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 Concept Videos

Regulation of Expression Occurs at Multiple Steps02:24

Regulation of Expression Occurs at Multiple Steps

Gene expression can be regulated at almost every step from gene to protein. Transcription is the step that is most commonly regulated. This involves the binding of proteins to short regulatory sequences on the DNA. This association can either promote or inhibit the transcription of a gene associated with the respective sequence.
Transcription results in the generation of precursor (pre-mRNA) that consists of both exons and introns, which needs further processing before being translated to a...
Regulation of Expression Occurs at Multiple Steps02:24

Regulation of Expression Occurs at Multiple Steps

Gene expression can be regulated at almost every step from gene to protein. Transcription is the step that is most commonly regulated. This involves the binding of proteins to short regulatory sequences on the DNA. This association can either promote or inhibit the transcription of a gene associated with the respective sequence.
Transcription results in the generation of precursor (pre-mRNA) that consists of both exons and introns, which needs further processing before being translated to a...
Neurogenesis and Regeneration of Nervous Tissue01:15

Neurogenesis and Regeneration of Nervous Tissue

In the CNS, neurogenesis, the birth of new neurons from stem cells, is limited to the hippocampus in adults. In other regions of the brain and spinal cord, neurogenesis is almost non-existent due to inhibitory influences from neuroglia, especially oligodendrocytes, and the absence of growth-stimulating cues. The myelin produced by oligodendrocytes in the CNS inhibits neuronal regeneration. Furthermore, astrocytes proliferate rapidly after neuronal damage, forming scar tissue that physically...
Regulation of Expression at Multiple Steps01:23

Regulation of Expression at Multiple Steps

The gene expression in cells is regulated at different stages: (i) transcription, (ii) RNA processing, (iii) RNA localization, and (iv) translation. Transcriptional regulation is mediated by regulatory proteins such as transcription factors, activators, or repressors—these control gene expression by initiating or inhibiting the transcription of genes. Once a precursor or pre-mRNA is produced, it undergoes post-transcriptional modification, including 5' capping, splicing, and the addition of a...
Co-activators and Co-repressors02:04

Co-activators and Co-repressors

Gene transcription is regulated by the synergistic action of several proteins that form a complex at a gene regulatory site. This is observed in eukaryotes, where the regulation of gene expression is a complex process. Regulatory proteins in eukaryotes can broadly be classified into two types – regulators that bind directly to specific DNA sequences and co-regulators that associate with regulatory proteins but cannot directly bind to the DNA. These co-regulators are further divided into...
Co-activators and Co-repressors02:04

Co-activators and Co-repressors

Gene transcription is regulated by the synergistic action of several proteins that form a complex at a gene regulatory site. This is observed in eukaryotes, where the regulation of gene expression is a complex process. Regulatory proteins in eukaryotes can broadly be classified into two types – regulators that bind directly to specific DNA sequences and co-regulators that associate with regulatory proteins but cannot directly bind to the DNA. These co-regulators are further divided into...

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

SMPD3 suppresses oligodendroglioma growth via dual autocrine-paracrine roles.

Communications biology·2026
Same author

Metabolic Assessment in Human Pluripotent Stem Cell-Derived Cerebral Organoids Using HR-MAS NMR Spectroscopy.

NMR in biomedicine·2026
Same author

Pathological disruption of CELF2 shuttling causes neuronal hyperactivity, learning deficits, and seizures.

The Journal of clinical investigation·2026
Same author

Plagl1 regulates the retinal progenitor cell to Müller glial cell transition.

PLoS genetics·2026
Same author

Composite Decellularized Corneal Hydrogel for Effective Corneal Injury Repair and Regeneration.

ACS applied bio materials·2026
Same author

Adhesive bioactive materials in ocular applications: Toward smart, regenerative, and minimally invasive therapies.

Bioactive materials·2026

Related Experiment Video

Updated: May 21, 2026

Induction of Protein Deletion Through In Utero Electroporation to Define Deficits in Neuronal Migration in Transgenic Models
12:01

Induction of Protein Deletion Through In Utero Electroporation to Define Deficits in Neuronal Migration in Transgenic Models

Published on: January 12, 2015

Neurog2 simultaneously activates and represses alternative gene expression programs in the developing neocortex.

Christopher Kovach1, Rajiv Dixit, Saiqun Li

  • 1University of Calgary, Hotchkiss Brain Institute, Alberta Children's Hospital Research Institute, Health Sciences Centre, Calgary, Alberta, Canada.

Cerebral Cortex (New York, N.Y. : 1991)
|June 28, 2012
PubMed
Summary
This summary is machine-generated.

Neurog2 acts as a master switch in the developing neocortex, activating specific genes while repressing others. This precise control ensures proper neuronal identity and prevents ventral fates during brain development.

Keywords:
Neurog2 proneural genebinary fate choicegenetic off-switchneocortical developmenttranscriptional activator or repressor

More Related Videos

Efficient Gene Delivery into Multiple CNS Territories Using In Utero Electroporation
13:12

Efficient Gene Delivery into Multiple CNS Territories Using In Utero Electroporation

Published on: June 23, 2011

Real-time Bioluminescence Imaging of Notch Signaling Dynamics during Murine Neurogenesis
10:25

Real-time Bioluminescence Imaging of Notch Signaling Dynamics during Murine Neurogenesis

Published on: December 12, 2019

Related Experiment Videos

Last Updated: May 21, 2026

Induction of Protein Deletion Through In Utero Electroporation to Define Deficits in Neuronal Migration in Transgenic Models
12:01

Induction of Protein Deletion Through In Utero Electroporation to Define Deficits in Neuronal Migration in Transgenic Models

Published on: January 12, 2015

Efficient Gene Delivery into Multiple CNS Territories Using In Utero Electroporation
13:12

Efficient Gene Delivery into Multiple CNS Territories Using In Utero Electroporation

Published on: June 23, 2011

Real-time Bioluminescence Imaging of Notch Signaling Dynamics during Murine Neurogenesis
10:25

Real-time Bioluminescence Imaging of Notch Signaling Dynamics during Murine Neurogenesis

Published on: December 12, 2019

Area of Science:

  • Neuroscience
  • Developmental Biology
  • Genetics

Background:

  • Cellular identity transitions are crucial for development, involving coordinated gene activation and repression.
  • The proneural gene Neurog2 plays a key role in neocortical development, but its precise regulatory mechanisms are not fully understood.

Purpose of the Study:

  • To investigate how the proneural gene Neurog2 simultaneously activates and represses gene expression programs during neocortical development.
  • To identify specific transcriptional targets and pathways regulated by Neurog2 that dictate neuronal identity.

Main Methods:

  • Comparison of wild-type Neurog2 with its transcriptional activator (Neurog2-VP16) and repressor (Neurog2-EnR) fusions.
  • Analysis of gene expression changes, including Pax6, Tbr2, Ebf1, Etv1, and Ascl1, in response to Neurog2 activity.
  • Investigating direct and indirect regulatory relationships between Neurog2 and its targets.

Main Results:

  • Neurog2 activates Pax6 repression and Tbr2 initiation in progenitor cells.
  • Neurog2 promotes dorsal (neocortical) neuronal identity and represses ventral fates.
  • Tbr2 directly represses the ventral gene Ebf1, and Neurog2 indirectly regulates Etv1 and Ascl1 to block ventral identity.

Conclusions:

  • Neurog2 employs multiple, distinct transcriptional off-switches to ensure specificity during neocortical development.
  • This study reveals a sophisticated mechanism by which Neurog2 prevents inappropriate gene expression and establishes correct neuronal identity.