Evidence map›Paper›PMID 20495880›Full record

ArticleMolecular imaging and biology2011

Conditional bicistronic Cre reporter line expressing both firefly luciferase and β-galactosidase.

Tomo-o Ishikawa, Harvey R Herschman

Open access · hybridAbstract read
In one paragraph

Article in Molecular imaging and biology, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.8field-weighted citation impact, top 24% 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

6 citing papers in PubMed, 12 citations in OpenAlex.

  1. Article
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  6. Applications of molecular imaging.Progress in molecular biology and translational science · 2010
    Review
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.

Tomo-o IshikawaDepartment of Molecular and Medical Pharmacology, Molecular Biology Institute, David Geffen School of Medicine, UCLA, 341 Boyer Hall, 611 Charles E. Young Drive East, Los Angeles, CA 90095, USA.
Harvey R Herschman
University of California, Los Angeles · US

Funding

Transductionally Redirected /Transcriptionally RestricteP50CA086306 · NCI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI HERSCHMAN, HARVEY R. · 2000 to 2014
$29.0M
IMAGING COX-2 GENE EXPRESSION IN INFLAMMATION AND TUMORSR01CA084572 · NCI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI HERSCHMAN, HARVEY R. · 2000 to 2009
$3.2M
The role of epidermal, fibroblast and endothelial cell COX-2 in skin cancerR01CA123055 · NCI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI HERSCHMAN, HARVEY R. · 2007 to 2011
$1.7M
NCI NIH HHS P50 CA086306NCI NIH HHS P50 CA86306NCI NIH HHS R01 CA084572NCI NIH HHS R01 CA123055NCI NIH HHS R01 CA84572
6 · The paper itself

Abstract

purposeThe Cre-loxP system has become an important strategy for conditional gene deletion and conditional gene expression in genetically engineered mice. To evaluate Cre recombinase expression, we generated reporter mice that permit both noninvasive imaging in living animals and either ex vivo histochemical/immunohistochemical tissue transgene expression analysis or quantitative enzyme analysis in the same animal. PROCEDURES: Transgenic reporter mice were generated in which a loxP-flanked enhanced green fluorescent protein (EGFP) reporter gene and STOP sequence are placed after the nearly ubiquitously expressed CAG promoter, but before a bicistronic transcriptional unit containing luciferase and β-galactosidase reporter gene coding sequences.

resultsAfter global deletion of the floxed STOP sequence by germ line Cre deletion, the reporter mouse expresses luciferase and β-galactosidase in all tissues examined. Tissue-specific expression of both reporter genes occurs in reporter mouse strains expressing Cre in skin (K14 keratin Cre), heart (myosin light chair Cre), or colon (Villin Cre).

conclusionThe luc-gal(Tg) reporter mouse allows noninvasive imaging of target Cre activation both in living animals and in tissues and cells following necropsy, using loss of EGFP expression, gain of luciferase expression, and gain of β-galactosidase expression as alternatives within the same animal for qualitative analysis of Cre expression.

Indexed as

Gene ExpressionGenetic TechniquesAnimalsbeta-GalactosidaseEmbryo, MammalianGene Knock-In TechniquesGenes, ReporterGreen Fluorescent ProteinsImmunohistochemistryIntegrasesLuciferases, FireflyMiceMice, TransgenicOrgan SpecificityWhole Body Imagingbeta-GalactosidaseCre recombinaseenhanced green fluorescent proteinGreen Fluorescent ProteinsIntegrasesLuciferases, Firefly

Identifiers

PMID20495880
PMCPMC3051074
OpenAlexW2077992873

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.