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Molecular and Cellular Biology, March 2001, p. 1953-1961, Vol. 21, No. 6
0270-7306/01/$04.00+0 DOI: 10.1128/MCB.21.6.1953-1961.2001
Copyright © 2001, American Society for Microbiology. All rights reserved.
A Truncated Form of the Human CAF-1 p150 Subunit Impairs the
Maintenance of Transcriptional Gene Silencing in Mammalian
Cells
Thierry
Tchénio,
Jean-François
Casella, and
Thierry
Heidmann
Unité des Rétrovirus
Endogènes et Eléments Rétroïdes des
Eucaryotes Supérieurs, CNRS UMR 1573, Institut Gustave
Roussy, 94805 Villejuif, France
Received 21 August 2000/Returned for modification 19 September
2000/Accepted 15 December 2000
Chromatin assembly factor 1 (CAF-1) is a protein complex
formed of three subunits, p150, p60, and p48, conserved
from the yeast Saccharomyces cerevisiae to humans, which
can promote nucleosome assembly onto newly replicated DNA. In S.
cerevisiae, deletion of the genes encoding any of the three
CAF-1 subunits (cac
mutants), although nonlethal,
results in a silencing defect of genes packaged into heterochromatin.
Here we report on a mammalian cell model that we devised to monitor
gene silencing and its reversal in a quantitative manner. This model
relies on the use of a cell line stably transfected with a reporter
gene in a silenced state. Reversal of reporter gene silencing was
achieved upon treatment of the cells with 5-azacytidine, which resulted
in the demethylation of the reporter gene copies. We show that
expression of a cDNA for the human p150 CAF-1 subunit harboring 5'
truncations, but not that of a cDNA encoding the full-length p150 CAF-1
subunit, increases by more than 500-fold the frequency at which
transcriptional silencing of the reporter gene copies is reversed in
these cells. Reversal of gene silencing is dependent upon expression of
a truncated protein, possibly acting as a dominant negative mutant
of the wild-type CAF-1, is associated with alterations in chromatin
structure as measured by an endonuclease sensitivity
assay and is not associated with detectable changes in the methylation
status of the silenced genes. These results suggest that the role
of CAF-1 in the epigenetic control of gene expression
has been conserved between yeast and mammals, despite the lack of DNA
methylation in yeast chromatin.
Molecular and Cellular Biology, March 2001, p. 1953-1961, Vol. 21, No. 6
0270-7306/01/$04.00+0 DOI: 10.1128/MCB.21.6.1953-1961.2001
Copyright © 2001, American Society for Microbiology. All rights reserved.
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