| Literature DB >> 29769402 |
Miguel Vasconcelos Almeida1, Sabrina Dietz2, Stefan Redl1, Emil Karaulanov3, Andrea Hildebrandt4, Christian Renz5, Helle D Ulrich5, Julian König4, Falk Butter2, René F Ketting6.
Abstract
Argonaute proteins and their associated small RNAs (sRNAs) are evolutionarily conserved regulators of gene expression. Gametocyte-specific factor 1 (Gtsf1) proteins, characterized by two tandem CHHC zinc fingers and an unstructured C-terminal tail, are conserved in animals and have been shown to interact with Piwi clade Argonautes, thereby assisting their activity. We identified the Caenorhabditis elegans Gtsf1 homolog, named it gtsf-1 and characterized it in the context of the sRNA pathways of C. elegans We report that GTSF-1 is not required for Piwi-mediated gene silencing. Instead, gtsf-1 mutants show a striking depletion of 26G-RNAs, a class of endogenous sRNAs, fully phenocopying rrf-3 mutants. We show, both in vivo and in vitro, that GTSF-1 interacts with RRF-3 via its CHHC zinc fingers. Furthermore, we demonstrate that GTSF-1 is required for the assembly of a larger RRF-3 and DCR-1-containing complex (ERIC), thereby allowing for 26G-RNA generation. We propose that GTSF-1 homologs may act to drive the assembly of larger complexes that act in sRNA production and/or in imposing sRNA-mediated silencing activities.Entities:
Keywords: zzm321990C. eleganszzm321990; zzm321990GTSFzzm321990; 26G‐RNA; RdRP; piRNA
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Year: 2018 PMID: 29769402 PMCID: PMC6003641 DOI: 10.15252/embj.201899325
Source DB: PubMed Journal: EMBO J ISSN: 0261-4189 Impact factor: 11.598