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. 2002 Nov;22(22):7802–7811. doi: 10.1128/MCB.22.22.7802-7811.2002

TABLE 1.

Regulation of various genes by dexamethasone

Gene Synonym(s) Expression level of gene (arbitrary units)a
Control 100 nM Dex 1 μM Dex
GAPDH 18,911 20,491 19,537
β-Actin 18,544 19,673 18,732
MT-1A 3,883 6,710 8,508
IκBα 1,726 3,206 3,109
IL-8 527 ND ND
DUSP1 MKP-1, CL-100, Erp 3,387 6,436 5,951
DUSP2 PAC-1 343 903 879
DUSP4 MKP-2, hVH2 230 389 339
DUSP5 hVH3 324 ND ND
DUSP10 MKP-5 288 305 356
DUSP11 PIR1 1,960 1,576 1,508
Wip1 685 573 506
a

HeLa-TO cells were treated for 2 h with vehicle (methanol) (control) or with 100 nM or 1 μM dexamethasone (Dex). Total RNA was prepared and analyzed using Affymetrix U95Av2 arrays as described in Materials and Methods. Raw data sets from the chip reader were normalized against one another using the mean expression level of all detected transcripts under each condition. Correction factors applied to the 100 nM and 1,000 nM dexamethasone data sets were 1.156 and 0.99, respectively. Normalization using the GAPDH or β-actin signals gave almost identical results. Normalization using internal control poly(A) mRNAs (added at the cRNA synthesis step) suggested slightly stronger up-regulation of MKP-1 gene expression by 100 and 1,000 nM dexamethasone (2.4- and 2.6-fold rather than 1.7-and 1.5-fold as shown above). An arbitrary cutoff of 200 expression units was employed, and genes expressed below this level were considered not detected (ND).