Literature DB >> 8174768

The E box is essential for activity of the cardiac actin promoter in skeletal but not in cardiac muscle.

I S Skerjanc1, M W McBurney.   

Abstract

The sequence CANNTG (E box) is frequently found in the promoters of muscle-specific genes and binds members of the basic helix-loop-helix (bHLH) family of transcription factors. We compared the need for the E box in the expression of a muscle-specific promoter normally expressed in both cardiac and skeletal muscle. The E box was mutated in a construct of the cardiac alpha-actin promoter driving the Escherichia coli lacZ gene. The wild-type and mutant constructs were transfected and stably integrated into the genomes of P19 embryonal carcinoma cells. The wild-type promoter was expressed in both cardiac and skeletal myocytes. The promoter lacking an E box was expressed in cardiac but not in skeletal muscle. Neither promoter was active in nonmuscle cells. Thus the E box is not necessary for the cardiac actin promoter activity in P19-derived cardiac muscle but is essential for its activity in skeletal muscle. This result is consistent with our inability to detect cardiac muscle-specific members of the MyoD family of bHLH transcription factors.

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Year:  1994        PMID: 8174768     DOI: 10.1006/dbio.1994.1128

Source DB:  PubMed          Journal:  Dev Biol        ISSN: 0012-1606            Impact factor:   3.582


  9 in total

1.  Factors in serum regulate muscle development in P19 cells.

Authors:  S Wilton; I Skerjanc
Journal:  In Vitro Cell Dev Biol Anim       Date:  1999-04       Impact factor: 2.416

2.  Factors in serum regulate Nkx2.5 and MEF2C function.

Authors:  M Jamali; C Karamboulas; S Wilton; I S Skerjanc
Journal:  In Vitro Cell Dev Biol Anim       Date:  2001 Nov-Dec       Impact factor: 2.416

3.  Analysis of muscle creatine kinase gene regulatory elements in skeletal and cardiac muscles of transgenic mice.

Authors:  D B Donoviel; M A Shield; J N Buskin; H S Haugen; C H Clegg; S D Hauschka
Journal:  Mol Cell Biol       Date:  1996-04       Impact factor: 4.272

4.  Functional characterization of a promoter polymorphism that drives ACSL5 gene expression in skeletal muscle and associates with diet-induced weight loss.

Authors:  Allen C T Teng; Kristi Adamo; Frédérique Tesson; Alexandre F R Stewart
Journal:  FASEB J       Date:  2009-02-13       Impact factor: 5.191

5.  Differences between MyoD DNA binding and activation site requirements revealed by functional random sequence selection.

Authors:  J Huang; T K Blackwell; L Kedes; H Weintraub
Journal:  Mol Cell Biol       Date:  1996-07       Impact factor: 4.272

6.  Cellular aggregation enhances MyoD-directed skeletal myogenesis in embryonal carcinoma cells.

Authors:  I S Skerjanc; R S Slack; M W McBurney
Journal:  Mol Cell Biol       Date:  1994-12       Impact factor: 4.272

7.  Oxytocin-Gly-Lys-Arg: a novel cardiomyogenic peptide.

Authors:  Bogdan A Danalache; Jolanta Gutkowska; Magdalena J Slusarz; Irena Berezowska; Marek Jankowski
Journal:  PLoS One       Date:  2010-10-26       Impact factor: 3.240

8.  Regulation of the murine alpha B-crystallin/small heat shock protein gene in cardiac muscle.

Authors:  R Gopal-Srivastava; J I Haynes; J Piatigorsky
Journal:  Mol Cell Biol       Date:  1995-12       Impact factor: 4.272

9.  Retinoic acid enhances skeletal muscle progenitor formation and bypasses inhibition by bone morphogenetic protein 4 but not dominant negative beta-catenin.

Authors:  Karen A M Kennedy; Tammy Porter; Virja Mehta; Scott D Ryan; Feodor Price; Vian Peshdary; Christina Karamboulas; Josée Savage; Thomas A Drysdale; Shun-Cheng Li; Steffany A L Bennett; Ilona S Skerjanc
Journal:  BMC Biol       Date:  2009-10-08       Impact factor: 7.364

  9 in total

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