INTRODUCTION: CELL TRANSFORMATION BY ONCOGENIC DNA VIRUSES Cell growth is a complex process resulting from a cascade of events regulated by both positively and negatively acting biological signals. Tumorigenic proliferation has been shown in some cases to be caused by alterations in genes encoding proteins involved in such signalling pathways (Klein, 1988). DNA tumour viruses have been extensively studied and widely used as molecular probes and models of cellular transformation. The oncogenes, i.e. tumour-inducing genes, from polyomavirus (Py), simian virus 40 (SV40) and adenovirus (Ad), are capable of inducing several distinct changes in cellular phenotype, including immortalization, secretion of growth factors, loss of contact inhibition, anchorage-independent growth and morphological transformation (Branton et al., 1985). However, unlike the transforming retroviruses, the DNA tumour viruses contain oncogenes with apparently no cellular counterparts (Bishop, 1985; Branton et al., 1985; Klein, 1988). Moreover, the proteins encoded by DNA viral oncogenes play an essential role in the lytic life-cycle of the virus in fully permissive host cells (Alwine et al., 1977; Harrison et al., 1977; Lassam et al., 1978), whereas transforming oncogenes of retroviruses are not required for lytic growth (Bishop, 1982). Adenovirus, like the other DNA tumour viruses, encodes a set of proteins that disturb cellular regulatory functions, thus reprogramming cell growth (Berk, 1986a; Branton et al., 1985; Branton & Rowe, 1985). The proteins encoded by oncogenes are termed 'oncoproteins'. Certain viral oncoproteins have been found to form stable complexes with host-cell proteins which also appear to be involved in transformation. This is the case for the Py middle T-pp60-8rc complex (Courtneidge & Smith, 1983), the SV40 large T-p53 complex (Lane & Crawford, 1983; Linzer & Levine, 1979; McCormick & Harlow, 1980), and the adenovirus E1B-p55:p53 complex (Sarnow et al., 1982a). The formation of these complexes may result in the potentiation of the transforming functions of these cellular proteins. The molecular mechanism might involve the alteration of a catalytic activity of the cellular protein, such as the protein kinase activity of pp6Oc-8rc (Bolen et al., 1984; Courtneidge, 1985), or a change in protein conformation and stability (e.g. p53; Oren et al., 1981; Reich et al., 1983). Cellular transformation by the adenovirus oncogenes involves a very elaborate mechanism at the molecular level. It seems to occur as a sequential process, involving two blocks of genes, ElA and E1B. EIA alone has the property of immortalizing primary