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脑皮质发育过程中 EphA7 基因表达的转录机制。

Transcriptional mechanisms of EphA7 gene expression in the developing cerebral cortex.

机构信息

Welbio and Institut de Recherches en Biologie Humaine et Moléculaire (IRIBHM) Université Libre de Bruxelles, B-1070 Brussels, Belgium.

出版信息

Cereb Cortex. 2012 Jul;22(7):1678-89. doi: 10.1093/cercor/bhr245. Epub 2011 Sep 21.

DOI:10.1093/cercor/bhr245
PMID:21940705
Abstract

The patterning of cortical areas is controlled by a combination of intrinsic factors that are expressed in the cortex and external signals such as inputs from the thalamus. EphA7 is a guidance receptor that is involved in key aspects of cortical development and is expressed in gradients within developing cortical areas. Here, we identified a regulatory element of the EphA7 promoter, named pA7, that can recapitulate salient features of the pattern of expression of EphA7, including cortical gradients. Using a pA7-Green fluorescent Protein (GFP) mouse reporter line, we isolated cortical neuron populations displaying different levels of EphA7/GFP expression. Transcriptome analysis of these populations enabled to identify many differentially expressed genes, including 26 transcription factors with putative binding sites in the pA7 element. Among these, Pbx1 was found to bind directly to the EphA7 promoter in the developing cortex. All genes validated further were confirmed to be expressed differentially in the developing cortex, similarly to EphA7. Their expression was unchanged in mutant mice defective for thalamocortical projections, indicating a transcriptional control largely intrinsic to the cortex. Our study identifies a novel repertoire of cortical neuron genes that may act upstream of, or together with EphA7, to control the patterning of cortical areas.

摘要

皮层区域的模式形成受内在因素和外部信号的共同控制,这些内在因素在皮层中表达,外部信号如来自丘脑的输入。EphA7 是一种导向受体,它参与皮质发育的关键方面,并在发育中的皮质区域内呈梯度表达。在这里,我们鉴定了 EphA7 启动子的一个调节元件,命名为 pA7,它可以重现 EphA7 表达模式的显著特征,包括皮质梯度。使用 pA7-GFP(绿色荧光蛋白)小鼠报告基因系,我们分离出显示不同 EphA7/GFP 表达水平的皮质神经元群体。对这些群体的转录组分析使我们能够鉴定出许多差异表达的基因,包括 26 个转录因子,它们在 pA7 元件中有潜在的结合位点。其中,Pbx1 被发现直接结合到发育中的皮质中的 EphA7 启动子。进一步验证的所有基因都被证实与 EphA7 相似,在发育中的皮质中表达存在差异。它们在丘脑皮质投射缺陷的突变小鼠中表达不变,表明这是一种主要发生在皮质内的转录控制。我们的研究鉴定了一组新的皮质神经元基因,它们可能在上游或与 EphA7 一起作用,以控制皮质区域的模式形成。

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