Ated that ERa could dose-dependently enhance MGARP transcriptional activity, indicating that this 23 kb upstream 374913-63-0 manufacturer region may either contain non-classic ERbinding site(s) or engage with ERa-interacting transactivator(s), including endogenous Sp1 (Figure 6A). Importantly, co-expressionof Sp1 with ERa can further increase ER-induced reporter activity, demonstrating significant synergistic effects on the MGARP promoters (Figure 6B). In addition, the synergistic effect was different for distinct regions of the MGARP promoter, with the promoters restricted to the GC Box1 2 
and Box1 producing the most greatest synergy, further supporting that it is primarily mediated by 12926553 Sp1 (Figure 6B). Since ERa can be activated by itsFigure 4. EMSA test indicates that Sp1 directly binds to the GC-boxes of the MGARP promoter. For the EMSA analysis, nuclear extracts (Nu) from HEK-293T or Y1 cells were incubated with Biotin-labeled oligonucleotides (Biotin-probe) spanning the GC-rich region (BOX1) of the MGARP promoter (23 kb). Competition reactions were performed with 200X of unlabeled cold competitor (cold), 200X of mutated-labeled competitors (mu) or Sp1 antibody (2 mg). The following cell lines were used: non-transfected or Sp1-overexpressed HEK-293T cells (A), non-transfected, Sp1overexpressed, or 630-RNAi transfected HEK-293T cells (B), and Y1 cells (C). doi:10.1371/journal.pone.0050053.gMGARP Is Regulated via Tandem Sp1 ElementsFigure 5. ChIP analysis indicates that Sp1 binds to MGARP promoter in vivo. ChIP was performed as described in the Materials and Methods. HEK-293T cells and antibodies for RNA polymerase II (Pol II) and Sp1 were used, with IgG as control. The immunoprecipitated chromatin was amplified by PCR with primers specific for the GC-rich region (BOX1 2) of the MGARP promoter (23 kb), with GAPDH locus as control. M: DNA Marker. doi:10.1371/journal.pone.0050053.gnatural ligand estrogen, we further studied the transactivation activity of ERa under the stimulation of estrogen. Our results indicated that estrogens could modestly enhance the transactivation activity of ERa on the MGARP promoter and markedly enhance the promoter activity in the presence of exogenous Sp1, while minimal effects were recorded on the control vector (Figure 6C). In contrast, in both the absence and presence of exogenous Sp1, knockdown of Sp1 significantly reduced the activation function of ERa on the MGARP promoter (Figure 6D). Furthermore, in ERa-transfected HEK-293T cells, estrogens could increase endogenous MGARP expression, while downregulation of Sp1 led to a reduction in endogenous MGARP mRNA expression, in the absence and presence of estrogens (Figure 6E). Together, these findings demonstrate that Sp1 and ERa up-regulate MGARP promoter activity in a synergistic manner and that ERa may act as a co-activator for Sp1 to regulate MGARP promoter activity.DiscussionGene transcription in eukaryotic organisms depends on the interplay ML-281 between transcription factors and regulatory elements in promoters. Transcription is regulated by chromatin-interacting factors, which bind to their specific DNA recognition sequences [29]. Sp1 is a general transcription factor driving gene expression in early development [30,31], containing a zinc finger motif that mediates binding to DNA with the consensus sequence 59-(G/ T)GGGCGG(G/A)(G/A)(C/T)-39 (GC box element). We demonstrated that the region spanning -150 to 0 bp of the MGARP promoter fragment has basic promoter properties and conta.Ated that ERa could dose-dependently enhance MGARP transcriptional activity, indicating that this 23 kb upstream region may either contain non-classic ERbinding site(s) or engage with ERa-interacting transactivator(s), including endogenous Sp1 (Figure 6A). Importantly, co-expressionof Sp1 with ERa can further increase ER-induced reporter activity, demonstrating significant synergistic effects on the MGARP promoters (Figure 6B). In addition, the synergistic effect was different for distinct regions of the MGARP promoter, with the promoters restricted to the GC Box1 2 and Box1 producing the most greatest synergy, further supporting that it is primarily mediated by 12926553 Sp1 (Figure 6B). Since ERa can be activated by itsFigure 4. EMSA test indicates that Sp1 directly binds to the GC-boxes of the MGARP promoter. For the EMSA analysis, nuclear extracts (Nu) from HEK-293T or Y1 cells were incubated with Biotin-labeled oligonucleotides (Biotin-probe) spanning the GC-rich region (BOX1) 
of the MGARP promoter (23 kb). Competition reactions were performed with 200X of unlabeled cold competitor (cold), 200X of mutated-labeled competitors (mu) or Sp1 antibody (2 mg). The following cell lines were used: non-transfected or Sp1-overexpressed HEK-293T cells (A), non-transfected, Sp1overexpressed, or 630-RNAi transfected HEK-293T cells (B), and Y1 cells (C). doi:10.1371/journal.pone.0050053.gMGARP Is Regulated via Tandem Sp1 ElementsFigure 5. ChIP analysis indicates that Sp1 binds to MGARP promoter in vivo. ChIP was performed as described in the Materials and Methods. HEK-293T cells and antibodies for RNA polymerase II (Pol II) and Sp1 were used, with IgG as control. The immunoprecipitated chromatin was amplified by PCR with primers specific for the GC-rich region (BOX1 2) of the MGARP promoter (23 kb), with GAPDH locus as control. M: DNA Marker. doi:10.1371/journal.pone.0050053.gnatural ligand estrogen, we further studied the transactivation activity of ERa under the stimulation of estrogen. Our results indicated that estrogens could modestly enhance the transactivation activity of ERa on the MGARP promoter and markedly enhance the promoter activity in the presence of exogenous Sp1, while minimal effects were recorded on the control vector (Figure 6C). In contrast, in both the absence and presence of exogenous Sp1, knockdown of Sp1 significantly reduced the activation function of ERa on the MGARP promoter (Figure 6D). Furthermore, in ERa-transfected HEK-293T cells, estrogens could increase endogenous MGARP expression, while downregulation of Sp1 led to a reduction in endogenous MGARP mRNA expression, in the absence and presence of estrogens (Figure 6E). Together, these findings demonstrate that Sp1 and ERa up-regulate MGARP promoter activity in a synergistic manner and that ERa may act as a co-activator for Sp1 to regulate MGARP promoter activity.DiscussionGene transcription in eukaryotic organisms depends on the interplay between transcription factors and regulatory elements in promoters. Transcription is regulated by chromatin-interacting factors, which bind to their specific DNA recognition sequences [29]. Sp1 is a general transcription factor driving gene expression in early development [30,31], containing a zinc finger motif that mediates binding to DNA with the consensus sequence 59-(G/ T)GGGCGG(G/A)(G/A)(C/T)-39 (GC box element). We demonstrated that the region spanning -150 to 0 bp of the MGARP promoter fragment has basic promoter properties and conta.