ARVCF catenin controls force production during vertebrate convergent extension

Dev Cell. 2022 May 9;57(9):1119-1131.e5. doi: 10.1016/j.devcel.2022.04.001. Epub 2022 Apr 26.

Abstract

The design of an animal's body plan is encoded in the genome, and the execution of this program is a mechanical progression involving coordinated movement of proteins, cells, and whole tissues. Thus, a challenge to understanding morphogenesis is connecting events that occur across various length scales. Here, we describe how a poorly characterized adhesion effector, Arvcf catenin, controls Xenopus head-to-tail axis extension. We find that Arvcf is required for axis extension within the intact organism but not within isolated tissues. We show that the organism-scale phenotype results from a defect in tissue-scale force production. Finally, we determine that the force defect results from the dampening of the pulsatile recruitment of cell adhesion and cytoskeletal proteins to membranes. These results provide a comprehensive understanding of Arvcf function during axis extension and produce an insight into how a cellular-scale defect in adhesion results in an organism-scale failure of development.

Keywords: Arvcf; biomechanics; cadherin; catenin; cell adhesion; convergent extension; morphogenesis.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Armadillo Domain Proteins* / genetics
  • Armadillo Domain Proteins* / metabolism
  • Cadherins / metabolism
  • Catenins*
  • Cell Adhesion Molecules / metabolism
  • Morphogenesis
  • Phosphoproteins / metabolism
  • Xenopus laevis / metabolism

Substances

  • Armadillo Domain Proteins
  • Cadherins
  • Catenins
  • Cell Adhesion Molecules
  • Phosphoproteins