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Trypanosome Tpt1 is a bifunctional enzyme composed of tandem DEDDh nuclease and RNA 2'-phosphotransferase domains.

Created on 17 Sep 2026

Authors

Apurba Sarkar, Shreya Ghosh, Beate Schwer, Stewart Shuman

Published in

RNA (New York, N.Y.). Sep 16, 2026. Epub Sep 16, 2026.

Abstract

RNA 2'-phosphotransferase Tpt1 is a widely distributed enzyme that removes an internal RNA 2'-phosphate by transfer to NAD+. Tpt1 is essential in fungi, where it erases the 2'-PO4 mark installed by tRNA ligase during tRNA splicing. Tpt1 enzymes from bacteria, archaea, fungi, and metazoa are monofunctional units composed of RNA-binding and NAD+-binding lobes. The lone exception to date is fission yeast Tpt1, which consists of an N-terminal RNA 2'-phosphotransferase catalytic domain fused to a C-terminal domain homologous to budding yeast iron-sulfur cluster assembly factor Yae1. Here we report that the Tpt1 homologs of kinetoplastid protozoa are bifunctional enzymes composed of an N-terminal DEDDh-type nuclease domain linked to a C-terminal 2'-phosphotransferase domain. Characterization of Trypanosoma brucei Tpt1 (TbrTpt1) revealed that: (i) the C-terminal domain TbrTpt1-(298-540) is an autonomous module that catalyzes 2'-PO4 transfer to NAD+ via an RNA-2'-phospho-(ADP-ribose) intermediate; (ii) TbrTpt1-(299-540) is active in tRNA splicing in vivo when expressed in budding yeast tpt1∆ cells; and (iii) TbrTpt1 is a manganese-dependent 3'-exonuclease adept at resecting DNA and RNA single strands. TbrTpt1's RNA exonuclease is blocked by a 2' terminal phosphate. TbrTpt1 and TbrTpt1-(298-540) can remove a 2'-terminal phosphate via transfer to NAD+, albeit much less efficiently than removal of an internal 2'-phosphate.

PMID:
42749356
Bibliographic data and abstract were imported from PubMed on 17 Sep 2026.

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