NHERF1 regulates actin cytoskeleton organization through modulation of α-actinin-4 stability

FASEB J. 2016 Feb;30(2):578-89. doi: 10.1096/fj.15-275586. Epub 2015 Oct 2.

Abstract

The actin cytoskeleton is composed of a highly dynamic network of filamentous proteins, yet the molecular mechanism that regulates its organization and remodeling remains elusive. In this study, Na(+)/H(+) exchanger regulatory factor (NHERF)-1 loss-of-function and gain-of-function experiments reveal that polymerized actin cytoskeleton (F-actin) in HeLa cells is disorganized by NHERF1, whereas actin protein expression levels exhibit no detectable change. To elucidate the molecular mechanism underlying actin cytoskeleton disorganization by NHERF1, a combined 2-dimensional electrophoresis-matrix-assisted laser desorption/ionization-time of flight mass spectrometry approach was used to screen for proteins regulated by NHERF1 in HeLa cells. α-Actinin-4, an actin cross-linking protein, was identified. Glutathione S-transferase pull-down and coimmunoprecipitation studies showed the α-actinin-4 carboxyl-terminal region specifically interacted with the NHERF1 postsynaptic density 95/disc-large/zona occludens-1 domain. The NHERF1/α-actinin-4 interaction increased α-actinin-4 ubiquitination and decreased its expression levels, resulting in actin cytoskeleton disassembly. Our study identified α-actinin-4 as a novel NHERF1 interaction partner and provided new insights into the regulatory mechanism of the actin cytoskeleton by NHERF1.

Keywords: F-actin; PDZ; protein interaction; stress fiber; ubiquitination.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Actinin / genetics
  • Actinin / metabolism*
  • Animals
  • COS Cells
  • Chlorocebus aethiops
  • Cytoskeleton / physiology*
  • Down-Regulation
  • Gene Expression Regulation / physiology
  • Gene Knockdown Techniques
  • HeLa Cells
  • Humans
  • Phosphoproteins / genetics
  • Phosphoproteins / metabolism*
  • Proteasome Endopeptidase Complex / metabolism
  • Sodium-Hydrogen Exchangers / genetics
  • Sodium-Hydrogen Exchangers / metabolism*
  • Ubiquitin / metabolism

Substances

  • ACTN4 protein, human
  • Phosphoproteins
  • Sodium-Hydrogen Exchangers
  • Ubiquitin
  • sodium-hydrogen exchanger regulatory factor
  • Actinin
  • Proteasome Endopeptidase Complex