Evidence map›Paper›PMID 34010626›Full record

ArticleCell chemical biology2021

Naturally occurring three-way junctions can be repurposed as genetically encoded RNA-based sensors.

Jared D Moon, Jiahui Wu, Sourav K Dey, Jacob L Litke, Xing Li, Hyaeyeong Kim, Samie R Jaffrey

Open access · bronzeAbstract read
In one paragraph

Article in Cell chemical biology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.3field-weighted citation impact, top 20% of its field
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

14 citing papers in PubMed, 27 citations in OpenAlex.

  1. Article
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  7. Review
  8. Fluorogenic CRISPR for genomic DNA imaging.Nature communications · 2024
    Article
  9. Review
  10. Article
  11. Review
  12. Article
  13. Article
  14. Engineering Fluorophore Recycling in a Fluorogenic RNA Aptamer.Angewandte Chemie (International ed. in English) · 2021
    Article
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

7 authors at 1 institution in 1 country.

Jared D MoonDepartment of Pharmacology, Weill Cornell Medicine, Cornell University, New York, NY 10065, USA; Weill Cornell/Rockefeller/Sloan Kettering Tri-Institutional MD-PhD Program, New York, NY 10065, USA.
Jiahui WuDepartment of Pharmacology, Weill Cornell Medicine, Cornell University, New York, NY 10065, USA.
Sourav K DeyDepartment of Pharmacology, Weill Cornell Medicine, Cornell University, New York, NY 10065, USA.
Jacob L LitkeDepartment of Pharmacology, Weill Cornell Medicine, Cornell University, New York, NY 10065, USA.
Xing LiDepartment of Pharmacology, Weill Cornell Medicine, Cornell University, New York, NY 10065, USA.
Hyaeyeong KimDepartment of Pharmacology, Weill Cornell Medicine, Cornell University, New York, NY 10065, USA.
Samie R JaffreyDepartment of Pharmacology, Weill Cornell Medicine, Cornell University, New York, NY 10065, USA. Electronic address: srj2003@med.cornell.edu.
Cornell University · US

Funding

Weill Cornell/Rockefeller/Sloan-Kettering MST ProgramT32GM007739 · NIGMS · WEILL MEDICAL COLL OF CORNELL UNIV · PI HSU, KATHARINE C · 1985 to 2023
$51.1M
New mechanisms and technologies for understanding post-transcriptional gene regulation in neuronsR35NS111631 · NINDS · WEILL MEDICAL COLL OF CORNELL UNIV · PI SAMIE R JAFFREY · 2019 to 2026
$8.6M
Engineering RNA-activated fluorescence switches for RNA imaging and analyte sensiR01NS064516 · NINDS · WEILL MEDICAL COLL OF CORNELL UNIV · PI JAFFREY, SAMIE R · 2009 to 2018
$3.6M
Engineered circular RNAs: A novel platform for genetically encoded RNA-based biosensors and their application as real-time viral infection reportersF31AI134100 · NIAID · WEILL MEDICAL COLL OF CORNELL UNIV · PI LITKE, JACOB · 2017 to 2019
$123k
NIAID NIH HHS F31 AI134100NIGMS NIH HHS T32 GM007739NINDS NIH HHS R01 NS064516NINDS NIH HHS R35 NS111631
6 · The paper itself

Abstract

Small molecules can be imaged in living cells using biosensors composed of RNA. However, RNA-based devices are difficult to design. Here, we describe a versatile platform for designing RNA-based fluorescent small-molecule sensors using naturally occurring highly stable three-way junction RNAs. We show that ligand-binding aptamers and fluorogenic aptamers can be inserted into three-way junctions and connected in a way that enables the three-way junction to function as a small-molecule-regulated fluorescent sensor in vitro and in cells. The sensors are designed so that the interhelical stabilizing interactions in the three-way junction are only induced upon ligand binding. We use these RNA-based devices to measure the dynamics of S-adenosylmethionine levels in mammalian cells in real time. We show that this strategy is compatible with diverse metabolite-binding RNA aptamers, fluorogenic aptamers, and three-way junctions. Overall, these data demonstrate a versatile method for readily generating RNA devices that function in living cells.

Indexed as

Biosensing TechniquesAptamers, NucleotideFemaleFluorescent DyesHEK293 CellsHeLa CellsHumansLigandsRNASmall Molecule LibrariesAptamers, NucleotideFluorescent DyesLigandsRNASmall Molecule Librariesaptamerscellular imagingfluorescencemetaboliteRNA probes

Identifiers

PMID34010626
PMCPMC8573057
OpenAlexW3160387308

What OpenQuestion holds

Textmetadata
LicenceTDM
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.