Evidence map›Paper›PMID 26289345›Full record

ArticleRNA (New York, N.Y.)2015

Expedited quantification of mutant ribosomal RNA by binary deoxyribozyme (BiDz) sensors.

Yulia V Gerasimova, Petro Yakovchuk, Larisa M Dedkova, Sidney M Hecht, Dmitry M Kolpashchikov

Abstract read
In one paragraph

Article in RNA (New York, N.Y.), 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing 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

13 citing papers in PubMed.

  1. DNA Nanomachine (DNM) Biplex Assay for DifferentiatingInternational journal of molecular sciences · 2023
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  12. DNA Antenna Tile-Associated Deoxyribozyme Sensor with Improved Sensitivity.Chembiochem : a European journal of chemical biology · 2016
    Article
  13. 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

5 authors.

Yulia V GerasimovaChemistry Department, University of Central Florida, Orlando, Florida 32816, USA.
Petro YakovchukCenter for BioEnergetics, Biodesign Institute, Arizona State University, Tempe, Arizona 85287, USA Department of Chemistry and Biochemistry, Arizona State University, Tempe, Arizona 85287, USA.
Larisa M DedkovaCenter for BioEnergetics, Biodesign Institute, Arizona State University, Tempe, Arizona 85287, USA Department of Chemistry and Biochemistry, Arizona State University, Tempe, Arizona 85287, USA.
Sidney M HechtCenter for BioEnergetics, Biodesign Institute, Arizona State University, Tempe, Arizona 85287, USA Department of Chemistry and Biochemistry, Arizona State University, Tempe, Arizona 85287, USA.
Dmitry M KolpashchikovChemistry Department, University of Central Florida, Orlando, Florida 32816, USA National Center for Forensic Science, University of Central Florida, Orlando, Florida 32816, USA Burnett School of Biomedical Sciences, University of Central Florida, Orlando, Florida 32816, USA.

Funding

Selection of Modified Ribosomes Using Novel PuromycinsR01GM103861 · NIGMS · ARIZONA STATE UNIVERSITY-TEMPE CAMPUS · PI HECHT, SIDNEY M. · 2013 to 2021
$1.6M
Deoxyribozyme sensor-based diagnostics for Mycobacterium tuberculosisR15AI103880 · NIAID · UNIVERSITY OF CENTRAL FLORIDA · PI KOLPASHCHIKOV, DMITRY MIKHAYLOVICH · 2013 to 2013
$430k
NIAID NIH HHS R15 AI103880NIAID NIH HHS R15AI10388001A1NIGMS NIH HHS 1R1GM103861-01A1NIGMS NIH HHS R01 GM103861
6 · The paper itself

Abstract

Mutations in ribosomal RNA (rRNA) have traditionally been detected by the primer extension assay, which is a tedious and multistage procedure. Here, we describe a simple and straightforward fluorescence assay based on binary deoxyribozyme (BiDz) sensors. The assay uses two short DNA oligonucleotides that hybridize specifically to adjacent fragments of rRNA, one of which contains a mutation site. This hybridization results in the formation of a deoxyribozyme catalytic core that produces the fluorescent signal and amplifies it due to multiple rounds of catalytic action. This assay enables us to expedite semi-quantification of mutant rRNA content in cell cultures starting from whole cells, which provides information useful for optimization of culture preparation prior to ribosome isolation. The method requires less than a microliter of a standard Escherichia coli cell culture and decreases analysis time from several days (for primer extension assay) to 1.5 h with hands-on time of ∼10 min. It is sensitive to single-nucleotide mutations. The new assay simplifies the preliminary analysis of RNA samples and cells in molecular biology and cloning experiments and is promising in other applications where fast detection/quantification of specific RNA is required.

Indexed as

Biosensing TechniquesMutationBase SequenceDNA, CatalyticEscherichia coliMolecular Sequence DataNucleic Acid ConformationNucleic Acid HybridizationRNA, BacterialRNA, RibosomalDNA, CatalyticRNA, BacterialRNA, Ribosomalbinary deoxyribozymefluorescent sensorsmix-and-read probesmutation analysisribosomal RNA

Identifiers

PMID26289345
PMCPMC4574759

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.