TABLE 2.
Comparison of differential gene expression levels determined by real-time RT-PCR and microarray hybridization
| Expt and gene | Fold change in transcript levelsa as determined by:
|
|
|---|---|---|
| RT-PCR | Microarray | |
| +/− riboflavin treatment | ||
| ribG | 3 | 2.0 |
| thiA | NC | NC |
| bioA | NC | NC |
| gap | NC | NC |
| +/− biotin treatment | ||
| ribG | NC | NC |
| thiA | NC | NC |
| bioA | 8 | >100 |
| gap | NC | NC |
| +/− thiamine treatment | ||
| ribG | NC | NC |
| thiA | 33 | 62 |
| bioA | NC | NC |
| gap | NC | NC |
Triplet real-time RT-PCRs were performed on cDNA prepared from total RNA isolated from cells grown to exponential phase in minimal medium in the presence or absence of riboflavin (200 μg/ml), biotin (0.1 μg/ml), or thiamine (0.34 μg/ml) as described in Materials and Methods. Values presented were calculated by dividing the average fold change from untreated cells by those from vitamin-treated cells. The fold change values determined by microarray analysis were taken from Table 1 for comparison. NC, no change in real-time RT-PCR values.