利用t - α1 α-微管蛋白启动子分析和调控神经元基因表达

Freda D. Miller , David Rogers , Shernaz X. Bamji , Ruth S. Slack , Andrew Gloster
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引用次数: 4

摘要

由于缺乏合适的模型系统,哺乳动物神经元分化的分子遗传机制分析一直受到阻碍。在这里,我们回顾了Tα1 α-微管蛋白基因代表这样一个模型系统的证据。内源性Tα1基因在发育和成熟神经元的生长过程中大量表达。在转基因小鼠中,来自Tα1基因5 '侧的1.1 kb序列足以将基因表达定向到早期发育的神经元,并作为神经元生长的功能调节其表达水平。对该启动子的分析初步阐明了神经元发育过程中基因表达所必需的序列元件。此外,Tα1启动子为转基因小鼠分化神经元的调控和分析提供了实验机制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Analysis and manipulation of neuronal gene expression using the Tα1 α-tubulin promoter

Analysis of the molecular genetic mechanisms underlying neuronal differentiation in mammals has been hampered by the lack of appropriate model systems. Here, we review the evidence that the Tα1 α-tubulin gene represents such a model system. The endogenous Tα1 gene is expressed at highly abundant levels during the growth of developing and mature neurons. In transgenic mice, 1·1 kb of 5′ flanking sequence from the Tα1 gene is sufficient to target gene expression to early developing neurons, and to regulate levels of expression as a function of neuronal growth. Analysis of this promoter has led to the initial elucidation of sequence elements essential for gene expression during neuronal development. Moreover, the Tα1 promoter provides an experimental mechanism for the manipulation and analysis of differentiating neurons in transgenic mice.

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