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本文引用的文献

1
The adeno-associated virus Rep78 major regulatory protein binds the cellular TATA-binding protein in vitro and in vivo.腺相关病毒Rep78主要调节蛋白在体外和体内均能与细胞TATA结合蛋白结合。
Virology. 1998 May 25;245(1):120-7. doi: 10.1006/viro.1998.9144.
2
Contributions of the TATA box sequence to rate-limiting steps in transcription initiation by RNA polymerase II.TATA盒序列对RNA聚合酶II转录起始限速步骤的贡献。
J Mol Biol. 1998 Apr 17;277(5):1015-31. doi: 10.1006/jmbi.1998.1651.
3
Overexpression of C/EBPbeta represses human papillomavirus type 18 upstream regulatory region activity in HeLa cells by interfering with the binding of TATA-binding protein.C/EBPβ的过表达通过干扰TATA结合蛋白的结合来抑制人乳头瘤病毒18型在HeLa细胞中的上游调控区活性。
J Virol. 1998 Mar;72(3):2113-24. doi: 10.1128/JVI.72.3.2113-2124.1998.
4
Adeno-associated virus Rep78 inhibits oncogenic transformation of primary human keratinocytes by a human papillomavirus type 16-ras chimeric.腺相关病毒Rep78抑制人乳头瘤病毒16型- ras嵌合体对原代人角质形成细胞的致癌转化作用。
Gynecol Oncol. 1997 Sep;66(3):487-94. doi: 10.1006/gyno.1997.4789.
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Mutational analysis of the adeno-associated virus type 2 Rep68 protein helicase motifs.2型腺相关病毒Rep68蛋白解旋酶基序的突变分析
J Virol. 1997 Sep;71(9):6996-7004. doi: 10.1128/JVI.71.9.6996-7004.1997.
6
The adeno-associated virus type 2 p40 promoter requires a proximal Sp1 interaction and a p19 CArG-like element to facilitate Rep transactivation.2型腺相关病毒p40启动子需要近端Sp1相互作用和一个p19 CArG样元件来促进Rep反式激活。
J Virol. 1997 Jun;71(6):4300-9. doi: 10.1128/JVI.71.6.4300-4309.1997.
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Mutational analysis of the adeno-associated virus Rep68 protein: identification of critical residues necessary for site-specific endonuclease activity.腺相关病毒Rep68蛋白的突变分析:位点特异性内切核酸酶活性所需关键残基的鉴定。
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8
The adeno-associated virus Rep78 major regulatory/transformation suppressor protein binds cellular Sp1 in vitro and evidence of a biological effect.腺相关病毒Rep78主要调节/转化抑制蛋白在体外与细胞Sp1结合及生物学效应的证据。
Cancer Res. 1996 Nov 15;56(22):5299-304.
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Papillomavirus infections--a major cause of human cancers.乳头瘤病毒感染——人类癌症的主要成因。
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10
High Sp1/Sp3 ratios in epithelial cells during epithelial differentiation and cellular transformation correlate with the activation of the HPV-16 promoter.在上皮分化和细胞转化过程中,上皮细胞中高Sp1/Sp3比率与HPV-16启动子的激活相关。
Virology. 1996 Oct 1;224(1):281-91. doi: 10.1006/viro.1996.0530.

腺相关病毒主要Rep78蛋白破坏TATA结合蛋白与人乳头瘤病毒16型p97启动子的结合。

Adeno-associated virus major Rep78 protein disrupts binding of TATA-binding protein to the p97 promoter of human papillomavirus type 16.

作者信息

Su P F, Chiang S Y, Wu C W, Wu F Y

机构信息

Division of Cancer Research, Institute of Biomedical Sciences, Academia Sinica, Taiwan, Republic of China.

出版信息

J Virol. 2000 Mar;74(5):2459-65. doi: 10.1128/jvi.74.5.2459-2465.2000.

DOI:10.1128/jvi.74.5.2459-2465.2000
PMID:10666281
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC111732/
Abstract

Adeno-associated virus type 2 (AAV) is known to inhibit the promoter activities of several oncogenes and viral genes, including the human papillomavirus type 16 (HPV-16) E6 and E7 transforming genes. However, the target elements of AAV on the long control region (LCR) upstream of E6 and E7 oncogenes are elusive. A chloramphenicol acetyltransferase assay was performed to study the effect of AAV on the transcription activity of the HPV-16 LCR in SiHa (HPV-positive) and C-33A (HPV-negative) cells. The results reveal that (i) AAV inhibited HPV-16 LCR activity in a dose-dependent manner, (ii) AAV-mediated inhibition did not require the HPV gene products, and (iii) the AAV replication gene product Rep78 was involved in the inhibition. Deletion mutation analyses of the HPV-16 LCR showed that regulatory elements outside the core promoter region of the LCR may not be direct targets of AAV-mediated inhibition. Further study with the electrophoretic mobility shift assay demonstrated that Rep78 interfered with the binding of TATA-binding protein (TBP) to the TATA box of the p97 core promoter more significantly than it disrupted the preformed TBP-TATA complex. These data thus suggest that Rep78 may inhibit transcription initiation of the HPV-16 LCR by disrupting the interaction between TBP and the TATA box of the p97 core promoter.

摘要

已知2型腺相关病毒(AAV)可抑制多种癌基因和病毒基因的启动子活性,包括人乳头瘤病毒16型(HPV - 16)的E6和E7转化基因。然而,AAV在E6和E7癌基因上游的长控制区(LCR)上的靶元件尚不清楚。进行了氯霉素乙酰转移酶试验,以研究AAV对SiHa(HPV阳性)和C - 33A(HPV阴性)细胞中HPV - 16 LCR转录活性的影响。结果显示:(i)AAV以剂量依赖性方式抑制HPV - 16 LCR活性;(ii)AAV介导的抑制作用不需要HPV基因产物;(iii)AAV复制基因产物Rep78参与了这种抑制作用。对HPV - 16 LCR的缺失突变分析表明,LCR核心启动子区域以外的调控元件可能不是AAV介导抑制作用的直接靶点。进一步通过电泳迁移率变动分析研究表明,Rep78对TATA结合蛋白(TBP)与p97核心启动子的TATA盒结合的干扰,比其对预先形成的TBP - TATA复合物的破坏更为显著。因此,这些数据表明Rep78可能通过破坏TBP与p97核心启动子的TATA盒之间的相互作用来抑制HPV - 16 LCR的转录起始。