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

Systematic variation in mRNA 3'-processing signals during mouse spermatogenesis.

Donglin Liu1, J Michael Brockman, Brinda Dass

  • 1The Jackson Laboratory, 600 Main Street, Bar Harbor, ME 04609, USA.

Nucleic Acids Research
|December 13, 2006
PubMed
Summary

Male germ cell maturation involves specialized gene processing. Alternative 3' processing and shorter 3' untranslated regions (3'-UTRs) in messenger RNAs (mRNAs) are key features during spermatogenesis.

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

A uniform tissue-clearing framework and mesoSPIM-ultra enable cm-scale single-neuron tracing.

bioRxiv : the preprint server for biology·2026
Same author

Erchen Decoction Induces Browning Tendency in White Adipose Tissue of Obese Rats via the SP1/ SREBP/UCP1 Signaling Pathway.

Endocrine, metabolic & immune disorders drug targets·2026
Same author

Structure-Guided Discovery of Neuroprotective Kromycin-Type Macrolides from <i>Streptomyces narbonensis</i> sp.

Journal of natural products·2026
Same author

Mesenchymal-derived neural progenitors underlie local <i>insulin</i> production and neuronal transdifferentiation during retina regeneration.

bioRxiv : the preprint server for biology·2026
Same author

Integration of a neuronal RNAseq dataset with the draft Gryllus bimaculatus transcriptome refines gene predictions and highlights potential systematic response to injury.

PloS one·2026
Same author

Regulatory provisions for post-release monitoring of genetically modified organisms in Africa.

Frontiers in bioengineering and biotechnology·2026

Area of Science:

  • Molecular Biology
  • Genetics
  • Reproductive Biology

Background:

  • Gene expression and processing are highly specialized during mouse male germ cell maturation (spermatogenesis).
  • Previous studies suggested a high incidence of alternative 3 eal-processing in male germ cell messenger RNAs (mRNAs), including reduced usage of the canonical polyadenylation signal (AAUAAA).

Purpose of the Study:

  • To identify 3 eal-processing sites used at various stages of spermatogenesis and in Sertoli cells.
  • To assess differences in 3 eal-processing characteristics and regulatory elements during male germ cell development.

Main Methods:

  • Utilized EST libraries from mouse testicular cells (spermatogonia, spermatocytes, round spermatids, Sertoli cells).
  • Employed a novel method for comparing degenerate regulatory elements between sequence samples.

Related Experiment Videos

  • Analyzed 3 eal-untranslated regions (3 eal-UTRs) for truncation and differences in processing sites.
  • Main Results:

    • Identified significant changes in the use of putative 3 eal-processing regulatory sequence elements across all spermatogenic cell types.
    • Observed a trend towards truncated 3 eal-UTRs, most pronounced in round spermatids.
    • Sertoli cells showed minimal 3 eal-UTR truncation and no significant difference in regulatory sequences.

    Conclusions:

    • Spermatogenesis exhibits developmental differences in polyadenylation site choice and regulatory elements.
    • Alternative 3 eal-processing and 3 eal-UTR truncation are specific features of male germ cell development.
    • Identified specific genes undergoing alternative 3 eal-processing during meiosis and postmeiotic development.