Related Experiment Video
Updated: Jun 4, 2026

Bead Aggregation Assays for the Characterization of Putative Cell Adhesion Molecules
Published on: October 17, 2014
Peroxiredoxin stabilization of DE-cadherin promotes primordial germ cell adhesion
Matthew DeGennaro1, Thomas Ryan Hurd, Daria Elisabeth Siekhaus
1Department of Cell Biology, HHMI and Kimmel Center for Biology and Medicine of the Skirball Institute, New York University School of Medicine, New York, NY 10016, USA.
Insights
Mutations in the Jafrac1 gene disrupt germ cell adhesion by affecting hydrogen peroxide levels, impacting DE-cadherin. This study reveals a peroxiredoxin
Area of Science:
- Cell Biology
- Developmental Biology
- Biochemistry
Background:
- Regulated cell adhesion is crucial for cell migration during development.
- Proper cell-environment interaction guides cell movement and tissue formation.
- Germ cell migration relies on precise adhesion mechanisms.
Purpose of the Study:
- To investigate the role of the Jafrac1 gene in Drosophila germ cell adhesion.
- To understand the molecular mechanisms underlying germ cell adhesion defects.
- To explore the link between hydrogen peroxide levels and cell adhesion.
Main Methods:
- Genetic screening in Drosophila to identify mutations affecting germ cell adhesion.
- Analysis of germ cell migration and adhesion in jafrac1 mutant embryos.
- Biochemical assays to assess hydrogen peroxide levels and DE-cadherin protein stability.
- Genetic rescue experiments to validate the role of DE-cadherin.
Main Results:
- Mutations in Jafrac1, a hydrogen peroxide-degrading enzyme, cause germ cell adhesion defects in Drosophila.
- jafrac1 mutant embryos exhibit disrupted primordial germ cell association with the midgut.
- Jafrac1-mediated reduction of hydrogen peroxide is essential for maintaining DE-cadherin protein levels.
- Increasing DE-cadherin levels rescues the germ cell adhesion defects in jafrac1 mutants.
Conclusions:
- Jafrac1 plays a critical role in regulating germ cell adhesion through modulation of hydrogen peroxide levels.
- The study provides in vivo evidence for a peroxiredoxin regulating DE-cadherin-mediated adhesion.
- This finding highlights a novel mechanism linking oxidative stress regulation to cell adhesion dynamics in early development.
Abstract:
Regulated adhesion between cells and their environment is critical for normal cell migration. We have identified mutations in a gene encoding the Drosophila hydrogen peroxide (H₂O₂)-degrading enzyme Jafrac1, which lead to germ cell adhesion defects. During gastrulation, primordial germ cells (PGCs) associate tightly with the invaginating midgut primordium as it enters the embryo; however, in embryos from jafrac1 mutant mothers this association is disrupted, leaving some PGCs trailing on the outside of the embryo. We observed similar phenotypes in embryos from DE-cadherin/shotgun (shg) mutant mothers and were able to rescue the jafrac1 phenotype by increasing DE-cadherin levels. This and our biochemical evidence strongly suggest that Jafrac1-mediated reduction of H₂O₂ is required to maintain DE-cadherin protein levels in the early embryo. Our results present in vivo evidence of a peroxiredoxin regulating DE-cadherin-mediated adhesion.
More Related Videos
10:57Examining the Dynamics of Cellular Adhesion and Spreading of Epithelial Cells on Fibronectin During Oxidative Stress
Published on: October 13, 2019
07:52In Vitro Reconstitution of Spatial Cell Contact Patterns with Isolated Caenorhabditis elegans Embryo Blastomeres and Adhesive Polystyrene Beads
Published on: November 26, 2019
Related Concept Videos
Cadherins in Tissue Organization
Cell Sorting During Development
Cell sorting plays an...
Structure of Cadherins
Desmosomes
Adherens Junctions
Adherens Junctions are Dynamic
The endothelial cells...
Role of Ephrin-Eph Signalling in Intestinal Stem Cell Renewal
Role Of Notch Signalling In Intestinal Stem Cell Renewal
Direct cell-to-cell contact is needed for the activation of Notch signaling. The signal is initiated when a notch ligand binds to a receptor on an adjacent cell, also...