TABLE 1.
Changes in gene expression identified by quantitative RT-PCR in nrf1−/− fetal livers and erythroid progenitorsa
Gene | Fold changeb (mean ± SD)
|
|
---|---|---|
Fetal liver | CFU-E from ES cells | |
Gclc | −2.9 ± 1.1 | 0.3 ± 0.4 |
Gclm | −3.7 ± 1.2 | −0.3 ± 0.5 |
Gpx-1 | −5.1 ± 1.7 | ND |
MT-1 | −4.0 ± 2.0 | 0.3 ± 0.3 |
MT-2 | −3.0 ± 2.0 | ND |
HO-1c | −2.1 ± 1.3 | NT |
The levels of expression of genes in each sample were quantitated relative to endogenous GAPDH levels as an internal reference. Expression levels relative to GAPDH levels were calculated as follows: 2(Ct of the test gene − Ct of the GAPDH gene).
The change in expression of the various genes was determined from the difference between the average expression levels of wild-type and Nrf1 mutant samples. Decreases are indicated by minus signs before the values. For fetal liver comparisons, the livers of five wild-type and six nrf1−/− mice were used. For comparisons of CFU of erythroid cells (CFU-E) from ES cells, cells from two wild-type and three nrf1−/− mice were used. ND, not determined; NT, not detected.
HO-1, heme oxygenase 1.