Smith, Tara C.
Crowley, Jessica Lynn
Palmieri, Stephen J.
Lifshitz, Lawrence M.
Ehrhardt, Anka G.
Hoffman, Laura M.
Beckerle, Mary C.
Luna, Elizabeth J.
UMass Chan AffiliationsProgram in Molecular Medicine
Department of Physiology
Department of Cell Biology
KeywordsAdaptor Proteins, Signal Transducing
Green Fluorescent Proteins
Myocytes, Smooth Muscle
Regulatory Sequences, Nucleic Acid
Medicine and Health Sciences
MetadataShow full item record
AbstractCell-substrate contacts, called focal adhesions (FAs), are dynamic in rapidly moving cells. We show that supervillin (SV)--a peripheral membrane protein that binds myosin II and F-actin in such cells--negatively regulates stress fibers, FAs, and cell-substrate adhesion. The major FA regulatory sequence within SV (SV342-571) binds to the LIM domains of two proteins in the zyxin family, thyroid receptor-interacting protein 6 (TRIP6) and lipoma-preferred partner (LPP), but not to zyxin itself. SV and TRIP6 colocalize within large FAs, where TRIP6 may help recruit SV. RNAi-mediated decreases in either protein increase cell adhesion to fibronectin. TRIP6 partially rescues SV effects on stress fibers and FAs, apparently by mislocating SV away from FAs. Thus, SV interactions with TRIP6 at FAs promote loss of FA structure and function. SV and TRIP6 binding partners suggest several specific mechanisms through which the SV-TRIP6 interaction may regulate FA maturation and/or disassembly.
J Cell Biol. 2006 Jul 31;174(3):447-58. Link to article on publisher's site
Permanent Link to this Itemhttp://hdl.handle.net/20.500.14038/50787
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