基因
生物
视网膜母细胞瘤蛋白
人口
克隆(编程)
遗传学
细胞生物学
细胞
病毒学
分子生物学
细胞周期
医学
计算机科学
环境卫生
程序设计语言
作者
Tracy M. Bryan,Ronald Redder
标识
DOI:10.1615/critrevoncog.v5.i4.10
摘要
For several decades simian virus 40 (SV40) early region genes have been used as a means of generating immortalized human cell lines; however, the molecular mechanisms of this process have begun to be understood only recently. SV40-induced immortalization proceeds via two phases. In the first phase ("lifespan extension"), cells continue proliferating for a limited number of population doublings beyond the point at which normal cells undergo senescence. This is mainly due to the ability of SV40 large T antigen (LTAg) to bind to the protein products of the p53 and retinoblastoma (Rb) genes. The second phase ("immortalization") occurs in only a small minority of cells, and cell hybridization analyses indicate that this is a gene inactivation event. The gene or genes involved are currently unknown, but chromosomal localization data are accumulating which should make their cloning and characterization possible in the near future.
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