TY - JOUR
T1 - Characterization of the DNA-binding properties of the Mohawk homeobox transcription factor
AU - Anderson, Douglas M.
AU - George, Rajani
AU - Noyes, Marcus B.
AU - Rowton, Megan
AU - Liu, Wenjin
AU - Jiang, Rulang
AU - Wolfe, Scot A.
AU - Wilson-Rawls, Jeanne
AU - Rawls, Alan
PY - 2012/10/12
Y1 - 2012/10/12
N2 - 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.
AB - 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.
UR - http://www.scopus.com/inward/record.url?scp=84867414332&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=84867414332&partnerID=8YFLogxK
U2 - 10.1074/jbc.M112.399386
DO - 10.1074/jbc.M112.399386
M3 - Article
C2 - 22923612
SN - 0021-9258
VL - 287
SP - 35351
EP - 35359
JO - Journal of Biological Chemistry
JF - Journal of Biological Chemistry
IS - 42
ER -