Specificity in the Biosynthesis of the Universal tRNA Nucleoside N6-Threonylcarbamoyl Adenosine (t6A) - TsaD is the Gatekeeper

Authors

William E. Swinehart, Portland State University
Christopher W. Deutsch, Portland State UniversityFollow
Kathryn L. Sarachan, University at Albany, State University of New York
Amit Luthra, San Diego State University
Jo Marie Bacusmo, University of Florida
Valérie de Crécy-Lagard, University of FloridaFollow
Manal A. Swairjo, San Diego State University
Paul F. Agris, University at Albany, State University of New York
Dirk Iwata-ReuylFollow

Published In

RNA

Document Type

Citation

Publication Date

6-1-2020

Abstract

N6-threonylcarbamoyl adenosine (t6A) is a nucleoside modification found in all kingdoms of life at position 37 of tRNAs decoding ANN codons, which functions in part to restrict translation initiation to AUG and suppress frameshifting at tandem ANN codons. In Bacteria the proteins TsaB, TsaC (or C2), TsaD, and TsaE, comprise the biosynthetic apparatus responsible for t6A formation. TsaC(C2) and TsaD harbor the relevant active sites, with TsaC(C2) catalyzing the formation of the intermediate threonylcarbamoyladenosine monophosphate (TC-AMP) from ATP, threonine, and CO2, and TsaD catalyzing the transfer of the threonylcarbamoyl moiety from TC-AMP to A37 of substrate tRNAs. Several related modified nucleosides, including hydroxynorvalylcarbamoyl adenosine (hn6A), have been identified in select organisms, but nothing is known about their biosynthesis. To better understand the mechanism and structural constraints on t6A formation, and to determine if related modified nucleosides are formed via parallel biosynthetic pathways or the t6A pathway, we carried out biochemical and biophysical investigations of the t6A systems from E. coli and T. maritima to address these questions. Using kinetic assays of TsaC(C2), tRNA modification assays, and NMR, our data demonstrate that TsaC(C2) exhibit relaxed substrate specificity, producing a variety of TC-AMP analogs that can differ in both the identity of the amino acid and nucleotide component, while TsaD displays more stringent specificity, but efficiently produces hn6A in E. coli and T. maritima tRNA. Thus, in organisms that contain modifications such as hn6A in their tRNA, we conclude that their origin is due to formation via the t6A pathway.

Description

Copyright © 2020 by the RNA Society

Locate the Document

http://doi.org/10.1261/rna.075747.120

DOI

10.1261/rna.075747.120

Persistent Identifier

https://archives.pdx.edu/ds/psu/32877

Citation Details

Swinehart, W. E., Deutsch, C. W., Sarachan, K. L., Luthra, A., Bacusmo, J. M., de Crécy-Lagard, V., ... & Iwata-Reuyl, D. (2020). Specificity in the Biosynthesis of the Universal tRNA Nucleoside N6-Threonylcarbamoyl Adenosine (t6A)-TsaD is the Gatekeeper. RNA, rna-075747.