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J Biol Chem, Vol. 274, Issue 17, 12095-12102, April 23, 1999
The CACC Box and Myocyte Enhancer Factor-2 Sites within the
Myosin Light Chain 2 Slow Promoter Cooperate in Regulating
Nerve-specific Transcription in Skeletal Muscle
Karyn
Esser ,
Tricia
Nelson¶,
Valerie
Lupa-Kimball , and
Eric
Blough ¶
From the School of Kinesiology and the
¶ Department of Physiology and Biophysics, University of Illinois
at Chicago, Illinois 60608
Previous experiments showed that activity of the
800-base pair MLC2slow promoter was 75-fold higher in the
innervated soleus (SOL) compared with the noninnervated SOL muscles.
Using in vivo DNA injection of MLC2slow promoter-luciferase
constructs, the aim of this project was to identify regulatory sites
and potential transcription factors important for slow
nerve-dependent gene expression. Three sites within the
proximal promoter (myocyte enhancer factor-2 (MEF2), E-box, and CACC
box) were individually mutated, and the effect on luciferase expression
was determined. There was no change in luciferase expression in the SOL
and extensor digitorum longus (EDL) muscles when the E-box was mutated.
In contrast, the MEF2 mutation resulted in a 30-fold decrease in expression in the innervated SOL muscles (10.3 versus 0.36 normalized relative light units (RLUs)). Transactivation of the
MLC2slow promoter by overexpressing MEF2 was only seen in
the innervated SOL (676,340 versus 2,225,957 RLUs;
p < 0.01) with no effect in noninnervated SOL or EDL
muscles. These findings suggest that the active MLC2slow
promoter is sensitive to MEF2 levels, but MEF2 levels alone do not
determine nerve-dependent expression. Mutation of the CACC
box resulted in a significant up-regulation in the EDL muscles (0.23 versus 4.08 normalized RLUs). With the CACC box mutated,
overexpression of MEF2 was sufficient to transactivate the MLC2slow
promoter in noninnervated SOL muscles (27,536 versus 1,605,797 RLUs). Results from electrophoretic mobility shift and supershift assays confirm MEF2 protein binding to the MEF2 site and
demonstrate specific binding to the CACC sequence. These results suggest a model for nerve-dependent regulation of the
MLC2slow promoter in which derepression occurs through the
CACC box followed by quantitative expression through enhanced MEF2 activation.
Copyright © 1999 by The American Society for Biochemistry and Molecular Biology, Inc.

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Copyright © 1999 by the American Society for Biochemistry and Molecular Biology.
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