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Ror beta regulates selective axon-target innervation in the mammalian midbrain

机译:ROR BETA在哺乳动物中脑中调节选择性轴突 - 目标支配

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Developmental control of long-range neuronal connections in the mammalian midbrain remains unclear. We explored the mechanisms regulating target selection of the developing superior colliculus (SC). The SC is a midbrain center that directs orienting behaviors and defense responses. We discovered that a transcription factor, Ror beta, controls establishment of axonal projections from the SC to two thalamic nuclei: the dorsal lateral geniculate nucleus (dLGN) and the lateral posterior nucleus (LP). A genetic strategy used to visualize SC circuits revealed that in control animals Ror beta(+) neurons abundantly innervate the dLGN but barely innervate the LP. The opposite phenotype was observed in global and conditional Rorb mutants: projections to the dLGN were strongly decreased, and projections to the LP were increased. Furthermore, overexpression of Rorb in the wild type showed increased projections to the dLGN and decreased projections to the LP. In summary, we identified Ror beta as a key developmental mediator of colliculo-thalamic innervation. Such regulation could represent a general mechanism orchestrating long-range neuronal connections in the mammalian brain.
机译:哺乳动物中脑中远程神经元连接的发育控制仍不清楚。我们探讨了调节展示型优势小集(SC)的目标选择的机制。 SC是一个引导定向行为和防御反应的中脑中心。我们发现转录因子,RORβ从SC到两个丘脑中的轴突突起的建立:背侧横向核细胞核(DLGN)和侧向后核(LP)。用于可视化SC电路的遗传策略表明,在对照动物中,RORβ(+)神经元大量地支配DLGN但几乎没有支配LP。在全局和有条件的下载突变体中观察到相对的表型:对DLGN的突起大大降低,并且增加了对LP的突出。此外,野生型中的RORB的过表达显示出对DLGN的突起增加并降低了LP的突起。总之,我们将ROL BETA作为Colliculo-Thalamic Undervation的关键发育介质。这种调节可以代表哺乳动物脑中协调长期神经元联系的一般机制。

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