Strated with direct immunoblotting of cell lysates with UBE2D3 and hTERT antibody (left panel or input), respectively. All experiments were repeated 3 times with similar results. doi:10.1371/journal.pone.0064660.gcyclin D1 expression after down-regulation of UBE2D3. Next, the effect of UBE2D3 on the viability of MCF-7 cells was determined using a CCK-8 assay. MCF-7 cells were transfected with Cated that 7 GOs were significantly regulated by the downregulated genes, whereas pshRNAUBE2D3 for different time periods (1, 2, 3, 4, 5, 6 and 7 days). Atime-dependent increase in cell viability was observed after repression of UBE2D3. The CCK-8 assay showed that after silencing of UBE2D3, there was a significant increase (P,0.05) in cell proliferation compared with the negative control (Figure 4).Down-regulation of UBE2D3 Enhanced Telomerase ActivityTelomerase activity is regarded as the primary determinant of tumor cell radiosensitivity. To examine the effect of UBE2D3 on telomerase activity, we treated MCF-7 cells with pshRNAUBE2D3 and negative control for 24 hr. Cell lysates were titrated between 0.001 and 2 mg protein per assay using a telomerase PCR-ELISA technique. MCF-7 cells transfected with pshRNAUBE2D3 showed higher telomerase activity compared to negativeFigure 3. The detection of protein(UBE2D3, hTERT, cyclin D1, bactin) expressions were illustrated. (A) Western blotting analysis showing the effect of 16985061 overexpression and R [3?] and disease [6,7]. In vitro cell migration assays are routinely used knockdown of UBE2D3 on UBE2D3 and hTERT levels in MCF-7 cells. Control cells were transfected with negative control shRNA. (B) Western blotting analysis showing the effect of knockdown of UBE2D3 on cyclin D1 levels in MCF-7 cells. (C) Western blotting analysis showing the effect of overexpression of hTERT on UBE2D3 and hTERT levels in MCF-7 cells. Experiments were repeated 3 times with similar results. doi:10.1371/journal.pone.0064660.gFigure 4. The MCF-7 cells proliferation were illustrated. After MCF-7 cells were transfected with pshRNA-UBE2D3, cell proliferation was examined by CCK-8 assay. The results were presented as the Means6SD of three independent experiments. *p,0.05. doi:10.1371/journal.pone.0064660.gUBE2D3 Regulates MCF-7 Cells Radiosensitivitycontrol (P,0.05) (Figure 5). On the basis of these preliminary results, we treated MCF-7 cells with 4 GY X-ray after transfection with the above plasmids. MCF-7 cells treated with X-rays after transfection with pshRNA-UBE2D3 showed higher telomerase activity compared with transfection with pshRNA-UBE2D3 alone, suggesting that UBE2D3-induced elevation of hTERT activity could be enhanced by radiation treatment.Down-regulation of UBE2D3 Weakened MCF-7 Cells RadiosensitivityAfter counting clones, the survival curves were plotted to evaluate the radiobiological parameters of each group. Compared to the negative control, the survival fractions of the pshRNAUBE2D3 group were much higher at each point in MCF-7 cells. Figure 6 shows that down-regulation of UBE2D3 reduced the radiosensitivity of MCF-7 cells. Similar results were observed in lung adenocarcinoma A549 cells (data not shown). Plating efficiency (PE) and survival fraction (SF) were calculated.DiscussionHere, we first performed Y2H to screen for hTERT-interacting proteins. We found evidence implicating UBE2D3 as a modulator of MCF-7 cell radiosensitivity by regulating hTERT and cyclin D1 protein expression. It is well established that telomerase activity requires the presence of the hTR and hTERT subunits. The present study of the relationship between hTERT and radiosensitivity indicates that in t.Strated with direct immunoblotting of cell lysates with UBE2D3 and hTERT antibody (left panel or input), respectively. All experiments were repeated 3 times with similar results. doi:10.1371/journal.pone.0064660.gcyclin D1 expression after down-regulation of UBE2D3. Next, the effect of UBE2D3 on the viability of MCF-7 cells was determined using a CCK-8 assay. MCF-7 cells were transfected with pshRNAUBE2D3 for different time periods (1, 2, 3, 4, 5, 6 and 7 days). Atime-dependent increase in cell viability was observed after repression of UBE2D3. The CCK-8 assay showed that after silencing of UBE2D3, there was a significant increase (P,0.05) in cell proliferation compared with the negative control (Figure 4).Down-regulation of UBE2D3 Enhanced Telomerase ActivityTelomerase activity is regarded as the primary determinant of tumor cell radiosensitivity. To examine the effect of UBE2D3 on telomerase activity, we treated MCF-7 cells with pshRNAUBE2D3 and negative control for 24 hr. Cell lysates were titrated between 0.001 and 2 mg protein per assay using a telomerase PCR-ELISA technique. MCF-7 cells transfected with pshRNAUBE2D3 showed higher telomerase activity compared to negativeFigure 3. The detection of protein(UBE2D3, hTERT, cyclin D1, bactin) expressions were illustrated. (A) Western blotting analysis showing the effect of 16985061 overexpression and knockdown of UBE2D3 on UBE2D3 and hTERT levels in MCF-7 cells. Control cells were transfected with negative control shRNA. (B) Western blotting analysis showing the effect of knockdown of UBE2D3 on cyclin D1 levels in MCF-7 cells. (C) Western blotting analysis showing the effect of overexpression of hTERT on UBE2D3 and hTERT levels in MCF-7 cells. Experiments were repeated 3 times with similar results. doi:10.1371/journal.pone.0064660.gFigure 4. The MCF-7 cells proliferation were illustrated. After MCF-7 cells were transfected with pshRNA-UBE2D3, cell proliferation was examined by CCK-8 assay. The results were presented as the Means6SD of three independent experiments. *p,0.05. doi:10.1371/journal.pone.0064660.gUBE2D3 Regulates MCF-7 Cells Radiosensitivitycontrol (P,0.05) (Figure 5). On the basis of these preliminary results, we treated MCF-7 cells with 4 GY X-ray after transfection with the above plasmids. MCF-7 cells treated with X-rays after transfection with pshRNA-UBE2D3 showed higher telomerase activity compared with transfection with pshRNA-UBE2D3 alone, suggesting that UBE2D3-induced elevation of hTERT activity could be enhanced by radiation treatment.Down-regulation of UBE2D3 Weakened MCF-7 Cells RadiosensitivityAfter counting clones, the survival curves were plotted to evaluate the radiobiological parameters of each group. Compared to the negative control, the survival fractions of the pshRNAUBE2D3 group were much higher at each point in MCF-7 cells. Figure 6 shows that down-regulation of UBE2D3 reduced the radiosensitivity of MCF-7 cells. Similar results were observed in lung adenocarcinoma A549 cells (data not shown). Plating efficiency (PE) and survival fraction (SF) were calculated.DiscussionHere, we first performed Y2H to screen for hTERT-interacting proteins. We found evidence implicating UBE2D3 as a modulator of MCF-7 cell radiosensitivity by regulating hTERT and cyclin D1 protein expression. It is well established that telomerase activity requires the presence of the hTR and hTERT subunits. The present study of the relationship between hTERT and radiosensitivity indicates that in t.
