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Mol. Cell. Biol., 05 1995, 2707-2718, Vol 15, No. 5
PS Naidu, DC Ludolph, RQ To, TJ Hinterberger and SF Konieczny
The basic helix-loop-helix muscle regulatory factor (MRF) gene family
encodes four distinct muscle-specific transcription factors known as MyoD,
myogenin, Myf-5, and MRF4. These proteins represent key regulatory factors
that control many aspects of skeletal myogenesis. Although the MRFs often
exhibit overlapping functional activities, their distinct expression
patterns during embryogenesis suggest that each protein plays a unique role
in controlling aspects of muscle development. As a first step in
determining how MRF4 gene expression is developmentally regulated, we
examined the ability of the MRF4 gene to be expressed in a muscle-specific
fashion in vitro. Our studies show that the proximal MRF4 promoter contains
sufficient information to direct muscle-specific expression. Located within
the proximal promoter are a single MEF2 site and E box that are required
for maximum MRF4 expression. Mutation of the MEF2 site or E box severely
impairs the ability of this promoter to produce a muscle-specific response.
In addition, the MEF2 site and E box function in concert to synergistically
activate the MRF4 gene in nonmuscle cells coexpressing MEF2 and myogenin
proteins. Thus, the MRF4 promoter is regulated by the MEF2 and basic
helix-loop-helix MRF protein family through a cross- regulatory circuitry.
Surprisingly, the MRF4 promoter itself is not transactivated by MRF4,
suggesting that this MRF gene is not subject to an autoregulatory pathway
as previously implied by other studies. Understanding the molecular
mechanisms regulating expression of each MRF gene is central to fully
understanding how these factors control developmental events.
Copyright © 1995, American Society for Microbiology
Myogenin and MEF2 function synergistically to activate the MRF4 promoter during myogenesis
Department of Biological Sciences, Purdue University, West Lafayette, Indiana 47907, USA.
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