Abstract
Retrotransposons and repetitive DNA elements in eukaryotes are silenced by small RNA-directed heterochromatin formation. In Arabidopsis, this process involves 24-nt siRNAs that bind to ARGONAUTE4 (AGO4) and facilitate the targeting of complementary loci via unknown mechanisms. Nuclear RNA polymerase V (Pol V) is an RNA silencing enzyme recently shown to generate noncoding transcripts at loci silenced by 24-nt siRNAs. We show that AGO4 physically interacts with these Pol V transcripts and is thereby recruited to the corresponding chromatin. We further show that DEFECTIVE IN MERISTEM SILENCING3 (DMS3), a structural maintenance of chromosomes (SMC) hinge-domain protein, functions in the assembly of Pol V transcription initiation or elongation complexes. Collectively, our data suggest that AGO4 is guided to target loci through base-pairing of associated siRNAs with nascent Pol V transcripts.
MeSH Terms
Arabidopsis/enzymology,genetics,metabolism
Arabidopsis Proteins/genetics,metabolism
Argonaute Proteins
Chromatin/metabolism
Chromosomal Proteins, Non-Histone/genetics,metabolism
DNA-Directed RNA Polymerases/metabolism
Models, Biological
RNA, Small Interfering/metabolism
Transcription, Genetic
Chemicals
AGO4 protein, Arabidopsis
Arabidopsis Proteins
Argonaute Proteins
Chromatin
Chromosomal Proteins, Non-Histone
DMS3 protein, Arabidopsis
RNA, Small Interfering
RNA polymerase V, Arabidopsis
DNA-Directed RNA Polymerases
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Wierzbicki Andrzej T
Biology Department, Washington University, St. Louis, Missouri, USA.
Ream Thomas S
Haag Jeremy R
Pikaard Craig S
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