Ritchie H H, Li X
Department of Cariology, Restorative Sciences and Endodontics, University of Michigan School of Dentistry, Ann Arbor 48109, USA.
Eur J Oral Sci. 2001 Oct;109(5):342-7. doi: 10.1034/j.1600-0722.2001.00093.x.
Dentin sialoprotein (DSP) is a major glycoprotein present in the mineralized dentin matrix that is expressed mainly by young and mature odontoblasts. Mutations in the DSP coding regions are linked to Dentinogenesis imperfecta I and II. indicating the importance of DSP in tooth formation. Previous studies have identified multiple mRNA transcripts in dentin that code for both DSP and phosphophoryns (PPs). Using reverse transcriptase-polymerase chain reaction (RT-PCR) to characterize these mRNA transcripts, we have identified a cDNA that codes for DSP, but not PP. This cDNA codes for a protein with 324 amino acids, 303 amino acids being identical to the published rat DSP sequence. However, the subsequent 21 amino acids are unique to this cDNA. Based on the coding sequence, the core protein is predicted to have a pI=4.24, a net charge of -34, and to contain four potential N-glycosylation sites and six potential sites for phosphorylation by casein kinase. That the corresponding mRNA was present in day 5 molar tooth germs was confirmed using RNA protection assays. These data, therefore, identify a novel transcript in rat tooth germs that codes only for DSP (designated as DSPII).
牙本质涎蛋白(DSP)是矿化牙本质基质中存在的一种主要糖蛋白,主要由年轻和成熟的成牙本质细胞表达。DSP编码区的突变与牙本质发育不全I型和II型相关,表明DSP在牙齿形成中的重要性。先前的研究已经在牙本质中鉴定出多种编码DSP和磷蛋白(PPs)的mRNA转录本。通过逆转录聚合酶链反应(RT-PCR)对这些mRNA转录本进行表征,我们鉴定出一种编码DSP而非PP的cDNA。该cDNA编码一种含有324个氨基酸的蛋白质,其中303个氨基酸与已发表的大鼠DSP序列相同。然而,随后的21个氨基酸是该cDNA所特有的。根据编码序列,预测核心蛋白的pI = 4.24,净电荷为 - 34,并含有四个潜在的N-糖基化位点和六个酪蛋白激酶磷酸化的潜在位点。使用RNA保护分析证实了相应的mRNA存在于第5天的磨牙牙胚中。因此,这些数据鉴定出大鼠牙胚中一种仅编码DSP的新型转录本(命名为DSPII)。