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Article
Novel interactors and a role for supervillin in early cytokinesis
Luna Lab Publications
  • Tara C. Smith, University of Massachusetts Medical School
  • Zhiyou Fang, University of Massachusetts Medical School
  • Elizabeth J. Luna, University of Massachusetts Medical School
UMMS Affiliation
Department of Cell Biology
Date
6-24-2010
Document Type
Article
Medical Subject Headings
Amino Acid Sequence; Animals; Biological Assay; COS Cells; Cattle; Cell Proliferation; Cercopithecus aethiops; *Cytokinesis; Cytoskeletal Proteins; Gene Knockdown Techniques; Green Fluorescent Proteins; Hela Cells; Humans; Membrane Proteins; Microfilament Proteins; Myosin Type II; Protein Binding; Protein Structure, Secondary; Protein Transport; Recombinant Fusion Proteins
Disciplines
Abstract
Supervillin, the largest member of the villin/gelsolin/flightless family, is a peripheral membrane protein that regulates each step of cell motility, including cell spreading. Most known interactors bind within its amino (N)-terminus. We show here that the supervillin carboxy (C)-terminus can be modeled as supervillin-specific loops extending from gelsolin-like repeats plus a villin-like headpiece. We have identified 27 new candidate interactors from yeast two-hybrid screens. The interacting sequences from 12 of these proteins (BUB1, EPLIN/LIMA1, FLNA, HAX1, KIF14, KIFC3, MIF4GD/SLIP1, ODF2/Cenexin, RHAMM, STARD9/KIF16A, Tks5/SH3PXD2A, TNFAIP1) co-localize with and mis-localize EGFP-supervillin in mammalian cells, suggesting associations in vivo. Supervillin-interacting sequences within BUB1, FLNA, HAX1, and MIF4GD also mimic supervillin over-expression by inhibiting cell spreading. Most new interactors have known roles in supervillin-associated processes, e.g. cell motility, membrane trafficking, ERK signaling, and matrix invasion; three (KIF14, KIFC3, STARD9/KIF16A) have kinesin motor domains; and five (EPLIN, KIF14, BUB1, ODF2/cenexin, RHAMM) are important for cell division. GST fusions of the supervillin G2-G3 or G4-G6 repeats co-sediment KIF14 and EPLIN, respectively, consistent with a direct association. Supervillin depletion leads to increased numbers of bi- and multi-nucleated cells. Cytokinesis failure occurs predominately during early cytokinesis. Supervillin localizes with endogenous myosin II and EPLIN in the cleavage furrow, and overlaps with the oncogenic kinesin, KIF14, at the midbody. We conclude that supervillin, like its interactors, is important for efficient cytokinesis. Our results also suggest that supervillin and its interaction partners coordinate actin and microtubule motor functions throughout the cell cycle.
Rights and Permissions
Citation: Cytoskeleton (Hoboken). 2010 Jun;67(6):346-64. Link to article on publisher's site
Related Resources
Link to Article in PubMed
PubMed ID
20309963
Citation Information
Tara C. Smith, Zhiyou Fang and Elizabeth J. Luna. "Novel interactors and a role for supervillin in early cytokinesis" Vol. 67 Iss. 6 (2010) ISSN: 1949-3592 (Electronic)
Available at: http://works.bepress.com/lunae/40/