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Apical domain polarization localizes actin-myosin activity to drive ratchet-like apical constriction

Apical constriction promotes epithelia folding, which changes tissue architecture. During Drosophila gastrulation, mesoderm cells exhibit repeated contractile pulses that are stabilized such that cells apically constrict like a ratchet. The transcription factor Twist is required to stabilize cell sh...

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Detalles Bibliográficos
Autores principales: Mason, Frank M., Tworoger, Michael, Martin, Adam C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3736338/
https://www.ncbi.nlm.nih.gov/pubmed/23831726
http://dx.doi.org/10.1038/ncb2796
Descripción
Sumario:Apical constriction promotes epithelia folding, which changes tissue architecture. During Drosophila gastrulation, mesoderm cells exhibit repeated contractile pulses that are stabilized such that cells apically constrict like a ratchet. The transcription factor Twist is required to stabilize cell shape, however it is unknown how Twist spatially coordinates downstream signals to prevent cell relaxation. We find that during constriction, Rho-associated kinase (Rok) is polarized to the middle of the apical domain (medioapical cortex), separate from adherens junctions (AJs). Rok recruits or stabilizes medioapical myosin II (Myo-II), which contracts dynamic medioapical actin cables. The formin Diaphanous mediates apical actin assembly to suppress medioapical E-Cadherin localization and form stable connections between the medioapical contractile network and AJs. Twist is not required for apical Rok recruitment, but instead polarizes Rok medioapically. Therefore, Twist establishes “radial” cell polarity of Rok/Myo-II and E-Cadherin and promotes medioapical actin assembly in mesoderm cells to stabilize cell shape fluctuations.