o-Ca cium- Calmodulin Kinase Mutant Mice
نویسندگان
چکیده
tuffs do not result from pyroclastic flow and hence are not true pyroclastic flow deposits. They do not explain the processes they envision, but in this situation pyroclastic emplacement without some form of lateral flow is clearly impossible, even in near-vent locations. 18. M. J. Branney and R. S. J. Sparks, J. Geol. Soc. London 147, 919 (1990). 19. For example, halloysite, smectites, sericite, montmorillonite, kaolinite, and illite. 20. R. L. Allen, Econ. Geol. 83,1424 (1988). 21. P. W. Lipman, Geol. Soc. Am. Bull. 87, 1397 (1976). 22. L. Draper, Marine Geol. 5, 133 (1966); P. D. Komar, J. Sed. Petrol. 44,169 (1974); B. Butnam et al., J. Geophys. Res. 84, 1182 (1979). 23. See K. T. Pickering et al., Deep Marine Environments (Unwin Hyman, London, 1989). 24. R. S. J. Sparks, Bull. Volcanol. 48, 3 (1986). 25. K. V. Cashman and R. S. Fiske, Science 253, 275 (1991). These authors described a fallout deposit resting above a coeval hot-emplaced (-4500C) flow deposit, which we suggest is most likely to have formed from the material that would not be incorporated into the convective column above the vent. 26. P. Kokelaar, Bull. Volcanol. 48, 275 (1986), figure 4. A bell-shaped exclusion zone postulated to occur above the vent was referred to in that case as a "cupola of steam," because the explosivity involves bulk incorporation of water in the eruptive conduit, so that the gas of the erupted dispersion is dominated by (nonmagmatic) steam; see P. Kokelaar, J. Geol. Soc. London 140, 939 (1983). 27. P. D. Rowey et al., U.S. Geol. Surv. Prof. Pap. 1250 (1981), p. 489. 28. Compare with R. S. Fiske and T. Matsuda, Am. J. Sci. 262, 76 (1964). 29. H. Ohmoto and B. J. Skinner, Econ. Geol. Monogr. 5, 1 (1983). 30. P. Kokelaar, Geol. Soc. Am. Bull., in press. 31. C. J. Busby-Spera and J. Saleeby, Geologic Guide to the Mineral King Area, Sequoia National Park, California (Society of Economic Paleontologists and Mineralogists, Los Angeles, 1987). 32. T. G. Gloppen and R. J. Steel, Soc. Econ. Paleontol. Mineral. Spec. Publ. 31, 49 (1981). 33. Supported by a NATO collaborative research grant 910549 and NSF grant EAR9018606 (to C.B.). We are grateful to G. Lloyd for assistance with production of the SEM image and to M. J. Branney, R. V. Fisher, S. Self, and R. S. J. Sparks for reviews of a draft of the article.
منابع مشابه
Ryanodine receptor phosphorylation by calcium/calmodulin-dependent protein kinase II promotes life-threatening ventricular arrhythmias in mice with heart failure.
BACKGROUND approximately half of patients with heart failure die suddenly as a result of ventricular arrhythmias. Although abnormal Ca(2+) release from the sarcoplasmic reticulum through ryanodine receptors (RyR2) has been linked to arrhythmogenesis, the molecular mechanisms triggering release of arrhythmogenic Ca(2+) remain unknown. We tested the hypothesis that increased RyR2 phosphorylation ...
متن کاملA Significant but Rather Mild Contribution of T286 Autophosphorylation to Ca2+/CaM-Stimulated CaMKII Activity
BACKGROUND Autophosphorylation of the Ca(2+)/calmodulin (CaM)-dependent protein kinase II (CaMKII) at T286 generates partially Ca(2+)/CaM-independent "autonomous" activity, which is thought to be required for long-term potentiation (LTP), a form of synaptic plasticity thought to underlie learning and memory. A requirement for T286 autophosphorylation also for efficient Ca(2+)/CaM-stimulated CaM...
متن کاملMolecular characterization of calmodulin trapping by calcium/calmodulin-dependent protein kinase II.
Autophosphorylation of alpha-Ca(2+)/calmodulin-dependent protein kinase II (CaM kinase II) at Thr(286) results in calmodulin (CaM) trapping, a >10,000-fold decrease in the dissociation rate of CaM from the enzyme. Here we present the first site-directed mutagenesis study on the dissociation of the high affinity complex between CaM and full-length CaM kinase II. We measured dissociation kinetics...
متن کاملCalcium-stimulated autophosphorylation site of plant chimeric calcium/calmodulin-dependent protein kinase.
The existence of two molecular switches regulating plant chimeric Ca(2+)/calmodulin-dependent protein kinase (CCaMK), namely the C-terminal visinin-like domain acting as Ca(2+)-sensitive molecular switch and calmodulin binding domain acting as Ca(2+)-stimulated autophosphorylation-sensitive molecular switch, has been described (Sathyanarayanan, P. V., Cremo, C. R., and Poovaiah, B. W. (2000) J....
متن کاملStimulation of unitary T-type Ca(2+) channel currents by calmodulin-dependent protein kinase II.
The effect of Ca(2+)/calmodulin-dependent protein kinase II (CaMKII) stimulation on unitary low voltage-activated (LVA) T-type Ca(2+) channel currents in isolated bovine adrenal glomerulosa (AG) cells was measured using the patch-clamp technique. In cell-attached and inside-out patches, LVA channel activity was identified by voltage-dependent inactivation and a single-channel conductance of app...
متن کاملInvolvement of neurogranin in the modulation of calcium/calmodulin-dependent protein kinase II, synaptic plasticity, and spatial learning: a study with knockout mice.
Neurogranin/RC3 is a neural-specific Ca(2+)-sensitive calmodulin (CaM)-binding protein whose CaM-binding affinity is modulated by phosphorylation and oxidation. Here we show that deletion of the Ng gene in mice did not result in obvious developmental or neuroanatomical abnormalities but caused an impairment of spatial learning and changes in hippocampal short- and long-term plasticity (paired-p...
متن کامل