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Analysis of trans activation by human papillomavirus type 16 E7 and adenovirus 12S E1A suggests a common mechanism.

作者信息

Phelps W C, Bagchi S, Barnes J A, Raychaudhuri P, Kraus V, Münger K, Howley P M, Nevins J R

机构信息

Division of Virology, Burroughs Wellcome Co., Research Triangle Park, North Carolina 27709.

出版信息

J Virol. 1991 Dec;65(12):6922-30. doi: 10.1128/JVI.65.12.6922-6930.1991.

DOI:10.1128/JVI.65.12.6922-6930.1991
PMID:1834862
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC250797/
Abstract

The human papillomavirus E7 gene product is an oncoprotein with properties similar to those of the adenovirus E1A proteins. The human papillomavirus E7 proteins possess substantial amino acid sequence similarity to portions of conserved regions 1 and 2 of E1A, and the human papillomavirus type 16 E7 protein trans-activates the adenovirus E2 early promoter. Analysis of point mutations in the E2 promoter indicated that the E2F recognition sites were critical to E7 stimulation. In contrast to the activation of the E2 promoter, E7 could not trans-activate various other E1A-inducible promoters. Although the promoter specificity for E7 differs from that of 13S E1A trans activation, it is very similar to activation by the E1A 12S product. Moreover, analysis of the E7 protein has suggested that amino acid sequences critical for trans activation include those shared with E1A within conserved region 2. Biochemical studies demonstrate that the E7 protein, like the 12S E1A product, can alter the interaction of cellular factors with the E2F transcription factor. We therefore conclude that E7 trans activation is functionally related to that mediated by the 12S E1A product.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/25fb/250797/ffe78ff9bfdf/jvirol00055-0563-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/25fb/250797/949da0ed6a9f/jvirol00055-0562-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/25fb/250797/ffe78ff9bfdf/jvirol00055-0563-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/25fb/250797/949da0ed6a9f/jvirol00055-0562-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/25fb/250797/ffe78ff9bfdf/jvirol00055-0563-a.jpg

相似文献

1
Analysis of trans activation by human papillomavirus type 16 E7 and adenovirus 12S E1A suggests a common mechanism.
J Virol. 1991 Dec;65(12):6922-30. doi: 10.1128/JVI.65.12.6922-6930.1991.
2
Chemical synthesis of human papillomavirus type 16 E7 oncoprotein: autonomous protein domains for induction of cellular DNA synthesis and for trans activation.人乳头瘤病毒16型E7癌蛋白的化学合成:诱导细胞DNA合成及反式激活的自主蛋白结构域
J Virol. 1990 Dec;64(12):6121-9. doi: 10.1128/JVI.64.12.6121-6129.1990.
3
Adenovirus E1A, simian virus 40 tumor antigen, and human papillomavirus E7 protein share the capacity to disrupt the interaction between transcription factor E2F and the retinoblastoma gene product.腺病毒E1A、猿猴病毒40肿瘤抗原和人乳头瘤病毒E7蛋白都具有破坏转录因子E2F与视网膜母细胞瘤基因产物之间相互作用的能力。
Proc Natl Acad Sci U S A. 1992 May 15;89(10):4549-53. doi: 10.1073/pnas.89.10.4549.
4
The human papillomavirus type 16 E7 protein complements adenovirus type 5 E1A amino-terminus-dependent transactivation of adenovirus type 5 early genes and increases ATF and Oct-1 DNA binding activity.人乳头瘤病毒16型E7蛋白可补充5型腺病毒E1A氨基末端依赖性的5型腺病毒早期基因反式激活作用,并增加ATF和Oct-1的DNA结合活性。
J Virol. 1996 Jan;70(1):332-40. doi: 10.1128/JVI.70.1.332-340.1996.
5
E1A 12S and 13S of the transformation-defective adenovirus type 12 strain CS-1 inactivate proteins of the RB family, permitting transactivation of the E2F-dependent promoter.转化缺陷型腺病毒12型毒株CS-1的E1A 12S和13S可使RB家族蛋白失活,从而实现E2F依赖性启动子的反式激活。
J Virol. 1997 Dec;71(12):9538-48. doi: 10.1128/JVI.71.12.9538-9548.1997.
6
The human papillomavirus type 16 E7 gene encodes transactivation and transformation functions similar to those of adenovirus E1A.人乳头瘤病毒16型E7基因编码的反式激活和转化功能与腺病毒E1A相似。
Cell. 1988 May 20;53(4):539-47. doi: 10.1016/0092-8674(88)90570-3.
7
Role of E2F transcription factor in E1A-mediated trans activation of cellular genes.E2F转录因子在E1A介导的细胞基因反式激活中的作用。
J Virol. 1991 Jul;65(7):3547-52. doi: 10.1128/JVI.65.7.3547-3552.1991.
8
Functional analysis of human papillomavirus type 16 E7 by complementation with adenovirus E1A mutants.
J Gen Virol. 1992 Aug;73 ( Pt 8):2135-9. doi: 10.1099/0022-1317-73-8-2135.
9
Structure-function analysis of the human papillomavirus type 16 E7 oncoprotein.人乳头瘤病毒16型E7癌蛋白的结构-功能分析
J Virol. 1992 Apr;66(4):2418-27. doi: 10.1128/JVI.66.4.2418-2427.1992.
10
Trans-activation of the adenovirus E2 promoter by human papillomavirus type 16 E7 is mediated by retinoblastoma-dependent and -independent pathways.人乳头瘤病毒16型E7对腺病毒E2启动子的反式激活由视网膜母细胞瘤依赖和非依赖途径介导。
J Gen Virol. 1993 Nov;74 ( Pt 11):2479-86. doi: 10.1099/0022-1317-74-11-2479.

引用本文的文献

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2
Angelman syndrome-associated point mutations in the Zn-binding N-terminal (AZUL) domain of UBE3A ubiquitin ligase inhibit binding to the proteasome.UBE3A 泛素连接酶 Zn 结合 N 端(AZUL)结构域中的 Angelman 综合征相关点突变抑制与蛋白酶体的结合。
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本文引用的文献

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Expression of early adenovirus genes requires a viral encoded acidic polypeptide.早期腺病毒基因的表达需要一种病毒编码的酸性多肽。
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Dissection of overlapping functions within the adenovirus type 5 E1A gene.5型腺病毒E1A基因重叠功能剖析
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The E7 proteins of low- and high-risk human papillomaviruses share the ability to target the pRB family member p130 for degradation.低风险和高风险人乳头瘤病毒的E7蛋白都具有将视网膜母细胞瘤家族成员p130作为降解靶点的能力。
Proc Natl Acad Sci U S A. 2006 Jan 10;103(2):437-42. doi: 10.1073/pnas.0510012103. Epub 2005 Dec 28.
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Interactions with pocket proteins contribute to the role of human papillomavirus type 16 E7 in the papillomavirus life cycle.与口袋蛋白的相互作用有助于人乳头瘤病毒16型E7蛋白在乳头瘤病毒生命周期中的作用。
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Proc Natl Acad Sci U S A. 1984 Jul;81(14):4381-5. doi: 10.1073/pnas.81.14.4381.
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Adenovirus 5 E2 transcription unit: an E1A-inducible promoter with an essential element that functions independently of position or orientation.腺病毒5型E2转录单元:一个E1A诱导型启动子,带有一个独立于位置或方向发挥作用的必需元件。
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Adenovirus 5 early region 1A host range mutants hr3, hr4, and hr5 contain point mutations which generate single amino acid substitutions.腺病毒5型早期区域1A宿主范围突变体hr3、hr4和hr5含有产生单个氨基酸取代的点突变。
J Virol. 1985 Oct;56(1):66-74. doi: 10.1128/JVI.56.1.66-74.1985.
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Proc Natl Acad Sci U S A. 1985 Jan;82(2):381-5. doi: 10.1073/pnas.82.2.381.
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Single-step purification of polypeptides expressed in Escherichia coli as fusions with glutathione S-transferase.以谷胱甘肽S-转移酶融合形式在大肠杆菌中表达的多肽的一步纯化。
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Human papillomavirus type 16 DNA cooperates with activated ras in transforming primary cells.16型人乳头瘤病毒DNA与激活的ras协同作用转化原代细胞。
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