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

Two genetic elements regulate murine beta-glucuronidase synthesis following transcript accumulation.

C J Wawrzyniak1, S A Meredith, R E Ganschow

  • 1Division of Basic Science Research, Children's Hospital Research Foundation, Cincinnati, Ohio 45229.

Genetics
|January 1, 1989
PubMed
Summary
This summary is machine-generated.

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

The epidemiology of hepatitis B virus infection in HIV-infected and HIV-uninfected pregnant women in the Western Cape, South Africa.

Vaccine·2013
Same author

Androgen responsiveness of mouse kidney beta-glucuronidase requires 5'-flanking and intragenic Gus-s sequences.

Molecular endocrinology (Baltimore, Md.)·1998
Same author

Characterization and functional expression of a cDNA encoding egasyn (esterase-22): the endoplasmic reticulum-targeting protein of beta-glucuronidase.

Genomics·1991
Same author

Androgen responsiveness of the murine beta-glucuronidase gene is associated with nuclease hypersensitivity, protein binding, and haplotype-specific sequence diversity within intron 9.

Molecular and cellular biology·1991
Same author

Characterization of a murine cDNA encoding a member of the carboxylesterase multigene family.

Genomics·1991
Same author

DNA determinants of structural and regulatory variation within the murine beta-glucuronidase gene complex.

Molecular and cellular biology·1989
Same journal

Coexistence of piRNA and KZFP defense systems: Evolutionary dynamics of layered defense against transposable elements.

Genetics·2026
Same journal

Creation and manipulation of bipartite expression transgenes in C. elegans using phiC31 recombinase.

Genetics·2026
Same journal

Inherited long telomeres induce a genome-wide transcriptional response in budding yeast.

Genetics·2026
Same journal

Adaptive Dynamics of Quantitative Traits in a Steadily Changing Environment.

Genetics·2026
Same journal

Functional Landscape of Zebrafish Gonadotropins and Receptors: A Comprehensive Genetic Analysis.

Genetics·2026
Same journal

Synergistic actions of Nup43 and Myosin VI drive actin cone assembly during Drosophila spermiogenesis.

Genetics·2026
See all related articles

Genetic regulatory elements impact beta-glucuronidase (GUS) activity in mice. These elements control GUS expression post-transcription, affecting GUS synthesis during early development.

Area of Science:

  • Genetics
  • Molecular Biology
  • Biochemistry

Background:

  • Beta-glucuronidase (GUS) activity levels vary among mouse haplotypes (A, B, H) due to genetic regulatory elements.
  • Two key elements, Gus-u and Gus-t, are linked to the GUS gene and influence its activity.
  • Previous research indicated differences in GUS synthesis rates explained combined element effects in adult mouse liver.

Purpose of the Study:

  • To investigate the distinct roles of Gus-u and Gus-t in regulating GUS synthesis during early postnatal development.
  • To determine the stage and mechanism by which these regulatory elements control GUS expression.

Main Methods:

  • Analysis of GUS activity levels in mice with different GUS haplotypes (A and H).
  • Assessment of GUS synthesis rates during specific early postnatal developmental periods.

Related Experiment Videos

  • S1 nuclease protection assays using radiolabeled GUS antisense RNA and liver RNA from adult mice of A and H haplotypes.
  • Main Results:

    • Gus-u exerts cis-active control on GUS activity across all tissues and times.
    • Gus-t regulates GUS activity in trans after the 12th postnatal day in specific tissues.
    • No significant differences in processed GUS transcript levels were observed between adult mouse haplotypes A and H.
    • The regulatory elements Gus-u and Gus-t appear to control GUS expression after transcript processing.

    Conclusions:

    • Gus-u and Gus-t exhibit distinct temporal and spatial regulatory patterns.
    • The control exerted by Gus-u and Gus-t on GUS expression occurs post-transcriptional accumulation.
    • Understanding these regulatory mechanisms is crucial for interpreting variations in GUS activity in different mouse models.