Evidence map›Paper›PMID 38110450›Full record

ArticleNature communications2023

Extending the toolbox for RNA biology with SegModTeX: a polymerase-driven method for site-specific and segmental labeling of RNA.

Raphael Haslecker, Vincent V Pham, David Glänzer, Christoph Kreutz, Theodore Kwaku Dayie, Victoria M D'Souza

Abstract read
In one paragraph

Article in Nature communications, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing 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

17 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Site-Specific Dual-Color Labeling of Long RNAs.Methods in molecular biology (Clifton, N.J.) · 2026
    Article
  5. Application of NMR to Large RNAs.Journal of molecular biology · 2025
    Review
  6. Article
  7. Review
  8. Ribozyme-Catalyzed Site-Specific Labeling of RNA Using OAngewandte Chemie (International ed. in English) · 2025
    Article
  9. Article
  10. Article
  11. Selective [9-Chembiochem : a European journal of chemical biology · 2025
    Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Enhanced TROSY Effect in [2-Angewandte Chemie (International ed. in English) · 2024
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors.

Raphael HasleckerDepartment of Molecular and Cellular Biology, Harvard University, Cambridge, MA, 02138, USA.ORCID 0000-0001-8001-9534
Vincent V PhamDepartment of Molecular and Cellular Biology, Harvard University, Cambridge, MA, 02138, USA.
David GlänzerInstitute of Organic Chemistry and Center for Molecular Biosciences Innsbruck (CMBI), University of Innsbruck, Innrain 80/82, 6020, Innsbruck, Austria.
Christoph KreutzInstitute of Organic Chemistry and Center for Molecular Biosciences Innsbruck (CMBI), University of Innsbruck, Innrain 80/82, 6020, Innsbruck, Austria.ORCID 0000-0002-7018-9326
Theodore Kwaku DayieDepartment of Chemistry and Biochemistry, University of Maryland, College Park, MD, 20782, USA.ORCID 0000-0002-7119-4362
Victoria M D'SouzaDepartment of Molecular and Cellular Biology, Harvard University, Cambridge, MA, 02138, USA. dsouza@g.harvard.edu.

Funding

Center for Structural Biology of HIV RNAU54AI170660 · NIAID · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI ALICE TELESNITSKY · 2022 to 2026
$32.1M
The Center for HIV RNA Studies (CRNA)U54GM103297 · NIGMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI TELESNITSKY, ALICE · 2017 to 2018
$10.2M
Inhibitor of FtsZ Polymerization in M. tuberculosisR01AI050470 · NIAID · SOUTHERN RESEARCH INSTITUTE · PI REYNOLDS, ROBERT C · 2002 to 2004
$1.7M
Austrian Science Fund FWF P 32773NIAID NIH HHS R01 AI050470NIAID NIH HHS U54 AI170660NIGMS NIH HHS U54 GM103297
6 · The paper itself

Abstract

RNA performs a wide range of functions regulated by its structure, dynamics, and often post-transcriptional modifications. While NMR is the leading method for understanding RNA structure and dynamics, it is currently limited by the inability to reduce spectral crowding by efficient segmental labeling. Furthermore, because of the challenging nature of RNA chemistry, the tools being developed to introduce site-specific modifications are increasingly complex and laborious. Here we use a previously designed Tgo DNA polymerase mutant to present SegModTeX - a versatile, one-pot, copy-and-paste approach to address these challenges. By precise, stepwise construction of a diverse set of RNA molecules, we demonstrate the technique to be superior to RNA polymerase driven and ligation methods owing to its substantially high yield, fidelity, and selectivity. We also show the technique to be useful for incorporating some fluorescent- and a wide range of other probes, which significantly extends the toolbox of RNA biology in general.

Indexed as

DNA-Directed RNA PolymerasesRNABiologyColoring AgentsMagnetic Resonance SpectroscopyColoring AgentsDNA-Directed RNA PolymerasesRNA

Identifiers

PMID38110450
PMCPMC10728113

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Registered trials

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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.