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Neuronal function of Tbx20 conserved from nematodes to vertebrates.

机译:Tbx20的神经元功能从线虫到脊椎动物都是保守的。

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The Tbx20 orthologue, mab-9, is required for development of the Caenorhabditis elegans hindgut, whereas several vertebrate Tbx20 genes promote heart development. Here we show that Tbx20 orthologues also have a role in motor neuron development that is conserved between invertebrates and vertebrates. mab-9 mutants exhibit guidance defects in dorsally projecting axons from motor neurons located in the ventral nerve cord. Danio rerio (Zebrafish) tbx20 morphants show defects in the migration patterns of motor neuron soma of the facial and trigeminal motor neuron groups. Human TBX20 is expressed in motor neurons in the developing hindbrain of human embryos and we show that human TBX20 can substitute for zebrafish tbx20 in promoting cranial motor neuron migration. mab-9 is also partially able to rescue the zebrafish migration defect, whereas other vertebrate T-box genes cannot. Conversely we show that the human TBX20 T-box domain can rescue motor neuron defects in C. elegans. These data suggest the functional equivalence of Tbx20 orthologues in regulating the development of specific motor neuron groups. We also demonstrate the functional equivalence of human and C. elegans Tbx20 T-box domains for regulating male tail development in the nematode even though these genes play highly diverged roles in organogenesis.
机译:Tbx20直系同源基因mab-9是秀丽隐杆线虫后肠的发育所必需的,而一些脊椎动物Tbx20基因则促进心脏发育。在这里,我们显示Tbx20直系同源物在无脊椎动物和脊椎动物之间保守的运动神经元发育中也有作用。 mab-9突变体在背腹神经索中的运动神经元的背突轴突中显示出指导缺陷。斑马鱼(Zebrafish)tbx20 morphant在面部和三叉神经运动神经元组的运动神经元体的迁移模式中显示出缺陷。人TBX20在人类胚胎发育中的后脑中的运动神经元中表达,我们证明了人TBX20可以代替斑马鱼tbx20促进颅神经运动神经元迁移。 mab-9也能够部分挽救斑马鱼的迁移缺陷,而其他脊椎动物T-box基因则不能。相反,我们表明人TBX20 T-box域可以挽救秀丽隐杆线虫的运动神经元缺陷。这些数据表明Tbx20直向同源物在调节特定运动神经元组发育中的功能等效性。我们还证明了人类和秀丽隐杆线虫Tbx20 T-box域在线虫中调节雄性尾巴发育的功能等效性,即使这些基因在器官发生中起着高度不同的作用。

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