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

Heterochromatin02:38

Heterochromatin

18.9K
The extent of chromatin compaction can be studied by staining chromatin using specific DNA binding dyes. Under the microscope, the dense-compacted regions that take up more dye are called heterochromatin. Heterochromatin is further classified into two forms – constitutive heterochromatin and facultative heterochromatin.
Constitutive heterochromatin: It is a highly compact region of chromatin that is mostly concentrated in the centromere and telomere. Unlike euchromatin, the amino acid at...
18.9K
Heterochromatin02:38

Heterochromatin

4.9K
4.9K
X-inactivation01:58

X-inactivation

6.7K
6.7K
X-Inactivation01:58

X-Inactivation

42.9K
The human X chromosome contains over ten times the number of genes as in the Y chromosome. Since males have only one X chromosome, and females have two, one might expect females to produce twice as many of the proteins, with undesirable results.
42.9K
Inheritance of Chromatin Structures03:17

Inheritance of Chromatin Structures

7.8K
Epigenetics is the study of inherited changes in a cell's phenotype without changing the DNA sequences. It provides a form of memory for the differential gene expression pattern to maintain cell lineage, position-effect variegation, dosage compensation, and maintenance of chromatin structures such as telomeres and centromeres. For example, the structure and location of the centromere on chromosomes are epigenetically inherited. Its functionality is not dictated or ensured by the underlying...
7.8K
Euchromatin01:01

Euchromatin

9.2K
The extent of chromatin compaction can be studied by staining chromatin using specific DNA binding dyes. Under the microscope, the dense-compacted regions take up more dye, appearing darker, while the less-compact areas take up less dye and appear lighter. Based on the compaction level, chromatins are classified into two primary forms – euchromatin and heterochromatin.
Euchromatin is the less dense region of the chromatin and stains lighter. Euchromatin contains histone H3 extensively...
9.2K

You might also read

Related Articles

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

Sort by
Same author

Feasibility of a depth camera-based center of mass feedback system for closed-loop functional electrical stimulation therapy and visual feedback balance training.

Biomedical physics & engineering express·2026
Same author

Clinical assessment and normative values of turning: The effects of age, sex, and military status on turning speed.

Gait & posture·2026
Same author

Assessment of influenza virus and coronavirus tropism, replication competence and disease severity in <i>ex vivo</i> and <i>in vitro</i> cultures of the human respiratory tract.

The Journal of general virology·2026
Same author

Examining ecological momentary assessment (EMA) alone versus EMA with personalized feedback for hazardous drinking among Korean college students.

Addictive behaviors·2026
Same author

Crude oil fractionation by means of mesoporous polyacrylonitrile membranes.

Nature·2026
Same author

Computational Insights Into Smart Bioelectronics in Digital Health Care (2020-2024): Topic Modeling Study.

JMIR medical informatics·2026

Related Experiment Video

Updated: Mar 17, 2026

Stem cell-like Xenopus Embryonic Explants to Study Early Neural Developmental Features In Vitro and In Vivo
11:13

Stem cell-like Xenopus Embryonic Explants to Study Early Neural Developmental Features In Vitro and In Vivo

Published on: February 2, 2016

8.5K

Chx10 Consolidates V2a Interneuron Identity through Two Distinct Gene Repression Modes.

Yoanne M Clovis1, So Yeon Seo2, Ji-Sun Kwon1

  • 1Pediatric Neuroscience Research Program, Papé Family Pediatric Research Institute, Department of Pediatrics, Oregon Health and Science University, Portland, OR 97239, USA.

Cell Reports
|August 2, 2016
PubMed
Summary

The paired homeodomain factor Chx10 is crucial for spinal V2a interneuron development. It promotes V2a cell fate and suppresses motor neuron programs, segregating related cell types during differentiation.

Keywords:
Chx10Lhx3Sox14V2a interneuronsVsx2developmentmotor neuronsspinal cordtranscription factor

More Related Videos

Subtype-selective Electroporation of Cortical Interneurons
06:42

Subtype-selective Electroporation of Cortical Interneurons

Published on: August 18, 2014

9.3K
HOX Loci Focused CRISPR/sgRNA Library Screening Identifying Critical CTCF Boundaries
10:10

HOX Loci Focused CRISPR/sgRNA Library Screening Identifying Critical CTCF Boundaries

Published on: March 31, 2019

8.8K

Related Experiment Videos

Last Updated: Mar 17, 2026

Stem cell-like Xenopus Embryonic Explants to Study Early Neural Developmental Features In Vitro and In Vivo
11:13

Stem cell-like Xenopus Embryonic Explants to Study Early Neural Developmental Features In Vitro and In Vivo

Published on: February 2, 2016

8.5K
Subtype-selective Electroporation of Cortical Interneurons
06:42

Subtype-selective Electroporation of Cortical Interneurons

Published on: August 18, 2014

9.3K
HOX Loci Focused CRISPR/sgRNA Library Screening Identifying Critical CTCF Boundaries
10:10

HOX Loci Focused CRISPR/sgRNA Library Screening Identifying Critical CTCF Boundaries

Published on: March 31, 2019

8.8K

Area of Science:

  • Developmental Biology
  • Neuroscience
  • Genetics

Background:

  • Closely related progenitor cells can give rise to distinct cell types expressing similar transcriptional regulators.
  • A mechanism is needed to segregate cell identities after initial fate commitment during differentiation.

Purpose of the Study:

  • Investigate the mechanism of spinal V2a interneuron fate specification.
  • Understand how V2a interneurons segregate from motor neurons (MNs) despite shared developmental genes.

Main Methods:

  • Studied the role of the paired homeodomain factor Chx10 in V2a interneuron fate specification.
  • Examined Chx10's function in postmitotic neurons and its interaction with the MN developmental program.

Main Results:

  • Chx10 is a critical determinant for V2a interneuron fate.
  • Chx10 actively promotes V2a fate downstream of Lhx3.
  • Chx10 suppresses the MN program by inhibiting MN-specific transcription complex binding and activation of MN genes.

Conclusions:

  • Chx10 actively separates V2a and MN developmental pathways.
  • This study reveals a gene regulatory principle for segregating related cell fates.