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同源框基因Dlx-1和Dlx-2的突变会破坏纹状体室下区以及晚期生成的纹状体神经元的分化。

Mutations of the homeobox genes Dlx-1 and Dlx-2 disrupt the striatal subventricular zone and differentiation of late born striatal neurons.

作者信息

Anderson S A, Qiu M, Bulfone A, Eisenstat D D, Meneses J, Pedersen R, Rubenstein J L

机构信息

Center for Neurobiology and Psychiatry, Department of Psychiatry, University of California at San Francisco, 94143, USA.

出版信息

Neuron. 1997 Jul;19(1):27-37. doi: 10.1016/s0896-6273(00)80345-1.

Abstract

The striatum has a central role in many neurobiological processes, yet little is known about the molecular control of its development. Inroads to this subject have been made, due to the discovery of transcription factors, such as the Dlx genes, whose expression patterns suggest that they have a role in striatal development. We report that mice lacking both Dlx-1 and Dlx-2 have a time-dependent block in striatal differentiation. In these mutants, early born neurons migrate into a striatum-like region, which is enriched for markers of the striosome (patch) compartment. However, later born neurons accumulate within the proliferative zone. Several lines of evidence suggest that mutations in Dlx-1 and Dlx-2 produce abnormalities in the development of the striatal subventricular zone and in the differentiation of striatal matrix neurons.

摘要

纹状体在许多神经生物学过程中起着核心作用,但对其发育的分子控制却知之甚少。由于发现了转录因子,如Dlx基因,其表达模式表明它们在纹状体发育中起作用,因此在这个问题上已经取得了进展。我们报告,同时缺乏Dlx-1和Dlx-2的小鼠在纹状体分化中存在时间依赖性阻滞。在这些突变体中,早期出生的神经元迁移到一个类似纹状体的区域,该区域富含纹状体小体(斑块)区室的标记物。然而,后期出生的神经元聚集在增殖区内。几条证据表明,Dlx-1和Dlx-2的突变会导致纹状体室下区发育异常以及纹状体基质神经元分化异常。

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