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

Polyamine sensing during antizyme mRNA programmed frameshifting.

Lorin M Petros1, Michael T Howard, Raymond F Gesteland

  • 1Department of Human Genetics, University of Utah, 15 N. 2030 E, Rm 7410, Salt Lake City, UT 84112-5330, USA.

Biochemical and Biophysical Research Communications
|November 5, 2005
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

Molecular architecture and diversity of StopGo/2A translational recoding.

Proceedings of the National Academy of Sciences of the United States of America·2026
Same author

Comprehensive analysis of yeast +1 ribosomal frameshifting unveils a novel stimulator supporting two distinct frameshifting mechanisms.

Nucleic acids research·2025
Same author

Programmed ribosomal frameshifting during <i>PLEKHM2</i> mRNA decoding generates a constitutively active proteoform that supports myocardial function.

Science advances·2025
Same author

Translon: a single term for translated regions.

Nature methods·2025
Same author

The dual luciferase assay does not support claims of stop codon readthrough on the AGO1 mRNA.

The EMBO journal·2025
Same author

Guidelines for minimal reporting requirements, design and interpretation of experiments involving the use of eukaryotic dual gene expression reporters (MINDR).

Nature structural & molecular biology·2025

Polyamines regulate cellular levels by controlling antizyme protein production through a ribosomal frameshift mechanism. This process involves specific mRNA elements and polyamine sensing for autoregulation.

Area of Science:

  • Molecular Biology
  • Genetics
  • Biochemistry

Background:

  • Antizyme protein is a key regulator of cellular polyamine levels across species.
  • Antizyme synthesis involves a programmed +1 ribosomal frameshift at the end of ORF1.
  • Frameshifting efficiency is modulated by polyamine concentrations, forming an autoregulatory loop.

Purpose of the Study:

  • To investigate the roles of specific mRNA elements in polyamine-mediated frameshifting.
  • To elucidate the mechanism of polyamine sensing during antizyme synthesis.
  • To examine the influence of polyamines on stop codon readthrough.

Main Methods:

  • Analysis of mRNA recoding signals for frameshifting.
  • Investigating the function of the ORF1 stop codon and 5' element.

Related Experiment Videos

  • Assessing the role of the 3' pseudoknot in frameshifting.
  • Studying polyamine-dependent stop codon readthrough.
  • Main Results:

    • The ORF1 stop codon and the 5' element are crucial for polyamine sensing.
    • The 3' pseudoknot enhances frameshifting independently of polyamine levels.
    • Polyamines are necessary to stimulate stop codon readthrough at the MuLV redefinition site.

    Conclusions:

    • The study identifies key elements controlling polyamine-regulated antizyme production.
    • A detailed mechanism for polyamine autoregulation via ribosomal frameshifting is presented.
    • Polyamines play a role in regulating gene expression through stop codon readthrough.