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Phosphorylation of phosphatidylinositol by transverse tubule vesicles and its possible role in excitation-contraction coupling

Phosphorylation of phosphatidylinositol to phosphatidylinositol 4-monophosphate and to phosphatidyl-inositol 4,5-bisphosphate was demonstrated in transverse-tubule membranes isolated from frog skeletal muscle using [γ- 32P]ATP as substrate. At millimolar concentrations of Mg 2+ both phosphorylation...

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Bibliographic Details
Published in:FEBS letters 1986-06, Vol.202 (1), p.69-73
Main Authors: Hidalgo, Cecilia, Carrasco, M.Angélica, Magendzo, Karin, Jaimovich, Enrique
Format: Article
Language:English
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Summary:Phosphorylation of phosphatidylinositol to phosphatidylinositol 4-monophosphate and to phosphatidyl-inositol 4,5-bisphosphate was demonstrated in transverse-tubule membranes isolated from frog skeletal muscle using [γ- 32P]ATP as substrate. At millimolar concentrations of Mg 2+ both phosphorylation reactions were completed within 15 s at 25°C. Isolated sarcoplasmic reticulum vesicles phosphorylated phosphatidyl-inositol to phosphatidylinositol 4-phosphate with a lower specific activity than the transverse tubules, and lacked the ability to produce phosphatidylinositol 4,5-bisphosphate. These findings show, for the first time, that isolated transverse-tubule membranes carry out one of the steps required to sustain a role for inositol trisphosphate as the physiological messenger in excitation-contraction coupling in skeletal muscle. The finding that 0.5 mM tetracaine apparently inhibits the phosphorylation of phosphatidylinositol 4-phosphate to phosphatidylinositol 4,5-bisphosphate also supports a role for these intermediates in excitation-contraction coupling.
ISSN:0014-5793
1873-3468
DOI:10.1016/0014-5793(86)80651-2