The expression of myosin genes in developing skeletal muscle in the mouse embryo
Journal Article
·
· Journal of Cell Biology; (USA)
- Pasteur Institute, Paris (France)
Using in situ hybridization, we have investigated the temporal sequence of myosin gene expression in the developing skeletal muscle masses of mouse embryos. The probes used were isoform-specific, 35S-labeled antisense cRNAs to the known sarcomeric myosin heavy chain and myosin alkali light chain gene transcripts. Results showed that both cardiac and skeletal myosin heavy chain and myosin light chain mRNAs were first detected between 9 and 10 d post coitum (p.c.) in the myotomes of the most rostral somites. Myosin transcripts appeared in more caudal somites at later stages in a developmental gradient. The earliest myosin heavy chain transcripts detected code for the embryonic skeletal (MHCemb) and beta-cardiac (MHC beta) isoforms. Perinatal myosin heavy chain (MHCpn) transcripts begin to accumulate at 10.5 d p.c., which is much earlier than previously reported. At this stage, MHCemb is the major MHC transcript. By 12.5 d p.c., MHCpn and MHCemb mRNAs are present to an equal extent, and by 15.5 d p.c. the MHCpn transcript is the major MHC mRNA detected. Cardiac MHC beta transcripts are always present as a minor component. In contrast, the cardiac MLC1A mRNA is initially more abundant than that encoding the skeletal MLC1F isoform. By 12.5 d p.c. the two MLC mRNAs are present at similar levels, and by 15.5 d p.c., MLC1F is the predominant MLC transcript detected. Transcripts for the ventricular/slow (MLC1V) and another fast skeletal myosin light chain (MLC3F) are not detected in skeletal muscle before 15 d p.c., which marks the beginning of the fetal stage of muscle development. This is the first stage at which we can detect differences in expression of myosin genes between developing muscle fibers. We conclude that, during the development of the myotome and body wall muscles, different myosin genes follow independent patterns of activation and acculumation.
- OSTI ID:
- 6324229
- Journal Information:
- Journal of Cell Biology; (USA), Journal Name: Journal of Cell Biology; (USA) Vol. 111:4; ISSN 0021-9525; ISSN JCLBA
- Country of Publication:
- United States
- Language:
- English
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Related Subjects
550201* -- Biochemistry-- Tracer Techniques
550801 -- Morphology-- Tracer Techniques
59 BASIC BIOLOGICAL SCIENCES
ANIMALS
BETA DECAY RADIOISOTOPES
BETA-MINUS DECAY RADIOISOTOPES
BODY
CARDIOVASCULAR SYSTEM
DAYS LIVING RADIOISOTOPES
DNA HYBRIDIZATION
EMBRYOS
EVEN-ODD NUCLEI
GENE REGULATION
GLOBULINS
HEART
HYBRIDIZATION
ISOENZYMES
ISOTOPE APPLICATIONS
ISOTOPES
LIGHT NUCLEI
MAMMALS
MESSENGER-RNA
MICE
MUSCLES
MYOSIN
NUCLEI
NUCLEIC ACIDS
NUCLEOPROTEINS
ORGANIC COMPOUNDS
ORGANS
PHENOTYPE
PROTEINS
RADIOISOTOPES
RNA
RODENTS
SULFUR 35
SULFUR ISOTOPES
TRACER TECHNIQUES
TRANSCRIPTION FACTORS
VERTEBRATES
550801 -- Morphology-- Tracer Techniques
59 BASIC BIOLOGICAL SCIENCES
ANIMALS
BETA DECAY RADIOISOTOPES
BETA-MINUS DECAY RADIOISOTOPES
BODY
CARDIOVASCULAR SYSTEM
DAYS LIVING RADIOISOTOPES
DNA HYBRIDIZATION
EMBRYOS
EVEN-ODD NUCLEI
GENE REGULATION
GLOBULINS
HEART
HYBRIDIZATION
ISOENZYMES
ISOTOPE APPLICATIONS
ISOTOPES
LIGHT NUCLEI
MAMMALS
MESSENGER-RNA
MICE
MUSCLES
MYOSIN
NUCLEI
NUCLEIC ACIDS
NUCLEOPROTEINS
ORGANIC COMPOUNDS
ORGANS
PHENOTYPE
PROTEINS
RADIOISOTOPES
RNA
RODENTS
SULFUR 35
SULFUR ISOTOPES
TRACER TECHNIQUES
TRANSCRIPTION FACTORS
VERTEBRATES