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p53-Dependent and -independent transactivation by the E6 protein of human papillomavirus type 16.

作者信息

Akutsu N, Shirasawa H, Asano T, Isono K, Simizu B

机构信息

Department of Microbiology, School of Medicine, Chiba University, Japan.

出版信息

J Gen Virol. 1996 Mar;77 ( Pt 3):459-63. doi: 10.1099/0022-1317-77-3-459.

DOI:10.1099/0022-1317-77-3-459
PMID:8601782
Abstract

The mechanism by which the E6 protein of human papillomavirus type 16 (HPV-16) transactivates heterologous virus promoters has not been established. In this study, the involvement of p53-mediated transcriptional repression in transactivation by the HPV-16 E6 protein was examined using several virus promoters. HPV-16 E6 transactivated the TATA box-containing simian virus 40 early promoter and the Rous sarcoma virus long terminal repeat in p53-containing cells but not in p53-deficient cells. In contrast, the adenovirus E2 promoter was transactivated both in p53-containing and p53-deficient cells. These results indicate that the transactivation activity of the HPV-16 E6 protein is mediated by p53-dependent and promoter-specific p53-independent pathways.

摘要

相似文献

1
p53-Dependent and -independent transactivation by the E6 protein of human papillomavirus type 16.
J Gen Virol. 1996 Mar;77 ( Pt 3):459-63. doi: 10.1099/0022-1317-77-3-459.
2
The domain of p53 required for binding HPV 16 E6 is separable from the degradation domain.与HPV 16 E6结合所需的p53结构域与降解结构域是可分离的。
Oncogene. 1995 Feb 2;10(3):457-65.
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The E6 protein of human papillomavirus type 16 functions as a transcriptional repressor in a mechanism independent of the tumor suppressor protein, p53.
Virology. 1994 Dec;205(2):583-5. doi: 10.1006/viro.1994.1684.
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Human papillomavirus E6 proteins bind p53 in vivo and abrogate p53-mediated repression of transcription.人乳头瘤病毒E6蛋白在体内与p53结合,并消除p53介导的转录抑制作用。
EMBO J. 1992 Aug;11(8):3045-52. doi: 10.1002/j.1460-2075.1992.tb05375.x.
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Telomerase activation by the E6 gene product of human papillomavirus type 16.人乳头瘤病毒16型E6基因产物对端粒酶的激活作用。
Nature. 1996 Mar 7;380(6569):79-82. doi: 10.1038/380079a0.
6
Dispensability of p53 degradation for tumorigenicity and decreased serum requirement of human papillomavirus type 16 E6.
Mol Carcinog. 1998 Mar;21(3):215-22.
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The E8 repression domain can replace the E2 transactivation domain for growth inhibition of HeLa cells by papillomavirus E2 proteins.E8 抑制结构域可替代 E2 反式激活结构域,用于乳头瘤病毒 E2 蛋白对 HeLa 细胞的生长抑制。
Int J Cancer. 2007 Nov 15;121(10):2284-92. doi: 10.1002/ijc.22907.
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Transcriptional activation of several heterologous promoters by the E6 protein of human papillomavirus type 16.人乳头瘤病毒16型E6蛋白对几种异源启动子的转录激活作用。
J Virol. 1992 Jan;66(1):325-33. doi: 10.1128/JVI.66.1.325-333.1992.
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The human papillomavirus type 16 E6 oncoprotein can down-regulate p53 activity by targeting the transcriptional coactivator CBP/p300.人乳头瘤病毒16型E6癌蛋白可通过靶向转录共激活因子CBP/p300来下调p53活性。
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Cellular steady-state levels of "high risk" but not "low risk" human papillomavirus (HPV) E6 proteins are increased by inhibition of proteasome-dependent degradation independent of their p53- and E6AP-binding capabilities.通过抑制蛋白酶体依赖性降解,“高危”而非“低危”人乳头瘤病毒(HPV)E6蛋白的细胞稳态水平会升高,且这一过程与其p53和E6相关蛋白(E6AP)结合能力无关。
Virology. 2002 Jul 20;299(1):72-87. doi: 10.1006/viro.2002.1502.

引用本文的文献

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Human papillomavirus 18 E6 inhibits phosphorylation of p53 expressed in HeLa cells.人乳头瘤病毒 18 E6 抑制 HeLa 细胞中表达的 p53 的磷酸化。
Cell Biosci. 2012 Jan 13;2:2. doi: 10.1186/2045-3701-2-2.
2
Human papillomavirus type 16 E6 protein transcriptionally modulates fibronectin gene expression by induction of protein complexes binding to the cyclic AMP response element.人乳头瘤病毒16型E6蛋白通过诱导与环磷酸腺苷反应元件结合的蛋白复合物,对纤连蛋白基因表达进行转录调控。
J Virol. 1997 Jun;71(6):4310-8. doi: 10.1128/JVI.71.6.4310-4318.1997.