Publication | Open Access
Calcium Regulates Transcriptional Repression of Myocyte Enhancer Factor 2 by Histone Deacetylase 4
165
Citations
34
References
2000
Year
Histone ModificationsEpigenetic ChangeCytoskeletonMuscle Cell DifferentiationHistone Deacetylase 4EpigeneticsCellular PhysiologyTranscriptional RepressionTranscriptional RegulationSignaling PathwayCell RegulationCell SignalingCell PhysiologyGene ExpressionCell BiologyTranscription RegulationChromatin FunctionChromatinCalmodulin-binding DomainsDevelopmental BiologySignal TransductionChromatin RemodelingNatural SciencesPhysiologyGene RegulationCalmodulin BindsTranscription FactorsMedicine
The myocyte enhancer factor 2 (MEF2) consists of a family of transcription factors that play important roles in a number of physiological processes from muscle cell differentiation to neuronal survival and T cell apoptosis. MEF2 has been reported to be associated with several distinct repressors including Cabin1(cain), MEF2-interacting transcriptional repressor (MITR), and HDAC4. It has been previously shown that Cabin1 is associated with MEF2 in a calcium-sensitive manner; activated calmodulin binds to Cabin1 and releases it from MEF2. However, it was not known whether the binding of HDAC4 and MITR to MEF2 is also regulated by calcium. We report that HDAC4 and MITR contain calmodulin-binding domains that overlap with their MEF2-binding domains. Binding of calmodulin to HDAC4 leads to its dissociation from MEF2, relieving MEF2 from the transcriptional repression by HDAC4. Together, HDAC4, MITR, and Cabin1 constitute a family of calcium-sensitive transcriptional repressors of MEF2.
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