EGFR-dependent actomyosin patterning coordinates morphogenetic movements between tissues.
D Nathaniel ClarkeAdam C MartinPublished in: bioRxiv : the preprint server for biology (2023)
The movements that give rise to the body's structure are powered by cell shape changes and rearrangements that are coordinated at supracellular scales. How such cellular coordination arises and integrates different morphogenetic programs is unclear. Using quantitative imaging, we found a complex pattern of adherens junction (AJ) levels in the ectoderm prior to gastrulation onset in Drosophila . AJ intensity exhibited a double-sided gradient, with peaks at the dorsal midline and ventral neuroectoderm. We show that this dorsal-ventral AJ pattern is regulated by epidermal growth factor (EGF) signaling and that this signal is required for ectoderm cell movement during mesoderm invagination and axis extension. We identify AJ levels and junctional actomyosin as downstream effectors of EGFR signaling. Overall, our study demonstrates a mechanism of coordination between tissue folding and convergent extension that facilitates embryo-wide gastrulation movements.
Keyphrases
- growth factor
- spinal cord
- small cell lung cancer
- single cell
- epidermal growth factor receptor
- neuropathic pain
- high resolution
- cell therapy
- tyrosine kinase
- deep brain stimulation
- public health
- spinal cord injury
- gene expression
- high intensity
- mass spectrometry
- bone marrow
- molecular dynamics simulations
- mesenchymal stem cells