Peripodial adherens junctions regulate Ajuba-Yorkie signaling to preserve fly eye morphology.
Dana F DeSantisScott J NealQingxiang ZhouFrancesca PignoniPublished in: Biology open (2023)
The Drosophila eye develops from the larval eye disc, a flattened vesicle comprised of continuous retinal and peripodial epithelia (PE). The PE is an epithelium that plays a supporting role in retinal neurogenesis, but gives rise to cuticle in the adult. We report here that the PE is also necessary to preserve the morphology of the retinal epithelium. Depletion of the adherens junction (AJ) components β-Catenin (β-Cat), DE-Cadherin or α-Catenin from the PE leads to altered disc morphology, characterized by retinal displacement (RDis); so too does loss of the Ajuba protein Jub, an AJ-associated regulator of the transcriptional coactivator Yorkie (Yki). Restoring AJs or overexpressing Yki in β-Cat deficient PE results in suppression of RDis. Additional suppressors of AJ-dependent RDis include knockdown of Rho kinase (Rok) and Dystrophin (Dys). Furthermore, knockdown of βPS integrin (Mys) from the PE results in RDis, while overexpression of Mys can suppress RDis induced by the loss of β-Cat. We thus propose that AJ-Jub-Yki signaling in PE cells regulates PE cell contractile properties and/or attachment to the extracellular matrix to promote normal eye disc morphology.
Keyphrases
- optical coherence tomography
- diabetic retinopathy
- extracellular matrix
- cell proliferation
- transcription factor
- epithelial mesenchymal transition
- single cell
- skeletal muscle
- stem cells
- oxidative stress
- brain injury
- tyrosine kinase
- signaling pathway
- subarachnoid hemorrhage
- cell death
- cell adhesion
- protein protein
- heat shock
- cerebral ischemia