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Association of the human papillomavirus type 16 E7 oncoprotein with the 600-kDa retinoblastoma protein-associated factor, p600

机译:人类乳头瘤病毒16型E7癌蛋白与600 kDa视网膜母细胞瘤蛋白相关因子p600的关联

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摘要

The human papillomavirus type 16 (HPV-16) E7 gene encodes a multifunctional oncoprotein that can subvert multiple cellular regulatory pathways. The best-known cellular targets of the HPV-16 E7 oncoprotein are the retinoblastoma tumor suppressor protein pRB and the related pocket proteins p107 and p130. However, there is ample evidence that E7 has additional cellular targets that contribute to its transforming potential. We isolated HPV-16 E7 associated cellular protein complexes by tandem affinity purification and mass spectrometry and identified the 600-kDa retinoblastoma protein associated factor, p600, as a cellular target of E7. Association of E7 with p600 is independent of the pocket proteins and is mediated through the N terminal E7 domain, which is related to conserved region 1 of the adenovirus E1A protein and importantly contributes to cellular transformation independent of pRB binding. Depletion of p600 protein levels by RNA interference substantially decreased anchorage-independent growth in HPV-positive and -negative human cancer cells. Therefore, p600 is a cellular target of E7 that regulates cellular pathways that contribute to anchorage-independent growth and cellular transformation.
机译:人类乳头瘤病毒16型(HPV-16)E7基因编码一种多功能癌蛋白,可以破坏多种细胞调节途径。 HPV-16 E7癌蛋白的最著名的细胞靶标是成视网膜细胞瘤抑癌蛋白pRB和相关的口袋蛋白p107和p130。但是,有充分的证据表明E7具有其他有助于其转化潜力的细胞靶标。我们通过串联亲和纯化和质谱分离了HPV-16 E7相关的细胞蛋白复合物,并确定了600 kDa视网膜母细胞瘤蛋白相关因子p600作为E7的细胞靶标。 E7与p600的结合独立于口袋蛋白,并通过N末端E7域介导,该区域与腺病毒E1A蛋白质的保守区1有关,并且重要地有助于细胞转化,而与pRB结合无关。 RNA干扰消耗的p600蛋白水平显着降低了HPV阳性和阴性人类癌细胞中锚定非依赖性生长。因此,p600是E7的细胞靶标,可调节有助于锚定非依赖性生长和细胞转化的细胞途径。

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