Figure 3
Figure 3. HOXB4 transcriptionally activates and binds to the promoter of Hemgn both ex vivo and in vivo. (A) Schematic illustration of the multiple putative HOXB4-binding sites on the promoter region of Hemgn (sites 1, 2, 3, and 4). (B) HOXB4-dependent increase in promoter activity of Hemgn-luciferase in MEL cell cotransfection experiments. *P < .05. (C) HOXB4-specific binding caused band shift of probes containing the putative HOXB4-binding site (site 1). Lanes 1 and 2 indicate biotin-labeled WT probe (−1562 bp to −1540 bp of Hemgn promoter); lanes 3 and 4, labeled WT probe: competitive unlabeled probe = 1:200; lanes 5 and 6, probe with “TAAT” core sequence mutated to “AGCA”; lanes 7 and 8, labeled WT probe plus anti HOXB4 antibody (I12); solid arrow indicates band shift by HOXB4; and open arrow, supershift by I12. #Degraded GST-HOXB4 caused band shift. (D) Semiquantitative PCR detected enrichment of the promoter fragments of Hemgn by HOXB4 specific binding after ChIP assay in 5-FU BM cells. (E) Quantitative real-time PCR detected relative enrichment of individual regions in Hemgn promoter by HOXB4 after ChIP assay in 5-FU BM cells. All values were normalized to the corresponding input control sample.

HOXB4 transcriptionally activates and binds to the promoter of Hemgn bothex vivoand in vivo. (A) Schematic illustration of the multiple putative HOXB4-binding sites on the promoter region of Hemgn (sites 1, 2, 3, and 4). (B) HOXB4-dependent increase in promoter activity of Hemgn-luciferase in MEL cell cotransfection experiments. *P < .05. (C) HOXB4-specific binding caused band shift of probes containing the putative HOXB4-binding site (site 1). Lanes 1 and 2 indicate biotin-labeled WT probe (−1562 bp to −1540 bp of Hemgn promoter); lanes 3 and 4, labeled WT probe: competitive unlabeled probe = 1:200; lanes 5 and 6, probe with “TAAT” core sequence mutated to “AGCA”; lanes 7 and 8, labeled WT probe plus anti HOXB4 antibody (I12); solid arrow indicates band shift by HOXB4; and open arrow, supershift by I12. #Degraded GST-HOXB4 caused band shift. (D) Semiquantitative PCR detected enrichment of the promoter fragments of Hemgn by HOXB4 specific binding after ChIP assay in 5-FU BM cells. (E) Quantitative real-time PCR detected relative enrichment of individual regions in Hemgn promoter by HOXB4 after ChIP assay in 5-FU BM cells. All values were normalized to the corresponding input control sample.

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