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本文引用的文献

1
Neurogenin1 expression in cell lineages of the cerebellar cortex in embryonic and postnatal mice.神经母细胞基因 1 在胚胎期和出生后小鼠小脑皮质细胞谱系中的表达。
Dev Dyn. 2009 Dec;238(12):3310-25. doi: 10.1002/dvdy.22165.
2
Histone marks and chromatin remodelers on the regulation of neurogenin1 gene in RA induced neuronal differentiation of P19 cells.组蛋白标记和染色质重塑因子对类风湿关节炎诱导的P19细胞神经元分化中神经生成素1基因的调控作用
J Cell Biochem. 2009 May 15;107(2):264-71. doi: 10.1002/jcb.22122.
3
ChIP-seq accurately predicts tissue-specific activity of enhancers.染色质免疫沉淀测序(ChIP-seq)能准确预测增强子的组织特异性活性。
Nature. 2009 Feb 12;457(7231):854-8. doi: 10.1038/nature07730.
4
Shadow enhancers as a source of evolutionary novelty.作为进化新奇性来源的影子增强子。
Science. 2008 Sep 5;321(5894):1314. doi: 10.1126/science.1160631.
5
Conserved non-coding sequences and transcriptional regulation.保守非编码序列与转录调控。
Brain Res Bull. 2008 Mar 18;75(2-4):225-30. doi: 10.1016/j.brainresbull.2007.11.010. Epub 2007 Dec 18.
6
Cross-regulation of Ngn1 and Math1 coordinates the production of neurons and sensory hair cells during inner ear development.在内耳发育过程中,Ngn1和Math1的交叉调节协调了神经元和感觉毛细胞的产生。
Development. 2007 Dec;134(24):4405-15. doi: 10.1242/dev.009118.
7
Deletion of ultraconserved elements yields viable mice.超保守元件的缺失产生可存活的小鼠。
PLoS Biol. 2007 Sep;5(9):e234. doi: 10.1371/journal.pbio.0050234.
8
Characterization of progenitor domains in the developing mouse thalamus.发育中小鼠丘脑祖细胞结构域的特征分析
J Comp Neurol. 2007 Nov 1;505(1):73-91. doi: 10.1002/cne.21467.
9
Genomic characterization of Gli-activator targets in sonic hedgehog-mediated neural patterning.音猬因子介导的神经模式形成中Gli激活因子靶点的基因组特征分析。
Development. 2007 May;134(10):1977-89. doi: 10.1242/dev.001966. Epub 2007 Apr 18.
10
Whole-genome ChIP-chip analysis of Dorsal, Twist, and Snail suggests integration of diverse patterning processes in the Drosophila embryo.对背腹因子、扭曲蛋白和蜗牛蛋白进行全基因组芯片分析,结果表明果蝇胚胎中多种模式形成过程存在整合现象。
Genes Dev. 2007 Feb 15;21(4):385-90. doi: 10.1101/gad.1509607.

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.

DOI:10.1016/j.ydbio.2010.02.012
PMID:20171205
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2854235/
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。