PIK-A49 is a 49-kDa soluble protein that was isolated as an activator of the plasma membrane phosphatidylinositol (PI) 4-kinase from carrot cells (Yang, W., Burkhart, W., Cavallius, J., Merrick, W. C., and Boss, W. F. (1993) J. Biol. Chem. 268, 392-398). PIK-A49 is a multifunctional protein that binds and bundles F-actin and has translational elongation factor-1 alpha activity. In this paper, we have investigated the mechanism of activation of PI 4-kinase by PIK-A49. PIK-A49 decreased the Km of PI 4-kinase for ATP from 0.40 to 0.19 mM. GTP and GDP, which affect the elongation factor-1 alpha function of the protein, inhibited the activation of PI 4-kinase by PIK-A49. Phosphorylation of purified PIK-A49 by a calcium-dependent protein kinase enhanced activation of PI 4-kinase. When dephosphorylated by alkaline phosphatase, PIK-A49 no longer activated PI 4-kinase; however, rephosphorylation of PIK-A49 by calcium-dependent protein kinase fully restored activation. Western blots using anti-PIK-A49 serum showed that PIK-A49 was associated with the plasma membrane and the F-actin fraction isolated from plasma membranes, indicating that PIK-A49 would be in a position to regulate plasma membrane PI 4-kinase. Based on these data, we propose a mechanism for feed-forward regulation of polyphosphoinositide biosynthesis in response to increases in cytosolic calcium.
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Wendy F. Boss (1994) studied this question.
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