Institute of Biosciences and Technology, Texas A & M University Health Science Center, Houston, Texas 77030, USA.
J Biol Chem. 2013 Jan 25;288(4):2485-500. doi: 10.1074/jbc.M112.402933. Epub 2012 Dec 10.
LHX6 is a LIM-homeobox transcription factor expressed during embryogenesis; however, the molecular mechanisms regulating LHX6 transcriptional activities are unknown. LHX6 and the PITX2 homeodomain transcription factor have overlapping expression patterns during tooth and craniofacial development, and in this report, we demonstrate new transcriptional mechanisms for these factors. PITX2 and LHX6 are co-expressed in the oral and dental epithelium and epithelial cell lines. Lhx6 expression is increased in Pitx2c transgenic mice and decreased in Pitx2 null mice. PITX2 activates endogenous Lhx6 expression and the Lhx6 promoter, whereas LHX6 represses its promoter activity. Chromatin immunoprecipitation experiments reveal endogenous PITX2 binding to the Lhx6 promoter. LHX6 directly interacts with PITX2 to inhibit PITX2 transcriptional activities and activation of multiple promoters. Bimolecular fluorescence complementation assays reveal an LHX6·PITX2 nuclear interaction in living cells. LHX6 has a dominant repressive effect on the PITX2 synergistic activation with LEF-1 and β-catenin co-factors. Thus, LHX6 acts as a transcriptional repressor and represses the expression of several genes involved in odontogenesis. We have identified specific defects in incisor, molar, mandible, bone, and root development and late stage enamel formation in Lhx6 null mice. Amelogenin and ameloblastin expression is reduced and/or delayed in the Lhx6 null mice, potentially resulting from defects in dentin deposition and ameloblast differentiation. Our results demonstrate that LHX6 regulates cell proliferation in the cervical loop and promotes cell differentiation in the anterior region of the incisor. We demonstrate new molecular mechanisms for LHX6 and an interaction with PITX2 for normal craniofacial and tooth development.
LHX6 是一种 LIM-homeobox 转录因子,在胚胎发生过程中表达;然而,调节 LHX6 转录活性的分子机制尚不清楚。LHX6 和 PITX2 同源结构域转录因子在牙齿和颅面发育过程中有重叠的表达模式,在本报告中,我们证明了这些因子的新转录机制。PITX2 和 LHX6 在口腔和牙上皮以及上皮细胞系中共同表达。Lhx6 在 Pitx2c 转基因小鼠中表达增加,在 Pitx2 缺失小鼠中表达减少。PITX2 激活内源性 Lhx6 表达和 Lhx6 启动子,而 LHX6 抑制其启动子活性。染色质免疫沉淀实验显示内源性 PITX2 结合到 Lhx6 启动子上。LHX6 直接与 PITX2 相互作用,抑制 PITX2 的转录活性和多个启动子的激活。双分子荧光互补测定显示活细胞中存在 LHX6·PITX2 核相互作用。LHX6 对 PITX2 的协同激活具有显性抑制作用,与 LEF-1 和 β-catenin 共因子协同激活。因此,LHX6 作为转录抑制因子,抑制参与牙发生的多个基因的表达。我们在 Lhx6 缺失小鼠中发现了门牙、磨牙、下颌骨、骨骼和牙根发育以及釉质形成后期的特定缺陷。Lhx6 缺失小鼠中釉原蛋白和釉蛋白的表达减少和/或延迟,可能是由于牙本质沉积和成釉细胞分化缺陷所致。我们的研究结果表明,LHX6 调节颈环中的细胞增殖,并促进门牙前区的细胞分化。我们为 LHX6 证明了新的分子机制,并证明了与 PITX2 的相互作用对于正常的颅面和牙齿发育是必要的。