2000
DOI: 10.1054/ceca.2000.0136
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The calmodulin multigene family as a unique case of genetic redundancy: multiple levels of regulation to provide spatial and temporal control of calmodulin pools?

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Cited by 100 publications
(77 citation statements)
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“…In addition, local CaM concentrations may also be translationally regulated as CaM mRNA is differentially distributed, a process that likely reflects the conservation of three non-allelic mammalian CaM genes encoding identical proteins but distinct 5Ј and 3Ј non-coding sequences. For example, one pool of CaM mRNA, derived from a specific CaM gene (CALM1) is abundant in the apical dendrites of cerebellar pyramidal cells and may give rise to local reservoirs of CaM; however, mRNAs derived from CALM1 and CALM2 genes are found in neurite outgrowths in nerve growth factor-stimulated PC12 cells, and CALM3-derived transcripts reside within the cell body (45)(46)(47). Base upon these factors, and the number and concentrations of CaM-binding proteins, it is possible that CaM availability is rate-limiting for SK channel surface expression (43).…”
Section: Discussionmentioning
confidence: 99%
“…In addition, local CaM concentrations may also be translationally regulated as CaM mRNA is differentially distributed, a process that likely reflects the conservation of three non-allelic mammalian CaM genes encoding identical proteins but distinct 5Ј and 3Ј non-coding sequences. For example, one pool of CaM mRNA, derived from a specific CaM gene (CALM1) is abundant in the apical dendrites of cerebellar pyramidal cells and may give rise to local reservoirs of CaM; however, mRNAs derived from CALM1 and CALM2 genes are found in neurite outgrowths in nerve growth factor-stimulated PC12 cells, and CALM3-derived transcripts reside within the cell body (45)(46)(47). Base upon these factors, and the number and concentrations of CaM-binding proteins, it is possible that CaM availability is rate-limiting for SK channel surface expression (43).…”
Section: Discussionmentioning
confidence: 99%
“…The heterogeneous expression of PMCA isoforms in brain may produce regional variation in the use-dependence of Ca 2+ clearance. Added variability might also result from differences in PMCA activation kinetics for different members of the calmodulin family of proteins (Toutenhoofd and Strehler 2000;Laube et al 2002). Alternative splicing also affects PDZ (Psd-95/Dlg/Zo-1) binding domains and phosphorylation consensus sites that alter the cellular localization and modulation of PMCA isoforms (Enyedi et al 1996;DeMarco and Strehler 2001).…”
Section: Discussionmentioning
confidence: 99%
“…The sequence of the last six Myo3A IQ motifs more closely resemble those of GAP-43 (neuromodulin) than the first three myosin neck IQ motifs. GAP-43 (neuromodulin) is a leading candidate for a calmodulin "storage" protein (Toutenhoofd and Strehler, 2000) that may be pertinent to the function of Myo3A.…”
Section: Class III Myosinsmentioning
confidence: 99%