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Alternative molecular mechanisms for force transmission at adherens junctions via β-catenin-vinculin interaction

Morales-Camilo, Nicole, Liu, Jingzhun, Ramirez, Manuel J, Canales-Salgado, Patricio, Alegria, Juan Jose, Liu, Xuyao, Ting Ong, Hui, Barrera, Nelso P, Fierro, Angelica, Toyama, Yusuke, and others. (2024) Alternative molecular mechanisms for force transmission at adherens junctions via β-catenin-vinculin interaction. Nature Communications, 15 (1). Article Number 5608. ISSN 2041-1723. (doi:10.1038/s41467-024-49850-5) (KAR id:106505)

Abstract

Force transmission through adherens junctions (AJs) is crucial for multicellular organization, wound healing and tissue regeneration. Recent studies shed light on the molecular mechanisms of mechanotransduction at the AJs. However, the canonical model fails to explain force transmission when essential proteins of the mechanotransduction module are mutated or missing. Here, we demonstrate that, in absence of α-catenin, β-catenin can directly and functionally interact with vinculin in its open conformation, bearing physiological forces. Furthermore, we found that β-catenin can prevent vinculin autoinhibition in the presence of α-catenin by occupying vinculin´s head-tail interaction site, thus preserving force transmission capability. Taken together, our findings suggest a multi-step force transmission process at AJs, where α-catenin and β-catenin can alternatively and cooperatively interact with vinculin. This can explain the graded responses needed to maintain tissue mechanical homeostasis and, importantly, unveils a force-bearing mechanism involving β-catenin and extended vinculin that can potentially explain the underlying process enabling collective invasion of metastatic cells lacking α-catenin.

Item Type: Article
DOI/Identification number: 10.1038/s41467-024-49850-5
Uncontrolled keywords: Vinculin, beta catenin, adherens junctions
Subjects: Q Science > QH Natural history > QH581.2 Cell Biology
Divisions: Divisions > Division of Natural Sciences > Biosciences
Funders: University of Kent (https://ror.org/00xkeyj56)
Depositing User: Ben Goult
Date Deposited: 06 Jul 2024 08:54 UTC
Last Modified: 05 Nov 2024 13:12 UTC
Resource URI: https://kar.kent.ac.uk/id/eprint/106505 (The current URI for this page, for reference purposes)

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