Characterization of tRNA splicing enzymes RNA ligase and tRNA 2'-phosphotransferase from the pathogenic fungi Mucorales Journal Article


Authors: Ghosh, S.; Dantuluri, S.; Jacewicz, A.; Sanchez, A. M.; Abdullahu, L.; Damha, M. J.; Schwer, B.; Shuman, S.
Article Title: Characterization of tRNA splicing enzymes RNA ligase and tRNA 2'-phosphotransferase from the pathogenic fungi Mucorales
Abstract: Fungal Trl1 is an essential trifunctional tRNA splicing enzyme that heals and seals tRNA exons with 2',3'-cyclic-PO4 and 5'-OH ends. Trl1 is composed of C-terminal cyclic phosphodiesterase and central polynucleotide kinase end-healing domains that generate the 3'-OH,2'-PO4 and 5'-PO4 termini required for sealing by an N-terminal ATP-dependent ligase domain. Trl1 enzymes are present in many human fungal pathogens and are promising targets for antifungal drug discovery because their domain structures and biochemical mechanisms are unique compared to the mammalian RtcB-type tRNA splicing enzyme. Here we report that Mucorales species (deemed high-priority human pathogens by WHO) elaborate a noncanonical tRNA splicing apparatus in which a monofunctional RNA ligase enzyme is encoded separately from any end-healing enzymes. We show that Mucor circinelloides RNA ligase (MciRNL) is active in tRNA splicing in vivo in budding yeast in lieu of the Trl1 ligase domain. Biochemical and kinetic characterization of recombinant MciRNL underscores its requirement for a 2'-PO4 terminus in the end-joining reaction, whereby the 2'-PO4 enhances the rates of RNA 5'-adenylylation (step 2) and phosphodiester synthesis (step 3) by ∼125-fold and ∼6200-fold, respectively. In the canonical fungal tRNA splicing pathway, the splice junction 2'-PO4 installed by RNA ligase is removed by a dedicated NAD+-dependent RNA 2'-phosphotransferase Tpt1. Here we identify and affirm by genetic complementation in yeast the biological activity of Tpt1 orthologs from three Mucorales species. Recombinant M. circinelloides Tpt1 has vigorous NAD+-dependent RNA 2'-phosphotransferase activity in vitro. © 2024 Ghosh et al.; Published by Cold Spring Harbor Laboratory Press for the RNA Society.
Keywords: genetics; animal; metabolism; animals; rna; chemistry; saccharomyces cerevisiae; mammal; transfer rna; rna, transfer; mammals; nad; trna splicing; polynucleotide 5' hydroxyl kinase; polynucleotide 5'-hydroxyl-kinase; rna ligase (atp); rna splicing; nicotinamide adenine dinucleotide; ligase; ligases; rna ligase; trna ligase; humans; human; fungal pathogen; mucorales; trna 2′-phosphotransferase
Journal Title: RNA
Volume: 30
Issue: 4
ISSN: 1355-8382
Publisher: Cold Spring Harbor Laboratory Press  
Date Published: 2024-04-01
Start Page: 367
End Page: 380
Language: English
DOI: 10.1261/rna.079911.123
PUBMED: 38238085
PROVIDER: scopus
PMCID: PMC10946426
DOI/URL:
Notes: Source: Scopus
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MSK Authors
  1. Stewart H Shuman
    548 Shuman
  2. Shreya Ghosh
    12 Ghosh
  3. Ana Maria Sanchez
    17 Sanchez