Abstract

The rate of 2-deoxyglucose uptake is approximately three times faster in actively growing BALB 3T3 cells than in resting cells, and another three times faster in polyoma or SV40-transformed cells than in actively growing untransformed cells. Uptake of 2-deoxyglucose increases approximately 10-fold after infection of resting cells by polyoma virus, and 3-fold after infection of growing cells. Uptake of 3- O-methylglucose also increases after infection of resting cells, showing that changes in the rate of 2-deoxyglucose uptake can be ascribed to changes in the rate of transport of hexose across the cell membrane. The increased rate of uptake in polyoma-infected cells begins about 12 hr after infection of resting cells at 37°, and occurs in the presence of cytosine arabinoside. The increase in uptake occurs after infection at 39° by a polyoma temperature-sensitive mutant, ts25, which is blocked in viral DNA synthesis at the restrictive temperature. The increase does not occur after infection with ts3, a mutant which is blocked in induction of cellular DNA synthesis, showing that an early viral gene product is required for increased uptake.

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