Regulation of human cardiac myosin heavy chain genes: The effect of catecholamine

The 5′-flanking regions of the α- and β-cardiac myosin heavy chain (MyHC) genes were excised from the cosmid human genomic clones using Hind III and Xbal for the α-MyHC gene, and the Hind III and Hind III sites for the β-MyHC gene. These fragments were linked to chloramphenicol acetyl transferase (C...

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Veröffentlicht in:Biochemical and biophysical research communications 1992-10, Vol.188 (2), p.547-553
Hauptverfasser: Chen, J.J., Wang, D.L., Shih, N.L., Hsu, K.H., Lien, W.P., Liew, C.C.
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Sprache:eng
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Zusammenfassung:The 5′-flanking regions of the α- and β-cardiac myosin heavy chain (MyHC) genes were excised from the cosmid human genomic clones using Hind III and Xbal for the α-MyHC gene, and the Hind III and Hind III sites for the β-MyHC gene. These fragments were linked to chloramphenicol acetyl transferase (CAT) vector to generate a chimeric fusion gene. These fusion genes were subsequently transfected to neonatal rat cardiac cultured cells to analyze the CAT activity. The α-MyHC gene is preferentially expressed as compared to the β-MyHC. In the presence of norepinephrine (NE) the β-MyHC gene is remarkably induced (within 24 hours following the addition of norepinephrine to the cardiocyte culture). However, the α-MyHC is also induced. Specific alpha andrenergic antagonists such as terazosin (Tz) partially suppressed both the α- and β-MyHC genes as revealed by the CAT activity. These findings suggest that catecholamine does activate the human cardiac MyHC genes but does not differentiate the specific expression of either the α- or β-MyHC genes.
ISSN:0006-291X
1090-2104
DOI:10.1016/0006-291X(92)91090-D