Indexing TNF-α gene expression using a gene-targeted reporter cell line
© Yan et al. 2009
Received: 03 October 2008
Accepted: 16 February 2009
Published: 16 February 2009
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© Yan et al. 2009
Received: 03 October 2008
Accepted: 16 February 2009
Published: 16 February 2009
Current cell-based drug screening technologies utilize randomly integrated reporter genes to index transcriptional activity of an endogenous gene of interest. In this context, reporter expression is controlled by known genetic elements that may only partially capture gene regulation and by unknown features of chromatin specific to the integration site. As an alternative technology, we applied highly efficient gene-targeting with recombinant adeno-associated virus to precisely integrate a luciferase reporter gene into exon 1 of the HeLa cell tumor necrosis factor-alpha (TNF-α) gene. Drugs known to induce TNF-α expression were then used to compare the authenticity of gene-targeted and randomly integrated transcriptional reporters.
TNF-α-targeted reporter activity reflected endogenous TNF-α mRNA expression, whereas randomly integrated TNF-α reporter lines gave variable expression in response to transcriptional and epigenetic regulators. 5,6-Dimethylxanthenone-4-acetic acid (DMXAA), currently used in cancer clinical trials to induce TNF-α gene transcription, was only effective at inducing reporter expression from TNF-α gene-targeted cells.
We conclude that gene-targeted reporter cell lines provide predictive indexing of gene transcription for drug discovery.
Transcriptional regulation provides an ideal target for therapeutic intervention. As such, tools for studying transcriptional modulators of disease genes will help to facilitate the development of novel therapeutics . Cell lines have been used to study the expression of specific genes involved in disease development or at signal transduction checkpoints, and are currently a front-line approach for early-stage drug discovery. A number of indirect techniques are available to assess gene transcription in cells including ELISA and gene arrays or quantitative PCR for measuring the gene transcript levels. However, these methods are time consuming, resource intensive and/or do not directly assess the transcriptional activity of an endogenous promoter. Moreover, they are not amenable to high-throughput screening (HTS) for efficient detection of drug-induced changes in disease gene expression.
Cell-based gene reporter assay systems were developed as an alternative system amenable to HTS over 10 years ago, and have been widely used to study transcription and gene regulation. Specifically, linking easily detectable reporter genes – such as luciferase, β-galactosidase or green fluorescent protein – to defined gene promoters and regulatory elements has resulted in the production of numerous reporter vectors. Transient transfection of such reporter vectors into cultured cells and quantitative analysis of the reporter gene product is a fast and efficient way to study disease gene expression. Moreover, the establishment of cell lines containing random stable integrants has made possible the development of cell-based reporter assays , which have now been successfully scaled-up for HTS following advances in robotics and fluorescence/luminescence plate-reader technologies [3, 4]. Recently, a novel reporter system was developed in which Flp recombinase is used to produce flippase recognition target (FRT) single site-specific integration of a reporter gene construct at a transcriptionally-active genomic locus in cultured cells . This approach has several advantages over randomly integrated reporter constructs including single copy construct integration and a single chromatin context within which the effects of promoter mutations or single nucleotide polymorphisms (SNPs) on gene expression can be studied . Moreover, this reporter system has been used to screen small molecules for inhibition of the pro-inflammatory cytokine, tumor necrosis factor (TNF) . Although randomly integrated and FRT single site-specific reporters are presumed to reflect endogenous regulation of the disease gene, this is a questionable assumption given the unknown epigenetic influences of chromatin structure on gene transcription along with missing genetic elements that regulate gene expression at the endogenous locus. To this end, optimal systems would utilize gene-targeted reporters controlled by endogenous regulatory sequences and governed by an inherited epigenetic program unique to a given disease gene locus. Although gene targeting in mouse embryonic stem cells makes it possible to precisely integrate exogenous DNA sequence into a predetermined 'target' gene locus , such systems have been much less effective in somatic cells. An alternative approach, utilizing single-stranded recombinant adeno-associated virus (rAAV) to promote homologous recombination between the targeting construct and the chromosome [8–11] has been widely applied to genetically modify endogenous genes by insertion, deletion/replacement, and point mutation [11–14]. The efficiency of gene targeting using single-stranded rAAV vectors is also much higher than that observed with adenovirus- or retrovirus-based vector systems . Self-complementary rAAV (scAAV) vectors have been shown to promote more efficient viral transduction than single-stranded rAAV vectors both in vitro and in vivo . However, these double-stranded vectors do not appear to contribute to the gene targeting reaction [13, 16].
The TNF-α gene maps to chromosome 6p21.3, contains four exons, and spans approximately 3 kb of DNA in human cells [17, 18]. TNF-α gene expression is cell type-specific and induced by a wide variety of stimuli such as phorbol 12-myristate 13-acetate (PMA) and lipopolysaccharide [19–21]. The TNF-α protein is a multifunctional cytokine, and is involved in the regulation of a broad spectrum of biological processes [22–24]. The TNF-α gene appears to be silenced in HeLa cells, as evidenced by undetectable levels of mRNA by northern blot and protein by ELISA . In the present study, we sought to engineer a HeLa cell line containing a targeted luciferase reporter in exon 1 of the TNF-α gene. We also sought to compare the patterns of Renilla luciferase (R-Luc) induction with endogenous TNF-α mRNA transcription between targeted and non-targeted cell lines in response to drug treatment. The production of a TNF-α gene-targeted reporter cell line will provide a sensitive and more predictive analytical tool for identifying molecules that modulate TNF-α gene transcription.
HeLa cells were infected with AV.TNF-RL.targ (Figure 1a) and re-plated for clonal expansion under Zeocin selection. Zeocin-resistant colonies were picked and transferred to replicate 96-well plates. Cells in replica plates were lysed for PCR screening with two sets of primers, which hybridize to sequences outside the right and left targeting arms and inside the exogenous insert. Clone #28 was identified as a positive targeted clone, from 192 clones screened, and its left-side PCR product was cloned into the pBlunt4PCR vector (Invitrogen) for sequence confirmation. Sequencing results revealed the presence of both the non-virus-derived flanking sequences and the expected in-frame fusion of the R-Luc cDNA in the TNF-α gene (data not shown). This positive clone (designated as Tg#28zeoR) was expanded and the genomic DNA was analyzed by digestion with several restriction enzymes (Figure 1b; lanes 2, 4 and 6). Genomic DNA from parental HeLa cells was used for comparison (Figure 1b; lanes 1, 3 and 5). The Southern blot was probed with TNF-α left arm-homologous sequences. The additional bands observed in the digested Tg#28zeoR samples (Figure 1b; lanes 2, 4 and 6) are indicative of targeted insertion of the R-Luc cDNA at the TNF-α gene locus. No additional random vector integration was observed (Figure 1b).
The exogenous PGK promoter and transcription of the Zeocin gene could affect the transcriptional activity of the targeted TNF-α gene. To eliminate any possible artificial induction in R-Luc activity, the selection cassette was removed from the targeted intermediate, Tg#28zeoR (Figure 1c). Flanked by a pair of LoxP sites, the PGK-Zeocin cassette can be easily excised from the targeting AAV genome. Cre recombinase-mediated excision was used to remove this selection cassette from the targeted Tg#28zeoR line and also from the non-targeted cell lines that harbor random integrations of the targeting virus. A recombinant adenoviral vector, Ad.Cre, was used to deliver Cre recombinase to the cells. Southern blot analysis with probes for TNF-α and PGK/Zeo demonstrated that Ad.Cre infection resulted in loss of the selection cassette from the targeted intermediate, producing the final TNF-α reporter cell line, Tg#28zeo- (Figure 1c and 1d).
Individual clones expanded from a single cell were isolated from the Zeocin-sensitive cell pool by limited dilution. Five independent lines were randomly selected and basal levels of R-Luc expression among these was compared. No apparent differences were observed between individual Tg#28zeo- lines, and the expression levels were very similar to that in the original cell pool (Figure 1e). However, basal R-Luc activity in the targeted intermediate was more than 300-fold higher than in the clones lacking the Zeocin selection cassette (Figure 1e). Thus, as predicted, this selection marker enhanced transcription from the TNF-α gene locus, arguing that R-Luc activity in Tg#28zeo- cells should more closely reflect endogenous TNF-α gene regulation than reporter activity in Tg#28zeoR cells.
Current TNF-α reporter vectors contain only about 1.0 kb of core promoter located upstream of the TNF-α gene (Invitrogen Corp., Carlsbad, CA; Panomics, Inc., Fremont, CA). In addition, these plasmid-based TNF-α/reporter constructs are randomly inserted into the host cell genome following transfection. In theory, the fidelity of TNF-α gene expression in these randomly integrated reporter cell lines may be influenced by missing regulatory sequences (enhancer and/or silencer) not part of the 1.0 kb core promoter of the TNF-α gene [20, 26, 27]. Indeed, recent studies have demonstrated that the regulation of TNF-α expression involves distal enhancers located over a 12 kb region, and that these enhancers interact to form a novel double-loop chromatin configuration. This structure circularizes the TNF-α gene and thereby facilitates transcription [28–30]. Moreover, epigenetic regulation is important for the control of TNF-α transcription  and key epigenetic modifications at the TNF-α locus may be missing from the regulatory elements governing reporter expression in the randomly integrated reporter cell lines. In addition to the lack of intact endogenous regulatory elements and epigenetic modifications associated with the self-contained TNF-α core promoter/reporter gene, expression of the randomly integrated reporters is very likely to be influenced by both genetic and epigenetic features associated with the insertion site, in a very unpredictable manner. Thus, we hypothesized that the TNF-α gene would be an ideal platform to test whether targeted reporter expression more closely reflects endogenous gene expression patterns than randomly integrated reporters.
Throughout the approximately one-year study period, the basal level of R-Luc activity remained low and the levels of PMA- and TSA-induced reporter expression remained constant in the targeted cell line (data not shown). However, we did not conduct a systematic analysis of drug-induced reporter activity at regular intervals during this time. Nevertheless, while the long-term affects from integration of reporter gene sequences are unknown, our data do not indicate a progressive transcriptional silencing of the R-Luc gene.
We conclude that gene-targeted reporter cell lines may more accurately index endogenous gene expression to facilitate predictive cell-based screening for drug discovery.
The human cervical adenocarcinoma cell line HeLa (ATCC CCL-2) was purchased from American Type Culture Collection (ATCC), and the cells were cultured in DMEM supplemented with 10% FBS. The Cre recombinase-expressing adenovirus vector, Ad.Cre, was obtained from the Vector Core of the Gene Therapy Center at The University of Iowa. PMA, DOX, Daunorubicin, Idarubicin, epirubicin, TSA and Aza-dC were purchased from Calbiochem. DMXAA was purchased from Sigma.
A 2.8 kb TNF-α DNA fragment was amplified by PCR, using AccuPrime Pfx supermix (Invitrogen), from genomic DNA extracted from cultured HeLa cells. Cloning primers were designed based on the published human TNF-α sequence (Gene Bank ID: AB202113). The forward primer used was 5'-GAGCTGTGGGGAGAACAAAAGGA-3' and the reverse primer used was 5'-TTGGCCCTTGAAGAGGACCTG-3'. The TNF-α start codon is located in the center of the PCR product, and 1.32 kb of the promoter and 5'untranslated sequences were included. The PCR product was cloned into the pBlunt4PCR vector using a Topo cloning kit (Invitrogen) and its identity confirmed by DNA sequencing. The resultant plasmid was designated pTopo-TNF2.8. We constructed a PGK promoter-driven Zeocin expression cassette by replacing the neomycin-resistant gene in pPGKneo with the zeocin resistant gene, retrieved from pSV40/Zeo (Invitrogen). The resultant pPGKzeo plasmid was also flanked by a pair of LoxP sites. 1.2 kb Renilla luciferase cDNA, plus an SV40 polyadenylation signal, was retrieved from pRL-SV40 (Promega) and linked to the 5'end of the PGK promoter in the plasmid pPGKzeo to obtain the cloning intermediate pRL-PGKzeo. 1.0 kb of the left homologous arm containing the TNF-α promoter and the first translation start codon was amplified from the plasmid clone pTopo-TNF2.8 using the forward primer subLF (5'-cccaagcttAGAGCCTCCAGGACCTCCAGGTAT-3'; lower-case font indicates the flanking restriction enzyme sites for cloning) and the reverse primer subLR (5'-aactttcgaagtCATGGTGTCCTTTCCAGGG-3'; bold font indicates the start codon). The PCR product was cut with HindIII and BstB1 and inserted into the plasmid pRL-PGKzeo, which resulted in the R-Luc cDNA being fused in frame to the TNF-α gene at the 3' end of the left homologous arm. The 1.0 kb right homologous arm was also amplified from the plasmid pTopo-TNF2.8, using the forward primer subRF (5'-cgagctaGCACTGAAAGCATGATCCGGG-3') and the reverse primer subRR (5'-ccatcgatGGGTTCGAGAAGATGATCCTGAAG-3'). The PCR product of the right arm, the DNA fragment containing the R-Luc-fused left arm and the PGK-Zeocin selectable marker were assembled and finally cloned into an AAV2 proviral plasmid, giving rise to a vector that harbors 2.0 kb of TNF-α genomic DNA fused in frame to the R-Luc cDNA and with a zeocin cassette inserted at the center. The AAV proviral vector was constructed in our laboratory with the AAV-2 inverted terminal repeats (ITRs) kindly provided by Targeted Genetics (Seattle, WA). The rAAV-2-targeting virus (AV.TNF-RL.targ, see Figure 1a) was produced as previously described, using a triple plasmid transfection procedure in 293 cells, and purified over an iodixanol cushion followed by ion exchange HPLC . The genome size of this single-stranded rAAV targeting vector, including the ITRs, is 4.7 kb.
5 × 105 HeLa cells were cultured in 60 mm dishes and infected with AV.TNF-RL.targ at a multiplicity of infection (MOI) of 100,000 particles per cell. On day 1 post-infection, HeLa cells were re-plated onto ten 100 mm dishes and selected in medium containing 150 μg/ml Zeocin for 16 days to allow for the expansion of Zeocin-resistant clones. One hundred and ninety-two well-separated colonies were picked, and expanded clonally in two 96-well plates. PCR screening was performed on one confluent replica plate using primer sequences outside the left vector homology arm and anchored within the R-Luc cDNA. Cells in the 96-well plates were then lysed by the addition of 10 μl per well of lysis buffer (50 mM KCL, 1.5 mM MgCl2, 10 mM Tris, pH 8.5, 0.5% NP40, 0.5% Tween 20), and 1/10 of the resultant cell lysate (1 μl) was used for PCR. The first round PCR primer set was as follows: F1 (5'-GGAAGCAAAGGAGAAGCTGAGAAGA-3') and intR1 (5'-AAGCGAAGGAGCAAAGCTGCTA-3'). One-fiftieth of each first-round PCR product was then used as a template for the second round of PCR with the following primers: F2 (5'-GCTCTGAGGAATGGGTTACAGGAG-3') and intR2 (5'-CCCAATCATGGCCGACAAAA-3'). The positive clones were confirmed by another nested PCR reaction targeting the right arm of the integration site, using the first round primer set: intF1 (5'-ACGTGACCCTGTTCATCAGCG-3') and R1 (5'-CGAGTCCTTCTCACATTGTCTCCAA-3'); and the second round nested primer set: intF2 (5'-TCGGAGGTCGTGTCCACGAACTT-3') and R2 (5'-CCTAGCCCTCCAAGTTCCAAGACA-3'). A single clone that was PCR-positive for both the left and right arms of the predicted integration event was expanded to 24-well plates, and eventually to 100 mm dishes, to generate sufficient cells for the preparation of genomic DNA and Southern blot confirmation of the integration event. Genomic DNAs were digested with either AseI or BamHI (both of which are unique sites in the targeting vector) and AvrII (which does not cut within the targeting vector). Southern blotting was carried out with a P32-labeled TNF-α left arm probe or PGK/Zeo probe (see Figure 1). LoxP/Cre-mediated cassette excision was used to remove the PGK/Zeo cassette from the Zeocin-resistant targeted intermediate and the AAV integrated non-targeted cells. Zeocin-resistant cells were infected with adenovirus encoding Cre (Ad.Cre) at 500 MOI per cell. Half of the cells were cultured and expanded in normal culture medium, and the remaining cells were cultured in Zeocin-containing medium to confirm the loss of drug resistance associated with Cre-mediated excision. Clonal cell lines were derived from cells grown in absence of Zeocin by limiting dilution. Southern blot analysis with TNF-α and PGK/Zeo probes was carried out to confirm cassette removal.
Enzyme activity was determined using the Renilla Luciferase Assay System (Promega) in a 20/20 luminometer equipped with an automatic injector (Turner Biosystems). Parental, targeted, and non-targeted HeLa cells were treated with different chemicals for specific periods of time prior to assaying luciferase activity. The drug induction period for PMA, TSA, DMXAA, and the anthracycline antibiotics (daunorubicin, doxorubicin, idarubicin and epirubicin) was 24 hours, and the period for Aza-dC was three days. Cells were dispensed onto 6-well or 24-well plates one day before drug addition. Cells (2 × 105) were lysed in 100 μl Renilla luciferase lysis buffer, and 1/10 of this cell lysate was assayed for luciferase activity. Four parallel samples were tested for each drug treatment. Cellular toxicity was assessed using the CellTiter-Blue Cell Viability Assay kit from Promega on the IVIS Biophotonic Imaging system, according to the manufacturer's instructions. In separate dose response experiments, Renilla Luciferase activity was also assessed using the IVIS Biophotonic Imaging system.
Total RNA was isolated from 1 × 106 cells, with or without drug treatment, and prepared using the RNAprotect Cell Reagent and the RNeasy Plus Mini kit (QiaGen). Total RNA samples eluted in a volume of 30 μl were used directly for reverse transcription (RT) or purified using the Micro-FastTract 2.0 mRNA Mini kit (Invitrogen) to enrich for polyA mRNA. The mRNA samples were resuspended in 10 μl RNase-free water. RT was performed using the High Capacity cDNA Reverse Transcription kit (ABI), through random priming. Either one-sixth (5 μl) of each total RNA sample or the entire volume of each mRNA sample (10 μl) was used for RT in a final reaction volume of 100 μl. The cDNA product (10 μl) from the RT reaction was used for TaqMan PCR quantification in a final reaction volume of 50 μl, using the TaqMan Universal PCR Master Mix (Applied Biosystems). A 20× mix of primers and FAM-labeled probe for the human TNF-α gene expression assay were purchased through ABI's Gene Expression Assay-on-Demand (Assay ID: Hs00174128_m1). The 20× mix of primers and FAM-labeled probe for the R-Luc expression assay were custom-ordered from ABI (Forward: 5'-GTGAAGTTCGTCGTCCAACATT-3'; Reverse: 5'-AACGTC AGGTTTACCACCTTTTACT-3'; TaqMan probe: 5'-FAM – CCTCGTGAAATCCCG). The housekeeping gene GAPDH was used for sample normalization, and the primer-limited VIC-labeled internal control for the GAPDH assay was also purchased from ABI. Relative quantification was performed using the TaqMan assay, and these data were collected and analyzed using a ABI-Prism 7900 HT Real-Time PCR Sequence Detection Systems (SDS v2.3). Conditions for the PCR reactions were 2 min at 50°C, 10 min at 95°C, and 40 cycles each consisting of 15 sec at 95°C and 1 min at 60°C. The experiments were performed in triplicate wells in a singleplex format when data were compared by the relative standard curve method, or in a multiplex format for both the FAM and VIC signals when data were analyzed by the comparative CT method.
This work was supported by a grant from the IOWA Centers for Enterprise (GHL and JFE), a Battelle Research and Commercialization Award – State of Iowa (GHL and JFE) and NIH RO1-DK51315 (JFE). The authors wish to thank Chengjie Huang for technical assistance and members of the University of Iowa Research Foundation for continued support. We also gratefully acknowledge the editorial assistance of Christine Blaumueller (University of Iowa).
This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.