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The T-box transcription factor Tbx18 maintains the separation of anterior and posterior somite compartments

机译:T-box转录因子Tbx18保持了前节和后节的分隔

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摘要

The compartmentalization of somites along their anterior–posterior (AP) axis is pivotal to the segmental organization of the vertebrate axial skeleton and the peripheral nervous system. Anterior and posterior somite halves contribute to different vertebral elements. They are also characterized by different proliferation rates and properties with respect to neural crest cell migration and spinal nerve passage. AP-somite polarity is generated in the anterior presomitic mesoderm by Mesp2 and Delta/Notch signaling. Here, we demonstrate that maintenance of AP-somite polarity is mediated by the T-box transcription factor Tbx18. Mice deficient for Tbx18 show expansion of pedicles with transverse processes and proximal ribs, elements derived from the posterior lateral sclerotome. AP-somite polarity is established in Tbx18 mutant embryos but is not maintained. During somite maturation, posterior somite compartments expand most likely because of posterior cells invading the anterior somite half. In the anterior lateral sclerotome, Tbx18 acts as an antiapoptotic factor. Ectopic expression experiments suggest that Tbx18 can promote anterior at the expense of posterior somite compartments. In summary, Tbx18 appears to act downstream of Mesp2 and Delta/Notch signaling to maintain the separation of anterior and posterior somite compartments.
机译:沿前-后(AP)轴划分的节段对脊椎动物轴向骨骼和周围神经系统的节段组织至关重要。前半部和后半部分别构成不同的椎骨元素。它们的特征还在于神经c细胞迁移和脊神经传递方面的不同增殖速率和特性。 AP-somite极性是通过Mesp2和Delta / Notch信号在前部前中胚层中产生的。在这里,我们证明了AP-Somite极性的维持是由T-box转录因子Tbx18介导的。缺乏Tbx18的小鼠显示出椎弓根扩张,横突和近端肋骨,其元素来自后侧硬骨膜刀。 AP-somite极性在Tbx18突变体胚胎中建立,但没有得到维持。在somite成熟期间,后部somite隔室最有可能膨胀,因为后部细胞侵入了前部somite的一半。在前外侧巩膜切除器中,Tbx18充当抗凋亡因子。异位表达实验表明,Tbx18可以促进前部,但以牺牲后部腹腔室为代价。总而言之,Tbx18似乎在Mesp2和Delta / Notch信号传导的下游起作用,以保持前后体节室的分离。

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