An Actomyosin-Arf-GEF Negative Feedback Loop for Tissue Elongation under Stress
Junior J West1, Teresa Zulueta-Coarasa2, Janna A Maier1
1Department of Cell & Systems Biology, University of Toronto, 25 Harbord Street, Toronto, ON M5S 3G5, Canada.
Cytohesins, like Steppke, are crucial for animal tissue elongation under stress by inhibiting actomyosin activity. This discovery reveals a negative feedback loop essential for preventing tissue tears during development.
Area of Science:
- Developmental Biology
- Cellular Mechanics
- Molecular Regulation
Background:
- Animal development involves tissue stretching due to localized contractions.
- Actomyosin activity drives these contractions, but its regulation of tissue physical properties under stress is unclear.
Purpose of the Study:
- To investigate the molecular mechanisms regulating tissue elongation under mechanical stress.
- To identify key proteins involved in controlling tissue tension during development.
Main Methods:
- Utilized Drosophila dorsal closure and zebrafish epiboly models.
- Employed protein localization, laser ablation, and genetic interaction studies.
- Performed live imaging to observe protein dynamics.
Main Results:
- Cytohesins, specifically Steppke, are essential for tissue elongation under stress.
- Steppke inhibits actomyosin activity at adherens junctions, reducing tissue tension.
- Loss of Steppke leads to embryogenesis failure due to myosin misregulation and tissue tears.
- Actomyosin network assembly triggers rapid, localized Steppke accumulation.
Conclusions:
- A rapid negative feedback loop involving cytohesins (Steppke) attenuates tissue tension.
- This mechanism allows for orderly tissue elongation under mechanical stress during animal development.
- Identified a novel molecular pathway regulating tissue physical properties in response to force.
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