Department of Biomedical Sciences, Texas A&M University Health Science Center Baylor College of Dentistry, Dallas, TX, USA.
Cells Tissues Organs. 2011;194(2-4):156-60. doi: 10.1159/000324747. Epub 2011 May 6.
For many years the molecular mechanisms governing bone morphogenetic protein 4 (Bmp4) expression in tooth bud mesenchyme could be explained by an uncomplicated model involving the interaction of the homeobox gene Msx1 and the paired domain gene Pax9 and a limited proximal promoter segment of Bmp4. New insights have led to major revisions, but we are still far from understanding the role of Msx1 and Pax9 in the complex processes that result in the expression of Bmp4 in the mesenchymal layer of the developing tooth bud. The objective of these studies was to gain further insight into the molecular relationship between Pax9, Msx1, and Bmp4 in dental mesenchyme and explore its association with nonsyndromic tooth agenesis in humans.
多年来,调控牙蕾间质中骨形态发生蛋白 4(Bmp4)表达的分子机制可以用一个简单的模型来解释,该模型涉及同源盒基因 Msx1 和配对结构域基因 Pax9 的相互作用,以及 Bmp4 的有限近端启动子片段。新的认识导致了重大修订,但我们仍远未理解 Msx1 和 Pax9 在导致牙蕾间质中 Bmp4 表达的复杂过程中的作用。这些研究的目的是进一步深入了解牙间质中 Pax9、Msx1 和 Bmp4 之间的分子关系,并探讨其与人类非综合征性牙齿缺失的关联。