Jones N C
Laboratory of Gene Regulation, Imperial Cancer Research Fund, London, UK.
Semin Cancer Biol. 1990 Dec;1(6):425-35.
Oncogenic transformation by the human adenoviruses involves the concerted action of two genes, E1A and E1B. Over the last few years the products of these genes have been characterised in considerable detail using genetic, immunological and biochemical means. The E1A gene by itself can immortalise primary cells and can cooperate to effect full morphological transformation not only with E1B but also with other known oncogenes. The immortalisation and cooperation activities of E1A require multiple functions that are directed by structurally and functionally independent regions of the E1A protein. These regions coincide with sites of protein: protein interaction between E1A and a variety of cellular polypeptides. One of these, the Rb protein, is a known regulator of the mammalian cell cycle. The E1B region encodes two proteins required for transformation, the larger of which binds to the p53 cellular protein. This protein has also been implicated as a negative regulator of cell growth. It appears therefore that E1A and E1B carry out their many functions associated with transformation at least in part by binding to and presumably modulating the activity of key cellular regulators.
人类腺病毒的致癌转化涉及两个基因E1A和E1B的协同作用。在过去几年中,已通过遗传学、免疫学和生物化学方法对这些基因的产物进行了相当详细的表征。单独的E1A基因可使原代细胞永生化,并且不仅可与E1B,还可与其他已知的癌基因协同作用以实现完全的形态转化。E1A的永生化和协同活性需要多种功能,这些功能由E1A蛋白的结构和功能独立区域指导。这些区域与E1A和多种细胞多肽之间的蛋白质:蛋白质相互作用位点一致。其中之一,即Rb蛋白,是哺乳动物细胞周期的已知调节因子。E1B区域编码转化所需的两种蛋白质,其中较大的一种与p53细胞蛋白结合。这种蛋白质也被认为是细胞生长的负调节因子。因此,似乎E1A和E1B至少部分地通过与关键细胞调节因子结合并可能调节其活性来执行与转化相关的许多功能。