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

Give it a REST!

Steven M Pollard1, Maria Angeles Marques-Torrejon1

  • 1MRC Centre for Regenerative Medicine, University of Edinburgh, Edinburgh, United Kingdom.

Elife
|January 9, 2016
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

Turning cancer against itself: Programmable genetic medicines for glioblastoma.

Molecular therapy : the journal of the American Society of Gene Therapy·2026
Same author

A comprehensive pharmacological survey across heterogeneous patient-derived glioblastoma stem cell models.

iScience·2026
Same author

Local Tumor Microenvironment Niches Correlate With Survival And Immunotherapy Response In Human Glioblastoma.

bioRxiv : the preprint server for biology·2026
Same author

Synthetic super-enhancers enable precision viral immunotherapy.

Nature·2026
Same author

CDK12/CDK13 inhibition disrupts transcriptional elongation and replication fork progression in glioblastoma.

EMBO molecular medicine·2026
Same author

Clinical and genetic determinants of glioblastoma survival: a retrospective study.

Frontiers in molecular neuroscience·2026
Same journal

Non-canonical amino acid incorporation enables minimally disruptive labeling of stress granule and TDP-43 proteinopathy.

eLife·2026
Same journal

Analysis of dendritic input currents during place field dynamics.

eLife·2026
Same journal

TopoMetry systematically learns and evaluates the latent geometry of single-cell data.

eLife·2026
Same journal

Navigating the path: Advice to physician-scientists on choosing a clinical specialty.

eLife·2026
Same journal

Neural activity profiles reveal overlapping, intermingled subpopulations spanning area borders in mouse sensorimotor cortex.

eLife·2026
Same journal

The exquisite mechanics of a tsetse bite.

eLife·2026
See all related articles

The REST protein prevents premature gene activation in mature neurons. New findings show REST also protects the genome within neural progenitor cells, crucial for brain development.

Area of Science:

  • Neuroscience
  • Molecular Biology
  • Genetics

Background:

  • The REST (RE1-Silencing Transcription factor) protein is known to regulate gene expression in the nervous system.
  • REST typically represses genes essential for mature neuronal function in non-neuronal cells and during early development.

Purpose of the Study:

  • To investigate the role of the REST protein beyond its known function in mature neurons.
  • To determine if REST has a protective role in the genome of neural progenitor cells.

Main Methods:

  • Utilized molecular biology techniques to study REST protein function.
  • Analyzed gene expression patterns and genomic stability in neural progenitor cells with and without REST.

Main Results:

Keywords:
REST complexdevelopmental biologygenomic instabilityknockout animalsmouseneurogenesisrepressionstem cellstranscription factors

Related Experiment Videos

  • REST protein was found to safeguard the genome of neural progenitor cells.
  • This protection mechanism is independent of REST's role in repressing mature neuron-specific genes.
  • Conclusions:

    • The REST protein plays a critical dual role in neuronal development and genome maintenance.
    • REST's function extends to protecting the genetic integrity of neural progenitor cells, vital for healthy neurogenesis.