Suppr超能文献

人纤维蛋白原α链基因5′侧翼区的特性分析

Characterization of the 5'-flanking region of the gene for the alpha chain of human fibrinogen.

作者信息

Hu C H, Harris J E, Davie E W, Chung D W

机构信息

Department of Biochemistry, University of Washington, Seattle 98195-7350, USA.

出版信息

J Biol Chem. 1995 Nov 24;270(47):28342-9. doi: 10.1074/jbc.270.47.28342.

Abstract

The 5'-flanking region of the gene coding for the alpha chain of human fibrinogen was isolated, sequenced, and characterized. The principal site of transcription initiation was determined by primer extension analysis and the RNase protection assay and shown to be at an adenine residue located 55 nucleotides upstream from the initiator methionine codon, or 13,399 nucleotides down-stream from the polyadenylation site of the gene coding for the gamma chain. Transient expression of constructs containing sequentially deleted 5'-flanking sequences of the alpha chain gene fused to the chloramphenicol acetyltransferase reporter gene showed that the promoter was liver-specific and inducible by interleukin 6 (IL-6). The shortest DNA fragment with significant promoter activity and full response to IL-6 stimulation encompassed the region from -217 to +1 base pairs (bp). Although six potential IL-6 responsive sequences homologous to the type II IL-6 responsive element were present, a single sequence of CTGGGA localized from -122 to -127 bp was shown to be a functional element in IL-6 induction. A hepatocyte nuclear factor 1 (HNF-1) binding site, present from -47 to -59 bp, in combination with other upstream elements, was essential for liver-specific expression of the gene. A functional CCAAT/enhancer binding protein site (C/EBP, -134 to -142 bp) was also identified within 217 bp from the transcription initiation site. An additional positive element (-1393 to -1133 bp) and a negative element (-1133 to -749 bp) were also found in the upstream region of the alpha-fibrinogen gene.

摘要

分离、测序并鉴定了人纤维蛋白原α链编码基因的5'-侧翼区域。通过引物延伸分析和核糖核酸酶保护试验确定了转录起始的主要位点,结果表明该位点位于起始甲硫氨酸密码子上游55个核苷酸处的腺嘌呤残基,即编码γ链的基因聚腺苷酸化位点下游13399个核苷酸处。将含有α链基因5'-侧翼序列依次缺失片段与氯霉素乙酰转移酶报告基因融合构建体进行瞬时表达,结果显示该启动子具有肝脏特异性,且可被白细胞介素6(IL-6)诱导。具有显著启动子活性并对IL-6刺激有完全反应的最短DNA片段包含从-217到+1碱基对(bp)的区域。尽管存在六个与II型IL-6反应元件同源的潜在IL-6反应序列,但位于-122至-127 bp的单个CTGGGA序列被证明是IL-6诱导中的功能元件。位于-47至-59 bp的肝细胞核因子1(HNF-1)结合位点与其他上游元件结合时,对该基因的肝脏特异性表达至关重要。在转录起始位点217 bp范围内还鉴定出一个功能性CCAAT/增强子结合蛋白位点(C/EBP,-134至-142 bp)。在α-纤维蛋白原基因的上游区域还发现了一个额外的正调控元件(-1393至-1133 bp)和一个负调控元件(-1133至-749 bp)。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验