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

A human tRNA(iMet) gene produces multiple transcripts.

C L Vnencak-Jones1, S Z Wahab, Z E Zehner

  • 1Department of Human Genetics, Medical College of Virginia, Virginia Commonwealth University, Richmond 23298.

Molecular and Cellular Biology
|November 1, 1987
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

Evaluating potential of multi-parametric MRI using co-registered histology: Application to a mouse model of glioblastoma.

Magnetic resonance imaging·2021
Same author

Rheo-NMR phenomena of wormlike micelles.

Soft matter·2020
Same author

Stacked in-plane histology for quantitative validation of non-invasive imaging biomarkers: Application to an infiltrative brain tumour model.

Journal of neuroscience methods·2019
Same author

Assessing the effects of Ang-(1-7) therapy following transient middle cerebral artery occlusion.

Scientific reports·2019
Same author

Quantitative histopathologic assessment of perfusion MRI as a marker of glioblastoma cell infiltration in and beyond the peritumoral edema region.

Journal of magnetic resonance imaging : JMRI·2018
Same author

miR-9 Acts as an OncomiR in Prostate Cancer through Multiple Pathways That Drive Tumour Progression and Metastasis.

PloS one·2016

Researchers identified a new human methionyl-transfer RNA (tRNA) gene (tRNA(iMet-3)). This gene uses inefficient termination signals, leading to multiple transcripts after polymerase readthrough, unlike other tRNA genes.

Area of Science:

  • Molecular Biology
  • Genetics
  • Biochemistry

Background:

  • The human methionyl-transfer RNA (tRNA) multigene family plays a crucial role in protein synthesis initiation.
  • Previous studies identified tRNA(iMet) loci with specific transcription termination signals.
  • Understanding tRNA gene regulation is vital for cellular processes.

Purpose of the Study:

  • To isolate and characterize a novel nonallelic locus of the human methionyl-tRNA multigene family, designated tRNA(iMet-3).
  • To investigate the transcription termination mechanisms of this new locus.
  • To analyze the resulting transcripts generated in vitro.

Main Methods:

  • Gene isolation and sequencing of the tRNA(iMet-3) locus.
  • In vitro transcription assays to study polymerase activity and termination.

Related Experiment Videos

  • Analysis of transcript products using molecular techniques.
  • Main Results:

    • A third nonallelic locus, tRNA(iMet-3), was identified in the human methionyl-tRNA multigene family.
    • Unlike other tRNA(iMet) loci, tRNA(iMet-3) lacks a canonical termination signal (run of T and C residues).
    • Three tandem, less efficient termination signals (short thymidylate runs) were found, causing polymerase readthrough and generating at least three distinct transcripts in vitro.
    • Significant variation in termination efficiency was observed at these sites.
    • All generated transcripts were processed in vitro.

    Conclusions:

    • The tRNA(iMet-3) locus exhibits a unique transcription termination strategy.
    • The inefficient termination signals result in the production of multiple transcripts.
    • These findings contribute to the understanding of tRNA gene regulation and transcript processing in humans.