Re-expression of ABP-120 rescues cytoskeletal, motility, and phagocytosis defects of ABP-120- Dictyostelium mutants

Mol Biol Cell. 1996 May;7(5):803-23. doi: 10.1091/mbc.7.5.803.

Abstract

The actin binding protein ABP-120 has been proposed to cross-link actin filaments in nascent pseudopods, in a step required for normal pseudopod extension in motile Dictyostelium amoebae. To test this hypothesis, cell lines that lack ABP-120 were created independently either by chemical mutagenesis or homologous recombination. Different phenotypes were reported in these two studies. The chemical mutant shows only a subtle defect in actin cross-linking, while the homologous recombinant mutants show profound defects in actin cross-linking, cytoskeletal structure, pseudopod number and size, cell motility and chemotaxis and, as shown here, phagocytosis. To resolve the controversy as to what the ABP-120- phenotype is, ABP-120 was re-expressed in an ABP-120- cell line created by homologous recombination. Two independently "rescued" cell lines that express wild-type levels of ABP-120 were analyzed. In both rescued cell lines, actin incorporation into the cytoskeleton, pseudopod formation, cell morphology, instantaneous velocity, phagocytosis, and chemotaxis were restored to wild-type levels. There is no alteration in the expression levels of several related actin binding proteins in either the original ABP-120- cell line or in the rescued cell lines, leading to the conclusion that neither the aberrant phenotype observed in ABP-120- cells nor the normal phenotype reasserted in rescued cells can be attributed to alterations in the levels of other abundant and related actin binding proteins. Re-expression of ABP-120 in ABP-120- cells reestablishes normal structural and behavioral parameters, demonstrating that the severity and properties of the structural and behavioral defects of ABP-120- cell lines produced by homologous recombination are the direct result of the absence of ABP-120.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Actins / genetics
  • Actins / metabolism
  • Animals
  • Blotting, Southern
  • Carrier Proteins / metabolism*
  • Cell Movement / drug effects
  • Cell Movement / genetics
  • Cell Movement / physiology*
  • Cell Size / genetics
  • Cell Size / physiology
  • Chemotaxis / drug effects
  • Cyclic AMP / pharmacology
  • Cytoskeleton / genetics
  • Cytoskeleton / metabolism*
  • Dictyostelium / genetics*
  • Dictyostelium / metabolism*
  • Gene Expression Regulation, Fungal
  • Microfilament Proteins / metabolism*
  • Microscopy, Confocal
  • Microscopy, Electron
  • Microscopy, Fluorescence
  • Phagocytosis / genetics
  • Phagocytosis / physiology
  • Pinocytosis / genetics
  • Pinocytosis / physiology
  • Pseudopodia / genetics
  • Pseudopodia / physiology*
  • Transformation, Genetic

Substances

  • Actins
  • Carrier Proteins
  • Microfilament Proteins
  • abpC protein, Dictyostelium
  • Cyclic AMP