Biological activities of v-myc and rearranged c-myc oncogenes in rat fibroblast cells in culture.

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Abstract
Two distinct forms of the myc oncogene were assayed for their ability to induce, in cultured rat fibroblast cells, the alterations of cellular growth controls observed upon transfer of the gene of polyoma virus encoding only the large T protein (plt). Both of these rearranged myc genes and the plt gene were previously shown to cooperate with ras oncogenes for transformation of rat embryo fibroblasts (REF) and were thought to induce the same early step (immortalization) of the tumoral transformation pathway. These 2 different oncogenes elicited the same response in the following biological assays: reduction of the requirements in serum factors for growth in culture of cells of the established FR3T3 line; expression of transformed properties in low serum medium after transfer into FR3T3 cells expressing only the middle T protein of polyoma virus (MTT lines); conferring on REF cells the ability to grow as clonal colonies after seeding at low cell density; conferring on REF cells the ability to grow continuously in cell culture. These congruent phenotypes suggest that the activities of the large T and myc proteins result in the induction of the same molecular events. These results also provide simple biological assays and selective systems for oncogenes of the myc class.