Hu Yuanyuan, Papagerakis Petros, Ye Ling, Feng Jerry Q, Simmer James P, Hu Jan C-C
Department of Orthodontics and Pediatric Dentistry, University of Michigan School of Dentistry, Ann Arbor, MI 48108, USA.
Eur J Oral Sci. 2008 Apr;116(2):113-23. doi: 10.1111/j.1600-0722.2007.00519.x.
Enamel formation is orchestrated by the sequential expression of genes encoding enamel matrix proteins; however, the mechanisms sustaining the spatio-temporal order of gene transcription during amelogenesis are poorly understood. The aim of this study was to characterize the cis-regulatory sequences necessary for normal expression of enamelin (Enam). Several enamelin transcription regulatory regions, showing high sequence homology among species, were identified. DNA constructs containing 5.2 or 3.9 kb regions upstream of the enamelin translation initiation site were linked to a LacZ reporter and used to generate transgenic mice. Only the 5.2-Enam-LacZ construct was sufficient to recapitulate the endogenous pattern of enamelin tooth-specific expression. The 3.9-Enam-LacZ transgenic lines showed no expression in dental cells, but ectopic beta-galactosidase activity was detected in osteoblasts. Potential transcription factor-binding sites were identified that may be important in controlling enamelin basal promoter activity and in conferring enamelin tissue-specific expression. Our study provides new insights into regulatory mechanisms governing enamelin expression.
釉质形成是由编码釉质基质蛋白的基因顺序表达所调控的;然而,在釉质发生过程中维持基因转录时空顺序的机制仍知之甚少。本研究的目的是鉴定釉蛋白(Enam)正常表达所需的顺式调控序列。鉴定出了几个在物种间具有高度序列同源性的釉蛋白转录调控区域。将含有釉蛋白翻译起始位点上游5.2或3.9 kb区域的DNA构建体与LacZ报告基因相连,并用于生成转基因小鼠。只有5.2-Enam-LacZ构建体足以重现釉蛋白牙齿特异性表达的内源性模式。3.9-Enam-LacZ转基因系在牙齿细胞中无表达,但在成骨细胞中检测到异位β-半乳糖苷酶活性。鉴定出了可能在控制釉蛋白基础启动子活性和赋予釉蛋白组织特异性表达方面起重要作用的潜在转录因子结合位点。我们的研究为调控釉蛋白表达的机制提供了新的见解。