Molecular Biology of the Cell click for ASCB 2009 Annual Meeting page

Home Help [Feedback] [For Subscribers] [Archive] [Search] [Contents]
 QUICK SEARCH:   [advanced]


     


Originally published as MBC in Press, 10.1091/mbc.E07-06-0628 on September 26, 2007

Vol. 18, Issue 12, 4731-4740, December 2007

This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Supplemental Materials
Right arrow All Versions of this Article:
E07-06-0628v1
18/12/4731    most recent
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Zhang, M.
Right arrow Articles by Saltiel, A. R.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Zhang, M.
Right arrow Articles by Saltiel, A. R.

Identification of CAP as a Costameric Protein that Interacts with Filamin CFormula

Mei Zhang, Jun Liu*, Alan Cheng, Stephanie M. DeYoung, and Alan R. Saltiel

Departments of Internal Medicine and Physiology, Life Sciences Institute, University of Michigan, Ann Arbor, MI 48109

Submitted July 2, 2007; Revised September 13, 2007; Accepted September 14, 2007
Monitoring Editor: Yu-li Wang

Cbl-associated protein (CAP) is an adaptor protein that interacts with both signaling and cytoskeletal proteins. Here, we characterize the expression, localization and potential function of CAP in striated muscle. CAP is markedly induced during myoblast differentiation, and colocalizes with vinculin during costamerogenesis. In adult mice, CAP is enriched in oxidative muscle fibers, and it is found in membrane anchorage complexes, including intercalated discs, costameres, and myotendinous junctions. Using both yeast two-hybrid and proteomic approaches, we identified the sarcomeric protein filamin C (FLNc) as a binding partner for CAP. When overexpressed, CAP recruits FLNc to cell–extracellular matrix adhesions, where the two proteins cooperatively regulate actin reorganization. Moreover, overexpression of CAP inhibits FLNc-induced cell spreading on fibronectin. In dystrophin-deficient mdx mice, the expression and membrane localization of CAP is increased, concomitant with the elevated plasma membrane content of FLNc, suggesting that CAP may compensate for the reduced membrane linkage of the myofibrils due to the loss of the dystroglycan–sarcoglycan complex in these mice. Thus, through its interaction with FLNc, CAP provides another link between the myofibril cytoskeleton and the plasma membrane of muscle cells, and it may play a dynamic role in the regulation and maintenance of muscle structural integrity.


This article was published online ahead of print in MBC in Press (http://www.molbiolcell.org/cgi/doi/10.1091/mbc.E07-06-0628) on September 26, 2007.

Formula The online version of this article contains supplemental material at MBC Online (http://www.molbiolcell.org).

* Present address: Kentucky Pediatric Research Institute, University of Kentucky School of Medicine, Lexington, KY 40536.

Address correspondence to: Alan R. Saltiel (saltiel{at}lsi.umich.edu).

Abbreviations used: CAP, cbl-associated protein; DGC, dystrophin-glycoprotein complex; ECM, extracellular matrix; FLNc, filamin C.




This article has been cited by other articles:


Home page
Hum Mol GenetHome page
D. Li, C. Long, Y. Yue, and D. Duan
Sub-physiological sarcoglycan expression contributes to compensatory muscle protection in mdx mice
Hum. Mol. Genet., April 1, 2009; 18(7): 1209 - 1220.
[Abstract] [Full Text] [PDF]


Home page
IOVSHome page
P. V. Rao and R. Maddala
Abundant Expression of Ponsin, a Focal Adhesion Protein, in Lens and Downregulation of Its Expression by Impaired Cytoskeletal Signaling
Invest. Ophthalmol. Vis. Sci., April 1, 2009; 50(4): 1769 - 1777.
[Abstract] [Full Text] [PDF]




Home Help [Feedback] [For Subscribers] [Archive] [Search] [Contents]
Copyright © 2007 by The American Society for Cell Biology. Terms of copyright protection, warranties, and disclaimers.