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J. Biol. Chem., Vol. 269, Issue 4, 2461-2467, 01, 1994
JP Merlie, J Mudd, TC Cheng and EN Olson
Several genes expressed in skeletal muscle are transcriptionally repressed
by electrical activity arising from motor innervation and are rapidly
induced following denervation. Among these are genes encoding the subunits
of the nicotinic acetylcholine receptor (AChR) and the myogenic
helix-loop-helix protein myogenin, which activates muscle- specific genes.
To understand how electrical activity arising from motor innervation is
converted into a transcriptional response, we have attempted to localize
cis-acting sequences in the AChR alpha subunit and myogenin genes
sufficient to direct activity-dependent transcription. Here we show that an
111-base pair and a 335-base pair region from the promoters of the AChR
alpha subunit and myogenin genes, respectively, can confer
activity-dependent regulation to a linked reporter gene in transgenic mice.
The presence of binding sites for myogenic helix-loop-helix proteins in
both of these regulatory regions is consistent with the hypothesis that
these myogenic regulators serve as nuclear targets for the signaling
cascade through which motor innervation leads to changes in gene
transcription in skeletal muscle.
Myogenin and acetylcholine receptor alpha gene promoters mediate transcriptional regulation in response to motor innervation
Department of Molecular Biology and Pharmacology, Washington University School of Medicine, St. Louis, Missouri 63110.
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