Evidence map›Paper›PMID 32713529›Full record

ArticleMethods in enzymology2020

A multicolor riboswitch-based platform for imaging of RNA in live mammalian cells.

Esther Braselmann, Amy E Palmer

Open access · greenAbstract read
In one paragraph

Article in Methods in enzymology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
2.4field-weighted citation impact, top 10% 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

5 citing papers in PubMed, 10 citations in OpenAlex.

  1. Article
  2. Article
  3. Translation Dynamics of Single mRNAs in Live Cells.Annual review of biophysics · 2024
    Review
  4. Article
  5. 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

2 authors at 1 institution in 1 country.

Esther BraselmannDepartment of Biochemistry, University of Colorado, Boulder, CO, United States; BioFrontiers Institute, University of Colorado, Boulder, CO, United States.
Amy E PalmerDepartment of Biochemistry, University of Colorado, Boulder, CO, United States; BioFrontiers Institute, University of Colorado, Boulder, CO, United States. Electronic address: amy.palmer@colorado.edu.
University of Colorado Boulder · US

Funding

Regulation of Cell Signaling by Transition Metal DynamicsDP1GM114863 · NIGMS · UNIVERSITY OF COLORADO · PI PALMER, AMY E · 2014 to 2018
$3.8M
Riboglow: a robust multi-color riboswitch-based platform for imaging RNA in living cellsR01GM133184 · NIGMS · UNIVERSITY OF COLORADO · PI BATEY, ROBERT T, PALMER, AMY E · 2019 to 2022
$1.2M
RNA tools for probing spliceosome dynamicsK99GM127752 · NIGMS · UNIVERSITY OF COLORADO · PI BRASELMANN, ESTHER · 2018 to 2020
$200k
NIGMS NIH HHS DP1 GM114863NIGMS NIH HHS K99 GM127752NIGMS NIH HHS R01 GM133184
6 · The paper itself

Abstract

A key approach to investigating RNA species in live mammalian cells is the ability to label them with fluorescent tags and track their dynamics in the complex cellular environment. The growing appreciation for the diversity of RNAs in nature, especially the roles of small, non-coding RNAs for cell function, calls for development of orthogonal RNA tagging systems. We previously developed Riboglow, a new RNA tagging system that features modular elements and hence the possibility to customize features for each application of choice. Riboglow consists of an RNA tag that is genetically fused to the RNA of interest and a small molecule that binds the RNA tag and elicits a fluorescence light up signal. Here, we present an overview of the Riboglow platform and compare and contrast the system with existing RNA tagging systems. Two step by step protocols for implementation of RNA imaging with Riboglow in live mammalian cells are presented, with special emphasis on guidelines that drive choices for modular elements in the Riboglow platform. Such modular elements include the RNA tag sequence and size, the number of RNA tag repeats per tagged RNA, the fluorescent color of the probe, the identity of the chemical linker in the probe, and the concentration of the probe used in live cells. Together, Riboglow is a new RNA tagging platform that enables robust live cell imaging of RNA dynamics, and this detailed protocol and guidelines for implementation will enable broad usage of Riboglow.

Indexed as

RiboswitchAnimalsFluorescenceFluorescent DyesIndicators and ReagentsRNAFluorescent DyesIndicators and ReagentsRiboswitchRNAFluorescent RNA tagsLive cell microscopymRNA localizationNon-coding RNA trackingSingle cell fluorescence microscopyStress granulesU-bodies

Identifiers

PMID32713529
PMCPMC7882419
OpenAlexW3046911702

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.