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PMID: 11171584 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Mutation of the IIB myosin heavy chain gene results in muscle fiber loss and compensatory hypertrophy.

American journal of physiology. Cell physiology ·Vol. 280 ·No. 3 ·2001-03-00 ·Pages C637-45

Allen DL, Harrison BC, Sartorius C, Byrnes WC, Leinwand LA

Abstract

The fast skeletal IIb gene is the source of most myosin heavy chain (MyHC) in adult mouse skeletal muscle. We have examined the effects of a null mutation in the IIb MyHC gene on the growth and morphology of mouse skeletal muscle. Loss in muscle mass of several head and hindlimb muscles correlated with amounts of IIb MyHC expressed in that muscle in wild types. Decreased mass was accompanied by decreases in mean fiber number, and immunological and ultrastructural studies revealed fiber pathology. However, mean cross-sectional area was increased in all fiber types, suggesting compensatory hypertrophy. Loss of muscle and body mass was not attributable to impaired chewing, and decreased food intake as a softer diet did not prevent the decrease in body mass. Thus loss of the major MyHC isoform produces fiber loss and fiber pathology reminiscent of muscle disease.

MeSH Terms
Adaptation, Physiological Animals Body Weight Feeding Behavior/physiology Hypertrophy Male Mice Motor Activity/physiology Muscle Fibers, Skeletal/pathology,ultrastructure Muscle, Skeletal/pathology Mutation/physiology Myosin Heavy Chains/genetics Organ Size Protein Isoforms/genetics Reference Values
Chemicals
Protein Isoforms Myosin Heavy Chains
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Allen D L
Department of Molecular, Cellular, and Developmental Biology, University of Colorado, Boulder, Colorado 80309, USA.
Harrison B C
Sartorius C
Byrnes W C
Leinwand L A
Article Info
Journal
American journal of physiology. Cell physiology
Abbr.
Am J Physiol Cell Physiol
ISSN
0363-6143
Published
2001-03-00
Pages
C637-45
Language
English
Region
United States
NLM ID
100901225
Subset
IM
Grants
NIGMS NIH HHS · R01 GM-29090-17 · United States
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