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Science 6 October 1989:
Vol. 246. no. 4926, pp. 121 - 124
DOI: 10.1126/science.2506643

Articles

Science, Vol 246, Issue 4926, 121-124
Copyright © 1989 by American Association for the Advancement of Science


articles

Fibroblasts transformed with v-src show enhanced formation of an inositol tetrakisphosphate

RM Johnson, WJ Wasilenko, RR Mattingly, MJ Weber, and JC Garrison

Department of Pharmacology, University of Virginia School of Medicine, Charlottesville 22908.

The tyrosine kinase pp60v-src, encoded by the v-src oncogene, seems to regulate phosphatidylinositol metabolism. The effect of pp60v-src on control points in inositol phosphate production was examined by measuring the amounts of inositol polyphosphates in Rat-1 cells expressing wild-type or mutant forms of the protein. Expression of v-src-resulted in a five- to sevenfold elevation in the steady-state amount of an isomer of inositol tetrakisphosphate, whereas the concentrations of inositol trisphosphates or other inositol tetrakisphosphates were not affected. The activity of a key enzyme in the formation of inositol tetrakisphosphates, inositol (1,4,5)-trisphosphate 3-kinase, was increased six- to eightfold in cytosolic extracts prepared from the v-src-transformed cells, suggesting that this enzyme may be one target for the pp60v-src kinase and that it may participate in the synthesis of novel, higher order inositol phosphates.


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