Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1947091 | Biochimica et Biophysica Acta (BBA) - Gene Structure and Expression | 2007 | 10 Pages |
Abstract
We have previously shown that the basic helix-loop-helix (bHLH) transcription factors coordinate NaV 1.4 Na+ channel gene expression in skeletal muscle, but the identity of the co-factors they direct is unknown. Using C2C12 muscle cells as a model system, we test the hypothesis that the bHLH factors counteract negative regulation exerted through a repressor E box (â 90/â 85) by recruiting positive-acting transcription factors to the nucleotides (â 135/â 57) surrounding the repressor E box. We used electrophoretic mobility shift assays to identify candidate factors that bound the repressor E box or these adjacent regions. Repressor E box-binding factors included the known transcription factor, ZEB/AREB6, and a novel repressor E box-binding factor designated REB. Mutations of the repressor E box that interfere with the binding of these factors prevented repression. The transcription factor, nuclear factor I (NFI), bound immediately upstream and downstream of the repressor E box. Mutation of the NFI-binding sites diminished the ability of myogenin and MRF4 to counteract repression. Based on these observations we suggest that bHLH factors recruit NFI to enhance skeletal muscle Na+ channel expression.
Keywords
CATdithiotheitolMrf4GABPZEBMyogeninREBbHLHAChRNMJSynaptogenesisPEBTFCDTTNFIDMEMDulbecco's modified Eagle's mediumElectrophoretic mobility shift assayNeuromuscular junctionbasic helix–loop–helixEMSA یا electrophoretic mobility shift assay Nuclear factor ISkeletal muscleGA-binding proteinchloramphenicol acetyltransferaseacetylcholine receptor
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Authors
Sadie L. Hebert, Christine Simmons, Amy L. Thompson, Catherine S. Zorc, Eric M. Blalock, Susan D. Kraner,