Evidence map›Paper›PMID 42316300›Full record

ArticleGenome biology2026

OTTR-seq profiling reveals dynamic tRNA modification landscapes across diverse archaeal species.

Jesse S Leavitt, Henry T Moore, Thomas J Santangelo, Todd M Lowe

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In one paragraph

Article in Genome biology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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1citing papers in PubMed
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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Jesse S LeavittDepartment of Biomolecular Engineering, Baskin School of Engineering, University of California Santa Cruz, Santa Cruz, CA, 95064, USA. jesse_leavitt@brown.edu.
Henry T MooreDepartment of Biomolecular Engineering, Baskin School of Engineering, University of California Santa Cruz, Santa Cruz, CA, 95064, USA.
Thomas J SantangeloDepartment of Biochemistry and Molecular Biology, Colorado State University, Fort Collins, CO, 80523, USA.
Todd M LoweDepartment of Biomolecular Engineering, Baskin School of Engineering, University of California Santa Cruz, Santa Cruz, CA, 95064, USA. tmjlowe@ucsc.edu.

Funding

A Unified Atlas of Dynamic tRNA FunctionR01HG006753 · NHGRI · UNIVERSITY OF CALIFORNIA SANTA CRUZ · PI LOWE, TODD MICHAEL · 2012 to 2022
$4.6M
Regulation of Archaeal TranscriptionR35GM143963 · NIGMS · COLORADO STATE UNIVERSITY · PI Thomas James Santangelo · 2022 to 2026
$1.8M
National Science Foundation, USA 2022065NHGRI NIH HHS R01 HG006753NIGMS NIH HHS R35 GM143963NIH HHS R35 GM143963USA National Aeronautics and Space Administration 80NSSC23K1354
6 · The paper itself

Abstract

backgroundTransfer RNA (tRNA) modifications are essential for structural integrity, decoding fidelity, and stress adaptation, yet their evolutionary dynamics remain poorly characterized in archaea. Here, we apply Ordered Two-Template Relay sequencing (OTTR-seq), a high-throughput approach that captures full-length tRNAs and modification-sensitive reverse transcription signatures, to systematically profile tRNA modification landscapes across diverse archaeal species.

resultsAcross nine archaeal species spanning thermophilic, acidophilic, halophilic, and mesophilic environments, we identify position-specific and clade-dependent patterns of tRNA modifications. We detect coordinated and mutually exclusive methylation at acceptor stem positions 6 and 67 in hyperthermophiles, as well as clade-specific co-modification at positions 10 and 26, which are typically known as tRNA modification anti-determinants. Comparative analyses also reveal lineage-specific divergence in the domain architectures of tRNA methyltransferases, including Trm1, Trm10, Trm11, and Trm14, linking enzymatic evolution to substrate specificity. We further refine known identity elements, such as the G10oU25 pairing, and identify novel structural features that may facilitate or prevent modification.

conclusionsThese findings exemplify the co-evolution of tRNAs and their modifying enzymes, providing new insights into how archaea may fine-tune translation in extreme environments. The broad scope of data and comparative analyses establishes a multispecies framework for future biochemical, mechanistic, and predictive modeling efforts.

Indexed as

ArchaeaRNA, ArchaealRNA Processing, Post-TranscriptionalRNA, TransferEvolution, MolecularRNA MethylationtRNA MethyltransferasesRNA, ArchaealRNA, TransfertRNA MethyltransferasesArchaeaEnzyme–substrate coevolutionHigh-throughput RNA modification mappingtRNA modification

Identifiers

PMID42316300
PMCPMC13520502

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.