Akhouayri Omar, Quélo Isabelle, St-Arnaud René
Genetics Unit, Shriners Hospital for Children, 1529 Cedar Avenue, Montréal, Québec, Canada H3G 1A6.
Mol Cell Biol. 2005 May;25(9):3452-60. doi: 10.1128/MCB.25.9.3452-3460.2005.
Since the c-Jun coactivator alphaNAC was initially identified in a differential screen for genes expressed in differentiated osteoblasts, we examined whether the osteocalcin gene, a specific marker of terminal osteoblastic differentiation, could be a natural target for the coactivating function of alphaNAC. We had also previously shown that alphaNAC can specifically bind DNA in vitro, but it remained unclear whether the DNA-binding function of alphaNAC is expressed in vivo or if it is required for coactivation. We have identified an alphaNAC binding site within the murine osteocalcin gene proximal promoter region and demonstrated that recombinant alphaNAC or alphaNAC from ROS17/2.8 nuclear extracts can specifically bind this element. Using transient transfection assays, we have shown that alphaNAC specifically potentiated the c-Jun-dependent transcription of the osteocalcin promoter and that this activity specifically required the DNA-binding domain of alphaNAC. Chromatin immunoprecipitation confirmed that alphaNAC occupies its binding site on the osteocalcin promoter in living osteoblastic cells expressing osteocalcin. Inhibition of the expression of endogenous alphaNAC in osteoblastic cells by use of RNA interference provoked a decrease in osteocalcin gene transcription. Our results show that the osteocalcin gene is a target for the alphaNAC coactivating function, and we propose that alphaNAC is specifically targeted to the osteocalcin promoter through its DNA-binding activity as a means to achieve increased specificity in gene transcription.
由于c-Jun共激活因子αNAC最初是在对分化成骨细胞中表达的基因进行差异筛选时被鉴定出来的,我们研究了骨钙素基因(终末成骨细胞分化的特异性标志物)是否可能是αNAC共激活功能的天然靶点。我们之前还表明αNAC在体外能特异性结合DNA,但αNAC的DNA结合功能在体内是否表达,或者它是否是共激活所必需的,仍不清楚。我们在小鼠骨钙素基因近端启动子区域内鉴定出一个αNAC结合位点,并证明重组αNAC或来自ROS17/2.8细胞核提取物的αNAC能特异性结合该元件。通过瞬时转染实验,我们表明αNAC能特异性增强骨钙素启动子的c-Jun依赖性转录,并且这种活性特别需要αNAC的DNA结合结构域。染色质免疫沉淀证实αNAC在表达骨钙素的活成骨细胞中占据其在骨钙素启动子上的结合位点。利用RNA干扰抑制成骨细胞中内源性αNAC的表达会导致骨钙素基因转录减少。我们的结果表明骨钙素基因是αNAC共激活功能的靶点,并且我们提出αNAC通过其DNA结合活性特异性地靶向骨钙素启动子,作为在基因转录中实现更高特异性的一种方式。