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Peer-reviewedCC BY 4.0International Journal of Molecular Sciences

Analysis of Ligation Activity in Miniaturized L1 Ligase Ribozyme Variants Down to 49 nt and in Split Ribozyme Forms

  • Yuki Nitta1
  • Misaki Kato1
  • Yunoka Takagi1
  • Yusuke Saga1
  • Tadashi Ando2,3
  • Hiromi Mutsuro-Aoki1
  • Koji Tamura1,3
  1. 1Department of Biological Science and Technology, Tokyo University of Science, 6-3-1 Niijuku, Katsushika-ku, Tokyo 125-8585, Japan
  2. 2Department of Applied Electronics, Tokyo University of Science, 6-3-1 Niijuku, Katsushika-ku, Tokyo 125-8585, Japan
  3. 3Research Institute for Science and Technology, Tokyo University of Science, 2641 Yamazaki, Noda 278-8510, Japan
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Abstract

Identifying the smallest active unit capable of ligating RNA in the absence of proteins is important to elucidate ribozyme evolution. Here, we aimed to construct an evolutionary model of the L1 ligase ribozyme. The miniaturized L1 ligase ribozyme (L1X6c2) consists of three stems: Stems A, B, and C. Mutants with shortened stems B and C were used to examine whether ligation occurred. In the mutant where both stems were simultaneously shortened, no ligation products were observed. We also constructed mutants with nucleotide deletions, measured their ligation-product signals after 24 h, and identified the structures crucial for ligation. A split mutant, formed by cleaving L1X6c2 at stem B, showed a ligation-product signal after 24 h close to that of L1X6c2, whereas another split mutant, formed by cleaving L1X6c2 at stem C, exhibited decreased activity. Although non-Watson–Crick base pairs near the ligation site did not affect ligation, the presence of G1 was important for ligation. Mutational analysis suggested that strong interactions between G1 and A51 in the G1–A51–U38 base triple are responsible for the base specificity of A51. Moreover, consecutive base pairs on each stem subtly contribute to the stability of the ribozyme folded into a compact structure to create a catalytic pocket.

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Cite

BibTeXRIS
BibTeX
@article{nitta2026analysis,
  title = {{Analysis of Ligation Activity in Miniaturized L1 Ligase Ribozyme Variants Down to 49 nt and in Split Ribozyme Forms}},
  author = {Yuki Nitta and Misaki Kato and Yunoka Takagi and Yusuke Saga and Tadashi Ando and Hiromi Mutsuro-Aoki and Koji Tamura},
  journal = {International Journal of Molecular Sciences},
  year = {2026},
  month = oct,
  doi = {10.3390/ijms27209107},
  url = {https://www.mdpi.com/1422-0067/27/20/9107},
  note = {CC BY 4.0},
}
RIS
TY  - JOUR
TI  - Analysis of Ligation Activity in Miniaturized L1 Ligase Ribozyme Variants Down to 49 nt and in Split Ribozyme Forms
AU  - Yuki Nitta
AU  - Misaki Kato
AU  - Yunoka Takagi
AU  - Yusuke Saga
AU  - Tadashi Ando
AU  - Hiromi Mutsuro-Aoki
AU  - Koji Tamura
PY  - 2026
DA  - 2026/10/01
JO  - International Journal of Molecular Sciences
DO  - 10.3390/ijms27209107
UR  - https://www.mdpi.com/1422-0067/27/20/9107
AB  - Identifying the smallest active unit capable of ligating RNA in the absence of proteins is important to elucidate ribozyme evolution. Here, we aimed to construct an evolutionary model of the L1 ligase ribozyme. The miniaturized L1 ligase ribozyme (L1X6c2) consists of three stems: Stems A, B, and C. Mutants with shortened stems B and C were used to examine whether ligation occurred. In the mutant where both stems were simultaneously shortened, no ligation products were observed. We also constructed mutants with nucleotide deletions, measured their ligation-product signals after 24 h, and identified the structures crucial for ligation. A split mutant, formed by cleaving L1X6c2 at stem B, showed a ligation-product signal after 24 h close to that of L1X6c2, whereas another split mutant, formed by cleaving L1X6c2 at stem C, exhibited decreased activity. Although non-Watson–Crick base pairs near the ligation site did not affect ligation, the presence of G1 was important for ligation. Mutational analysis suggested that strong interactions between G1 and A51 in the G1–A51–U38 base triple are responsible for the base specificity of A51. Moreover, consecutive base pairs on each stem subtly contribute to the stability of the ribozyme folded into a compact structure to create a catalytic pocket.
SN  - 1422-0067
ER  -