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J. Biol. Chem., Vol. 276, Issue 10, 7500-7506, March 9, 2001
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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.
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.
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