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本文引用的文献

1
Characterization of the mouse gene that encodes the delta/YY1/NF-E1/UCRBP transcription factor.编码δ/YY1/NF-E1/UCRBP转录因子的小鼠基因的特性分析。
Proc Natl Acad Sci U S A. 1993 Jun 15;90(12):5559-63. doi: 10.1073/pnas.90.12.5559.
2
Protein-DNA interactions in the epsilon-globin gene silencer.ε-珠蛋白基因沉默子中的蛋白质-DNA相互作用
J Biol Chem. 1993 Feb 15;268(5):3430-7.
3
Different regulatory sequences control creatine kinase-M gene expression in directly injected skeletal and cardiac muscle.不同的调控序列控制直接注射的骨骼肌和心肌中肌酸激酶-M基因的表达。
Mol Cell Biol. 1993 Feb;13(2):1264-72. doi: 10.1128/mcb.13.2.1264-1272.1993.
4
The intracisternal A-particle upstream element interacts with transcription factor YY1 to activate transcription: pleiotropic effects of YY1 on distinct DNA promoter elements.脑池内A颗粒上游元件与转录因子YY1相互作用以激活转录:YY1对不同DNA启动子元件的多效性作用。
Mol Cell Biol. 1993 Nov;13(11):6621-8. doi: 10.1128/mcb.13.11.6621-6628.1993.
5
Cross-coupling of the NF-kappa B p65 and Fos/Jun transcription factors produces potentiated biological function.核因子-κB p65与Fos/Jun转录因子的交叉偶联产生增强的生物学功能。
EMBO J. 1993 Oct;12(10):3879-91. doi: 10.1002/j.1460-2075.1993.tb06066.x.
6
Interactions of human papillomavirus transforming proteins with the products of tumor suppressor genes.人乳头瘤病毒转化蛋白与肿瘤抑制基因产物的相互作用。
FASEB J. 1993 Jul;7(10):872-9. doi: 10.1096/fasebj.7.10.8393818.
7
Identification of a transcriptional initiator element in the cytochrome c oxidase subunit Vb promoter which binds to transcription factors NF-E1 (YY-1, delta) and Sp1.细胞色素c氧化酶亚基Vb启动子中转录起始元件的鉴定,该元件可与转录因子NF-E1(YY-1,δ)和Sp1结合。
J Biol Chem. 1993 Feb 25;268(6):4188-96.
8
Nuclear protein-binding sites in a transcriptional control region of the rabbit alpha-globin gene.兔α-珠蛋白基因转录控制区中的核蛋白结合位点。
Mol Cell Biol. 1993 Sep;13(9):5439-49. doi: 10.1128/mcb.13.9.5439-5449.1993.
9
Evidence for physical interaction between the zinc-finger transcription factors YY1 and Sp1.锌指转录因子YY1和Sp1之间存在物理相互作用的证据。
Proc Natl Acad Sci U S A. 1993 Jul 1;90(13):6145-9. doi: 10.1073/pnas.90.13.6145.
10
Phylogenetic footprinting reveals unexpected complexity in trans factor binding upstream from the epsilon-globin gene.系统发育足迹分析揭示了ε-珠蛋白基因上游反式作用因子结合中意想不到的复杂性。
Proc Natl Acad Sci U S A. 1993 Jul 1;90(13):6018-22. doi: 10.1073/pnas.90.13.6018.

一个转换区域决定了YY1对人乳头瘤病毒18型启动子活性的细胞类型特异性正向或负向作用。

A switch region determines the cell type-specific positive or negative action of YY1 on the activity of the human papillomavirus type 18 promoter.

作者信息

Bauknecht T, Jundt F, Herr I, Oehler T, Delius H, Shi Y, Angel P, Zur Hausen H

机构信息

Forschungsschwerpunkt Angewandte Tumorvirologie, Deutsches Krebsforschungszentrum Heidelberg, Germany.

出版信息

J Virol. 1995 Jan;69(1):1-12. doi: 10.1128/JVI.69.1.1-12.1995.

DOI:10.1128/JVI.69.1.1-12.1995
PMID:7983700
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC188542/
Abstract

YY1 is a zinc finger transcription factor which acts as either a repressor or an activator dependent on the promoter context. YY1 is a potent activator of the genuine human papillomavirus type 18 (HPV-18) upstream regulatory region (URR) in HeLa cells, which are known for high-level expression of the HPV-18 early genes. The activating activity of YY1 is dependent on the presence of a newly identified switch region located upstream of the YY1 binding site. Deletion of this region causes YY1 to act as a repressor of HPV-18 promoter activity. In vivo footprinting of the HPV-18 URR and an in vitro electrophoretic mobility shift assay identified proteins binding to the switch region. Site-directed mutagenesis of the switch region and YY1 binding sites suggests that these two regions work in concert to yield high-level HPV-18 URR activity in HeLa cells but not in HepG2 cells, where HPV-18 is almost inactive. These data identified a novel mode of cell type-specific regulation of HPV-18 promoter activity by positive or negative action of YY1, determined by the switch region binding factor(s).

摘要

YY1是一种锌指转录因子,根据启动子环境,它既可以作为阻遏物,也可以作为激活物。YY1是HeLa细胞中真正的人乳头瘤病毒18型(HPV - 18)上游调控区(URR)的有效激活物,HeLa细胞以HPV - 18早期基因的高水平表达而闻名。YY1的激活活性取决于位于YY1结合位点上游的一个新发现的开关区域的存在。删除该区域会导致YY1作为HPV - 18启动子活性的阻遏物。对HPV - 18 URR进行体内足迹分析和体外电泳迁移率变动分析,鉴定出与开关区域结合的蛋白质。对开关区域和YY1结合位点进行定点诱变表明,这两个区域协同作用,在HeLa细胞中产生高水平的HPV - 18 URR活性,但在HPV - 18几乎无活性的HepG2细胞中则不然。这些数据确定了一种由YY1通过开关区域结合因子的正向或负向作用对HPV - 18启动子活性进行细胞类型特异性调控的新模式。