C).
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