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Originally published In Press as doi:10.1074/jbc.M008234200 on November 28, 2000

J. Biol. Chem., Vol. 276, Issue 10, 7500-7506, March 9, 2001
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The Dynamics of Myogenin Site-specific Demethylation Is Strongly Correlated with Its Expression and with Muscle Differentiation*

Marco Lucarelli, Andrea Fuso, Roberto Strom, and Sigfrido ScarpaDagger

From the Department of Cellular Biotechnologies and Hematology and I Department of Surgery, University of Rome "La Sapienza," Viale Regina Elena 324-00161 Rome, Italy

The molecular mechanisms underlying the activation of tissue-specific genes have not yet been fully clarified. We analyzed the methylation status of specific CCGG sites in the 5'-flanking region and exon 1 of myogenin gene, a very important myogenic differentiation factor. We demonstrated a loss of methylation, at the onset of C2C12 muscle cell line differentiation, limited to the CCGG site of myogenin 5'-flanking region, which was strongly correlated with the transcriptional activation of this gene and with myogenic differentiation. The same CCGG site was also found to be hypomethylated, in vivo, in embryonic mouse muscle (a myogenin-expressing tissue), as opposed to nonmuscle (nonexpressing) tissues that had a fully methylated site. In a C2C12-derived clone with enhanced myogenic ability, demethylation occurred within 2 h of induction of differentiation, suggesting the involvement of some active demethylation mechanism(s) that occur in the absence of DNA replication. Exposure to drugs that inhibit DNA methylation by acting on the S-adenosylmethionine metabolism produced a further reduction, to a few minutes, in the duration of the demethylation dynamics. These effects suggest that the final site-specific DNA methylation pattern of tissue-specific genes is defined through a continuous, relatively fast interplay between active DNA demethylation and re-methylation mechanisms.


* This work was supported by the University of Rome "La Sapienza," Progetti di Ateneo (1998) and by the 1998 National Program on AIDS.The costs of publication of this article were defrayed in part by the payment of page charges. The article must therefore be hereby marked "advertisement" in accordance with 18 U.S.C. Section 1734 solely to indicate this fact.

Dagger To whom correspondence should be addressed: Dept. Biotecnologie Cellulari ed Ematologia, c/o Laboratorio I Clinica Chirurgica, Via A. Scarpa 14, 00161 Rome, Italy. Tel.: 39-06-49766600; Fax: 39-06-49766606; E-mail: scarpa@bce.med.uniroma1.it.


Copyright © 2001 by The American Society for Biochemistry and Molecular Biology, Inc.


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