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. 2011 Oct 7;6(10):e26064. doi: 10.1371/journal.pone.0026064

Figure 2. Hif1α increases transcription of the CHD4 and MTA3 genes.

Figure 2

(A) MCF-7 cells stably expressing either a non-specific shRNA (shRNACon) or shRNA targeting Hif1α (shRNAHif1α) were exposed to DMOG (1 mM) or CoCl2 (200 µM) for 24 hrs. Cell extracts were prepared and then examined by western blot (WB) analysis to monitor levels of Hif1α. β-actin levels are shown to demonstrate equal loading. (B–E) MCF-7 cells stably expressing either a non-specific shRNA (shRNACon) or shRNA targeting Hif1α (shRNAHif1α) were exposed to solvent (open bars) or CoCl2 (200 µM; filled bars) for 8 hr. mRNA levels for the indicated genes were measured by RT-PCR as described in methods. Results ± SE (n = 3). (F) MCF7 cells stably expressing either a non-specific shRNA (shRNACon) or shRNA targeting Hif1α (shRNAHif1α) were exposed to CoCl2 (200 µM) for indicated number of hours. Cell extracts were prepared and then examined by western blot (WB) analysis to monitor levels of CHD4, MTA3 and Hif1α. β-actin levels are shown to demonstrate equal loading.