4.6 Article

Escherichia coli tRNA 2-Selenouridine Synthase (SelU): Elucidation of Substrate Specificity to Understand the Role of S-Geranyl-tRNA in the Conversion of 2-Thio- into 2-Selenouridines in Bacterial tRNA

Journal

CELLS
Volume 11, Issue 9, Pages -

Publisher

MDPI
DOI: 10.3390/cells11091522

Keywords

tRNA 2-selenouridine synthase; MBP-SelU fusion protein; modified nucleoside; 2-thiouridine; S-geranyl 2-thiouridine; 2-selenouridine

Categories

Funding

  1. National Science Center of Poland [UMO2018/29/B/ST5/02509]
  2. Statutory Funds for the Centre of Molecular and Macromolecular Studies, Polish Academy of Sciences

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This study characterized the substrate requirements of the bacterial enzyme SelU, identified SelU-associated tRNAs and their specific modifications in the wobble position. It explained the sequence of steps in the selenation of tRNA and found that the recognition by SelU is influenced by the S2U position within the RNA chain, the flanking sequence of the modification, and the length of the RNA substrate.
The bacterial enzyme tRNA 2-selenouridine synthase (SelU) is responsible for the conversion of 5-substituted 2-thiouridine (R5S2U), present in the anticodon of some bacterial tRNAs, into 5-substituted 2-selenouridine (R5Se2U). We have already demonstrated using synthetic RNAs that transformation S2U -> Se2U is a two-step process, in which the S2U-RNA is geranylated and the resulting geS2U-RNA is selenated. Currently, the question is how SelU recognizes its substrates and what the cellular pathway of R5S2U -> R5Se2U conversion is in natural tRNA. In the study presented here, we characterized the SelU substrate requirements, identified SelU-associated tRNAs and their specific modifications in the wobble position. Finally, we explained the sequence of steps in the selenation of tRNA. The S2U position within the RNA chain, the flanking sequence of the modification, and the length of the RNA substrate, all have a key influence on the recognition by SelU. MST data on the affinity of SelU to individual RNAs confirmed the presumed process. SelU binds the R5S2U-tRNA and then catalyzes its geranylation to the R5geS2U-tRNA, which remains bound to the enzyme and is selenated in the next step of the transformation. Finally, the R5Se2U-tRNA leaves the enzyme and participates in the translation process. The enzyme does not directly catalyze the R5S2U-tRNA selenation and the R5geS2U-tRNA is the intermediate product in the linear sequence of reactions.

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