Extremophilic Archaea employ diverse RNA modifications for survival. Our understanding of the modified nucleosides and their functions in Archaea is far from complete. Here, we establish an extensive profile of nucleoside modifications in thermophilic and mesophilic Archaea. Through liquid chromatography-tandem mass spectrometry (LC-MS/MS) and rigorous non-coding RNA depletion, we identify four previously unannotated modifications in archaeal mRNA. Nucleoside analysis conducted on total, large, small, and mRNA-enriched subfractions of hyperthermophile Thermococcus kodakarensis reveals modifications whose relative abundance is dynamically responsive to growth temperatures. To predict archaeal RNA-modifying enzymes, we leverage open-access databases to compare putative functional domains with previously annotated enzymes. Our approach leads to the discovery of a methyltransferase responsible for the installation of m(7)G in the P loop of 23S rRNA peptidyl transferase center in T. kodakarensis. The methyltransferase activity is confirmed in vitro with synthetic substrates and in vivo by assessing the presence of the m(7)G modification in a genetic deletion strain.
Comprehensive nucleoside analysis of archaeal RNA modification profiles reveals an m(7)G in the conserved P loop of 23S rRNA.
对古细菌 RNA 修饰谱的全面核苷分析揭示了 23S rRNA 保守 P 环中的 m(7)G
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作者:Tsai Yueh-Lin, Wolf Eric J, Fluke Kristin A, Fuchs Ryan T, Dai Nan, Johnson Sean R, Sun Zhiyi, Elkins Liam, Burkhart Brett W, Santangelo Thomas J, Corrêa Ivan R Jr
| 期刊: | Cell Reports | 影响因子: | 6.900 |
| 时间: | 2025 | 起止号: | 2025 Apr 22; 44(4):115471 |
| doi: | 10.1016/j.celrep.2025.115471 | 研究方向: | 微生物学 |
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