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Nat Commun. 2017 May 25;8:15332. doi: 10.1038/ncomms15332.

Tailing and degradation of Argonaute-bound small RNAs protect the genome from uncontrolled RNAi.

Author information

1
Department of Biochemistry, Gene Center, University of Munich, 81377 Munich, Germany.

Abstract

RNAi is a conserved mechanism in which small RNAs induce silencing of complementary targets. How Argonaute-bound small RNAs are targeted for degradation is not well understood. We show that the adenyl-transferase Cid14, a member of the TRAMP complex, and the uridyl-transferase Cid16 add non-templated nucleotides to Argonaute-bound small RNAs in fission yeast. The tailing of Argonaute-bound small RNAs recruits the 3'-5' exonuclease Rrp6 to degrade small RNAs. Failure in degradation of Argonaute-bound small RNAs results in accumulation of 'noise' small RNAs on Argonaute and targeting of diverse euchromatic genes by RNAi. To protect themselves from uncontrolled RNAi, cid14Δ cells exploit the RNAi machinery and silence genes essential for RNAi itself, which is required for their viability. Our data indicate that surveillance of Argonaute-bound small RNAs by Cid14/Cid16 and the exosome protects the genome from uncontrolled RNAi and reveal a rapid RNAi-based adaptation to stress conditions.

PMID:
28541282
PMCID:
PMC5458512
DOI:
10.1038/ncomms15332
[Indexed for MEDLINE]
Free PMC Article

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