Characterization of the DNA-binding Properties of the Mohawk Homeobox Transcription Factor

被引:25
作者
Anderson, Douglas M. [1 ,2 ]
George, Rajani [1 ,2 ]
Noyes, Marcus B. [4 ,5 ]
Rowton, Megan [1 ,2 ]
Liu, Wenjin [6 ,7 ]
Jiang, Rulang [6 ,7 ]
Wolfe, Scot A. [4 ,5 ]
Wilson-Rawls, Jeanne [1 ]
Rawls, Alan [1 ,3 ]
机构
[1] Arizona State Univ, Sch Life Sci, Tempe, AZ 85287 USA
[2] Arizona State Univ, Mol & Cellular Biol Grad Program, Tempe, AZ 85287 USA
[3] Arizona State Univ, Ctr Evolutionary Med & Informat, Biodesign Inst, Tempe, AZ 85287 USA
[4] Univ Massachusetts, Med Ctr, Program Gene Funct & Express, Worcester, MA 01605 USA
[5] Univ Massachusetts, Med Ctr, Dept Biochem & Mol Pharmacol, Worcester, MA 01605 USA
[6] Univ Rochester, Sch Med & Dent, Dept Biomed Genet, Rochester, NY 14642 USA
[7] Univ Rochester, Sch Med & Dent, Ctr Oral Biol, Rochester, NY 14642 USA
基金
美国国家卫生研究院; 美国国家科学基金会;
关键词
GENE-EXPRESSION; NEGATIVE AUTOREGULATION; MOUSE DEVELOPMENT; SKELETAL-MUSCLE; FIBER-TYPE; SOX6; FAMILY; DIFFERENTIATION; IDENTIFICATION; SPECIFICITIES;
D O I
10.1074/jbc.M112.399386
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
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.
引用
收藏
页码:35351 / 35359
页数:9
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