DNA-mediated transfer of cAMP resistance in CHO cells

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Abstract
Chinese hamster ovary (CHO) strain 10215 carries a dominant mutation which confers resistant to cAMP by virtue of an altered catalytic subunit of the cAMP‐dependent protein kinase (Evain et al., 1979). This mutation was transferred to wild‐type CHO cells by DNA‐mediated gene transfer. Based on the absence of cAMP growth inhibition, seven transformant colonies were isolated. One of these, 11586, was studied in detail. This transformant showed the same phenotype as the mutant, including resistance to the morphological changes and growth inhibitory effects of 1 mM 8‐Br‐cAMP, reduced total cAMP dependent protein kinase activity and lowered sensitivity of the kinase to cAMP activation. When the cAMP‐dependent protein kinase was fractionated on a DEAE‐cellulose column, the transformant was lacking in type II cAMP dependent protein activity, to the same degree as the mutant. The transformant and mutant, but not wild‐type cells, also failed to phosphorylate a 52,000‐dalton protein in a cAMP‐dependent manner. These characteristics support the conclusion that the gene for the mutant cAMP‐dependent protein kinase has been transferred. The ability to transfer this gene by DNA‐mediated transfer suggests that this methodology may be useful for the molecular isolation of the gene encoding the catalytic subunit of cAMP‐dependent protein kinase.