Evidence map›Paper›PMID 29662072›Full record

ArticleScientific reports2018

A Firefly Luciferase Dual Color Bioluminescence Reporter Assay Using Two Substrates To Simultaneously Monitor Two Gene Expression Events.

Bruce R Branchini, Tara L Southworth, Danielle M Fontaine, Dawn Kohrt, Catherine M Florentine, Martha J Grossel

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
1.9field-weighted citation impact, top 13% 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

26 citing papers in PubMed, 50 citations in OpenAlex.

  1. Article
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  3. Reporter-expressing viruses for antiviral drug discovery research.Frontiers in cellular and infection microbiology · 2025
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  6. Uncovering the role of sorbitol inBiochemistry and biophysics reports · 2024
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  7. Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. C-Series Coelenterazine-Driven Bioluminescence Signature Imaging.International journal of molecular sciences · 2022
    Article
  13. Article
  14. Article
  15. Multiplex Hextuple Luciferase Assaying.Methods in molecular biology (Clifton, N.J.) · 2022
    Article
  16. Article
  17. Article
  18. Review
  19. Article
  20. A Novel Potent Carrier for Unconventional Protein Export inFrontiers in cell and developmental biology · 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

6 authors at 1 institution in 1 country.

Bruce R BranchiniDepartment of Chemistry, Connecticut College, New London, Connecticut, 06320, USA. brbra@conncoll.edu.
Tara L SouthworthDepartment of Chemistry, Connecticut College, New London, Connecticut, 06320, USA.
Danielle M FontaineDepartment of Chemistry, Connecticut College, New London, Connecticut, 06320, USA.
Dawn KohrtDepartment of Biology, Connecticut College, New London, Connecticut, 06320, USA.
Catherine M FlorentineDepartment of Chemistry, Connecticut College, New London, Connecticut, 06320, USA.
Martha J GrosselDepartment of Biology, Connecticut College, New London, Connecticut, 06320, USA.
Connecticut College · US

Funding

Mechanism of Differentiation Functions of Cyclin Dependent Kinase 6 (Cdk6)R15CA125731 · NCI · CONNECTICUT COLLEGE · PI GROSSEL, MARTHA J. · 2007 to 2015
$1.0M
NCI NIH HHS R15 CA125731
6 · The paper itself

Abstract

Effective methods for monitoring eukaryotic gene expression and regulation based on bioluminescence - the emission of light by living organisms - are well established. Typically, the expression of a gene of interest is reported on with high sensitivity and over a wide dynamic range by the emission of light from a variety of engineered luciferase genes from beetles and marine organisms. The luciferase reporter genes are expressed downstream of the target gene or promoter and detected after exogenous addition of luciferin substrates. We describe a novel bioluminescence reporter method for the simultaneous monitoring of two genes expressing engineered firefly luciferase variants that emit readily distinguishable green and red light signals. The key feature is the selectivity of the enzymes for two luciferin substrates that determine each emission color. To validate our method, we performed a complex promoter transactivation experiment side-by-side with the Dual-Luciferase Reporter protocol and obtained essentially identical results. Additional comparative experiments demonstrated that our assay system provided improvements in background, cell normalization, and detectability compared to representative available methods. With access to a luminometer equipped with two optical filters, this method is an excellent choice for genetic reporter assays that can be performed with a single reagent solution.

Indexed as

Gene ExpressionGenes, ReporterFirefly LuciferinHEK293 CellsHumansLuciferases, FireflyLuminescent AgentsLuminescent MeasurementsPromoter Regions, GeneticProtein EngineeringSubstrate SpecificityTranscriptional ActivationTransfectionFirefly LuciferinLuciferases, FireflyLuminescent Agents

Identifiers

PMID29662072
PMCPMC5902630
OpenAlexW2801483177

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.