An epithelial cell-transforming virus could be of great use, both in the culture of epithelial cell lines and in the study of carcinogenesis. Since the adenoviral ElA gene has been shown to partially transform some epithelial cells from primary rat cell cultures, we constructed retrovirus vectors containing either the 12S or 13S ElA cDNA sequences to facilitate the transfer of these genes into a variety of primary cell types. The 12S ElA virus induced proliferation and immortalization of epithelial cells in rat kidney, liver, heart, pancreas, and thyroid primary cultures. In the two cases tested, heart and liver cultures, ElA-immortalized cells were nontumorigenic, but could be completely transformed by subsequent introduction of the ras oncogene. To our surprise, the 13S virus had a greatly reduced immortalization potential. We discuss these data in light of the model of Spindler et al. (K. R. Spindler, C. Y. Eng, and A.-J. Berk, J. Virol. 53:742-750, 1985), in which the 12S ElA protein is required for the complete induction of the cellular DNA replication machinery in the quiescent human epithelial cells in which adenoviruses normally replicate.The culture of normal epithelial cells from primary tissues has been a difficult task, often requiring the precise definition of a hormonally supplemented, serum-free medium for each cell type (3, 31). Unlike fibroblasts, many epithelial cell types will not grow in high concentrations of serum, perhaps owing to the presence of one or more inhibitory factors (2,12, 20). Although some oncogenic viruses have been useful for the transformation of specific differentiated cell types in vitro, such as the transformation of pre-B cells by Abelson virus (34), no viruses have been consistently successful in the transformation of diverse epithelial cells (33).The human adenoviruses have been shown to transform a few epithelial cell types, allowing their continuous growth in serum-supplemented medium (7,25,35). However, adenovirus transformation of many rodent tissues, and most human tissues tested, is extremely inefficient. It is likely that the inefficiency of adenovirus transformation results from a variety of factors such as (i) the lytic properties of adenovirus in many cell types (ii) the low frequency with which adenoviral DNA integrates into the host chromosome, and (iii) a possible tissue specificity of expression and/or function of the adenoviral transforming proteins.To examine the propensity for epithelial cell transformation of one of the adenoviral transforming genes in a variety of primary cells, without the constraints of adenovirus infection, and in the absence of other adenoviral gene products, we have constructed and describe here the properties of retrovirus vectors containing either the 12S or 13S early-region 1A (E1A) sequences from adenovirus type 2-adenovirus type 5 hybrid cDNAs. DNAs, rvl2S and rvl3S, were transfected into qs2 cells (19) by CaPO4 precipitation. Transiently expressed viral particles were harvested from the medium 24 h posttransfection to inf...