Bloem L J, Chen Y, Liu J, Bye L S, Yu L
Department of Medical and Molecular Genetics, Indiana University School of Medicine, Indianapolis 46202.
Brain Res Mol Brain Res. 1993 Mar;17(3-4):194-200. doi: 10.1016/0169-328x(93)90002-7.
The serotonin 1c (5-HT1C) receptor is found in many brain regions, but is particularly enriched on the epithelial cells of the choroid plexus. A major challenge in neurobiology is to delineate the molecular processes that regulate the specific pattern of neuronal gene expression in the brain. As an initial step towards identifying cis-acting DNA sequences that control the expression of the 5-HT1C receptor, we have isolated the promoter sequence of its gene. Sequence analysis of a 1.8 kb fragment indicated that the 3' end of this fragment overlaps with the 5' untranslated region of the 5-HT1C receptor mRNA, and primer extension using mouse brain poly(A)+ RNA mapped the transcription initiation site within this fragment. There are a number of sequence elements upstream from the transcription initiation site that are homologous to regulatory elements found in other eucaryotic genes. To determine the promoter activity, a plasmid was constructed that contains this fragment as promoter region and the cDNA for the 5-HT1C receptor as the reporter. When injected into the nucleus of Xenopus oocytes, this construct resulted in functional expression of the reporter gene. Primer extension using the RNA extracted from the injected oocytes indicated a single transcription initiation site of the reporter mRNA. These results suggest that the 5-HT1C receptor was functionally expressed under the promoter activity of the 1.8 kb 5' sequence of its gene. This system will be useful for further analysis of the cis-acting elements in the promoter region of the 5-HT1C receptor gene and the trans-acting factors that regulate tissue-specific expression of the receptor.
5-羟色胺1c(5-HT1C)受体存在于许多脑区,但在脉络丛上皮细胞中尤其丰富。神经生物学中的一个主要挑战是描绘调节大脑中神经元基因表达特定模式的分子过程。作为鉴定控制5-HT1C受体表达的顺式作用DNA序列的第一步,我们分离了其基因的启动子序列。对一个1.8 kb片段的序列分析表明,该片段的3'端与5-HT1C受体mRNA的5'非翻译区重叠,并且使用小鼠脑多聚腺苷酸加尾RNA进行的引物延伸将转录起始位点定位在该片段内。转录起始位点上游有许多序列元件,它们与其他真核基因中发现的调控元件同源。为了确定启动子活性,构建了一个质粒,该质粒包含此片段作为启动子区域以及5-HT1C受体的cDNA作为报告基因。当注入非洲爪蟾卵母细胞核时,该构建体导致报告基因的功能性表达。使用从注入的卵母细胞中提取的RNA进行引物延伸表明报告基因mRNA有一个单一的转录起始位点。这些结果表明在其基因1.8 kb 5'序列的启动子活性下5-HT1C受体功能性表达。该系统将有助于进一步分析5-HT1C受体基因启动子区域中的顺式作用元件以及调节该受体组织特异性表达的反式作用因子。