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

Dosage Compensation02:50

Dosage Compensation

In animals, gender is determined by the number and type of sex chromosome. For example, human females have two X chromosomes, and males have one X and one Y chromosome, whereas C.elegans with one X chromosome is a male, and the one with two X chromosomes is a hermaphrodite.
In addition to sexual development, the X chromosome has genes involved in autosomal functions such as brain development and the immune system. Therefore, males and females with  distinct numbers of X chromosomes will have...
X-Inactivation01:58

X-Inactivation

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.
The Ratio of X Chromosome to Autosomes02:45

The Ratio of X Chromosome to Autosomes

In most organisms, sex is determined by the ratio of X and Y chromosomes. However, in some organisms, such as Drosophila and C.elegans, sex is determined by the ratio of the number of X chromosomes to the number of sets of autosomes. The Y chromosome in Drosophila is active but does not determine sex. It contains genes responsible for the production of sperms in adult flies.  
Normal male Drosophila has a ratio of one X chromosome to two sets of autosomes. In contrast, normal female Drosophila...

You might also read

Related Articles

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

Sort by
Same author

Bidirectional fibrogenic cross-talk revealed in a human iPSC-derived epithelial-mesenchymal co-culture model of pulmonary fibrosis.

bioRxiv : the preprint server for biology·2026
Same author

Clinical Interventions and Inflammatory Signaling Shape the Transcriptional and Cellular Architecture of the Early Postnatal Lung.

bioRxiv : the preprint server for biology·2025
Same author

Purinergic ecto-enzyme CD73 is a context-dependent tumor suppressor in colorectal cancer.

The Journal of biological chemistry·2025
Same author

A scalable long-term <i>in vitro</i> model of human colonic epithelium with continuous barrier function.

bioRxiv : the preprint server for biology·2025
Same author

Primitive means first, not worst: Critical roles for primitive endoderm in embryos and embryo models.

Developmental biology·2025
Same author

AKR1B1 Expression in the Colorectal Tumor Microenvironment Contributes Towards Its Prognostic Significance.

Cancer medicine·2025
Same journal

Dissecting planar and vertical organiser signals in early chick neural development.

Development (Cambridge, England)·2026
Same journal

Real-time transcriptomic profiling of hPSC-derived cartilage during development identifies a key role for the extracellular matrix in homeostasis and protection.

Development (Cambridge, England)·2026
Same journal

In preprints - housekeeping the housekeeping genes.

Development (Cambridge, England)·2026
Same journal

In preprints - light, cluster, friction: a cell dance on the gastrulation stage.

Development (Cambridge, England)·2026
Same journal

PBX-dependent and -independent Hox programs establish and maintain motor neuron terminal identity.

Development (Cambridge, England)·2026
Same journal

NUDT21 regulates 3'UTR dynamics in epididymal principal cells to preserve sperm integrity.

Development (Cambridge, England)·2026
See all related articles

Related Experiment Video

Updated: May 18, 2026

Determining the Role of Maternally-Expressed Genes in Early Development with Maternal Crispants
10:08

Determining the Role of Maternally-Expressed Genes in Early Development with Maternal Crispants

Published on: December 21, 2021

Maternal Cdx2 is dispensable for mouse development.

Stephanie Blij1, Tristan Frum, Aytekin Akyol

  • 1Department of Molecular, Cell, and Developmental Biology, University of California Santa Cruz, Santa Cruz, CA 95064, USA.

Development (Cambridge, England)
|September 21, 2012
PubMed
Summary
This summary is machine-generated.

Maternal CDX2 (caudal type homeobox 2) is not essential for mouse development. Genetic ablation confirmed that this transcription factor does not play a critical role in early embryonic cell fate determination.

More Related Videos

Quantitative Analysis of Protein Expression to Study Lineage Specification in Mouse Preimplantation Embryos
11:25

Quantitative Analysis of Protein Expression to Study Lineage Specification in Mouse Preimplantation Embryos

Published on: February 22, 2016

Generation of Maternal Mutants Using zpc:cas9 Knock-in Zebrafish
09:17

Generation of Maternal Mutants Using zpc:cas9 Knock-in Zebrafish

Published on: July 22, 2025

Related Experiment Videos

Last Updated: May 18, 2026

Determining the Role of Maternally-Expressed Genes in Early Development with Maternal Crispants
10:08

Determining the Role of Maternally-Expressed Genes in Early Development with Maternal Crispants

Published on: December 21, 2021

Quantitative Analysis of Protein Expression to Study Lineage Specification in Mouse Preimplantation Embryos
11:25

Quantitative Analysis of Protein Expression to Study Lineage Specification in Mouse Preimplantation Embryos

Published on: February 22, 2016

Generation of Maternal Mutants Using zpc:cas9 Knock-in Zebrafish
09:17

Generation of Maternal Mutants Using zpc:cas9 Knock-in Zebrafish

Published on: July 22, 2025

Area of Science:

  • Developmental biology
  • Genetics
  • Molecular biology

Background:

  • Cell fate determination in many species relies on maternal determinants.
  • The role of caudal domain transcription factor CDX2 as a maternal determinant in mammalian embryogenesis is controversial.
  • Previous studies using RNA interference have yielded conflicting results regarding maternal CDX2's essentiality.

Purpose of the Study:

  • To definitively resolve the requirement of maternal CDX2 in mouse development.
  • To investigate the role of maternal CDX2 in regulating cell fate decisions during early embryogenesis.
  • To overcome the limitations of previous RNA interference-based studies.

Main Methods:

  • Genetic ablation of the maternal Cdx2 gene using a Cre/lox strategy in mice.
  • Analysis of embryonic development following maternal Cdx2 deletion.

Main Results:

  • Maternal CDX2 is not essential for mouse development.
  • The genetic deletion of maternal Cdx2 did not impede embryonic development.
  • This study provides unambiguous evidence regarding the non-essential role of maternal CDX2.

Conclusions:

  • Maternal CDX2 does not function as a critical determinant for cell fate in mouse embryogenesis.
  • The findings challenge previous hypotheses regarding deterministic mechanisms in mammalian development regulated by maternal factors.
  • Genetic ablation provides a definitive method for assessing the necessity of maternal genes in development.