Evidence map›Paper›PMID 11708652›Full record

ArticleTransgenic research2001

Rapid in vivo functional analysis of transgenes in mice using whole body imaging of luciferase expression.

W Zhang, J Q Feng, S E Harris, P R Contag, D K Stevenson, C H Contag

Abstract read
PubMed Publisher
In one paragraph

Article in Transgenic research, 2001. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
4.5field-weighted citation impact, top 5% 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

30 citing papers in PubMed, 117 citations in OpenAlex.

  1. Heme, Heme Oxygenase-1, Statins, and SARS-CoV-2.Antioxidants (Basel, Switzerland) · 2023
    Article
  2. Distinct Regulations ofMolecular and cellular biology · 2021
    Article
  3. Article
  4. Molecular Imaging with Reporter Genes: Has Its Promise Been Delivered?Journal of nuclear medicine : official publication, Society of Nuclear Medicine · 2019
    Review
  5. Article
  6. Glucuronidation of D-Luciferin In Vitro: Isoform Selectivity and Kinetics Characterization.European journal of drug metabolism and pharmacokinetics · 2019
    Article
  7. Article
  8. MiR-196a regulates heme oxygenase-1 by silencing Bach1 in the neonatal mouse lung.American journal of physiology. Lung cellular and molecular physiology · 2016
    Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. William A Silverman lecture.Journal of perinatology : official journal of the California Perinatal Association · 2014
    Article
  14. Article
  15. Article
  16. Article
  17. Enhanced in vivo bioluminescence imaging using liposomal luciferin delivery system.Journal of controlled release : official journal of the Controlled Release Society · 2010
    Article
  18. Article
  19. Article
  20. 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 4 institutions in 1 country.

W ZhangDepartment of Pediatrics, Stanford University Medical Center, Stanford University, CA 94305-5208, USA.
J Q Feng
S E Harris
P R Contag
D K Stevenson
C H Contag
Stanford Medicine · USStanford University · USThe University of Texas Health Science Center at San Antonio · USUniversity of Missouri–Kansas City · US

Funding

XOLAIR IN SUBJECTS WITH MODERATE TO SEVERE ATOPIC DERMATITIS WITH FOOD ALLERGYM01RR000070 · NCRR · STANFORD UNIVERSITY · PI RASGON, NATALIE L · 1985 to 2008
$32.4M
REGULATION OF HEME OXYGENASE IN NEONATAL ANIMALSR01HL058013 · NHLBI · STANFORD UNIVERSITY · PI STEVENSON, DAVID K · 1998 to 2005
$1.1M
NCRR NIH HHS RR00070NHLBI NIH HHS 1R01 HL58013
6 · The paper itself

Abstract

The use of transgenic animals in biomedical research is increasing rapidly and may be the best means of determining gene function. Generating transgenic animals typically requires time-consuming screening processes, and gene function is assessed by an array of difficult phenotypic and biochemical assays performed ex vivo. To address the unmet need in transgenic research for functional assays performed with ease in living animals, we demonstrate here that in vivo detection of luciferase enzyme as a transcriptional reporter facilitates rapid screening for both the presence and function of transgenes in intact living mice. Using this approach we identified three bioluminescent transgenic founders where the transgene consisted of the heme oxygenase promoter fused to the modified coding sequence of the luciferase gene. These founders were identified from 183 pups and confirmed by PCR analysis. Identification of HO-1-luc homozygotes from back- crossed F2 littermates was then accelerated by in vivo imaging. In another transgenic mouse line, where the transgene was comprised of the bone morphogenic-4 (BMP4) promoter fused to the modified luciferase gene, we were able to identify transgenic animals and in each line we were able to visualize patterns of expression in living animals over time. The light production from these transgenic mice indicated that the desired DNA fragment was functional and different expression profiles apparent at different ages and after gene induction.

Indexed as

Luminescent MeasurementsMice, TransgenicAnimalsBone Morphogenetic Protein 4Bone Morphogenetic ProteinsFemaleGene Expression ProfilingGenetic EngineeringHeme Oxygenase (Decyclizing)HomozygoteLuciferasesMaleMicePromoter Regions, GeneticTransgenesBmp4 protein, mouseBone Morphogenetic Protein 4Bone Morphogenetic ProteinsHeme Oxygenase (Decyclizing)Luciferases

Identifiers

PMID11708652
OpenAlexW1932389800

What OpenQuestion holds

Textmetadata
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.