Dhamija S, Krebsbach P H
University of Michigan School of Dentistry, Department of Oral Medicine, Pathology, and Oncology, Ann Arbor, Michigan 48109-1078, USA.
J Biol Chem. 2001 Sep 14;276(37):35159-64. doi: 10.1074/jbc.M010719200. Epub 2001 Jul 12.
Ameloblastin is a tooth-specific extracellular matrix protein that is thought to play a role in enamel crystal formation in the developing dentition. The murine ameloblastin promoter functions in a cell type-specific manner and contains cis-acting elements that function both to enhance and to suppress transcription. The objective of this study was to determine whether the transcription factor Cbfa1, known to be essential for transcription of other mineralized tissue genes, is also required for ameloblastin transcription. Site-directed mutagenesis of the Cbfa1-binding site (-248 base pairs) termed osteoblast-specific element 2 (OSE2) decreased ameloblastin promoter activity by greater than 50% in ameloblast-like cells. No differences in promoter activity were observed in two other oral tissue-derived cell lines transfected with similar constructs. Nuclear factor binding to the ameloblastin promoter was also shown to be cell type-specific and was altered by site-specific mutations in the OSE2 site. Cbfa1 was specifically shown to participate in the DNA-protein complexes between nuclear factors and the ameloblastin OSE2 site by supershift electrophoretic mobility shift assays. The findings that Cbfa1 interacts with functionally important regions of the ameloblastin promoter while promoter activity is diminished in constructs containing site-directed mutations in the Cbfa1 site indicate that Cbfa1 possesses an important function in transcription of the ameloblastin gene.
成釉蛋白是一种牙齿特异性细胞外基质蛋白,被认为在发育中的牙列的釉质晶体形成中发挥作用。小鼠成釉蛋白启动子以细胞类型特异性方式发挥作用,并包含顺式作用元件,这些元件兼具增强和抑制转录的功能。本研究的目的是确定转录因子Cbfa1(已知对其他矿化组织基因的转录至关重要)是否也是成釉蛋白转录所必需的。对称为成骨细胞特异性元件2(OSE2)的Cbfa1结合位点(-248个碱基对)进行定点诱变,在成釉细胞样细胞中使成釉蛋白启动子活性降低了50%以上。在用类似构建体转染的另外两种口腔组织来源的细胞系中未观察到启动子活性的差异。与成釉蛋白启动子结合的核因子也显示出细胞类型特异性,并因OSE2位点的定点突变而改变。通过超迁移电泳迁移率变动分析明确显示Cbfa1参与核因子与成釉蛋白OSE2位点之间的DNA-蛋白质复合物。Cbfa1与成釉蛋白启动子的功能重要区域相互作用,而在Cbfa1位点含有定点突变的构建体中启动子活性降低,这些发现表明Cbfa1在成釉蛋白基因的转录中具有重要功能。