Synthesis and RNA transcription of colored 4-selenouridine triphosphate with atom mutagenesis

  1. Zhen Huang1,2
  1. 1Key Laboratory of Bio-Resource and Eco-Environment of Ministry of Education, The College of Life Sciences, Sichuan University, Chengdu, Sichuan 610064, China
  2. 2SeNA Research Institute and Szostak Large Nucleic Acids Institute, College of Life Sciences, Hubei University, Wuhan, Hubei 430062, China
  3. 3State Key Laboratory of Southwestern Chinese Medicine Resources, Chengdu University of Traditional Chinese Medicine, Chengdu, Sichuan 610075, China
  1. Corresponding authors: huang{at}senaresearch.org; peixjin{at}163.com
  1. 4 These authors contributed equally to this work.

  2. Handling editor: Adrian Ferre-D'Amare

Abstract

4-Selenouridine (4SeU) is one of the naturally occurring modifications of tRNAs, possibly maintaining the three-dimensional structural stability of tRNA and playing a critical role in stress responses. By using the 4-Se-atomic probe, previously we have revealed more insights into the RNA noncanonical interactions and uridine participation in diversified RNA functions and structures. To further explore the Se-atomic probe, herein we report the first synthesis of 4-selenouridine triphosphate (4SeUTP) and the enzymatic incorporation of 4SeUTP into RNAs. Interestingly, we found that 4SeUTP possessed unique properties, including red-shifted base absorption (365 nm), colored base (yellow), and higher base acidity (pKa = 7.85) reduced by an Se-atom. Further, 4SeUTP was recognized by T7 RNA polymerase as well as UTP counterpart, and its transcription of RNAs (such as 4SeU-hammerhead ribozyme RNA) was up to the native level. Furthermore, the transcribed 4SeU-hammerhead ribozyme had higher cleaving activity (∼1.8-fold) than the corresponding native ribozyme. In conclusion, 4SeUTP can be a fine substrate of RNA polymerase, and the 4SeU-RNAs can be enzymatically synthesized with better catalytic activity, opening a new avenue for investigating the biochemical functions and structures of RNAs, especially catalytic RNAs.

Keywords

  • Received October 16, 2025.
  • Accepted February 20, 2026.

This article is distributed exclusively by the RNA Society for the first 12 months after the full-issue publication date (see http://rnajournal.cshlp.org/site/misc/terms.xhtml). After 12 months, it is available under a Creative Commons License (Attribution-NonCommercial 4.0 International), as described at http://creativecommons.org/licenses/by-nc/4.0/.

| Table of Contents