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Biochem Biophys Res Commun. 1994 Jun 15;201(2):603-9.

Potent transforming activity of the G13 alpha subunit defines a novel family of oncogenes.

Author information

1
Molecular Signalling Unit, National Institute of Dental Research, NIH, Bethesda, Maryland 20892.

Abstract

The finding of GTPase inhibiting mutations in genes for alpha subunits of Gs and Gi2 in certain endocrine tumors suggests that heterotrimeric G proteins might contribute to neoplasia. Expression of these activated forms of alpha s or alpha i2 in NIH 3T3 murine fibroblasts induces certain alterations in cell growth, but is weakly transforming. Mutationally activated forms of the alpha subunit of another G protein family, Gq, are fully oncogenic in NIH 3T3 cells, although with a very low potency. In contrast, we have recently shown that overexpression of the alpha subunit of a novel G protein, G12, is itself transforming, and an activated mutant of alpha 12 behaves as one of the most potent oncogenes known. In this study, we have explored whether another member of the G alpha 12 family, G alpha 13, harbors transforming potential. Our data demonstrate that G alpha 13 can behave as a potent dominant acting oncogene. These findings strongly suggest that the G12 family of G proteins represents a novel class of oncogenes.

PMID:
8002992
DOI:
10.1006/bbrc.1994.1744
[Indexed for MEDLINE]

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