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A role for nuclear inositol 1,4,5-trisphosphate kinase in transcriptional control.


AUTHORS

Odom| Stahlberg| Wente| York AR| A| SR| JDA R| A| S R| J D . Science (New York, N.Y.). 2000 3 17; 287(5460). 2026-9

ABSTRACT

Phospholipase C and two inositol polyphosphate (IP) kinases constitute a signaling pathway that regulates nuclear messenger RNA export through production of inositol hexakisphosphate (IP6). The inositol 1,4,5-trisphosphate kinase of this pathway in Saccharomyces cerevisiae, designated Ipk2, was found to be identical to Arg82, a regulator of the transcriptional complex ArgR-Mcm1. Synthesis of inositol 1,4,5,6-tetrakisphosphate, but not IP6, was required for gene regulation through ArgR-Mcm1. Thus, the phospholipase C pathway produces multiple IP messengers that modulate distinct nuclear processes. The results reveal a direct mechanism by which activation of IP signaling may control gene expression.



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