| Literature DB >> 33789107 |
Jonathan J Ipsaro1, Paul A O'Brien2, Shibani Bhattacharya3, Arthur G Palmer2, Leemor Joshua-Tor4.
Abstract
The Piwi-interacting RNA (piRNA) pathway safeguards genomic integrity by silencing transposable elements (transposons) in the germline. While Piwi is the central piRNA factor, others including Asterix/Gtsf1 have also been demonstrated to be critical for effective silencing. Here, using enhanced crosslinking and immunoprecipitation (eCLIP) with a custom informatic pipeline, we show that Asterix/Gtsf1 specifically binds tRNAs in cellular contexts. We determined the structure of mouse Gtsf1 by NMR spectroscopy and identified the RNA-binding interface on the protein's first zinc finger, which was corroborated by biochemical analysis as well as cryo-EM structures of Gtsf1 in complex with co-purifying tRNA. Consistent with the known dependence of long terminal repeat (LTR) retrotransposons on tRNA primers, we demonstrate that LTR retrotransposons are, in fact, preferentially de-repressed in Asterix mutants. Together, these findings link Asterix/Gtsf1, tRNAs, and LTR retrotransposon silencing and suggest that Asterix exploits tRNA dependence to identify transposon transcripts and promote piRNA silencing.Entities:
Keywords: Asterix; Gtsf1; LTR; NMR; RNA; cryoEM; eCLIP; piRNA; retrotransposon; tRNA
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Year: 2021 PMID: 33789107 PMCID: PMC8283736 DOI: 10.1016/j.celrep.2021.108914
Source DB: PubMed Journal: Cell Rep Impact factor: 9.423