
doi: 10.1038/15640
pmid: 10559984
Nucleoplasmic calcium ions (Ca2+) influence nuclear functions as critical as gene transcription, apoptosis, DNA repair, topoisomerase activation and polymerase unfolding. Although both inositol trisphosphate receptors and ryanodine receptors, types of Ca2+ channel, are present in the nuclear membrane, their role in the homeostasis of nuclear Ca2+ remains unclear. Here we report the existence in the inner nuclear membrane of a functionally active CD38/ADP-ribosyl cyclase that has its catalytic site within the nucleoplasm. We propose that the enzyme catalyses the intranuclear cyclization of nicotinamide adenine dinucleotide to cyclic adenosine diphosphate ribose. The latter activates ryanodine receptors of the inner nuclear membrane to trigger nucleoplasmic Ca2+ release.
Cell Nucleus, Adenosine Diphosphate Ribose, Cyclic ADP-Ribose, Membrane Glycoproteins, Microscopy, Confocal, Immunoblotting, 3T3 Cells, Inositol 1,4,5-Trisphosphate, Cell Fractionation, NAD, ADP-ribosyl Cyclase 1, Antigens, Differentiation, Mice, NAD+ Nucleosidase, Antigens, CD, Genes, Reporter, Multienzyme Complexes, Animals, Calcium, ADP-ribosyl Cyclase
Cell Nucleus, Adenosine Diphosphate Ribose, Cyclic ADP-Ribose, Membrane Glycoproteins, Microscopy, Confocal, Immunoblotting, 3T3 Cells, Inositol 1,4,5-Trisphosphate, Cell Fractionation, NAD, ADP-ribosyl Cyclase 1, Antigens, Differentiation, Mice, NAD+ Nucleosidase, Antigens, CD, Genes, Reporter, Multienzyme Complexes, Animals, Calcium, ADP-ribosyl Cyclase
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