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Genetic specification of left–right asymmetry in the diaphragm muscles and their motor innervation

机译:the肌左右不对称的遗传特征及其运动神经

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摘要

The diaphragm muscle is essential for breathing in mammals. Its asymmetric elevation during contraction correlates with morphological features suggestive of inherent left–right (L/R) asymmetry. Whether this asymmetry is due to L versus R differences in the muscle or in the phrenic nerve activity is unknown. Here, we have combined the analysis of genetically modified mouse models with transcriptomic analysis to show that both the diaphragm muscle and phrenic nerves have asymmetries, which can be established independently of each other during early embryogenesis in pathway instructed by Nodal, a morphogen that also conveys asymmetry in other organs. We further found that phrenic motoneurons receive an early L/R genetic imprint, with L versus R differences both in Slit/Robo signaling and MMP2 activity and in the contribution of both pathways to establish phrenic nerve asymmetry. Our study therefore demonstrates L–R imprinting of spinal motoneurons and describes how L/R modulation of axon guidance signaling helps to match neural circuit formation to organ asymmetry.>DOI:
机译:diaphragm肌对于哺乳动物的呼吸必不可少。它在收缩过程中的不对称升高与暗示固有的左右(L / R)不对称的形态特征相关。这种不对称性是由于肌肉还是the神经活动的L对R差异所致尚不清楚。在这里,我们将转基因小鼠模型的分析与转录组学分析相结合,显示the肌和神经都具有不对称性,这可以在Nodal指示的途径的早期胚胎发生过程中彼此独立地建立,这也是一种吗啡原。其他器官的不对称性。我们进一步发现运动神经元收到了早期的L / R遗传印记,Slit / Robo信号传导和MMP2活性以及建立both神经不对称性的两种途径的贡献均具有L对R差异。因此,我们的研究证明了脊髓运动神经元的L–R印记,并描述了轴突引导信号的L / R调节如何帮助将神经回路形成与器官不对称相匹配。> DOI:

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