MyoD induces myogenic differentiation through cooperation of its NH2- and COOH-terminal regions

• DOI: 10.1083/jcb.200502101
• Publication Date: 2005-11-07T20:02:47Z
• Authors: Jeff Ishibashi; Robert L. Perry; Atsushi Asakura; Michael A. Rudnicki
• Keywords: Mice, Knockout; Transcriptional Activation; 0303 health sciences; Cell Differentiation; Protein Structure, Tertiary; Myoblasts; Mice; 03 medical and health sciences; Gene Expression Regulation; Animals; Myogenic Regulatory Factor 5; Muscle, Skeletal; Research Articles; Cells, Cultured; Cell Proliferation; MyoD Protein; Oligonucleotide Array Sequence Analysis

MyoD and Myf5 are basic helix-loop-helix transcription factors that play key but redundant roles in specifying myogenic progenitors during embryogenesis. However, there are functional differences between the two transcription factors that impact myoblast proliferation and differentiation. Target gene activation could be one such difference. We have used microarray and polymerase chain reaction approaches to measure the induction of muscle gene expression by MyoD and Myf5 in an in vitro model. In proliferating cells, MyoD and Myf5 function very similarly to activate the expression of likely growth phase target genes such as L-myc, m-cadherin, Mcpt8, Runx1, Spp1, Six1, IGFBP5, and Chrnβ1. MyoD, however, is strikingly more effective than Myf5 at inducing differentiation-phase target genes. This distinction between MyoD and Myf5 results from a novel and unanticipated cooperation between the MyoD NH2- and COOH-terminal regions. Together, these results support the notion that Myf5 functions toward myoblast proliferation, whereas MyoD prepares myoblasts for efficient differentiation.