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tRNA 2′-O-methylation by a duo of TRM7/FTSJ1 proteins modulates small RNA silencing in Drosophila
Author(s) -
Margarita T. Angelova,
Dilyana G. Dimitrova,
Bruno da Silva,
Virginie Marchand,
Caroline Jacquier,
Cyrinne Achour,
Mira Brazane,
Catherine Goyenvalle,
Valérie BourguigIgel,
Salman Shehzada,
Souraya Khouider,
Tina Lenče,
Vincent Guérineau,
JeanYves Roignant,
Christophe Antoniewski,
Laure Teysset,
Damien Brégeon,
Yuri Motorin,
Matthias Schaefer,
Clément Carré
Publication year - 2020
Publication title -
nucleic acids research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 9.008
H-Index - 537
eISSN - 1362-4954
pISSN - 0305-1048
DOI - 10.1093/nar/gkaa002
Subject(s) - biology , transfer rna , methylation , drosophila (subgenus) , gene silencing , genetics , rna , rna silencing , rna induced transcriptional silencing , dna methylation , rna interference , trans acting sirna , microbiology and biotechnology , gene , gene expression
2'-O-Methylation (Nm) represents one of the most common RNA modifications. Nm affects RNA structure and function with crucial roles in various RNA-mediated processes ranging from RNA silencing, translation, self versus non-self recognition to viral defense mechanisms. Here, we identify two Nm methyltransferases (Nm-MTases) in Drosophila melanogaster (CG7009 and CG5220) as functional orthologs of yeast TRM7 and human FTSJ1. Genetic knockout studies together with MALDI-TOF mass spectrometry and RiboMethSeq mapping revealed that CG7009 is responsible for methylating the wobble position in tRNAPhe, tRNATrp and tRNALeu, while CG5220 methylates position C32 in the same tRNAs and also targets additional tRNAs. CG7009 or CG5220 mutant animals were viable and fertile but exhibited various phenotypes such as lifespan reduction, small RNA pathways dysfunction and increased sensitivity to RNA virus infections. Our results provide the first detailed characterization of two TRM7 family members in Drosophila and uncover a molecular link between enzymes catalyzing Nm at specific tRNAs and small RNA-induced gene silencing pathways.

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