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Stereospecific Inositol 1,4,5-[32P]Trisphosphate Binding to Isolated Rat Liver Nuclei: Evidence for Inositol Trisphosphate Receptor-Mediated Calcium Release from the Nucleus

It is well known that inositol 1,4,5-trisphosphate binding and release of calcium are mediated by the same protein. Several reports have indicated the location of the inositol 1,4,5-trisphosphate receptor in organelles other than endoplasmic reticulum. Immunocytochemical studies on the subcellular l...

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Bibliographic Details
Published in:Proceedings of the National Academy of Sciences - PNAS 1990-12, Vol.87 (23), p.9270-9274
Main Authors: Malviya, A. N., Rogue, P., Vincendon, G.
Format: Article
Language:English
Subjects:
ATP
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Summary:It is well known that inositol 1,4,5-trisphosphate binding and release of calcium are mediated by the same protein. Several reports have indicated the location of the inositol 1,4,5-trisphosphate receptor in organelles other than endoplasmic reticulum. Immunocytochemical studies on the subcellular localization of 1,4,5-trisphosphate receptor in the Purkinje cells from two laboratories have given contradictory results regarding the nuclear location of this receptor. In this paper, a high-affinity inositol 1,4,5-[32P]trisphosphate binding site (Kd= 0.11 nM) on nuclei isolated from rat liver and devoid of any microsomal, mitochondrial, or plasma membrane constituents is documented. Furthermore, we present data demonstrating that inositol 1,4,5-trisphosphate is capable of releasing45Ca2+from the intact isolated liver nuclei. A rapid and transient release of calcium that was taken up by nuclei in the presence of ATP is observed. The role of inositol 1,4,5-trisphosphate in the coupling between cytoplasmic second messengers and nuclear events activated during signal transduction is postulated.
ISSN:0027-8424
1091-6490
DOI:10.1073/pnas.87.23.9270