Identification of FHOD1-binding proteins and mechanisms of FHOD1-regulated actin dynamics

J Cell Biochem. 2004 May 1;92(1):29-41. doi: 10.1002/jcb.20031.

Abstract

Formin homology-2-domain containing protein 1 (FHOD1) regulates gene transcription, actin-cytoskeleton structure, and cell migration. To gain insight into the mechanisms by which FHOD1 mediates these diverse activities, a yeast-two-hybrid screen was performed to identify FHOD1-binding proteins. Three proteins specifically interacted with the carboxy-terminal two-thirds of FHOD1, which includes the FH1, FH2, and diaphanous activating domains (DAD). The newly identified FHOD1-binding proteins are protein kinase C binding protein 1 (PRKCBP1), cyclophilin B, and an isoform of WASP-interacting SH3-domain protein/diaphanous-interacting protein 1 (WISH/DIP1), named WISH-B. The proline-rich FH1 domain of FHOD1 was sufficient to interact with the central portion of PRKCP1 and full-length cyclophilin B. The FH1 domain also interacted with full-length WISH-B, but the extreme amino-terminus was sufficient to associate with WISH-B as well. WISH-B altered the solubility of FHOD1 in vitro and a truncation mutant containing the amino-terminal 227 residues of WISH-B disrupted FHOD1-induced stress fibers. WISH-B did not affect FHOD1-induced gene transcription through the serum response factor (SRF) recognition site on the skeletal alpha actin promoter (SkA). However, stabilization of F-actin prevented FHOD1 dependent activation of this promoter in presence of high, but not low serum concentrations. Thus, the identification of a new FHOD1-binding protein provides insight into the mechanisms by which FHOD1 regulates actin polymerization and transcription.

Publication types

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

MeSH terms

  • Actins / genetics*
  • Adaptor Proteins, Signal Transducing / metabolism
  • Animals
  • Carrier Proteins / metabolism*
  • Cell Line
  • Cyclophilins / metabolism
  • Fetal Proteins / genetics
  • Fetal Proteins / metabolism*
  • Formins
  • Humans
  • Mice
  • Muscle Proteins / metabolism
  • Nuclear Proteins / genetics
  • Nuclear Proteins / metabolism*
  • Peptidylprolyl Isomerase
  • Promoter Regions, Genetic / genetics
  • Protein Binding
  • Protein Interaction Mapping
  • Protein Structure, Tertiary
  • Receptors for Activated C Kinase
  • Receptors, Cell Surface / metabolism
  • Response Elements / genetics
  • Stress Fibers / metabolism*
  • Stress Fibers / ultrastructure
  • Transcriptional Activation / genetics
  • Tumor Suppressor Proteins
  • Two-Hybrid System Techniques

Substances

  • Actins
  • Adaptor Proteins, Signal Transducing
  • Carrier Proteins
  • FHOD1 protein, human
  • Fetal Proteins
  • Formins
  • Muscle Proteins
  • Nckipsd protein, mouse
  • Nuclear Proteins
  • Receptors for Activated C Kinase
  • Receptors, Cell Surface
  • Tumor Suppressor Proteins
  • ZMYND8 protein, human
  • cyclophilin B
  • Cyclophilins
  • Peptidylprolyl Isomerase