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Cell type-specific gene expression in the neuroendocrine system. A neuroendocrine-specific regulatory element in the promoter of chromogranin A, a ubiquitous secretory granule core protein.

机译:神经内分泌系统中细胞类型特异性基因的表达。嗜铬粒蛋白A(一种普遍存在的分泌性颗粒核心蛋白)启动子中的神经内分泌特异性调节元件。

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摘要

The acidic secretory protein chromogranin A universally occurs in amine and peptide hormone and neurotransmitter storage granules throughout the neuroendocrine system. What factors govern the activity of the chromogranin A gene, to yield such a widespread yet neuroendocrine-selective pattern of expression? To address this question, we isolated the mouse chromogranin A gene promoter. The promoter conferred cell type-specific expression in several neuroendocrine cell types (adrenal medullary chromaffin cells, anterior pituitary corticotropes, and anterior pituitary somatolactotropes) but not in control (fibroblast or kidney) cells. In neuroendocrine cells, analysis of promoter deletions established both positive and negative transcriptional regulatory domains. A distal positive domain (-4.8/-2.2 kbp) was discovered, as well as negative (-258/-181 bp) and positive (-147/-61 bp) domains in the proximate promoter. The proximate promoter contained a minimal neuroendocrine-specific element between -77 and -61 bp. Sequence alignment of the mouse promoter with corresponding regions in rat and bovine clones indicated that the mouse sequence shares over 85% homology with rat and 52% with bovine promoters. DNaseI footprinting and electrophoretic gel mobility shift assays demonstrated the presence of nuclear factors in neuroendocrine cells that recognized the proximate promoter. We conclude that the chromogranin A promoter contains both positive and negative domains governing its cell type-specific pattern of transcription, and that a small proximate region of the promoter, containing novel as well as previously described elements, interacts specifically with neuroendocrine nuclear proteins, and is thereby sufficient to ensure widespread neuroendocrine expression of the gene.
机译:酸性分泌蛋白嗜铬粒蛋白A普遍存在于整个神经内分泌系统的胺和肽激素以及神经递质存储颗粒中。哪些因素控制嗜铬粒蛋白A基因的活性,以产生如此广泛而又神经内分泌的选择性表达模式?为了解决这个问题,我们分离了小鼠嗜铬粒蛋白A基因启动子。启动子在几种神经内分泌细胞类型(肾上腺髓质嗜铬细胞,垂体前叶皮质激素和垂体前体促乳腺激素)中赋予细胞类型特异性表达,但在对照(成纤维细胞或肾脏)细胞中却没有。在神经内分泌细胞中,对启动子缺失的分析建立了正和负转录调节域。发现了远端启动子中的远端正结构域(-4.8 / -2.2 bp),以及负(-258 / -181 bp)和正结构域(-147 / -61 bp)。最接近的启动子在-77和-61 bp之间包含最小的神经内分泌特异性元件。小鼠启动子与大鼠和牛克隆中相应区域的序列比对表明,小鼠序列与大鼠具有超过85%的同源性,与牛启动子具有52%的同源性。 DNaseI足迹法和电泳凝胶迁移率迁移分析法证明了神经内分泌细胞中识别邻近启动子的核因子的存在。我们得出的结论是,嗜铬粒蛋白A启动子包含控制其细胞类型特异性转录模式的正结构域和负结构域,并且该启动子的一小部分邻近区域(包含新的以及先前描述的元件)与神经内分泌核蛋白特异性相互作用,并且因此足以确保该基因广泛的神经内分泌表达。

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