Mind bomb 2 promotes cell migration and epithelial structure by regulating adhesion complexes and the actin cytoskeleton.

Cell migration is essential in animal development and co-opted during metastasis and inflammatory diseases. Some cells migrate collectively, which requires them to balance epithelial characteristics such as stable cell-cell adhesions with features of motility like rapid turnover of adhesions and dynamic cytoskeletal structures. How this is regulated is not entirely clear but important to understand. While investigating Drosophila oogenesis, we found that the putative E3 ubiquitin ligase, Mind bomb 2 (Mib2), is required to promote epithelial stability and the collective cell migration of border cells. Through biochemical analysis, we identified components of Mib2 complexes, which include E-cadherin and α- and β-catenins, as well as actin regulators. We also found that three Mib2 interacting proteins, RhoGAP19D, Supervillin, and Myosin heavy chain-like, affect border cell migration. mib2 mutant main body follicle cells have drastically reduced E-cadherin-based adhesion complexes and diminished actin filaments. We conclude that Mib2 acts to stabilize E-cadherin-based adhesion complexes and promote a robust actin cytoskeletal network, which is important for maintenance of epithelial integrity. The interaction with cadherin adhesion complexes and other cytoskeletal regulators contribute to its role in collective cell migration. Since Mib2 is well conserved, it may have similar functional significance in other organisms. [Display omitted] • Drosophila Mind bomb 2, an E3 ligase, is highly expressed in ovarian follicle cells. • mind bomb 2 is required for border cell migration and epithelial character. • Mind bomb 2 interactors, RhoGAP19D, Myosin heavy chain-like , and Supervillin , act in migration. • Loss of mind bomb 2 results in reduced adhesion complexes and F-actin. Summary statement: Mind bomb 2, an E3 ubiquitin ligase, enables collective cell migration in Drosophila and promotes epithelial character by stabilizing adhesion complexes and cytoskeletal proteins. [ABSTRACT FROM AUTHOR]