Literature DB >> 2447874

Proto-oncogene expression in proliferating and differentiating cardiac and skeletal muscle.

W C Claycomb1, N A Lanson.   

Abstract

We have examined the expression of 13 proto-oncogenes in proliferating and terminally differentiated cardiac and skeletal muscle. Total RNA was prepared from intact ventricular cardiac-muscle tissue and from purified ventricular cardiac-muscle cells of neonatal and adult rats and from cultured proliferating and terminally differentiated L6A1 rat skeletal-muscle cells. cDNA probes for histone H4, thymidine kinase, myosin heavy chain and M-creatine kinase were used to assess cellular proliferation and differentiation. Oncogenes c-myc, c-raf, c-erb-A, c-ras-H, c-ski, and c-sis were expressed in both proliferating and differentiated cardiac muscle tissue and cells, whereas c-myb expression was not observed in either. c-src was expressed only in neonatal cardiac muscle tissue and cells. c-fms, c-abl, and c-ras-K were expressed in tissue from both neonatal and adult animals but only in purified cells from neonatal animals. c-fes/fps was expressed only in neonatal cardiac muscles cells. c-fos expression was not observed in cardiac-muscle tissue from either neonatal or adult rats, but surprisingly was abundantly expressed in freshly isolated cardiac-muscle cells from animals of both ages. These results emphasize that biochemical analysis using intact cardiac-muscle tissue may not necessarily reflect muscle-specific cell processes. They also show that the expression of c-fos can be activated by the cell isolation procedure. c-myc, c-ski, c-ras-H, c-ras-K, c-abl, c-raf and c-erb-A were expressed in both proliferating and terminally differentiated skeletal-muscle cells, whereas c-myb, c-fos, c-src and c-fms transcripts were observed only in proliferating cells. c-fes/fps and c-sis were not expressed in dividing or fused skeletal-muscle cells. These results demonstrate unique tissue and cell-specific patterns of proto-oncogene expression and suggest that these genes may be involved with the regulation of cellular proliferation and terminal differentiation in striated muscle.

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Year:  1987        PMID: 2447874      PMCID: PMC1148469          DOI: 10.1042/bj2470701

Source DB:  PubMed          Journal:  Biochem J        ISSN: 0264-6021            Impact factor:   3.857


  34 in total

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Journal:  Adv Exp Med Biol       Date:  1983       Impact factor: 2.622

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Authors:  H D Bradshaw
Journal:  Proc Natl Acad Sci U S A       Date:  1983-09       Impact factor: 11.205

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  9 in total

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6.  Hypertrophic stimuli induce transforming growth factor-beta 1 expression in rat ventricular myocytes.

Authors:  N Takahashi; A Calderone; N J Izzo; T M Mäki; J D Marsh; W S Colucci
Journal:  J Clin Invest       Date:  1994-10       Impact factor: 14.808

7.  Expression of c-myc and c-fos in rat skeletal muscle. Evidence for increased levels of c-myc mRNA during hypertrophy.

Authors:  P F Whitelaw; J E Hesketh
Journal:  Biochem J       Date:  1992-01-01       Impact factor: 3.857

8.  Atrial-natriuretic-factor mRNA is developmentally regulated in heart ventricles and actively expressed in cultured ventricular cardiac muscle cells of rat and human.

Authors:  W C Claycomb
Journal:  Biochem J       Date:  1988-10-15       Impact factor: 3.857

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  9 in total

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