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首页> 外文期刊>Molecular and Cellular Endocrinology >DNase I hypersensitivity analysis of non-pituitary human prolactin gene expression.
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DNase I hypersensitivity analysis of non-pituitary human prolactin gene expression.

机译:DNase I超敏性分析非垂体人类催乳素基因的表达。

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The expression of non-pituitary human PRL is initiated at a unique 5' untranslated exon located approximately 5.7 kb upstream of the pituitary-specific transcriptional start site. Unlike pituitary PRL expression, transcriptional regulation from the upstream promoter does not rely on the POU-homeodomain protein Pit-1. We have used DNase I mapping of chromatin from PRL-producing and non-producing human lymphoblastoid cell lines to identify hypersensitive sites unique to the PRL expressing phenotype. Analysis of 22 kb of 5' flanking DNA revealed DNase I hypersensitive sites in intron A-1 separating the pituitary from non-pituitary specific transcription start site which were only detected in the PRL-producing cell line. Transient transfection showed strong transcriptional activity directed by this region only in the antisense orientation and in a non cell-type specific manner. Transfection experiments with deletion mutants of 5259 bp of the non-pituitary PRL promoter region also revealed promoter activity not restricted to the PRL expressing phenotype. These data suggest that non-pituitary PRL gene expression may be regulated by elements located in intron A-1 and that recapitulation of cell-specific expression requires a unique cellular context and chromatin assembly.
机译:非垂体人类PRL的表达始于位于垂体特异性转录起始位点上游约5.7 kb的独特5'非翻译外显子。与垂体PRL表达不同,上游启动子的转录调控不依赖于POU-同源结构域蛋白Pit-1。我们已经使用DNase I映射来自PRL生产和非生产人淋巴母细胞细胞系的染色质,以识别PRL表达表型独特的超敏位点。对22 kb 5'侧翼DNA的分析显示,内含子A-1中的DNase I超敏位点将垂体和非垂体特异性转录起始位点分开,仅在产生PRL的细胞系中检测到。瞬时转染仅在反义方向上以非细胞类型特异性方式显示了由该区域定向的强转录活性。用非垂体PRL启动子区域的5259bp的缺失突变体进行的转染实验还显示了启动子活性不限于表达PRL的表型。这些数据表明非垂体PRL基因表达可能受到位于A-1内含子中的元件的调节,而细胞特异性表达的概括需要独特的细胞背景和染色质组装。

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