首页> 美国卫生研究院文献>Journal of Virology >Negative regulation of the bovine papillomavirus E5 E6 and E7 oncogenes by the viral E1 and E2 genes.
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Negative regulation of the bovine papillomavirus E5 E6 and E7 oncogenes by the viral E1 and E2 genes.

机译:病毒E1和E2基因对牛乳头瘤病毒E5E6和E7癌基因的负调控。

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摘要

Papillomaviruses induce benign squamous epithelial lesions that infrequently are associated with uncontrolled growth or malignant conversion. The virus-encoded oncogenes are clearly under negative regulation since papillomaviruses can latently infect cells and since different levels of viral oncogene expression are seen within the layers of differentiating infected epitheliomas. We used bovine papillomavirus type 1 (BPV-1) to investigate the mechanisms involved in the negative regulation of transformation. We found that the following two distinct and interacting mechanisms negatively regulate BPV-1 transformation effected by virally encoded trans-acting factors: (i) E2 repressors suppress transformation by the E6 and E7 oncogenes, and (ii) E1 and the E2 transactivator suppress transformation by the E6, E7, and E5 oncogenes. These systems interact in that the E2 repressors function to relieve the transformation suppression effected by the E1 and E2 transactivator genes. A BPV-1 mutant that lacked E2 repressors and E1 had greatly augmented transformation capacity. Analysis of this mutant revealed that the enhanced transformation was due to expression of the E6 and E7 genes in the absence of E5, revealing a previously unappreciated potency and synergy for the BPV-1 E6 and E7 oncogenes.
机译:乳头瘤病毒可诱发良性鳞状上皮病变,这种病变很少与生长不受控制或恶变有关。病毒编码的癌基因显然处于负调控之下,因为乳头瘤病毒可以潜伏地感染细胞,并且由于在区分感染的上皮瘤的各层中发现了不同水平的病毒癌基因表达。我们使用牛乳头瘤病毒1型(BPV-1)来研究参与负调控转化的机制。我们发现以下两种不同且相互作用的机制对病毒编码的反式作用因子产生的BPV-1转化产生负调控:(i)E2阻遏物抑制E6和E7癌基因的转化,以及(ii)E1和E2反式激活物抑制转化由E6,E7和E5癌基因引起。这些系统的相互作用在于E2阻遏物的功能是减轻E1和E2反式激活基因对转化的抑制。缺少E2阻遏物和E1的BPV-1突变体大大增强了转化能力。对该突变体的分析表明,增强的转化是由于在不存在E5的情况下E6和E7基因的表达所致,从而揭示了BPV-1 E6和E7癌基因以前未曾意识到的效力和协同作用。

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