Published
in: Mammalian Genome: 11:347-355 (May 5, 2000):
"Reactivation of Heritably Silenced Gene Expression in Mice".
Heidi G.E. Sutherland, Margot Kearns, Hugh D. Morgan,
Alexander P. Headley, Christine Morris, David I.K. Martin, Emma Whitelaw
Abstract
Epigenetic modifications that suppress gene activity in mammals are
generally considered to be cleared in the germline, restoring totipotency
of the genome. Here we report the germline inheritance of transcriptional
silencing in mice, and reversion to activity after as many as three generations
in the silent state. In a series of lines made with a LacZ transgene, one
line exhibits variable expressivity: genotypically identical littermates
have proportions of beta-Gal-positive erythrocytes that vary over at least
four orders of magnitude, and in some offspring expression is completely
silenced. The silent state of the transgene is inherited for multiple generations
in the founder strain irrespective of the sex of the parent, implying maintenance
of the epigenetic state through meiosis. Crosses of silenced mice with
C57BL/6 mice result in reactivation of the transgene in approximately a
third of F1 littermates. The silencing involves a stochastic,
all-or-none mechanism. Furthermore, silencing is transcriptional and correlates
with methylation of the transgene as well as an inaccessible chromatin
structure; these changes are reversed when expression is reactivated. This
work supports the notion that silent genetic information in mammals can
be inherited and later reactivated, and implies a mode of phenotypic inheritance
that is less stable than Mendelian inheritance.
Additional References:
1. "RNAi: Double-Stranded
RNA Directs the ATP-Dependent Cleavage of mRNA at 21 to 23 Nucleotide Intervals".
2. "Oncogenes
as Molecular Targets within Active Chromatin".
3. "Nuclear RNA
Species Activate DNA Transcription within Chromatin".
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euchromatin: "the most active portion of the genome within the cell
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