Evidence map›Paper›PMID 40064876›Full record

ArticleNature communications2025

Systematic analysis of cotranscriptional RNA folding using transcription elongation complex display.

Skyler L Kelly, Eric J Strobel

Abstract read
In one paragraph

Article in Nature communications, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

2 authors.

Skyler L KellyDepartment of Biological Sciences, The University at Buffalo, Buffalo, NY, 14260, USA.
Eric J StrobelDepartment of Biological Sciences, The University at Buffalo, Buffalo, NY, 14260, USA. estrobel@buffalo.edu.ORCID http://orcid.org/0000-0002-7082-2881

Funding

Mechanisms of cotranscriptional RNA structure formationR35GM147137 · NIGMS · STATE UNIVERSITY OF NEW YORK AT BUFFALO · PI Eric J Strobel · 2022 to 2026
$2.0M
NIGMS NIH HHS R35 GM147137SUNY | University at Buffalo (SUNY Buffalo) Laboratory startup fundsU.S. Department of Health & Human Services | NIH | National Institute of General Medical Sciences (NIGMS) R35GM147137
6 · The paper itself

Abstract

RNA can fold into structures that mediate diverse cellular functions. Understanding how RNA primary sequence directs the formation of functional structures requires methods that can comprehensively assess how changes in an RNA sequence affect its structure and function. Here we have developed a platform for performing high-throughput cotranscriptional RNA biochemical assays, called Transcription Elongation Complex display (TECdisplay). TECdisplay measures RNA function by fractionating a TEC library based on the activity of cotranscriptionally displayed nascent RNA. In this way, RNA function is measured as the distribution of template DNA molecules between fractions of the transcription reaction. This approach circumvents typical RNA sequencing library preparation steps that can cause technical bias. We used TECdisplay to characterize the transcription antitermination activity of >1 million variants of the Clostridium beijerinckii pfl ZTP riboswitch designed to perturb steps within its cotranscriptional folding pathway. Our findings establish TECdisplay as an accessible platform for high-throughput RNA biochemical assays.

Indexed as

RNA, BacterialRNA FoldingTranscription Elongation, GeneticTranscription, GeneticGene LibraryNucleic Acid ConformationRiboswitchRiboswitchRNA, Bacterial

Identifiers

PMID40064876
PMCPMC11894091

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.