GTSF‐1 is required for formation of a functional RNA‐dependent RNA Polymerase complex in Caenorhabditis elegans |
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Authors: | Miguel Vasconcelos Almeida Sabrina Dietz Stefan Redl Emil Karaulanov Andrea Hildebrandt Christian Renz Helle D Ulrich Julian König Falk Butter René F Ketting |
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Affiliation: | 1. Biology of Non‐coding RNA Group, Institute of Molecular Biology, Mainz, Germany;2. Quantitative Proteomics Group, Institute of Molecular Biology, Mainz, Germany;3. Bioinformatics Core Facility, Institute of Molecular Biology, Mainz, Germany;4. Genomic Views of Splicing Regulation Group, Institute of Molecular Biology, Mainz, Germany;5. Maintenance of Genome Stability Group, Institute of Molecular Biology, Mainz, Germany |
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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. |
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Keywords: | 26G‐RNA
C.  elegans
GTSF
piRNA RdRP |
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