Faha B, Harlow E, Lees E
Massachusetts General Hospital Cancer Center, Charlestown 02129.
J Virol. 1993 May;67(5):2456-65. doi: 10.1128/JVI.67.5.2456-2465.1993.
The adenovirus E1A oncoproteins form stable complexes with several cellular proteins. Association of E1A with these proteins has been shown to be important for the oncogenic potential of E1A. Several of these proteins have been identified and include the product of the retinoblastoma gene and a key cell cycle regulatory protein, cyclin A. E1A also associates with a potent histone H1 kinase. The two major components of this activity are the cyclin E-p33cdk2 and cyclin A-p33cdk2 complexes. Both the cyclin E-p33cdk2 and cyclin A-p33cdk2 complexes have been implicated in regulatory events controlling entry into or passage through DNA synthesis. Although the architecture of such interactions remains unclear, it is likely that by targeting such complexes, adenovirus is affecting some aspect of cell cycle control.
腺病毒E1A癌蛋白与多种细胞蛋白形成稳定复合物。E1A与这些蛋白的结合已被证明对E1A的致癌潜能很重要。其中几种蛋白已被鉴定出来,包括视网膜母细胞瘤基因的产物和一种关键的细胞周期调节蛋白——细胞周期蛋白A。E1A还与一种强效组蛋白H1激酶相关联。这种活性的两个主要成分是细胞周期蛋白E-p33cdk2和细胞周期蛋白A-p33cdk2复合物。细胞周期蛋白E-p33cdk2和细胞周期蛋白A-p33cdk2复合物都与控制进入或通过DNA合成的调节事件有关。尽管这种相互作用的结构仍不清楚,但腺病毒很可能通过靶向这些复合物来影响细胞周期控制的某些方面。