Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Experiment Videos

Extracellular superoxide dismutase polymorphism in mice.

Anson Pierce1, Jason Whitlark, Ladislav Dory

  • 1Department of Molecular Biology & Immunology, University of North Texas Health Science Center at Fort Worth, USA.

Arteriosclerosis, Thrombosis, and Vascular Biology
|August 2, 2003
PubMed
Summary

Researchers identified a new extracellular superoxide dismutase (ecSOD) allele in mice. This allele significantly impacts ecSOD activity, highlighting the importance of genetic background in research.

Related Concept Videos

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

Quantitation of TAK-981 in human plasma via LC-MS/MS and its application in clinical trials.

Bioanalysis·2025
Same author

Hyperbaric oxygen alleviates selective domains of cognitive and motor deficits in female 5xFAD mice.

GeroScience·2023
Same author

Heat shock factor 1 drives regulatory T-cell induction to limit murine intestinal inflammation.

Mucosal immunology·2023
Same author

Superoxide-mediated oxidative stress accelerates skeletal muscle atrophy by synchronous activation of proteolytic systems.

GeroScience·2020
Same author

Extracellular Superoxide Dismutase Enhances Recruitment of Immature Neutrophils to the Liver.

Infection and immunity·2016
Same author

Overexpression of heat shock factor 1 maintains TAR DNA binding protein 43 solubility via induction of inducible heat shock protein 70 in cultured cells.

Journal of neuroscience research·2016

Area of Science:

  • Genetics
  • Biochemistry
  • Mouse Models

Background:

  • Extracellular superoxide dismutase (ecSOD) plays a crucial role in antioxidant defense.
  • Understanding genetic variations in ecSOD is essential for interpreting research findings, particularly in mouse models.

Purpose of the Study:

  • To identify and characterize a novel murine extracellular superoxide dismutase (ecSOD) allele.
  • To investigate the distribution of this ecSOD allele across different mouse strains.
  • To determine the impact of the identified ecSOD allele on the ecSOD phenotype.

Main Methods:

  • Polymerase chain reaction (PCR) analysis of genomic and cDNA.
  • DNA sequencing and genotyping.
  • Measurement of free and heparin-releasable ecSOD activities.

Related Experiment Videos

  • Immunoblotting to assess plasma enzyme mass.
  • Main Results:

    • Two distinct ecSOD transcripts and alleles were identified: a short variant (10-bp deletion in 3'UTR and a single nucleotide substitution) and a long form.
    • The 129P3/J strain carries the short ecSOD allele, while other strains carry the long form.
    • Mice with the short ecSOD allele exhibit over 3-fold higher ecSOD activity and enzyme mass compared to mice with the long allele.
    • A clear allele dose-dependent effect on ecSOD activity was observed in F2 hybrid mice.

    Conclusions:

    • Allele-specific effects on the ecSOD phenotype are demonstrated, independent of other strain-specific factors.
    • The findings underscore the necessity of backcrossing genetically modified mice to control for genetic background variations.
    • Accurate characterization of ecSOD alleles is critical for reproducible research in cardiovascular and metabolic disease models.