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Mol. Cell. Biol., Aug 1996, 4156-4162, Vol 16, No. 8
M Khosla, GB Spiegelman and G Weeks
Transformants that expressed either the wild-type rasG gene, an activated
rasG-G12T gene, or a dominant negative rasG-S17N gene, all under the
control of the folate-repressible discoidin (dis1gamma) promoter, were
isolated. All three transformants expressed high levels of Ras protein
which were reduced by growth in the presence of folate. All three
transformants grew slowly, and the reduction in growth rate correlated with
the amount of RasG protein produced, suggesting that RasG is important in
regulating cell growth. The pVEII-rasG transformant containing the
wild-type rasG gene developed normally despite the presence of high levels
of RasG throughout development. This result indicates that the down
regulation of rasG that normally occurs during aggregation of wild-type
strains is not essential for the differentiation process. Dictyostelium
transformants expressing the dominant negative rasG-S17N gene also
differentiated normally. Dictyostelium transformants that overexpressed the
activated rasG-G12T gene did not aggregate. The defect occurred very early
in development, since the expression of car1 and pde, genes that are
normally induced soon after the initiation of development, was repressed.
However, when the transformant cells were pulsed with cyclic AMP,
expression of both genes returned to wild-type levels. The transformants
exhibited chemotaxis to cyclic AMP, and development was synergized by
mixing with wild-type cells. Furthermore, cells that were pulsed with
cyclic AMP for 4 h before being induced to differentiate by plating on
filters produced small, but otherwise normal, fruiting bodies. These
results suggest that the rasG-G12T transformants are defective in cyclic
AMP production and that RasG - GTP blocks development by interfering with
the initial generation of cyclic AMP pulses.
Copyright © 1996, American Society for Microbiology
Overexpression of an activated rasG gene during growth blocks the initiation of Dictyostelium development
Department of Microbiology and Immunology, University of British Columbia, Vancouver, Canada.
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