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首页> 外文期刊>Developmental neurobiology >Zebrafish transgenic constructs label specific neurons in Xenopus laevis Xenopus laevis spinal cord and identify frog V0v spinal neurons
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Zebrafish transgenic constructs label specific neurons in Xenopus laevis Xenopus laevis spinal cord and identify frog V0v spinal neurons

机译:斑马鱼转基因构建标记特异性神经元在Xenopus Laevis Xenopus Laevis脊髓,识别Frog V0V脊髓神经元

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ABSTRACT A correctly functioning spinal cord is crucial for locomotion and communication between body and brain but there are fundamental gaps in our knowledge of how spinal neuronal circuitry is established and functions. To understand the genetic program that regulates specification and functions of this circuitry, we need to connect neuronal molecular phenotypes with physiological analyses. Studies using Xenopus laevis tadpoles have increased our understanding of spinal cord neuronal physiology and function, particularly in locomotor circuitry. However, the X. laevis tetraploid genome and long generation time make it difficult to investigate how neurons are specified. The opacity of X. laevis embryos also makes it hard to connect functional classes of neurons and the genes that they express. We demonstrate here that Tol2 transgenic constructs using zebrafish enhancers that drive expression in specific zebrafish spinal neurons label equivalent neurons in X. laevis and that the incorporation of a Gal4:UAS amplification cassette enables cells to be observed in live X. laevis tadpoles. This technique should enable the molecular phenotypes, morphologies and physiologies of distinct X. laevis spinal neurons to be examined together in vivo . We have used an islet1 enhancer to label Rohon‐Beard sensory neurons and evx enhancers to identify V0v neurons, for the first time, in X. laevis spinal cord. Our work demonstrates the homology of spinal cord circuitry in zebrafish and X. laevis , suggesting that future work could combine their relative strengths to elucidate a more complete picture of how vertebrate spinal cord neurons are specified, and function to generate behavior. ? 2017 Wiley Periodicals, Inc. Develop Neurobiol 77: 1007–1020, 2017
机译:摘要脊髓正确运作的脊髓对于身体和大脑之间的运动和沟通至关重要,但我们知道如何确定脊神经元电路的知识以及功能。要了解调节该电路的规范和功能的遗传计划,我们需要用生理分析连接神经元分子表型。使用Xenopus Laevis Tadpoles的研究提高了我们对脊髓神经元生理学和功能的理解,特别是在运动电路中。然而,X. Laevis四倍体基因组和长的一代时间使得难以调查神经元的特征方式。 X. Laevis Embryos的不透明性也使其难以连接功能阶级的神经元和所表达的基因。我们展示了使用斑马鱼增强剂的Tol2转基因构建体,其在X. Laevis中驱动特定斑马鱼脊髓神经元标记等效神经元的表达,并且掺入GAL4:UAS扩增盒使得能够在Laevis Tadpoles的Lavis Tadpoles中观察到细胞。该技术应使得不同X.劳埃维斯脊髓神经元的分子表型,形态和生理学在体内一起检查。我们使用了islet1增强剂来标记Rohon-Beard感官神经元和EVX增强剂,首次在X. Laevis脊髓中识别V0V神经元。我们的作品展示了斑马鱼和X. Laevis中的脊髓电路的同源性,这表明未来的工作可以将其相对优势结合起来,以阐明如何指定脊椎动物神经元的更完整的图像,并且可以产生行为。还2017 Wiley期刊,Inc。开发Neurobiol 77:1007-1020,2017

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