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神经母细胞瘤 1 基因(Neurog1)在脊索管腹侧的表达受一个独特增强子的调控,并优先标记腹侧中间神经元谱系。

Neurogenin 1 (Neurog1) expression in the ventral neural tube is mediated by a distinct enhancer and preferentially marks ventral interneuron lineages.

机构信息

Department of Neuroscience, University of Texas Southwestern Medical Center, 5323 Harry Hines Blvd, Dallas, TX 75390-9111, USA.

出版信息

Dev Biol. 2010 Apr 15;340(2):283-92. doi: 10.1016/j.ydbio.2010.02.012. Epub 2010 Feb 18.

Abstract

The bHLH transcription factor Neurog1 (Ngn1, Neurod3, neurogenin 1) is involved in neuronal differentiation and cell-type specification in distinct regions of the developing nervous system. Here, transgenic mouse models were developed that use a Bacterial Artificial Chromosome (BAC) containing 208kb flanking the Neurog1 gene to efficiently drive expression of GFP and Cre in all Neurog1 domains. Two characteristics of Neurog1 gene regulation were uncovered. First, a 4kb region previously shown to be sufficient for driving expression of a reporter gene to a subset of the Neurog1 pattern in the developing midbrain, hindbrain, and spinal cord is required uniformly for high levels of expression in all Neurog1 domains, even those not originally identified as being regulated by this region. Second, a 0.8 kb enhancer was identified that is sufficient to drive Neurog1-like expression specifically in the ventral neural tube. Furthermore, Neurog1 progenitor cells in the ventral neural tube are largely fated to interneuron lineages rather than to motoneurons. These studies provide new tools for directing tissue specific expression in the developing neural tube, define Neurog1 lineages in the spinal cord, and further define the complex genomic structure required for obtaining the correct levels and spatial restriction of the neuronal differentiation gene Neurog1.

摘要

bHLH 转录因子 Neurog1(Ngn1、Neurod3、神经基因 1)参与发育中神经系统不同区域的神经元分化和细胞类型特化。在这里,开发了使用包含 208kb 侧翼 Neurog1 基因的细菌人工染色体 (BAC) 的转基因小鼠模型,以有效地在所有 Neurog1 结构域中驱动 GFP 和 Cre 的表达。揭示了 Neurog1 基因调控的两个特征。首先,先前已显示足以驱动报告基因在发育中的中脑、后脑和脊髓中的一部分 Neurog1 模式中表达的 4kb 区域,对于所有 Neurog1 结构域中高水平的表达是必需的,即使这些区域最初并未被认为受该区域调控。其次,鉴定出一个 0.8kb 的增强子,足以特异性地驱动腹侧神经管中的 Neurog1 样表达。此外,腹侧神经管中的 Neurog1 祖细胞主要命运为中间神经元谱系,而不是运动神经元。这些研究为在发育中的神经管中指导组织特异性表达提供了新的工具,定义了脊髓中的 Neurog1 谱系,并进一步定义了获得神经元分化基因 Neurog1 的正确水平和空间限制所需的复杂基因组结构。

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