School of Life Sciences, Biodesign Institute, Arizona State University, Tempe, Arizona 85287-4501; Molecular and Cellular Biology Graduate Program, Biodesign Institute, Arizona State University, Tempe, Arizona 85287-4501.
Program in Gene Function and Expression, University of Massachusetts Medical School, Worcester, Massachusetts 01605; Department of Biochemistry and Molecular Pharmacology, University of Massachusetts Medical School, Worcester, Massachusetts 01605.
J Biol Chem. 2012 Oct 12;287(42):35351-35359. doi: 10.1074/jbc.M112.399386. Epub 2012 Aug 24.
The homeobox transcription factor Mohawk (Mkx) is a potent transcriptional repressor expressed in the embryonic precursors of skeletal muscle, cartilage, and bone. MKX has recently been shown to be a critical regulator of musculoskeletal tissue differentiation and gene expression; however, the genetic pathways through which MKX functions and its DNA-binding properties are currently unknown. Using a modified bacterial one-hybrid site selection assay, we determined the core DNA-recognition motif of the mouse monomeric Mkx homeodomain to be A-C-A. Using cell-based assays, we have identified a minimal Mkx-responsive element (MRE) located within the Mkx promoter, which is composed of a highly conserved inverted repeat of the core Mkx recognition motif. Using the minimal MRE sequence, we have further identified conserved MREs within the locus of Sox6, a transcription factor that represses slow fiber gene expression during skeletal muscle differentiation. Real-time PCR and immunostaining of in vitro differentiated muscle satellite cells isolated from Mkx-null mice revealed an increase in the expression of Sox6 and down-regulation of slow fiber structural genes. Together, these data identify the unique DNA-recognition properties of MKX and reveal a novel role for Mkx in promoting slow fiber type specification during skeletal muscle differentiation.
同源盒转录因子 Mohawk(Mkx)是一种在骨骼肌、软骨和骨骼的胚胎前体细胞中表达的强效转录抑制剂。MKX 最近被证明是肌肉骨骼组织分化和基因表达的关键调节因子;然而,MKX 发挥作用的遗传途径及其 DNA 结合特性目前尚不清楚。我们使用改良的细菌单杂交位点选择测定法,确定了小鼠单体 Mkx 同源域的核心 DNA 识别基序为 A-C-A。通过细胞测定法,我们在 Mkx 启动子内鉴定出一个最小的 Mkx 反应元件(MRE),该元件由核心 Mkx 识别基序的高度保守反向重复组成。使用最小的 MRE 序列,我们在 Sox6 的基因座内进一步鉴定出保守的 MRE,Sox6 是一种转录因子,在骨骼肌分化过程中抑制慢肌纤维基因的表达。从 Mkx 缺失小鼠分离的体外分化的肌肉卫星细胞的实时 PCR 和免疫染色显示 Sox6 的表达增加,慢肌纤维结构基因的下调。这些数据共同确定了 MKX 的独特 DNA 识别特性,并揭示了 Mkx 在促进骨骼肌分化过程中慢肌纤维类型特化中的新作用。