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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.

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。

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