Hebert Sadie L, Simmons Christine, Thompson Amy L, Zorc Catherine S, Blalock Eric M, Kraner Susan D
Department of Molecular and Biomedical Pharmacology, University of Kentucky Medical Center, Lexington, KY 40536, USA.
Biochim Biophys Acta. 2007 Nov-Dec;1769(11-12):649-58. doi: 10.1016/j.bbaexp.2007.08.004. Epub 2007 Sep 14.
We have previously shown that the basic helix-loop-helix (bHLH) transcription factors coordinate Na(V) 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.
我们之前已经表明,碱性螺旋-环-螺旋(bHLH)转录因子可协调骨骼肌中Na(V) 1.4 Na(+)通道基因的表达,但它们所指导的辅助因子的身份尚不清楚。利用C2C12肌肉细胞作为模型系统,我们检验了这样一个假设:bHLH因子通过招募正向作用的转录因子至阻遏物E框(-90/-85)周围的核苷酸(-135/-57),来对抗通过阻遏物E框施加的负调控。我们使用电泳迁移率变动分析来鉴定与阻遏物E框或这些相邻区域结合的候选因子。与阻遏物E框结合的因子包括已知的转录因子ZEB/AREB6,以及一个新的与阻遏物E框结合的因子,命名为REB。干扰这些因子结合的阻遏物E框突变可阻止抑制作用。转录因子核因子I(NFI)结合在阻遏物E框的紧邻上游和下游。NFI结合位点的突变降低了生肌调节因子和MRF4对抗抑制的能力。基于这些观察结果,我们认为bHLH因子招募NFI以增强骨骼肌Na(+)通道的表达。