A non-canonical E-box within the MyoD core enhancer is necessary for circadian expression in skeletal muscle

• Published in: Nucleic acids research 2012-04, Vol.40 (8), p.3419-3430
• Main Authors: Zhang, Xiping, Patel, Samir P, McCarthy, John J, Rabchevsky, Alexander G, Goldhamer, David J, Esser, Karyn A
• Format: Article
• Language: English
• Subjects: Animals; ARNTL Transcription Factors - metabolism; BMAL1 protein; Brain; Cell Line; Cell Respiration - genetics; Circadian Rhythm - genetics; Circadian rhythms; CLOCK protein; CLOCK Proteins - genetics; CLOCK Proteins - metabolism; Differentiation; E-Box Elements; Enhancers; Gene expression; Gene Expression Regulation; Gene Regulation, Chromatin and Epigenetics; Informatics; Mice; Mice, Inbred C57BL; Mitochondria; Mitochondria, Muscle - metabolism; Muscle Fibers, Skeletal - metabolism; Muscle, Skeletal - metabolism; Mutation; MyoD gene; MyoD protein; MyoD Protein - genetics; MyoD Protein - metabolism; myogenesis; Oscillations; Respiration; Respiratory function; Skeletal muscle; Transcription factors
• ISSN: 0305-1048; 1362-4962
• DOI: 10.1093/nar/gkr1297

The myogenic differentiation 1 (MyoD) gene is a master regulator of myogenesis. We previously reported that the expression of MyoD mRNA oscillates over 24 h in skeletal muscle and that the circadian clock transcription factors, BMAL1 (brain and muscle ARNT-like 1) and CLOCK (circadian locomotor output cycles kaput), were bound to the core enhancer (CE) of the MyoD gene in vivo. In this study, we provide in vivo and in vitro evidence that the CE is necessary for circadian expression of MyoD in adult muscle. Gel shift assays identified a conserved non-canonical E-box within the CE that is bound by CLOCK and BMAL1. Functional analysis revealed that this E-box was required for full activation by BMAL1/CLOCK and for in vitro circadian oscillation. Expression profiling of muscle of CE(loxP/loxP) mice found approximately 1300 genes mis-expressed relative to wild-type. Based on the informatics results, we analyzed the respiratory function of mitochondria isolated from wild-type and CE(loxP/loxP) mice. These assays determined that State 5 respiration was significantly reduced in CE(loxP/loxP) muscle. The results of this work identify a novel element in the MyoD enhancer that confers circadian regulation to MyoD in skeletal muscle and suggest that loss of circadian regulation leads to changes in myogenic expression and downstream mitochondrial function.