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Molecular Cell
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Molecular Cell
Article . 2008
License: Elsevier Non-Commercial
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Molecular Cell
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Multimegabase Silencing in Nucleolar Dominance Involves siRNA-Directed DNA Methylation and Specific Methylcytosine-Binding Proteins

Authors: Preuss, Sasha B.; Costa-Nunes, Pedro; Tucker, Sarah; Pontes, Olga; Lawrence, Richard J.; Mosher, Rebecca; Kasschau, Kristin D.; +4 Authors

Multimegabase Silencing in Nucleolar Dominance Involves siRNA-Directed DNA Methylation and Specific Methylcytosine-Binding Proteins

Abstract

In genetic hybrids, the silencing of nucleolar rRNA genes inherited from one progenitor is the epigenetic phenomenon known as nucleolar dominance. An RNAi knockdown screen identified the Arabidopsis de novo cytosine methyltransferase, DRM2, and the methylcytosine binding domain proteins, MBD6 and MBD10, as activities required for nucleolar dominance. MBD10 localizes throughout the nucleus, but MBD6 preferentially associates with silenced rRNA genes and does so in a DRM2-dependent manner. DRM2 methylation is thought to be guided by siRNAs whose biogenesis requires RNA-DEPENDENT RNA POLYMERASE 2 (RDR2) and DICER-LIKE 3 (DCL3). Consistent with this hypothesis, knockdown of DCL3 or RDR2 disrupts nucleolar dominance. Collectively, these results indicate that in addition to directing the silencing of retrotransposons and noncoding repeats, siRNAs specify de novo cytosine methylation patterns that are recognized by MBD6 and MBD10 in the large-scale silencing of rRNA gene loci.

Keywords

Arabidopsis Proteins, Arabidopsis, Cell Biology, DNA Methylation, Models, Biological, Protein Structure, Tertiary, Cytosine, Protein Transport, RNA, Plant, RNA, Ribosomal, Heterochromatin, Nucleolus Organizer Region, DNA, Intergenic, RNA Interference, DNA (Cytosine-5-)-Methyltransferases, Gene Silencing, RNA, Small Interfering, Molecular Biology, Base Pairing, Cell Nucleolus, Protein Binding

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    influence
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    This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
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selected citations
These citations are derived from selected sources.
This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Citations provided by BIP!
popularity
This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
BIP!Popularity provided by BIP!
influence
This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Influence provided by BIP!
impulse
This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
BIP!Impulse provided by BIP!
125
Top 10%
Top 10%
Top 10%
hybrid