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Notch1 基因座中的顺式作用元件参与调节中间神经元祖细胞中的基因表达。

A cis-element in the Notch1 locus is involved in the regulation of gene expression in interneuron progenitors.

机构信息

Department of Biomedical Engineering, Rutgers University, 599 Taylor Road, Piscataway, NJ 08854, USA.

出版信息

Dev Biol. 2012 Dec 15;372(2):217-28. doi: 10.1016/j.ydbio.2012.09.015. Epub 2012 Sep 27.

Abstract

Interneurons comprise approximately one third of the total cortical neurons in the mammalian cerebral cortex. Studies have revealed many details in the generation of this cell type. However, the mechanism that defines interneuron-lineage specific gene expression is not well understood. Gene regulatory elements, e.g., promoters, enhancers, and trans-acting factors, are essential for the proper control of gene expression. Here, we report that a novel evolutionarily conserved cis-element in the second intron of the Notch1 locus plays an important role in regulating gene expression in interneuron progenitors. The spatiotemporal activity of the cis-element in the developing central nervous system (CNS) was determined by both transient reporter expression in the developing chick and a transgenic mouse model. Its activity is well correlated with neurogenesis in both the chick and mouse and restricted to neural progenitor cells in the ganglionic eminence that are fated to differentiate into GABAergic interneurons of the neocortex. We further demonstrate that the cis-element activity requires the binding motif for trans-acting factors Gsh1/Barx2/Brn3. Deletion of this binding motif abolishes reporter gene expression. Together, these data provide new insights into the regulatory mechanisms of interneuron development in the vertebrate CNS.

摘要

中间神经元约占哺乳动物大脑皮层总皮质神经元的三分之一。研究已经揭示了这种细胞类型产生的许多细节。然而,定义中间神经元谱系特异性基因表达的机制尚不清楚。基因调控元件,例如启动子、增强子和反式作用因子,对于基因表达的正确调控至关重要。在这里,我们报告 Notch1 基因座第二个内含子中的一个新的进化上保守的顺式元件在调节中间神经元祖细胞中的基因表达中起着重要作用。通过在发育中的鸡和转基因小鼠模型中瞬时报告基因表达,确定了顺式元件在发育中的中枢神经系统(CNS)中的时空活性。其活性与鸡和小鼠中的神经发生密切相关,并局限于神经前体细胞,这些细胞注定要分化为新皮层的 GABA 能中间神经元。我们进一步证明,顺式元件活性需要反式作用因子 Gsh1/Barx2/Brn3 的结合基序。该结合基序的缺失会导致报告基因表达的丧失。总之,这些数据为脊椎动物中枢神经系统中间神经元发育的调控机制提供了新的见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/540d/3518388/58b30a406f7d/nihms416638f1.jpg

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