牙釉蛋白 C 端对于牙釉质的发育是必需的。
The amelogenin C-terminus is required for enamel development.
机构信息
Department of Anatomy and Cell Biology, University of Pennsylvania School of Dental Medicine, Philadelphia, 19104-6030, USA.
出版信息
J Dent Res. 2010 Feb;89(2):165-9. doi: 10.1177/0022034509358392. Epub 2009 Dec 30.
The abundant amelogenin proteins are responsible for generating proper enamel thickness and structure, and most amelogenins include a conserved hydrophilic C-terminus. To evaluate the importance of the C-terminus, we generated transgenic mice that express an amelogenin lacking the C-terminal 13 amino acids (CTRNC). MicroCT analysis of TgCTRNC29 teeth (low transgene number) indicated that molar enamel density was similar to that of wild-type mice, but TgCTRNC18 molar enamel (high transgene number) was deficient, indicating that extra transgene copies were associated with a more severe phenotype. When amelogenin-null (KO) and TgCTRNC transgenic mice were mated, density and volume of molar enamel from TgCTRNCKO offspring were not different from those of KO mice, indicating that neither TgCTRNC18 nor TgCTRNC29 rescued enamel's physical characteristics. Because transgenic full-length amelogenin partially rescues both density and volume of KO molar enamel, it was concluded that the amelogenin C-terminus is essential for proper enamel density, volume, and organization.
丰富的釉原蛋白负责产生适当的釉质厚度和结构,大多数釉原蛋白都包含一个保守的亲水 C 末端。为了评估 C 末端的重要性,我们生成了表达缺乏 C 末端 13 个氨基酸(CTRNC)的釉原蛋白的转基因小鼠。TgCTRNC29 牙齿(转基因数量低)的 MicroCT 分析表明,磨牙釉质密度与野生型小鼠相似,但 TgCTRNC18 磨牙釉质(转基因数量高)缺乏,表明额外的转基因拷贝与更严重的表型相关。当釉原蛋白缺失(KO)和 TgCTRNC 转基因小鼠交配时,TgCTRNCKO 后代的磨牙釉质密度和体积与 KO 小鼠没有差异,表明 TgCTRNC18 和 TgCTRNC29 都没有挽救釉质的物理特性。由于转基因全长釉原蛋白部分挽救了 KO 磨牙釉质的密度和体积,因此可以得出结论,釉原蛋白 C 末端对于适当的釉质密度、体积和组织是必不可少的。