Li Y P, Chen W, Stashenko P
Department of Cytokine Biology, Forsyth Dental Center, Boston, MA 02115, USA.
Nucleic Acids Res. 1995 Dec 25;23(24):5064-72. doi: 10.1093/nar/23.24.5064.
Osteocalcin, the major non-collagenous protein in bone, is transcribed in osteoblasts at the onset of extracellular matrix mineralization. In this study it was demonstrated that sequences located in the first exon of the human osteocalcin gene possess a differentiation-related osteocalcin silencer element (OSE). Osteocalcin was rendered transcribable in UMR-106 cells and proliferating normal osteoblasts after deletion of the -3 to +51 region. Site-specific mutagenesis of this region revealed that a 7 bp sequence (TGGCCCT) (+29 to +35) is critical for silencing function. Mobility shift assays demonstrated that a nuclear factor bound to the OSE. The OSE binding protein was present in proliferating normal pre-osteoblasts and in UMR-106 and ROS 17/2.8 osteosarcoma cells, but was absent from post-proliferative normal osteoblasts. The binding protein was inhibited by fragments containing the +29/+35 sequence, but not by other promoter fragments or by the consensus oligomers of unrelated nuclear factors AP-1 and Sp1. DNase 1 footprinting demonstrated that the OSE binding-protein protected the +17 to +36 portion of the first exon, consistent with the results of mapping studies and competitive mobility shift assays. It is hypothesized that this silencer is activated by complexing of the OSE binding protein to the OSE during the osteoblast proliferation stage and that the OSE binding protein is down-regulated at the onset of extracellular matrix mineralization.
骨钙素是骨骼中主要的非胶原蛋白,在细胞外基质矿化开始时由成骨细胞转录。本研究表明,位于人骨钙素基因第一外显子的序列具有一个与分化相关的骨钙素沉默元件(OSE)。在缺失-3至+51区域后,骨钙素在UMR-106细胞和增殖的正常成骨细胞中变得可转录。该区域的位点特异性诱变表明,一个7bp序列(TGGCCCT)(+29至+35)对沉默功能至关重要。凝胶迁移试验表明,一种核因子与OSE结合。OSE结合蛋白存在于增殖的正常前成骨细胞、UMR-106和ROS 17/2.8骨肉瘤细胞中,但在增殖后的正常成骨细胞中不存在。结合蛋白被含有+29/+35序列的片段抑制,但不被其他启动子片段或无关核因子AP-1和Sp1的共有寡聚体抑制。DNA酶I足迹试验表明,OSE结合蛋白保护第一外显子的+17至+36部分,这与定位研究和竞争性凝胶迁移试验的结果一致。据推测,在成骨细胞增殖阶段,该沉默子通过OSE结合蛋白与OSE的复合而被激活,并且OSE结合蛋白在细胞外基质矿化开始时被下调。