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Human Papillomavirus Type 16 E7 Oncoprotein Associates with the Cullin 2 Ubiquitin Ligase Complex, Which Contributes to Degradation of the Retinoblastoma Tumor Suppressor▿

机译:人乳头瘤病毒16型E7癌蛋白与Cullin 2泛素连接酶复合物相关,可导致视网膜母细胞瘤肿瘤抑制因子的降解。

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摘要

Human papillomavirus type 16 (HPV16) and other high-risk HPVs are etiologically linked to the development of cervical carcinomas and contribute to a number of other tumors of the anogenital tract, as well as oral cancers. The high-risk HPV E6 and E7 oncoproteins are consistently expressed in cervical cancer cells and are necessary for the induction and maintenance of the transformed phenotype. An important aspect of HPV16 E7's oncogenic activities is destabilization of the retinoblastoma tumor suppressor (pRB) through a ubiquitin/proteasome-dependent mechanism, although the exact molecular mechanism is unknown. Here, we report that HPV16 E7 is associated with an enzymatically active cullin 2 ubiquitin ligase complex and that the HPV16 E7/pRB complex contains cullin 2. Depletion of cullin 2 by RNA interference causes increased steady-state levels and stability of pRB in HPV16 E7-expressing cells, and ectopic expression of HPV16 E7 and the cullin 2 complex leads to pRB ubiquitination in vivo. Hence, we propose that the HPV16 E7-associated cullin 2 ubiquitin ligase complex contributes to aberrant degradation of the pRB tumor suppressor in HPV16 E7-expressing cells.
机译:人类乳头瘤病毒16型(HPV16)和其他高危HPV在病因上与宫颈癌的发生有关,并导致许多其他生殖道肿瘤以及口腔癌。高危HPV E6和E7癌蛋白始终在宫颈癌细胞中表达,并且对于诱导和维持转化的表型是必需的。 HPV16 E7致癌活性的一个重要方面是通过泛素/蛋白酶体依赖性机制使视网膜母细胞瘤肿瘤抑制因子(pRB)失稳,尽管确切的分子机制尚不清楚。在这里,我们报告HPV16 E7与酶活性的cullin 2泛素连接酶复合物相关,并且HPV16 E7 / pRB复合物包含cullin2。由于RNA干扰而使cullin 2耗尽会导致HPV16 E7中pRB的稳态水平和稳定性增加。表达细胞,HPV16 E7和cullin 2复合体的异位表达导致体内pRB泛素化。因此,我们建议HPV16 E7相关的cullin 2泛素连接酶复合物有助于表达HPV16 E7的细胞中pRB肿瘤抑制物的异常降解。

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