Calcium/calmodulin-dependent protein kinase type IV Is a target gene of the Wnt/?-catenin signaling pathway

Arrázola M.S.; Varela-Nallar, L; Colombres M.; Toledo E.M.; Inestrosa, N. C.; Cruzat F.; Montecino, M.; Pavez, L.; Gonzalez, M.; Assar, R; Aravena, A.; Maass A.; Martínez, S.

Keywords: behavior, model, disorder, proteins, neurons, rat, tests, mouse, region, animals, expression, transcription, binding, culture, biology, rats, protein, cell, gene, chloride, disease, calcium, tcf, beta, genome, physiology, mice, memory, prediction, metabolism, embryo, strains, line, experiment, humans, transduction, transgenic, human, genetics, strain, lithium, cytology, nerve, targeting, hippocampus, signal, rna, drug, catenin, pathology, article, kinase, factor, promoter, enhancer, wnt, iv, alzheimer, vivo, calmodulin, bioinformatics, genetic, transfection, test, type, controlled, animal, factors, study, 4, 1, rattus, priority, spatial, in, nonhuman, journal, Rats,, effect, Behavior,, Messenger, Models,, Inbred, t, Computational, Mice,, dependent, lymphoid, Neuropsychological, Mus, Wnt3a, Regions,, Elements,, calcium-calmodulin-dependent, Wnt3

Abstract

Calcium/calmodulin-dependent protein kinase IV (CaMKIV) plays a key role in the regulation of calcium-dependent gene expression. The expression of CaMKIV and the activation of CREB regulated genes are involved in memory and neuronal survival. We report here that: (a) a bioinformatic analysis of 15,476 promoters of the human genome predicted several Wnt target genes, being CaMKIV a very interesting candidate; (b) CaMKIV promoter contains TCF/LEF transcription motifs similar to those present in Wnt target genes; (c) biochemical studies indicate that lithium and the canonical ligand Wnt-3a induce CaMKIV mRNA and protein expression levels in rat hippocampal neurons as well as CaMKIV promoter activity; (d) treatment of hippocampal neurons with Wnt-3a increases the binding of b-catenin to the CaMKIV promoter: (e) In vivo activation of the Wnt signaling improve spatial memory impairment and restores the expression of CaMKIV in a mice double transgenic model for Alzheimer's disease which shows decreased levels of the kinase. We conclude that CaMKIV is regulated by the Wnt signaling pathway and that its expression could play a role in the neuroprotective function of the Wnt signaling against the Alzheimer's amyloid peptide. © 2009 Wiley-Liss, Inc.

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Título de la Revista: JOURNAL OF CELLULAR PHYSIOLOGY
Volumen: 221
Número: 3
Editorial: Wiley
Fecha de publicación: 2009
Página de inicio: 658
Página final: 667
URL: http://www.scopus.com/inward/record.url?eid=2-s2.0-70449699789&partnerID=q2rCbXpz