| Literature DB >> 34715329 |
James P Simmer1, Jan C-C Hu2, Yuanyuan Hu3, Shelly Zhang4, Tian Liang5, Shih-Kai Wang6, Jung-Wook Kim7, Yasuo Yamakoshi8, Yong-Hee Chun9, John D Bartlett10, Charles E Smith11.
Abstract
The revolution in genetics has rapidly increased our knowledge of human and mouse genes that are critical for the formation of dental enamel and helps us understand how enamel evolved. In this graphical review we focus on the roles of 41 genes that are essential for the secretory stage of amelogenesis when characteristic enamel mineral ribbons initiate on dentin and elongate to expand the enamel layer to the future surface of the tooth. Based upon ultrastructural analyses of genetically modified mice, we propose a molecular model explaining how a cell attachment apparatus including collagen 17, α6ß4 and αvß6 integrins, laminin 332, and secreted enamel proteins could attach to individual enamel mineral ribbons and mold their cross-sectional dimensions as they simultaneously elongate and orient them in the direction of the retrograde movement of the ameloblast membrane.Entities:
Keywords: ACP4; Amelogenesis; Basement membrane; Biomineralization; Evolution; SLC13A5
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Year: 2021 PMID: 34715329 PMCID: PMC8665125 DOI: 10.1016/j.jsb.2021.107805
Source DB: PubMed Journal: J Struct Biol ISSN: 1047-8477 Impact factor: 2.867