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瞬时和稳定导入的CCAAT/增强子结合蛋白基因在培养细胞中持续表达。

Transiently and stably introduced CCAAT/enhancer-binding-protein genes are constitutively expressed in cultured cells.

作者信息

Xanthopoulos K G, Cannon P D, Robinson G S, Mirkovitch J, Darnell J E

机构信息

Karolinska Institute, Center for Biotechnology, Novum, Sweden.

出版信息

Eur J Biochem. 1992 Sep 1;208(2):501-9. doi: 10.1111/j.1432-1033.1992.tb17214.x.

Abstract

CCAAT/enhancer-binding protein (C/EBP) is expressed in certain cell types including hepatocytes and adipocytes. In order to understand the mechanisms that control the expression of the mouse C/EBP gene in the liver as well as in adipocytes, we have studied both the endogenous gene and transfected C/EBP gene constructs. The initiation site of transcription was identified and a strong liver-specific DNase-I hypersensitive site located at -3 kb, which does not appear to contribute functionally to the regulation of the gene in a variety of either transiently or stably transfected cells with constructs which include sequences up to 6-kb upstream of the transcription start. C/EBP gene expression during the transition from preadipocytes to adipocytes was shown to be controlled at the level of transcription. However, adipocytes stably transfected with constructs that include -3.3 kb upstream of the C/EBP gene do not express the reporter genes in a differentiation-specific manner. We detected several DNA-binding proteins that interact with the upstream sites of the C/EBP gene. Those include two labile and two heat-stable site-specific DNA-binding proteins that are present in nuclear extracts from several tissues and cultured cell lines.

摘要

CCAAT/增强子结合蛋白(C/EBP)在包括肝细胞和脂肪细胞在内的某些细胞类型中表达。为了了解控制小鼠C/EBP基因在肝脏以及脂肪细胞中表达的机制,我们研究了内源性基因和转染的C/EBP基因构建体。确定了转录起始位点,并发现一个位于-3 kb处的强肝脏特异性DNase-I超敏位点,在用包含转录起始上游达6 kb序列的构建体进行瞬时或稳定转染的多种细胞中,该位点在功能上似乎对基因调控没有贡献。从前脂肪细胞向脂肪细胞转变过程中的C/EBP基因表达显示在转录水平受到调控。然而,用包含C/EBP基因上游-3.3 kb的构建体稳定转染的脂肪细胞,不会以分化特异性方式表达报告基因。我们检测到几种与C/EBP基因上游位点相互作用的DNA结合蛋白。其中包括两种不稳定和两种热稳定的位点特异性DNA结合蛋白,它们存在于几种组织和培养细胞系的核提取物中。

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