Farin Henner F, Mansouri Ahmed, Petry Marianne, Kispert Andreas
Institute for Molecular Biology, Medizinische Hochschule Hannover, OE5250, Carl-Neuberg-Strasse 1, D-30625 Hannover, Germany and the.
Department of Molecular Cell Biology, Max-Planck-Institute of Biophysical Chemistry, 37077 Göttingen, Germany.
J Biol Chem. 2008 Sep 12;283(37):25372-25380. doi: 10.1074/jbc.M802723200. Epub 2008 Jul 21.
The compartmentalization of somites along their anterior-posterior axis is crucial to the segmental organization of the vertebral column. Anterior-posterior somite polarity is generated in the anterior presomitic mesoderm by Mesp2 and Delta/Notch signaling and is further maintained by two transcriptional regulators, Uncx4.1 and Tbx18, acting in the posterior and anterior somite compartment, respectively. Here, we report that the paired box transcription factor Pax3 cooperates with the T-box protein Tbx18 in maintaining anterior somite half identity. Our findings that both genes are co-expressed in the anterior presomitic mesoderm and in early somites, that Pax3 and Tbx18 proteins physically interact, and that the loss of Pax3 gene function enhances the vertebral defects (i.e. the gain of vertebral elements derived from posterior somite halves in Tbx18 mutant mice) suggests that the two proteins cooperatively regulate the gene expression program necessary for maintaining anterior-posterior somite polarity. Genetic interaction of Pax3 with Tbx18 and the closely related T-box gene Tbx15 was also observed in the development of the scapula blade, indicating an additional cooperative function for these genes in the paraxial mesoderm.
体节沿前后轴的分区对于脊柱的节段组织至关重要。前后体节极性在前体节中胚层由Mesp2和Delta/Notch信号产生,并分别由两个转录调节因子Uncx4.1和Tbx18在后体节区室和前体节区室中发挥作用来进一步维持。在此,我们报道配对盒转录因子Pax3与T盒蛋白Tbx18协同维持前体节半体身份。我们的研究发现这两个基因在前体节中胚层和早期体节中共同表达,Pax3和Tbx18蛋白发生物理相互作用,并且Pax3基因功能的丧失增强了脊柱缺陷(即Tbx18突变小鼠中源自后体节半体的椎骨成分增加),这表明这两种蛋白协同调节维持前后体节极性所需的基因表达程序。在肩胛骨的发育过程中也观察到Pax3与Tbx18以及密切相关的T盒基因Tbx15之间的遗传相互作用,表明这些基因在近轴中胚层中具有额外的协同功能。