- Methodology article
- Open Access
Application of four dyes in gene expression analyses by microarrays
© Staal et al; licensee BioMed Central Ltd. 2005
- Received: 25 February 2005
- Accepted: 25 July 2005
- Published: 25 July 2005
DNA microarrays are widely used in gene expression analyses. To increase throughput and minimize costs without reducing gene expression data obtained, we investigated whether four mRNA samples can be analyzed simultaneously by applying four different fluorescent dyes.
Following tests for cross-talk of fluorescence signals, Alexa 488, Alexa 594, Cyanine 3 and Cyanine 5 were selected for hybridizations. For self-hybridizations, a single RNA sample was labelled with all dyes and hybridized on commercial cDNA arrays or on in-house spotted oligonucleotide arrays. Correlation coefficients for all combinations of dyes were above 0.9 on the cDNA array. On the oligonucleotide array they were above 0.8, except combinations with Alexa 488, which were approximately 0.5. Standard deviation of expression differences for replicate spots were similar on the cDNA array for all dye combinations, but on the oligonucleotide array combinations with Alexa 488 showed a higher variation.
In conclusion, the four dyes can be used simultaneously for gene expression experiments on the tested cDNA array, but only three dyes can be used on the tested oligonucleotide array. This was confirmed by hybridizations of control with test samples, as all combinations returned similar numbers of differentially expressed genes with comparable effects on gene expression.
- HepG2 Cell
- Oligonucleotide Array
- cDNA Array
- Microarray Slide
DNA microarray technology is widely used for gene expression analysis studies [1–5], as it is a high throughput technique by which the expression of all genes in a whole genome can be studied in a single assay. For many microarrays, the probe consists of cDNA or oligonucleotides spotted on a glass slide, and the target is fluorescent labelled cDNA (or cRNA). Both direct as well as indirect labelling protocols are applied: either, one target cDNA or cRNA is labelled with a single dye and hybridized on a microarray slide, or two targets are labelled with two different dyes, one for the reference and one for the test sample, and co-hybridized on a microarray slide. In dual label experiments, most often Cyanine 3 (Cy3) and Cyanine 5 (Cy5) are used as fluorescent dyes, although other dyes have been suggested . In this way differential expression for thousands of genes between two different RNA samples can be measured simultaneously. Usually these experiments are time consuming, and, because microarray slides and fluorescent labels are expensive, the experiments are also high in costs. Moreover, several replicates need to be performed to increase statistical significance and to detect small differences in gene expression [7, 8].
The application of four different dyes to label targets would be a major advantage as fewer microarrays will be required, leading to a reduction of costs and time without compromising gene expression data. A larger number of samples can be compared directly on a single microarray by labelling with more dyes, suggesting that fewer arrays will be required and that the hybridization design can be further optimized [9, 10]. For instance, in the case that four samples need to be compared in all combinations, a dual-label common reference design requires four arrays for a single analysis of each sample, whereas a four-label design would require no common reference because all samples can be hybridized on a single array and only one array for a single analysis of each sample is needed. This will reduce variation, since variation between signal intensities for two dyes on a single spot is much smaller than variation between spots on different arrays . Furthermore, day to day variation is reduced since it is possible to achieve more hybridizations on the same day . In toxicogenomics assessments, as well as in other research areas, the approach to use multiple dyes can be of high value as it allows comparing several exposure conditions or time series simultaneously.
Forster et al  were the first to study the feasibility of using a third dye (Alexa 594) for labelling in microarray based gene expression analyses. Although they found that Alexa 594 gave a small signal in the Cy3 channel during scanning and Cy3 gave a small signal in the Alexa 594 channel, they concluded that Alexa 594 could be used besides Cy3 and Cy5 for direct comparison of two experimental samples and measuring these samples in relation to a reference sample.
The goal of our study was to investigate whether more than three different fluorescent dyes can be applied in gene expression studies using DNA microarrays. This was studied using microarrays with cDNA and oligonucleotide probes by hybridizing with a single sample labelled with four dyes (a quadruple self-hybridization or further stated as self-hybridization). Self-hybridization experiments are useful for measuring microarray data variability since any deviation from the expected value of 0 (for log transformed data) is caused by systemic or technical variation [13, 14]. We also studied the application of more than two dyes for gene expression changes caused by exposure of cells to benzo[a]pyrene, to verify that the new dyes can be applied simultaneously in microarray studies. In the present study, we demonstrate that on our cDNA arrays four dyes can be applied, but that hybridization on the oligonucleotide arrays should be restricted to three dyes.
Selection of fluorescent dyes
Cross-fluorescence of tested dyes. Fluorescence of dyes at scanner settings of all dyes expressed as a percentage of fluorescence at its own settings (the latter was set to 100%).
Optimizing laser power and PMT gain settings
In the scatter plots of data of one scan versus another, in general the data points indicate parallel lines when the settings are varied between the scans, implying that the fluorescent signals are consistent for all levels of gene expression when targets are labelled with these dyes. The larger distribution of the data points at low signals is a normal effect, which is due to reduced accuracy to measure signals from low expressed genes. Compared to Alexa 594, varying laser settings gave similar results for Alexa 488. For Cy3 and Cy5, the data points in the scatter plots run parallel for each setting. Varying laser settings gave similar results for all tested dyes. The Alexa 488 and Alexa 594 graphs, however, show a minor disturbance in the lines of the data points when the laser is varied (shown for Alexa 594 in Figure 1a). This suggests that for these two dyes, a fixed laser power should always be applied, whereas the other dyes allow some variation. Furthermore, these data indicate that laser power and PMT gain can be varied to some extend without affecting relative gene expression levels, as long as there is no saturation of signal intensities.
Correlation coefficients between dyes at different laser power settings
Correlation coefficients between gene expression measured for different dyes at various laser settings for the cDNA array. Correlation coefficients for all genes on the PHASE-I cDNA array between combinations of dyes at different scanner settings for 1 array, and at laser power 100 settings for 5 arrays.
laser power = 100 (n = 5)
laser = 70
laser = 100
mean ± stdev
Alexa 488 vs Alexa 594
0.953 ± 0.020
Alexa 488 vs Alexa Cy3
0.923 ± 0.044
Alexa 488 vs Cy5
0.942 ± 0.014
Alexa 594 vs Cy3
0.938 ± 0.053
Alexa 594 vs Cy5
0.986* ± 0.005
Cy3 vs Cy5
0.926* ± 0.062
0.945 ± 0.025
The reproducibility was tested by several other self-hybridizations of different RNA samples. Table 2 shows the results for the correlation coefficients calculated for all combinations of dyes. Numerical data from the table indicate that correlation coefficients for the repeated experiments are similar with mean correlation coefficients varying between 0.923 (Alexa 488 and Cy3) and 0.986 (Alexa 594 and Cy5).
Correlation coefficients between gene expression measured for different dyes at various laser settings for the oligonucleotide array. Correlation coefficients for all genes on the oligonucleotide array between combinations of dyes at different scanner on 1 array, and at laser power 100 settings for 7 arrays. Alexa 488 labelled samples were only hybridized on the first array.
laser power = 100 (n = 7)
laser = 70
laser = 100
mean ± stdev
Alexa 488 vs Alexa 594
Alexa 488 vs Alexa Cy3
Alexa 488 vs Cy5
Alexa 594 vs Cy3
0.855 ± 0.032
Alexa 594 vs Cy5
0.853 ± 0.027
Cy3 vs Cy5
0.890* ± 0.052
0.843 ± 0.072
To reduce the background binding on the oligonucleotide arrays, we applied several different hybridisation and washing protocols. We varied BSA concentration in the hybridization buffer, added tRNA, Cot1 or PolyA and used a commercial hybridization buffer (DIG Easy Hyb granules, Roche, Germany). We also varied the concentrations SSC and SDS in the washing buffers. The best results for all dyes were obtained by using the hybridization protocol as described in "Microarray hybridizations" of the Methods section. The data from this most optimal protocol are presented here.
With the exclusion of Alexa 488, the other dyes were tested in several more self-hybridizations with for each array a different RNA sample in order to confirm the reproducibility. Table 3 shows the correlation coefficients for all combinations of the 3 dyes. The correlation coefficients are similar for all repetitive experiments with mean values varying between 0.854 and 0.891.
Standard deviation in relation to spot intensity for all combinations of dyes
Identification of modulated genes for various dye combinations
Labelling schedule for B[a]P exposed samples. Each HepG2 sample is labelled with each fluorescent dye. Rat liver samples were labelled as shown by array number 1–3, without the application of Alexa 488.
Performance of a dye combination in revealing modulated genes in B[a]P (3 μM) treated HepG2 cells using a cDNA array.
Performance of a dye combination in revealing modulated genes in B[a]P (10 μM) treated HepG2 cells using a cDNA array.
Performance of a dye combination in revealing modulated genes in B[a]P (30 μM) treated HepG2 cells using a cDNA array.
Performance of a dye combination in revealing modulated genes in B[a]P treated liver slices using an oligonucleotide array.
Cy5 – Cy3
Cy3 – A594
Cy3 – Cy5
A594 – Cy3
Cy5 – A594
A594 – Cy5
We have investigated the applicability of four fluorescent dyes in gene-expression analysis by microarrays. By using more than two dyes in microarray experiments, without lessening the data obtained, costs and time can be decreased as fewer microarrays are needed.
Initially, several dyes were tested for cross-talk on the ScanArrayExpress reader, and ultimately 4 dyes were tested for parallel use in microarray experiments. Today, Cy3 and Cy5 are the most widely used dyes in microarray experiments and much research has been done on these dyes [4, 8, 11, 15, 16], although Alexa 555 and Alexa 647 have been suggested by Cox et al . It was our intention to select dyes that could complement Cy3 and Cy5 and we show that Alexa 488 and Alexa 594 are suited for this and can be used for parallel hybridization in microarray experiments. All dyes were applicable on the tested cDNA arrays. On the tested oligonucleotide arrays, however, only three dyes, namely Alexa 594, Cy3 and Cy5, could be used.
Selection of fluorescent dyes
Based on cross-talk signals, four dyes – Alexa 488, Alexa 594, Cy3 and Cy5 – were found suitable for hybridization on microarrays and some cross-talk did occur for this combination. The highest fluorescence for a dye at settings of another dye was observed for Cy5, namely 13% cross-talk at the settings for Alexa 594. This cross-talk may influence differential gene expression analyses, especially if the signals for Cy5 and Alexa 594 differ drastically within a spot. Therefore, in order to minimize artificial gene expression differences, scan settings should be optimized such that emission intensities are gross similar (e.g. by assuring that the brightest spots are on the edge of saturation). Furthermore, dye swap design on replicate arrays will reduce the bias resulting from cross-talk, and algorithms can be developed to eliminate this bias.
Dye bias is the difference in labelling efficiency between different dyes as one dye can be better incorporated than another; this can affect the gene expression data [17–19]. When using more than one dye, dye bias may occur and most likely, it is enhances with increasing number of dyes. Dye bias can be reduced by using the indirect amino-allyl labelling instead of direct labelling, but it is not clear whether dye bias is fully eliminated . However, dye bias can be eliminated by LOWESS normalization of the data, combined with a labelling and hybridization design in which each target is labelled with each different dye . Liang et al  showed that the correlation between predicted and observed gene expression ratios increased by adding a second microarray with dye switching. This confirms that accuracy can be improved by adding dye swap replicates and applying a balanced labelling design. A balanced labelling design with four dyes may increase the number of required arrays, but still saves the total number of arrays. For example, when 3 treatments and a control are to be compared using 4 data points per comparison, 16 microarrays are needed for a common reference design, 12 arrays for a block design (treatment vs. control on an array), 8 when using a loop design, but only 4 with 4 dyes and the design shown in Table 4.
Applicability of selected dyes
The applicability of the dyes was analyzed in four different ways. First by calculating the correlation coefficients between dyes in self-hybridizations, second by calculating the standard deviation of their log ratio per gene for replicate spots in the self-hybridizations, third by comparing numbers of modulated genes for all dye combinations in samples exposed to B[a]P and finally by comparing gene expression modulation for several genes from samples exposed to B[a]P.
When applied on the cDNA array, all combinations of dyes gave high correlation coefficients (>0.9) and thus seem suitable for parallel hybridization in microarray experiments. On the oligonucleotide array, the correlation coefficients were high for all combinations (>0.8), except for combinations with Alexa 488 (≌0.5). The correlation coefficients for all combinations of dyes on both arrays are constant in multiple repeated hybridizations. These results are supported by the plots for the standard deviation of the replicate spots. For the cDNA array, the standard deviation is equal for all combinations of dyes at high gene expression level. However, for the oligonucleotide array the standard deviation of the signal intensity of high expressed genes for all combinations with Alexa 488 is higher than the standard deviation for all other combinations of dyes. Since the correlation coefficient of Alexa 488 with other dyes is low and the standard deviation for Alexa 488 is high, it is not advisable to use Alexa 488 for labelling and hybridization on the oligonucleotide array.
The correlation coefficients observed for all combinations of Alexa 488 with any other dye on the oligonucleotide array are lower than any of the other correlation coefficients. This was due to a high background signal and a lower signal-to-noise ratio in the Alexa 488 channel, which can not be attributed to auto fluorescence. This background signal was much less pronounced on the cDNA array, which may be explained by a different coating of the microarray slides. Alexa dyes have a net negative charge, which may cause non-specific electrostatic interaction with positively charged molecules . This may be a reason for why the dye adhered differently to the two different microarray slides. However, this does not explain why the background binding for Alexa 594 is much less in comparison to that of Alexa 488.
For all dyes tested on the oligonucleotide array, many genes showed a low gene expression level compared to the cDNA array. In general, weak signals are detected with lower accuracy than strong ones . This is reflected by the higher standard deviations for lower signals in the plots for the cDNA and oligonucleotide array (Figure 4). Lyng et al  showed that reliable data for mean signal intensities were only achieved within a range of 200 to 50,000 (no background correction performed). This clarifies the lower correlation coefficients found for the oligonucleotide array compared to the cDNA array.
For all dye combinations, percentages of modulated genes relative to modulated genes for all dye combinations combined are generally equal (Tables 5 and 6). This indicates that any dye combination has approximately the same sensitivity to identify differentially expressed genes, and that the traditional combination of Cy3-Cy5 is not necessarily preferable above the others. Therefore, we consider all dyes suitable for usage in gene expression studies by microarrays. This was further substantiated by the observation for several differentially expressed genes that the level of modulation is in the same range for all dye combinations.
Although Forster et al  used a different approach to test the use of Alexa 594 besides Cy3 and Cy5 in microarray analysis, their conclusions are in agreement with that of this study. Forster et al  tested the use of different combinations of two dyes in hybridization, and found some cross-talk between Cy3 and Alexa 594 and between Cy5 and Alexa 594. Although, some cross-talk was observed between Cy5 and Alexa 594 (13%), only small cross-talk was noticed (<3%) for Cy3 and Alexa 594 in this study. Forster et al  also found a more linear relation between Cy3 and Alexa 594 than for Cy3 and Cy5. However, we noticed only a small difference in correlation coefficient for Cy3 / Cy5 and for Alexa 594 / Cy3 (Table 2 and 3). These differences could be due to the different testing methods and different arrays used.
All our experiments demonstrate that for gene expression analyses on microarrays Alexa 594 is best suited as a third dye in addition to Cy3 and Cy5, and that Alexa 488 can be applied as a fourth dye on some microarray platforms, but unfortunately not on all array platforms. The general applicability of four dyes on other microarray systems is therefore uncertain, and needs to be investigated on a case-by-case basis.
Cross-talk analysis of fluorescent dyes
Two ARES™ Alexa fluor® dyes (Alexa 488 and 594) (Molecular Probes, Leiden, The Netherlands) and conventionally used Cyanine3 (Cy3) and Cyanine5 (Cy5) (Amersham Biosciences, Uppsala, Sweden) were tested for cross-talk of excitation / emission signals. All dyes were dissolved according to the producer's manual and applied on a glass slide. The slide was scanned with a ScanArrayExpress microarray scanner (Packard BioChip Technologies, Perkin Elmer life sciences, Boston, USA) with laser wavelengths for Alexa 488, Cy3, Alexa 594 and of 488, 543.8, 594 and 632.8 nm respectively, and emission filter of 522, 570, 614 and 670 nm respectively. The images were analyzed with ImaGene (BioDiscovery, USA). Fluorescence of each dye at the scanning settings of all tested dyes was measured and four dyes were selected for further use (see Results).
Source of RNA samples
RNA was isolated from cultured HepG2 cells or from rat liver or precision-cut liver slices and used for the microarray hybridizations. HepG2 cells were cultured in Minimal Essential Medium (MEM) supplemented with 1% non-essential amino acids, 1% sodium-pyruvate, 2% penicillin/streptomycin and 10% Foetal Bovine Serum (all from Gibco/BRL, Breda, The Netherlands) in T25 culture flasks at 37°C and 5% CO2. HepG2 cells were exposed to 3, 10 or 30 μM of Benzo[a]pyrene (B[a]P, from Sigma-Aldrich, the Netherlands) and a vehicle control (DMSO) during 6 hours in two independent experiments. DMSO concentration in de cell culture media was 0.1%. After exposure, media was removed and 1 ml Trizol (Gibco/BRL, Breda, The Netherlands) was immediately added to the cells.
A male Wistar albino rat (200 g) was killed by cervical dislocation, and the liver after removal, was snap frozen in liquid nitrogen and stored at -80°C. Liver tissue (8.6 g) was crushed using a mortar and pester. An amount of 0.05 g crushed liver tissue was dissolved in 1 ml Trizol reagent. Additionally, precision-cut liver slices were obtained by using a Krumdieck tissue slicer . Cylindrical liver cores with a diameter of 8 mm were sliced into 250 μm thick slices. In the two independent experiments, slices were exposed to 3, 10 or 30 μM B[a]P or a solvent control (DMSO 0.067%) during 24 hours. After exposure, slices were snap frozen in liquid nitrogen and RNA was isolated in a manner similar to that of the whole liver tissue.
RNA isolation and cDNA synthesis
RNA was isolated from the Trizol solutions according to the producer's manual and purified with the RNeasy mini kit (Qiagen Westburg bv., Leusden, The Netherlands). RNA quantity was measured on a spectrophotometer and the quality was determined on a BioAnalyzer (Agilent Technologies, Breda, The Netherlands). Only RNA samples which showed clear 18S and 28S peaks were used for labelling and hybridization. In order to generate sufficient large uniform samples for the multiple self hybridizations, RNA samples from several isolations were pooled.
RNA was reverse transcribed into cDNA in quadruplicate with amino allyl labelled dUTP (Sigma-Aldrich, St Louis, USA) and subsequently labelled with one of the dyes (based on Van Delft et al ). For each sample, a mixture of 10 μg of RNA and 6 μg of random hexamer primers were incubated in 18.5 μl at 70°C for 10 minutes and snap frozen on dry ice / ethanol for 30 seconds. Thereafter DTT (final concentration 10 mM), 0.5 mM dATP, dCTP and dGTP, 0.3 mM dTTP, 0.2 mM 5-(3-aminoallyl)-2'deoxyuridine-5'-triphosphate (aa-dUTP), and 400 U Superscript II reverse transcriptase (Invitrogen, Life Technologies, Breda, The Netherlands) were added to a final volume of 30.1 μl and incubated overnight at 42°C. RNA was hydrolyzed by adding 10 μl of 1 M NaOH and 10 μl of 0.5 M EDTA followed by an incubation of 15 minutes at 65°C. To neutralize, 10 μl of 1 M HCl was added. cDNA samples were purified to remove unincorporated amino allyl dUTP and buffers using a QIAquick PCR Purification Kit (Qiagen Westburg bv., Leusden, The Netherlands) according to the producer's manual. However, in order to eliminate interference of amines during labelling, buffers were substituted by phosphate buffers (wash buffer: 5 mM KPO4 pH 8.0, 80% ethanol; elution buffer: 4 mM KPO4 pH 8.5). The sample was eluted in duplicate using 30 μl elution buffer and dried in vacuo. Following amino-allyl labelling, cDNA targets were resolved in 4.5 μl of 0.1 M Na2CO3 pH 9.0 and 4.5 μl of a 2.25 μM of Cy™5 or Cy™3 Monofunctional Reactive Dye esters (Amersham Biosciences, Uppsala, Sweden) was added. Samples were incubated in the dark at room temperature for 1 hour. Targets to be labelled with Alexa dyes were resolved in 5 μl of MilliQ, 3 μl of labelling buffer (Sodium bicarbonate, prepared according to the producers' manual) and 2 μl of a 6.3 μM of ARES™ Alexa Fluor® (Molecular Probes, Leiden, The Netherlands) (dissolved in DMSO according to the producers' manual) was added. The sample was incubated for 1 hour in the dark at room temperature. After incubation 35 μl of 100 mM NaAc pH 5.2 was added to the Cy-labelled targets and 90 μl MilliQ was added to the Alexa labelled targets. The samples were purified using a QIAquick PCR Purification Kit (Qiagen Westburg bv, Leusden, The Netherlands) to remove unincorporated dyes. To the rat liver targets, additional 4 μl of 100 U/ml Poly-dA (Amersham Biosciences, Uppsala, Sweden) and 3 μl of 1 mg/ml mouse Cot1-DNA (Invitrogen, Breda, The Netherlands) were added to block an unspecific binding of the targets to the array. The targets were dried in vacuo.
HepG2 targets were hybridized to the PHASE-1 Microarray Human-600 (PHASE-1 Molecular Toxicology, Santa Fe, USA), containing 597 sequence verified cDNA clones from human genes, representing a number of toxicologically relevant, as well as control, genes, each printed in quadruplicate. Hybridization and washing was done according to the producer's manual as previously described . The labelled cDNA target was dissolved in 30 μl hybridization buffer (50% formamide, 5× SSC, 0.1% SDS, 0.1 mg/ml Salmon Sperm DNA) and incubated for 15 minutes in the dark at room temperature. The target was denatured by heating for 5 minutes at 95°C, centrifuged for 3 minutes at maximum speed, and placed in a heat block at 70°C until further use. The target (28 μl) was applied on the cover slip (24–32 mm) and the microarray was placed on top of the cover slip. The slide was hybridized overnight in a humidified hybridization chamber (Corning, Life Sciences, The Netherlands) in a water bath at 42°C. After incubation, the slide was placed in wash buffer (2× SSC, 30–34°C) to remove the cover slip, and washed 5 minutes in 2× SSC / 0.1% SDS, 5 minutes in 0.1× SSC / 0.1% SDS, 2 times 5 minutes in 0.1× SSC at 32°C, and 1 minute in MilliQ all at room temperature. The slide was centrifuged to dry.
Rat liver targets were hybridized on an Operon rat oligonucleotide array containing 5700 oligonucleotides (Operon, Qiagen, Venlo, The Netherlands) printed in triplicate on Corning UltraGAPS Coated Slides (Corning Life Sciences, New York, USA) by the Genome Centre Maastricht (Maastricht University, Maastricht, The Netherlands). Hybridization and washing was done according to Corning's protocol for oligonucleotide arrays. The labelled cDNA target was dissolved in 65 μl hybridization buffer (30% formamide; 5× SSC; 0.1% SDS) and incubated for 15 minutes in the dark at room temperature. The target was denatured by heating for 5 minutes at 95°C, centrifuged for 2 minutes at maximum speed, and kept at room temperature until further use. The microarray slide and cover slip (24 × 60 mm) were prehybridized for 45 minutes in preheated prehybridization buffer (5× SSC; 0.1% SDS; 1% BSA) at 42°C. Slides and cover slips were washed several times in MilliQ followed by dipping in isopropanol and centrifugation to dry. The target (60 μl) was applied on the cover slip and the microarray was placed on top of the cover slip. The slide was hybridized overnight in a humidified hybridization chamber (Corning, Life Sciences, The Netherlands) in a water bath at 42°C. After incubation, the slide was placed in wash buffer (2× SSC / 0.1% SDS) at 42°C to remove the cover slip. The slide was washed for 2 times 5 minutes in 2× SSC / 0,1% SDS at 42°C, 2 times 10 minutes in 0.1× SSC / 0.1% SDS at room temperature and 4 times 1 minute in 0.1× SSC at room temperature. The slide was centrifuged to dryness.
Microarray data analysis
The microarray slides were scanned on a ScanArrayExpress (Packard Biochip Technologies, Perkin Elmer life sciences, Boston, USA). All four channels were scanned at several different settings for laser power and / or photo multiplier tube (PMT Gain). Settings were optimized such that the signal of the highest fluorescent spots is just below the maximum measurable level. Laser power settings were set at 100% and PMT Gain was adjusted, unless otherwise stated. The images (10 micron resolution; 16 bit tiff) were processed with ImaGene 5.0 software (BioDiscovery Inc., Los Angeles, USA) to quantify spot signals. Irregular spots were manually or automatically flagged and not included in the data analysis.
For the self-hybridizations, data from ImaGene were exported to Microsoft Excel (Microsoft, USA) for transformations and analysis. For each spot, mean local background signal was subtracted from the mean spot signal, negative signals were excluded, and the resulting net spot signal data were log transformed. These log transformed background corrected expression signals for all combinations of dyes at all scanner settings were plotted and analyzed by linear regression and correlation coefficients (R2) were calculated. Furthermore, standard deviations of 10log transformed expression ratios for each gene (for 3 or 4 replicate spots, depending on the array used), were plotted against the mean 10log transformed expression signals and analyzed by regression analysis.
For the B[a]P exposed samples, data from ImaGene were transported to GeneSight software version 4.1.5 (BioDiscovery Inc, Los Angeles, USA) for transformations and analyses. For each spot, background was subtracted; flagged spots and spots with a net expression level below 5 were omitted. Data were log base 2 transformed and expression difference between exposed and control were calculated. Data normalization was done by LOWESS and centring expression differences by subtracting mean values (the latter only for the oligonucleotide arrays). Data of replicate spots were combined while omitting outliers (>2 standard deviations). In order to estimate the number of differentially expressed genes following a treatment, the confidence analysis tool from GeneSight was used. For confidence analyses, for each B[a]P concentration, data of the two replicate arrays with the same dye combination were combined. Up-regulated and down-regulated genes were identified at 99% confidence intervals with up-regulation or down regulation levels set at 0.2 (2log-scale) for the cDNA arrays and respectively 99.5% and 0.5 for the oligonucleotide arrays.
The authors thank Dr. C Ioannides and his colleagues for his help in making and the exposure of the rat liver slices and Ms D. Pushparajah for her help in correcting the English language. The research was carried out in the context of the AMBIPAH project (mechanism-based approaches to improved cancer risk assessment of ambient air polycyclic aromatic hydrocarbons), funded by the European Union (No. QLRT-2001-02402).
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