Institute of Biotechnology, Developmental Biology Program, PO Box 56, University of Helsinki, FIN-00014, Helsinki, Finland.
Dev Biol. 2010 Apr 15;340(2):355-68. doi: 10.1016/j.ydbio.2010.01.019. Epub 2010 Jan 25.
Teeth form as appendages of the ectoderm and their morphogenesis is regulated by tissue interactions mediated by networks of conserved signal pathways. Micro-RNA (miRNA) pathway has emerged as important regulator of various aspects of embryonic development, but its function in odontogenesis has not been elucidated. We show that the expression of RNAi pathway effectors is dynamic during tooth morphogenesis and differentiation of dental cells. Based on microarray profiling we selected 8 miRNAs expressed during morphogenesis and 7 miRNAs in the incisor cervical loop containing the stem cell niche. These miRNAs were mainly expressed in the dental epithelium. Conditional deletion of Dicer-1 in the epithelium (Dcr(K14)(-)(/)(-)) resulted in rather mild but significant aberrations in tooth shape and enamel formation. The cusp patterns of the Dcr(K14)(-)(/)(-) molar crowns resembled the patterns of both ancestral muroid rodents and mouse mutants with modulated signal pathways. In the Dcr(K14)(-)(/)(-) incisors, longitudinal grooves formed on the labial surface and these were shown to result from ectopic budding of the progenitor epithelium in the cervical loop. In addition, ameloblast differentiation was impaired and resulted in deficient enamel formation in molars and incisors. To help the identification of candidate target genes of the selected tooth enriched miRNAs, we constructed a new ectodermal organ oriented database, miRTooth. The predicted targets of the selected miRNAs included several components of the main morphogenetic signal pathways regulating tooth development. Based on our findings we suggest that miRNAs modulate tooth morphogenesis largely by fine tuning conserved signaling networks and that miRNAs may have played important roles during tooth evolution.
牙齿是外胚层的附属物,其形态发生受组织间相互作用的调节,这些组织间相互作用是由保守信号通路网络介导的。微小 RNA (miRNA) 通路已成为胚胎发育各个方面的重要调节因子,但它在牙发生中的作用尚未阐明。我们发现,在牙齿形态发生和牙齿细胞分化过程中,RNAi 通路效应物的表达是动态的。基于微阵列分析,我们选择了 8 种在形态发生过程中表达的 miRNA 和 7 种在包含干细胞龛的切牙颈环中的 miRNA。这些 miRNA 主要在牙上皮中表达。上皮细胞中 Dicer-1 的条件缺失 (Dcr(K14)(-)(/)(-)) 导致牙齿形状和釉质形成出现相当轻微但显著的异常。Dcr(K14)(-)(/)(-)磨牙牙冠的尖峰模式类似于调节信号通路的祖始鼠科啮齿动物和小鼠突变体的模式。在 Dcr(K14)(-)(/)(-)切牙中,唇面形成了纵向沟,这些沟是由于颈环中的祖细胞上皮异位芽生所致。此外,成釉细胞分化受损,导致磨牙和切牙釉质形成不足。为了帮助鉴定所选牙齿富集 miRNA 的候选靶基因,我们构建了一个新的外胚层器官定向数据库 miRTooth。所选 miRNA 的预测靶基因包括调节牙齿发育的主要形态发生信号通路的几个组成部分。基于我们的发现,我们认为 miRNA 通过微调保守信号网络来调节牙齿形态发生,并且 miRNA 在牙齿进化过程中可能发挥了重要作用。
Dev Genes Evol. 2000-5
J Taibah Univ Med Sci. 2024-12-30
Oral Sci Int. 2021-1
Front Cell Dev Biol. 2021-8-25
Hum Mol Genet. 2021-9-15