SPIN90 associates with mDia1 and the Arp2/3 complex to regulate cortical actin organization

Nat Cell Biol. 2020 Jul;22(7):803-814. doi: 10.1038/s41556-020-0531-y. Epub 2020 Jun 22.

Abstract

Cell shape is controlled by the submembranous cortex, an actomyosin network mainly generated by two actin nucleators: the Arp2/3 complex and the formin mDia1. Changes in relative nucleator activity may alter cortical organization, mechanics and cell shape. Here we investigate how nucleation-promoting factors mediate interactions between nucleators. In vitro, the nucleation-promoting factor SPIN90 promotes formation of unbranched filaments by Arp2/3, a process thought to provide the initial filament for generation of dendritic networks. Paradoxically, in cells, SPIN90 appears to favour a formin-dominated cortex. Our in vitro experiments reveal that this feature stems mainly from two mechanisms: efficient recruitment of mDia1 to SPIN90-Arp2/3 nucleated filaments and formation of a ternary SPIN90-Arp2/3-mDia1 complex that greatly enhances filament nucleation. Both mechanisms yield rapidly elongating filaments with mDia1 at their barbed ends and SPIN90-Arp2/3 at their pointed ends. Thus, in networks, SPIN90 lowers branching densities and increases the proportion of long filaments elongated by mDia1.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Actin Cytoskeleton / physiology*
  • Actin-Related Protein 2-3 Complex / genetics
  • Actin-Related Protein 2-3 Complex / metabolism*
  • Actins / metabolism*
  • Adaptor Proteins, Signal Transducing / genetics
  • Adaptor Proteins, Signal Transducing / metabolism*
  • Animals
  • Blastula / cytology
  • Blastula / metabolism
  • Cell Shape
  • Embryo, Nonmammalian / cytology
  • Embryo, Nonmammalian / metabolism
  • Formins / genetics
  • Formins / metabolism*
  • Humans
  • Melanoma / genetics
  • Melanoma / metabolism
  • Melanoma / pathology*
  • Muscle Proteins / genetics
  • Muscle Proteins / metabolism*
  • Xenopus laevis / growth & development
  • Xenopus laevis / metabolism

Substances

  • Actin-Related Protein 2-3 Complex
  • Actins
  • Adaptor Proteins, Signal Transducing
  • DIAPH1 protein, human
  • Formins
  • Muscle Proteins
  • NCKIPSD protein, human