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亨廷顿舞蹈症(HD)基因启动子的功能分析

Functional analysis of the Huntington's disease (HD) gene promoter.

作者信息

Coles R, Caswell R, Rubinsztein D C

机构信息

Department of Medical Genetics, University of Cambridge, Box 158, Addenbrooke's NHS Trust, Hills Road, Cambridge CB2 2QQ, UK.

出版信息

Hum Mol Genet. 1998 May;7(5):791-800. doi: 10.1093/hmg/7.5.791.

Abstract

The basis for the highly specific neuronal vulnerability seen in Huntington's disease (HD) has not been determined. Recent studies have demonstrated that variation in HD protein expression occurs in the striatum, with affected regions showing increased HD immunoreactivity. Experiments in HD and SCA1 transgenic mice suggest a correlation between phenotypic severity and expression of the mutant transgene. To gain insights into control of HD gene expression, and to investigate the possibility of cell-cell differences in transcription, we have analysed the 5' upstream region of the HD gene in a neuronal (SK-N-SH) and a non-neuronal (JEG3) cell line. Reporter gene assays demonstrated the presence of a key positive-acting region apparently arising from two Sp1 sites in a tandem repeat acting synergistically. This site is polymorphic, and a single Sp1 site is associated with reduced levels of transcription. These experiments also reveal differences in control of expression between neuronal and non-neuronal cell lines.

摘要

亨廷顿舞蹈症(HD)中高度特异性的神经元易损性的基础尚未确定。最近的研究表明,HD蛋白表达的变化发生在纹状体中,受影响区域显示出HD免疫反应性增加。在HD和SCA1转基因小鼠中的实验表明,表型严重程度与突变转基因的表达之间存在相关性。为了深入了解HD基因表达的调控,并研究转录过程中细胞间差异的可能性,我们分析了神经元(SK-N-SH)和非神经元(JEG3)细胞系中HD基因的5'上游区域。报告基因检测表明存在一个关键的正性作用区域,该区域显然由串联重复中的两个Sp1位点协同作用产生。该位点具有多态性,单个Sp1位点与转录水平降低有关。这些实验还揭示了神经元和非神经元细胞系在表达调控上的差异。

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