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1 Department of Biology, Williams College, Williamstown, Massachusetts 01267; and 2 Program in Molecular Genetics, Ottawa Hospital Research Institute, Ottawa, Ontario K1H 8L6, Canada
A strong
correlative pattern between MyoD gene expression and myosin heavy chain
IIB (MHC IIB) gene expression exists. To test whether this correlative
relationship is causative, MHC gene expression in muscles from
MyoD(
/
) mice was analyzed. The MHC IIB gene was not detectable in
the MyoD(
/
) diaphragm, whereas the MHC IIB protein made up
10.0 ± 1.7% of the MHC protein pool in the wild-type (WT) mouse
diaphragm. Furthermore, the MHC IIA protein was not detectable in the
MyoD(
/
) biceps brachii, and the MHC IIB protein was overexpressed
in the masseter. To examine whether MyoD is required for the
upregulation of the MHC IIB gene within slow muscle after disuse,
MyoD(
/
) and WT hindlimb musculature was unweighted. MyoD(
/
)
exhibited a diminished response in the upregulation of the MHC IIB mRNA
within the soleus muscle as a result of the hindlimb unweighting.
Collectively, these data suggest that MyoD plays a role in the MHC
profile in a muscle-specific fashion.
basic helix-loop-helix; fiber type; transcription factor; myogenic regulatory factor
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