TY - JOUR
T1 - Differential expression of muscle regulatory factor genes in normal and denervated adult rat hindlimb muscles
AU - Voytik, Sherry L.
AU - Przyborski, Maryjo
AU - Badylak, Stephen F.
AU - Konieczny, Stephen F.
PY - 1993/11
Y1 - 1993/11
N2 - Skeletal muscle represents an excellent model system in which to examine regulatory mechanisms that modulate gene expression in the mature adult organism. Individual muscle fibers can be categorized as fast‐ or slow‐twitch based upon several physiological and molecular criteria, including metabolic enzyme activity and contractile protein isoforms. Each property can be influenced by a variety of factors such as changes in motor neuron activity or alterations in hormone levels, although the molecular pathways by which environmental factors affect gene expression remain largely unknown. As a first step in identifying potential regulators of fiber‐type diversity, the expression patterns of four basic/helix‐loop‐helix muscle regulatory factors (MRFs), referred to as MyoD, myogenin, Myf‐5, and MRF4, were examined in normal adult rat muscles which differed in their phenotypic properties. As expected, all four MRFs were expressed at detectable levels in the muscles studied. However, different muscles accumulated different proportions and combinations of MRF transcripts. For example, myogenin expression was maximally detected in slow‐twitch muscles whereas MyoD transcripts were found predominantly in muscles exhibiting a fast‐twitch phenotype. Induced phenotypic changes in two fast‐twitch muscles via denervation lead to a large and rapid increase in transcript levels of all four MRFs as early as 24 hr following denervation, with myogenin transcripts approaching 150–200‐fold higher levels than innervated contralateral muscles within 7 days. These results suggest that myogenin, as well as the other three MRFs, may be involved in both the initial establishment as well as maintenance of fiber‐type diversity in the developing organism. © 1993 Wiley‐Liss, Inc.
AB - Skeletal muscle represents an excellent model system in which to examine regulatory mechanisms that modulate gene expression in the mature adult organism. Individual muscle fibers can be categorized as fast‐ or slow‐twitch based upon several physiological and molecular criteria, including metabolic enzyme activity and contractile protein isoforms. Each property can be influenced by a variety of factors such as changes in motor neuron activity or alterations in hormone levels, although the molecular pathways by which environmental factors affect gene expression remain largely unknown. As a first step in identifying potential regulators of fiber‐type diversity, the expression patterns of four basic/helix‐loop‐helix muscle regulatory factors (MRFs), referred to as MyoD, myogenin, Myf‐5, and MRF4, were examined in normal adult rat muscles which differed in their phenotypic properties. As expected, all four MRFs were expressed at detectable levels in the muscles studied. However, different muscles accumulated different proportions and combinations of MRF transcripts. For example, myogenin expression was maximally detected in slow‐twitch muscles whereas MyoD transcripts were found predominantly in muscles exhibiting a fast‐twitch phenotype. Induced phenotypic changes in two fast‐twitch muscles via denervation lead to a large and rapid increase in transcript levels of all four MRFs as early as 24 hr following denervation, with myogenin transcripts approaching 150–200‐fold higher levels than innervated contralateral muscles within 7 days. These results suggest that myogenin, as well as the other three MRFs, may be involved in both the initial establishment as well as maintenance of fiber‐type diversity in the developing organism. © 1993 Wiley‐Liss, Inc.
KW - Denervation
KW - Fast‐twitch muscle
KW - MRF4
KW - Muscle regulatory factor
KW - Myf‐5
KW - MyoD
KW - Myogenin
KW - Rat muscle
KW - Slow‐twitch muscle
UR - http://www.scopus.com/inward/record.url?scp=0027722905&partnerID=8YFLogxK
U2 - 10.1002/aja.1001980307
DO - 10.1002/aja.1001980307
M3 - Article
C2 - 8136525
AN - SCOPUS:0027722905
SN - 1058-8388
VL - 198
SP - 214
EP - 224
JO - Developmental Dynamics
JF - Developmental Dynamics
IS - 3
ER -