Institute of Oral Biology, Center of Dental Medicine, Faculty of Medicine, University of Zurich, 8032 Zurich, Switzerland.
Clin Genet. 2011 Oct;80(4):319-29. doi: 10.1111/j.1399-0004.2011.01762.x. Epub 2011 Aug 23.
Teeth arise from sequential and reciprocal interactions between the oral epithelium and the cranial neural crest-derived mesenchyme. Their formation involves a precisely orchestrated series of molecular and morphogenetic events. Numerous regulatory genes that have been primarily found in organisms such as Drosophila, zebrafish, xenopus and mouse are associated with all stages of tooth formation (patterning, morphogenesis, cytodifferentiation and mineralization). Most of these genes belong to evolutionary conserved signaling pathways that regulate communication between epithelium and mesenchyme during embryonic development. These signaling molecules together with specific transcription factors constitute a unique molecular imprint for odontogenesis and contribute to the generation of teeth with various and function-specific shapes. Mutations in several genes involved in tooth formation cause developmental absence and/or defects of teeth in mice. In humans, the odontogenic molecular program is not as well known as that of mice. However, some insight can be obtained from the study of mutations in regulatory genes, which lead to tooth agenesis and/or the formation of defective dental tissues.
牙齿由口腔上皮和颅神经嵴衍生的间充质之间的顺序和相互作用产生。它们的形成涉及一系列精确协调的分子和形态发生事件。许多已在果蝇、斑马鱼、爪蟾和小鼠等生物中发现的调节基因与牙齿形成的所有阶段(模式形成、形态发生、细胞分化和矿化)有关。这些基因中的大多数属于进化保守的信号通路,在胚胎发育过程中调节上皮和间充质之间的通讯。这些信号分子与特定的转录因子一起构成了牙发生的独特分子印记,并有助于生成具有各种功能特异性形状的牙齿。参与牙齿形成的几个基因的突变会导致小鼠牙齿的发育缺失和/或缺陷。在人类中,牙发生的分子程序不如小鼠那么为人所知。然而,从调节基因的突变研究中可以获得一些见解,这些突变导致牙齿缺失和/或形成有缺陷的牙组织。
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