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首页> 外文期刊>Archives of Biochemistry and Biophysics >Molecular cloning of the cDNA and the promoter of the hamster uteroglobin Clara cell 10-kDa gene (ug/cc10): Tissue-specific and hormonal regulation
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Molecular cloning of the cDNA and the promoter of the hamster uteroglobin Clara cell 10-kDa gene (ug/cc10): Tissue-specific and hormonal regulation

机译:cDNA分子克隆和仓鼠子宫珠状克拉拉细胞10-kDa基因(ug / cc10)的启动子:组织特异性和激素调节

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摘要

Using the polymerase chain reaction on first-strand cDNAs from lung as well as on genomic DNA, we have cloned and sequenced both the cDNA and 1.5 kb of the promoter of the gene coding for hamster-uteroglobin/Clara cell 10-kDa protein (UG/CC10), a secretory protein mainly synthesized in the pulmonary Clara cells. The amino acid sequence deduced from the cDNA indicated a preprotein of 96 residues, 19 of which corresponded to the signal peptide. The promoter region contained transcriptional regulatory elements conserved between species. Northern blot and SP resistance assays detected high expression of ug/cc10 in lung but not st all in other tissues. Expression in lung was positively controlled by glucocorticoids and was also subjected tee a biphasic developmental regulation after birth. in agreement with the tissue-specific expression observed in vivo, the hamster promoter preferentially directed the expression of a reporter gene in cells derived from Clara cells. The results indicated that the tissue-specific expression and the regulation of ug/cc10 varied considerably between species but all of them had a high expression in lung. (C) 1998 Academic Press. [References: 58]
机译:使用聚合酶链反应对肺部第一链cDNA和基因组DNA进行克隆和测序,我们对仓鼠-子宫珠蛋白/克拉拉细胞10-kDa蛋白(UG / CC10),一种分泌蛋白,主要在肺克拉拉细胞中合成。从cDNA推导的氨基酸序列表明有96个残基的前蛋白,其中19个对应于信号肽。启动子区域包含物种之间保守的转录调控元件。 Northern印迹和SP抗性测定法检测到肺中ug / cc10的高表达,但在其他组织中并非全部。肺中的表达受到糖皮质激素的正向控制,并且在出生后也经历了双相发育调节。与体内观察到的组织特异性表达一致,仓鼠启动子优先指导报道基因在源自Clara细胞的细胞中表达。结果表明,物种之间的组织特异性表达和ug / cc10的调控差异很大,但它们在肺中均高表达。 (C)1998年学术出版社。 [参考:58]

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