Evidence map›Paper›PMID 39231532›Full record

ArticleJournal of the American Chemical Society2024

Mass Spectrometry-Based Direct Sequencing of tRNAs De Novo and Quantitative Mapping of Multiple RNA Modifications.

Xiaohong Yuan, Yue Su, Benjamin Johnson, Michele Kirchner, Xudong Zhang, Sihang Xu, Sophia Jiang, Jing Wu, Shundi Shi, James J Russo and 2 more

Abstract read
In one paragraph

Article in Journal of the American Chemical Society, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

26 citing papers in PubMed.

  1. Article
  2. Compendium of RNA modifications for bacterial stress adaptation.Microbiology and molecular biology reviews : MMBR · 2026
    Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Integrating mass spectrometry with Nanopore direct RNA sequencing forbioRxiv : the preprint server for biology · 2026
    Article
  8. Review
  9. Article
  10. SnoRNA Expression and RNA 2'-O-Methylation inbioRxiv : the preprint server for biology · 2026
    Article
  11. Article
  12. Article
  13. Article
  14. Review
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors.

Xiaohong YuanDepartment of Biological and Chemical Sciences, New York Institute of Technology, New York, New York 10023, United States.ORCID 0000-0002-9165-5197
Yue SuDepartment of Biological and Chemical Sciences, New York Institute of Technology, New York, New York 10023, United States.
Benjamin JohnsonDepartment of Biological and Chemical Sciences, New York Institute of Technology, New York, New York 10023, United States.
Michele KirchnerDepartment of Biological and Chemical Sciences, New York Institute of Technology, New York, New York 10023, United States.
Xudong ZhangMolecular Medicine Program, Department of Human Genetics, and Division of Urology, Department of Surgery, University of Utah School of Medicine, Salt Lake City, Utah 84132, United States.
Sihang XuDepartment of Biological and Chemical Sciences, New York Institute of Technology, New York, New York 10023, United States.
Sophia JiangDepartment of Biological and Chemical Sciences, New York Institute of Technology, New York, New York 10023, United States.
Jing WuDepartment of Biological and Chemical Sciences, New York Institute of Technology, New York, New York 10023, United States.
Shundi ShiDepartment of Chemical Engineering, Columbia University, New York, New York 10027, United States.
James J RussoDepartment of Chemical Engineering, Columbia University, New York, New York 10027, United States.
Qi ChenMolecular Medicine Program, Department of Human Genetics, and Division of Urology, Department of Surgery, University of Utah School of Medicine, Salt Lake City, Utah 84132, United States.ORCID 0000-0001-6353-9589
Shenglong ZhangDepartment of Biological and Chemical Sciences, New York Institute of Technology, New York, New York 10023, United States.ORCID 0000-0001-8003-7484

Funding

Center for Multi-Scale Analysis of the Human EpitranscriptomeRM1HG011563 · NHGRI · WEILL MEDICAL COLL OF CORNELL UNIV · PI SAMIE R JAFFREY, Kathryn D Meyer · 2021 to 2026
$22.2M
Technology Development Coordinating CenterU24HG011735 · NHGRI · JACKSON LABORATORY · PI Mark D ADAMS · 2021 to 2026
$8.1M
Sperm tsRNAs/rsRNAs and their RNA modifications in diet-induced epigenetic inheritanceR01HD092431 · NICHD · UTAH STATE HIGHER EDUCATION SYSTEM--UNIVERSITY OF UTAH · PI Qi Chen, David S Milstone · 2017 to 2026
$3.5M
Role of PXR in EDC-induced cardiovascular diseaseR35ES035015 · NIEHS · UNIVERSITY OF CALIFORNIA RIVERSIDE · PI Changcheng Zhou · 2023 to 2026
$3.4M
Development of Next-Generation Mass Spectrometry-based de novo RNA Sequencing for all ModificationsR01HG012853 · NHGRI · STATE UNIVERSITY OF NEW YORK AT ALBANY · PI Shenglong Zhang · 2023 to 2026
$2.6M
Decoding the signature of sperm RNA & RNA modification of environmental stressors on the intergenerational transmission of metabolic phenotypesR01ES032024 · NIEHS · UNIVERSITY OF UTAH · PI CHEN, QI, ZHOU, TONG · 2020 to 2024
$2.1M
Development of LC/MS-Based Direct RNA Sequencing with Concomitant Basecalling and Modification Analysis CapabilityR21HG009576 · NHGRI · NEW YORK INST OF TECHNOLOGY · PI LI, WENJIA, ZHANG, SHENGLONG · 2017 to 2019
$569k
LC/MS-Based Direct RNA Sequencing with Concomitant Capability to Sequence Multiple Base Modifications at Single-base ResolutionR56HG011099 · NHGRI · NEW YORK INST OF TECHNOLOGY · PI ZHANG, SHENGLONG · 2020 to 2020
$350k
NHGRI NIH HHS R01 HG012853NHGRI NIH HHS R21 HG009576NHGRI NIH HHS R56 HG011099NHGRI NIH HHS RM1 HG011563NHGRI NIH HHS U24 HG011735NICHD NIH HHS R01 HD092431NIEHS NIH HHS R01 ES032024NIEHS NIH HHS R35 ES035015
6 · The paper itself

Abstract

Despite the extensive use of next-generation sequencing (NGS) of RNA, simultaneous direct sequencing and quantitative mapping of multiple RNA nucleotide modifications remains challenging. Mass spectrometry (MS)-based sequencing can directly sequence all RNA modifications without being limited to specific ones, but it requires a perfect MS ladder that few tRNAs can provide. Here, we describe an MS ladder complementation sequencing approach (MLC-Seq) that circumvents the perfect ladder requirement, allowing de novo MS sequencing of full-length heterogeneous cellular tRNAs with multiple nucleotide modifications at single-nucleotide precision. Unlike NGS-based methods, which lose RNA modification information, MLC-Seq preserves RNA sequence diversity and modification information, revealing new detailed stoichiometric tRNA modification profiles and their changes upon treatment with the dealkylating enzyme AlkB. It can also be combined with reference sequences to provide quantitative analysis of diverse tRNAs and modifications in total tRNA samples. MLC-Seq enables systematic, quantitative, and site-specific mapping of RNA modifications, revealing the truly complete informational content of tRNA.

Indexed as

RNA, TransferHigh-Throughput Nucleotide SequencingHumansMass SpectrometryRNA Processing, Post-TranscriptionalSequence Analysis, RNARNA, Transfer

Identifiers

PMID39231532
PMCPMC11421004

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

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.