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The lung enriched transcription factor TTF-1 and the ubiquitously expressed proteins Sp1 and Sp3 interact with elements located in the minimal promoter of the rat Clara cell secretory protein gene

机译:富含肺的转录因子TTF-1和普遍表达的蛋白Sp1和Sp3与位于大鼠Clara细胞分泌蛋白基因最小启动子中的元件相互作用

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pThe mechanisms that direct expression of the Clara cell secretory protein (CCSP) gene to the bronchiolar epithelial cells of the lung remain to be elucidated. Previous studies have identified a number of proteins which bind to a functionally important region (Region 1) located -132 to -76 bp from the transcription start site in the rat CCSP gene. Subsequently we have shown that while Region 1 is an important positive regulator of CCSP gene expression, sequences 3′ of this region (-75 to +38) are sufficient to confer tissue-specific expression of a reporter gene. In the present study we have used transient transfections with a deletion series of CCSP–CAT reporter plasmids (where CAT is chloramphenicol acetyltransferase) and gel mobility shift assays with a series of overlapping oligonucleotides covering the whole minimal promoter region to study protein–DNA interactions within this region. These studies have identified a conserved functional binding site for the lung and thyroid enriched homeodomain transcription factor TTF-1, located between positions -51 and -42 from the transcription start site. CCSP–CAT chimaeric reporters containing this region are specifically activated by TTF-1 in co-transfection assays, and nuclear extracts from cells which express TTF-1 bind to this region, as does iin vitro/i translated rat TTF-1. Three additional conserved regions were identified, and in further gel mobility shift studies with an oligonucleotide spanning the conserved region immediately 5′ to the TTF-1 site we identified a binding site for the ubiquitously expressed zinc-finger-containing proteins Sp1 and Sp3. These studies suggest that cell-type-restricted and ubiquitous nuclear proteins may play a combined role in the regulation of the CCSP gene within the bronchiolar epithelium by interacting with the minimal promoter region./p
机译:>将克拉拉细胞分泌蛋白(CCSP)基因表达导向肺的细支气管上皮细胞的机制仍有待阐明。先前的研究已经鉴定出许多蛋白质,它们与大鼠CCSP基因转录起始位点-132至-76 bp的功能重要区域(区域1)结合。随后我们发现,虽然区域1是CCSP基因表达的重要正调控因子,但该区域的3'序列(-75至+38)足以赋予报告基因组织特异性表达。在本研究中,我们使用了一系列缺失的CCSP–CAT报告基因质粒(其中CAT是氯霉素乙酰转移酶)进行瞬时转染,并使用了一系列覆盖整个最小启动子区域的重叠寡核苷酸进行凝胶迁移率迁移分析,以研究其中的蛋白质–DNA相互作用。这个地区。这些研究已经确定了富含肺和甲状腺的同源结构域转录因子TTF-1的保守功能结合位点,位于转录起始位点的-51和-42之间。在共转染实验中,含有TSF-1的CCSP-CAT嵌合报告基因被TTF-1特异性激活,表达TTF-1的细胞的核提取物与该区域结合,体外翻译的大鼠TTF也是如此。 -1。确定了三个额外的保守区域,在进一步的凝胶迁移率迁移研究中,使用一个寡核苷酸跨越一个保守区域,紧接TTF-1位点5',我们确定了一个普遍表达的含锌指蛋白Sp1和Sp3的结合位点。这些研究表明,受细胞类型限制和普遍存在的核蛋白可能通过与最小启动子区域相互作用而在支气管上皮内CCSP基因的调节中共同发挥作用。

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