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Basic helix-loop-helix factors recruit nuclear factor I to enhance expression of the NaV 1.4 Na+ channel gene

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9 Scopus citations

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 (- 90/- 85) by recruiting positive-acting transcription factors to the nucleotides (- 135/- 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.

Original languageEnglish
Pages (from-to)649-658
Number of pages10
JournalBiochimica et Biophysica Acta - Gene Structure and Expression
Volume1769
Issue number11-12
DOIs
StatePublished - Nov 2007

Bibliographical note

Funding Information:
This work is supported by NIH grants AR 46477 (S.D.K.) and AG000242 (A.L.T.).

Funding

This work is supported by NIH grants AR 46477 (S.D.K.) and AG000242 (A.L.T.).

FundersFunder number
National Institutes of Health (NIH)AR 46477
National Institutes of Health (NIH)
National Institute on AgingT32AG000242
National Institute on Aging

    Keywords

    • GABP
    • MRF4
    • Myogenin
    • NFI
    • Neuromuscular junction
    • Skeletal muscle
    • Synaptogenesis

    ASJC Scopus subject areas

    • Structural Biology
    • Biophysics
    • Biochemistry
    • Genetics

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