Simultaneous quantitative and allele-specific expression analysis with real competitive PCR
© Ding et al; licensee BioMed Central Ltd. 2004
Received: 20 February 2004
Accepted: 05 May 2004
Published: 05 May 2004
For a diploid organism such as human, the two alleles of a particular gene can be expressed at different levels due to X chromosome inactivation, gene imprinting, different local promoter activity, or mRNA stability. Recently, imbalanced allelic expression was found to be common in human and can follow Mendelian inheritance. Here we present a method that employs real competitive PCR for allele-specific expression analysis.
A transcribed mutation such as a single nucleotide polymorphism (SNP) is used as the marker for allele-specific expression analysis. A synthetic mutation created in the competitor is close to a natural mutation site in the cDNA sequence. PCR is used to amplify the two cDNA sequences from the two alleles and the competitor. A base extension reaction with a mixture of ddNTPs/dNTP is used to generate three oligonucleotides for the two cDNAs and the competitor. The three products are identified and their ratios are calculated based on their peak areas in the MALDI-TOF mass spectrum. Several examples are given to illustrate how allele-specific gene expression can be applied in different biological studies.
This technique can quantify the absolute expression level of each individual allele of a gene with high precision and throughput.
Keywordsallele-specific gene expression MALDI-TOF mass spectrometry PCR heterozygous
Mutations in the human genome can cause biochemical changes in protein products, or mRNA expression levels . Epigenetic modifications such as DNA methylation can also change gene expression. Abnormal methylation is frequently detected in cancer (for review, see ). Allele-specific expression of heterozygotic genes (either a mutant allele or a wild type allele is expressed at a higher level than the other allele) might be one reason that carriers have different disease manifestations. Recently, Lo and colleagues showed that allelic variation in gene expression is common in the human genome . Out of the 602 heterozygous genes surveyed in the kidney and lung tissues from seven individuals, 326 (54%) showed preferential expression of one allele in at least one individual. Bray and colleagues showed that skewed allelic expression in the human brain occurs due to cis-acting variations . In addition, Yan and colleagues found that allelic variation of gene expression can follow Mendelian inheritance .
Fluorescent dideoxy terminators and capillary gel electrophoresis , microarrays (Affymetrix HuSNP oligo arrays), real time PCR  and polymerase colonies  have been used for allele-specific expression. However, direct analysis of allelic expression has been limited for technological reasons. For example, capillary gel electrophoresis sometimes has difficulty detecting and quantifying extension products from the two different alleles. Real time PCR, when used for allele-specific detections, requires substantial optimization so that the two alleles can have sufficient annealing temperature difference. The technical difficulties have caused experimental inconsistencies such as debates over whether APOE ε 3/4 brain mRNA shows allele-specific expression [7, 8].
Here we present a method that employs real competitive PCR  for allele-specific expression analysis. Real competitive PCR combines competitive PCR, primer extension reaction and matrix-assisted laser desorption/ionization – time of flight mass spectrometry (MALDI-TOF MS). Real competitive PCR can be used for high-throughput (>7,000 reactions/day using one mass spectrometer), absolute quantification of RNA transcripts with high precision (coefficient of variation < 10% with no assay optimization). To distinguish the two transcripts of a gene from the two alleles, transcribed single nucleotide polymorphisms (SNPs) or rare disease mutations in carriers are used as markers. MALDI-TOF MS can distinguish two oligonucleotides (in the 4000–9000 Da range) with molecular weight difference as small as a few Da, and thus can unambiguously detect the two alleles and the competitor. This technique can be used to quantify simultaneously the absolute expression level of each individual allele of a gene with high precision and throughput.
Results and Discussion
Recently, matrix-assisted laser desorption ionization – time of flight mass spectrometry (MALDI-TOF MS) was adapted for quantitative gene expression analysis . This technique, dubbed as real competitive PCR, combines competitive PCR, primer extension reaction and MALDI-TOF MS. After isolation of RNA and reverse transcription, cDNA is spiked with a synthetic oligonucleotide (the competitor) with an identical sequence except one single base roughly in the middle of the sequence to the cDNA of interest. The competitor and the cDNA of interest are co-amplified by PCR. Excess dNTPs are removed by shrimp alkaline phosphatase treatment after PCR. Then, a base extension reaction is carried out with an extension primer, a combination of three different ddNTPs and one dNTP and a ThermoSequenase. The base extension primer hybridizes right next to the mutation site and either one or two bases are added for the competitor and the cDNA, yielding two oligonucleotide products with different molecular weights (typically around 300 Da difference). In a typical molecular weight window of 4,000 to 9,000 Da, MALDI-TOF MS can easily distinguish two oligonucleotides if they differ by more than 10 Da. These two extension products are thus readily identified, and the ratio of their concentrations is quantified by MALDI-TOF MS.
Since the amount of competitor spiked in is known, the absolute concentration of each of the two cDNAs can be easily calculated. Thus, it is possible to simultaneously quantify the gene expression levels from the two alleles of one gene. The competitor and the two cDNAs are virtually identical in sequence and are amplified with the same kinetics. The allele specificity is superior due to the high precision of MALDI-TOF MS in molecular weight determination.
We next tested allele-specific expression of the lexA gene in Escherichia coli. Gene expression perturbation in E. coli was used for gene network studies . Expression perturbation was achieved by introducing an exogenous copy for each gene of interest in an inducible expression plasmid. The expression of each gene potentially in a gene regulatory network was perturbed via the induction of the exogenous gene expression, and the expression changes of other genes were analyzed. These perturbed gene expression levels were then fed into a multiple linear regression algorithm to estimate the network interactions. This approach appears to be a powerful tool for functional genomics analysis. However, self-regulatory interactions such as positive and negative self-feedbacks can only be resolved by measuring the exogenous and endogenous gene expression separately. In the original study on the E. coli network, a reporter gene (luciferase), expressed under identical conditions as the gene of interest, was used to estimate the exogenous gene expression. However, this estimate is likely to be inaccurate since the expression level of the luciferase gene is likely to be different from the exogenous genes, even when they are under the control of the same promoter. If we can directly and separately quantify the expressions of the exogenous and the endogenous gene, we will be able to obtain significantly more accurate estimates of self-regulatory interactions in gene networks. To this end, an exogenous lexA was introduced into E. coli via the pBADX53 vector. The exogenous lexA gene is distinguishable from the endogenous lexA gene by a silent mutation (TCC to TCG silent mutation at codon 103). The exogenous lexA expression was induced with arabinose. Without arabinose, only endogenous lexA transcript was detected (Figure 2B). With an intermediate arabinose induction, exogenous lexA was expressed at about 20% level compared with the endogenous lexA (Figure 2B).
In the third example, we tested allele-specific expression of the ABCD-1 gene (located on the X chromosome) involved in X-linked adrenoleukodystrophy (XALD). The manifestation of symptoms in XALD carriers was previously shown to be associated with a higher degree of non-random X chromosome inactivation . A non-random X chromosome inactivation is likely to cause a preferential expression down-regulation of one of the ABCD-1 allele. If the wild type allele is inactivated, the mutant allele will be predominantly expressed. Thus, the individual might show symptoms similar to a homozygous mutant. X chromosome inactivation studies can only provide a genome-wide, indirect picture while direct allele-specific gene expression can provide the direct link between gene expression and disease manifestation. We thus carried out allele-specific gene expression for three carriers with three different ABCD-1 mutations (S108W, S213C and Q672X). The S108W carrier showed predominant (>99%) mutant allele expression while the S213C and Q672X showed predominant wild type allele (89% and >99%, respectively) expression (Figure 2C). This result is in complete concordance with results obtained previously .
We present here a straightforward method for quantitative and allele-specific gene expression analysis with real competitive PCR. The allele specificity for gene expression analysis is based on the superior molecular weight determination ability of the MALDI-TOF MS technology. Highly precise (CV 4% – 9%) and absolute gene expression analysis is achieved. In addition, the real competitive PCR is based on the highly automated MassARRAY system (SEQUENOM), and is ideal for high-throughput (7000 reactions/day/instrument) analysis. The high-throughput and low cost features of this technique can easily be exploited in large-scale allele-specific expression studies.
cDNA and oligonucleotides
Interleukin 6 gene expression analysis
Complementary DNA for interleukin 6 gene expression analysis was prepared from cell line IMR-90 (ATCC). The PCR primer sequences for the interleukin 6 gene expression analysis are, 5'-ACGTTGGATGGCAGGACATGACAACTCATC-3' and 5'-ACGTTGGATGCCATGCTACATTTGCCGAAG-3'. The extension primer sequence is 5'-CGCAGCTTTAAGGAGTT-3'. The synthetic competitor sequence is 5'-GCCCATGCTACATTTGCCGAAGAGCCCTCAGGCTGGACTGCATAAACTCCTTAAAGCTGCGCAGAATGAGATGAGTTGTCATGTCCTGCAG-3'. All oligonucleotides were purchased from Integrated DNA Technologies (Coralville, IA). The synthetic competitor was PAGE purified by the vendor and absorbance at 260 nm was measured in our laboratory.
lexA gene expression analysis
RNA samples for lexA gene expression analysis were provided by Dr. Timothy Gardner (Boston University). The exogenous lexA gene has a TCC to TCG silent mutation at codon 103 so that it can be distinguished from the endogenous lexA gene. The exogenous lexA gene was cloned in the vector pBADX53. Bacterial culture and RNA extraction were carried out as previously described . The PCR primer sequences for the lexA gene expression analysis are, 5'-ACGTTGGATGGCGCAACAGCATATTGAAGG-3' and 5'-ACGTTGGATGACATCCCGCTGACGCGCAGC-3'. The extension primer sequence is 5'-ATCAGCATTCGGCTTGAATA-3'. The synthetic competitor sequence is 5'-ACATCCCGCTGACGCGCAGCAGGAAATCAGCATTCGGCTTGAATATGGAAGGATCGACCTGATAATGACCTTCAATATGCTGTTGCGC-3'. The synthetic competitor was PAGE purified by the vendor and absorbance at 260 nm was measured in our laboratory.
ABCD-1 gene expression analysis
Complementary DNA and genomic DNA samples for ABCD-1 gene expression analysis were prepared as previously described . Three ABCD-1 carriers, S108W, S213C and Q672X, were used in this study. PCR primers for the three mutations are: 5'-ACGTTGGATGAGCAGCTGCCAGCCAAAAGC-3' and 5'-ACGTTGGATGACTCGGCCGCCTTGGTGAG-3' for S108W, 5'-ACGTTGGATGTAGGAAGTCACAGCCACGTC-3' and 5'-ACGTTGGATGAACCCTGACCAGTCTCTGAC-3' for S213C, and 5'-ACGTTGGATGTCCCTGTGGAAATACCACAC-3' and 5'-ACGTTGGATGAGTCCAGCTTCTCGAACTTC-3' for Q672X. The extension primers are: 5'-GGCGGGCCACATACACC-3' for S108W, 5'-AGTGGCTTGGTCAGGTTG-3' for S213C and 5'-AATACCACACACACTTGCTA-3' for Q672X.
Real competitive PCR
Real competitive PCR was carried out as was previously described .
Step 1: PCR amplification
Each PCR reaction contains 1 μL diluted cDNA (0.025 ng/μL), 0.5 μL 10× HotStar Taq PCR buffer, 0.2 μL MgCl2 (25 mM), 0.04 μL dNTP mix (25 mM each), 0.02 μL HotStar Taq Polymerase (50 U/μL, Qiagen), 0.1 μL competitor oligonucleotide (5 × 10-9 μM), 1 μL forward and reverse primer (1 μM each) and 2.14 μL ddH2O. The PCR condition was: 95°C for 15 min for hot start, followed by denaturing at 94°C for 20 sec, annealing at 56°C for 30 sec and extension at 72°C for 1 min for 45 cycles, and finally incubated at 72°C for 3 min.
Step 2: Shrimp alkaline phosphatase treatment
PCR products were treated with shrimp alkaline phosphatase to remove excess dNTPs. A mixture of 0.17 μL hME buffer (SEQUENOM), 0.3 μL shrimp alkaline phosphatase (SEQUENOM) and 1.53 μL ddH2O was added to each PCR reaction. The reaction solutions (now 7 μL each) were incubated at 37°C for 20 min, followed by 85°C for 5 min to inactive the enzyme.
Step 3: Single base extension reaction
For each base extension reaction, 0.2 μL of selected ddNTPs/dNTP mixture (SEQUENOM), 0.108 μL of selected extension primer, 0.018 μL of ThermoSequenase (32 U/μL, SEQUENOM) and 1.674 μL ddH2O were added. The base extension condition was, 94°C for 2 min, followed by 94°C for 5 sec, 52°C for 5 sec and 72°C for 5 sec for 40 cycles. The ddNTPs/dNTP mixtures are: ddATP/ddCTP/ddGTP/dTTP for interleukin 6 and ABCD-1 Q672X, ddTTP/ddCTP/ddGTP/dATP for lexA, and ddATP/ddCTP/ddTTP/dGTP for ABCD-1 S108W and S213C.
Step 4: Liquid dispensing and MALDI-TOF MS
The final base extension products were treated with SpectroCLEAN (SEQUENOM) resin to remove salts in the reaction buffer. This step was carried out with a Multimek (Beckman) 96 channel auto-pipette and 16 μL resin/water solution was added into each base extension reaction, making the total volume 25 μL. After a quick centrifugation (2,500 rpm, 3 min) in a Sorvall legend RT centrifuge, approximately 10 nL of reaction solution was dispensed onto a 384 format SpectroCHIP (SEQUENOM) pre-spotted with a matrix of 3-hydroxypicolinic acid (3-HPA) by using a MassARRAY Nanodispenser (SEQUENOM). A modified Bruker Biflex MALDI-TOF mass spectrometer was used for data acquisitions from the SpectroCHIP. Mass spectrometric data were automatically imported into the SpectroTYPER (SEQUENOM) database for automatic analysis such as noise normalization and peak area analysis.
We thank Timothy Gardner from Boston University for the RNA samples for lexA analysis. This work is supported by a grant from SEQUENOM to Boston University.
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