Literature DB >> 3431550

Differential patterns of transcript accumulation during human myogenesis.

P Gunning1, E Hardeman, R Wade, P Ponte, W Bains, H M Blau, L Kedes.   

Abstract

We evaluated the extent to which muscle-specific genes display identical patterns of mRNA accumulation during human myogenesis. Cloned satellite cells isolated from adult human skeletal muscle were expanded in culture, and RNA was isolated from low- and high-confluence cells and from fusing cultures over a 15-day time course. The accumulation of over 20 different transcripts was compared in these samples with that in fetal and adult human skeletal muscle. The expression of carbonic anhydrase 3, myoglobin, HSP83, and mRNAs encoding eight unknown proteins were examined in human myogenic cultures. In general, the expression of most of the mRNAs was induced after fusion to form myotubes. However, several exceptions, including carbonic anhydrase and myoglobin, showed no detectable expression in early myotubes. Comparison of all transcripts demonstrated little, if any, identity of mRNA accumulation patterns. Similar variability was also seen for mRNAs which were also expressed in nonmuscle cells. Accumulation of mRNAs encoding alpha-skeletal, alpha-cardiac, beta- and gamma-actin, total myosin heavy chain, and alpha- and beta-tubulin also displayed discordant regulation, which has important implications for sarcomere assembly. Cardiac actin was the only muscle-specific transcript that was detected in low-confluency cells and was the major alpha-actin mRNA at all times in fusing cultures. Skeletal actin was transiently induced in fusing cultures and then reduced by an order of magnitude. Total myosin heavy-chain mRNA accumulation lagged behind that of alpha-actin. Whereas beta- and gamma-actin displayed a sharp decrease after initiation of fusion and thereafter did not change, alpha- and beta-tubulin were transiently induced to a high level during the time course in culture. We conclude that each gene may have its own unique determinants of transcript accumulation and that the phenotype of a muscle may not be determined so much by which genes are active or silent but rather by the extent to which their transcript levels are modulated. Finally, we observed that patterns of transcript accumulation established within the myotube cultures were consistent with the hypothesis that myoblasts isolated from adult tissue recapitulate a myogenic developmental program. However, we also detected a transient appearance of adult skeletal muscle-specific transcripts in high-confluence myoblast cultures. This indicates that the initial differentiation of these myoblasts may reflect a more complex process than simple recapitulation of development.

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Year:  1987        PMID: 3431550      PMCID: PMC368081          DOI: 10.1128/mcb.7.11.4100-4114.1987

Source DB:  PubMed          Journal:  Mol Cell Biol        ISSN: 0270-7306            Impact factor:   4.272


  51 in total

1.  Intricate combinatorial patterns of exon splicing generate multiple regulated troponin T isoforms from a single gene.

Authors:  R E Breitbart; H T Nguyen; R M Medford; A T Destree; V Mahdavi; B Nadal-Ginard
Journal:  Cell       Date:  1985-05       Impact factor: 41.582

2.  The relationship between stress fiber-like structures and nascent myofibrils in cultured cardiac myocytes.

Authors:  A A Dlugosz; P B Antin; V T Nachmias; H Holtzer
Journal:  J Cell Biol       Date:  1984-12       Impact factor: 10.539

3.  Evolution of the human sarcomeric-actin genes: evidence for units of selection within the 3' untranslated regions of the mRNAs.

Authors:  P Gunning; T Mohun; S Y Ng; P Ponte; L Kedes
Journal:  J Mol Evol       Date:  1984       Impact factor: 2.395

4.  Expression of human cardiac actin in mouse L cells: a sarcomeric actin associates with a nonmuscle cytoskeleton.

Authors:  P Gunning; P Ponte; L Kedes; R J Hickey; A I Skoultchi
Journal:  Cell       Date:  1984-03       Impact factor: 41.582

5.  Analysis of cloned mRNA sequences encoding subfragment 2 and part of subfragment 1 of alpha- and beta-myosin heavy chains of rabbit heart.

Authors:  C J Kavinsky; P K Umeda; J E Levin; A M Sinha; J M Nigro; S Jakovcic; M Rabinowitz
Journal:  J Biol Chem       Date:  1984-03-10       Impact factor: 5.157

6.  alpha-Cardiac actin is the major sarcomeric isoform expressed in embryonic avian skeletal muscle.

Authors:  B M Paterson; J D Eldridge
Journal:  Science       Date:  1984-06-29       Impact factor: 47.728

7.  Synthesis and accumulation of myosin isozymes in tissue culture.

Authors:  R G Whalen; L B Bugaisky; G S Butler-Browne; M S Ecob; C Pinset
Journal:  Adv Exp Med Biol       Date:  1985       Impact factor: 2.622

8.  Cloning, expression in Escherichia coli, and reconstitution of human myoglobin.

Authors:  R Varadarajan; A Szabo; S G Boxer
Journal:  Proc Natl Acad Sci U S A       Date:  1985-09       Impact factor: 11.205

9.  Organization of the human myoglobin gene.

Authors:  P Weller; A J Jeffreys; V Wilson; A Blanchetot
Journal:  EMBO J       Date:  1984-02       Impact factor: 11.598

10.  Fate of microtubule-organizing centers during myogenesis in vitro.

Authors:  A M Tassin; B Maro; M Bornens
Journal:  J Cell Biol       Date:  1985-01       Impact factor: 10.539

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  39 in total

1.  Identification of skeletal muscle precursor cells in vivo by use of MyoD1 and myogenin probes.

Authors:  M D Grounds; K L Garrett; M C Lai; W E Wright; M W Beilharz
Journal:  Cell Tissue Res       Date:  1992-01       Impact factor: 5.249

2.  The human skeletal alpha-actin gene is regulated by a muscle-specific enhancer that binds three nuclear factors.

Authors:  G E Muscat; S Perry; H Prentice; L Kedes
Journal:  Gene Expr       Date:  1992

3.  Four sarcomeric myosin heavy chain genes are expressed by human fetal skeletal muscle cells differentiating in culture.

Authors:  R Feghali; I Karsch-Mizrachi; L A Leinwand; D S Kohtz
Journal:  Gene Expr       Date:  1992

4.  A combination of closely associated positive and negative cis-acting promoter elements regulates transcription of the skeletal alpha-actin gene.

Authors:  K L Chow; R J Schwartz
Journal:  Mol Cell Biol       Date:  1990-02       Impact factor: 4.272

5.  Involvement of a cell surface protein and an ecto-protein kinase in myogenesis.

Authors:  X Y Chen; T C Lo
Journal:  Biochem J       Date:  1991-10-15       Impact factor: 3.857

6.  Multiple 5'-flanking regions of the human alpha-skeletal actin gene synergistically modulate muscle-specific expression.

Authors:  G E Muscat; L Kedes
Journal:  Mol Cell Biol       Date:  1987-11       Impact factor: 4.272

7.  Myoblast transfer of human erythropoietin gene in a mouse model of renal failure.

Authors:  Y Hamamori; B Samal; J Tian; L Kedes
Journal:  J Clin Invest       Date:  1995-04       Impact factor: 14.808

8.  Context-dependent functional substitution of alpha-skeletal actin by gamma-cytoplasmic actin.

Authors:  Michele A Jaeger; Kevin J Sonnemann; Daniel P Fitzsimons; Kurt W Prins; James M Ervasti
Journal:  FASEB J       Date:  2009-03-11       Impact factor: 5.191

9.  A common factor regulates skeletal and cardiac alpha-actin gene transcription in muscle.

Authors:  G E Muscat; T A Gustafson; L Kedes
Journal:  Mol Cell Biol       Date:  1988-10       Impact factor: 4.272

10.  Identification of FHL1 as a regulator of skeletal muscle mass: implications for human myopathy.

Authors:  Belinda S Cowling; Meagan J McGrath; Mai-Anh Nguyen; Denny L Cottle; Anthony J Kee; Susan Brown; Joachim Schessl; Yaqun Zou; Josephine Joya; Carsten G Bönnemann; Edna C Hardeman; Christina A Mitchell
Journal:  J Cell Biol       Date:  2008-12-15       Impact factor: 10.539

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