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The data on the transforming activity of intact DNA of human adenovirus type 6 and that fragmented by restrictases Bam H I (31.3% of the genome), Bgl 2 (9.3% of the genome), and Hind 3 (7.6% of the genome) in a primary culture of rat kidney cells are presented. The activity of the specimens varied within 1.1-2.1 foci per 1 microgram of DNA. From the transformation foci 5 cell lines were derived and their properties (T-antigen production, integration of adenovirus genome, phenotypic features) were studied.

Methods for generation of cell lines transformed by highly oncogenic simian adenovirus SA7, nononcogenic human adenovirus type 6 and their DNAs are described. WAG rat kidney cells were used for transformation. To produce 1 focus of transformation, 1.7 X 10(6) PFU of SA7 virus is required. Intact and fragmented DNA of both viruses may be quite effectively used for transformation. For production of 1 transformation focus 1.2 microgram SA7 DNA and 1.1 microgram type 6 adenovirus DNA is required. In most cases, DNA fragmentation increases the transforming activity which has been shown to be associated with the left genome region of both viruses under study.

Liposomes connected with influenza viral glycoproteins increase by 1-2 orders the specific infectiousness of DNA from SV-40 or monkey adenovirus SA7 as compared with the one registered when the standard method of calcium precipitation is used.