Pinal C S, Cortessis V, Tobin A J
Department of Biology, University of California, Los Angeles 90095-1761, USA.
Dev Neurosci. 1997;19(6):465-75. doi: 10.1159/000111244.
GAD65 and GAD67, the two forms of GABA-synthesizing enzyme, are usually coexpressed, but their levels are regulated independently. The GAD67 promoter has been described. We have now characterized transcriptional regulatory elements in the 5' flanking region of the GAD65 gene, extending 2.4 kb from the ATG translation initiation site. Primer extension assays revealed that transcription begins at -228 in both adult rat brain and in P19 embryonal carcinoma cells, with additional start sites at -280 in brain and at -360 in P19 cells. These sites are in a GC-rich (72%) region lacking a TATA box. Transient transfection assays revealed that the basal promoter is between -740 and -60, and elements conferring cell-type specificity are further 5'. DNA sequences between -1652 and -1420 can 'silence' transcription from a heterologous promoter. GAD65 and GAD67 promoters share little sequence identity, consistent with differences in their transcriptional regulation.
GABA合成酶的两种形式GAD65和GAD67通常共同表达,但其水平是独立调节的。GAD67启动子已被描述。我们现在已对GAD65基因5'侧翼区域的转录调控元件进行了特征分析,该区域从ATG翻译起始位点延伸2.4 kb。引物延伸分析表明,在成年大鼠脑和P19胚胎癌细胞中,转录均起始于-228,在脑中还有-280处的额外起始位点,在P19细胞中有-360处的额外起始位点。这些位点位于富含GC(72%)且缺乏TATA框的区域。瞬时转染分析表明,基础启动子位于-740至-60之间,赋予细胞类型特异性的元件则更靠5'端。-1652至-1420之间的DNA序列可使来自异源启动子的转录“沉默”。GAD65和GAD67启动子的序列一致性很少,这与它们转录调控的差异相一致。