Utrophin and dystrophin present two large proteins that link the intracellular actin cytoskeleton to the extracellular matrix via the C-terminal-associated protein complex. Here we describe a novel short N-terminal isoform of utrophin and its protein product in various rat tissues (N-utro, 62kDa, amino acids 1-539, comprising the actin-binding domain plus the first two spectrin repeats). Using different N-terminal recombinant utrophin fragments, we show that actin binding exhibits pronounced negative cooperativity (affinity constants K 1= ∼ 5×10 6 and K 2= ∼1 × 10 5M -1) and is Ca 2+-insensitive. Expression of the different fragments in COS7 cells and in myotubes indicates that the actin-binding domain alone binds exlusively to actin filaments. The recombinant N-utro analogue binds in vitro to actin and in the cells associates to the membranes. The results indicate that N-utro may be responsible for the anchoring of the cortical actin cytoskeleton to the membranes in muscle and other tissues. Copyright © 2011 Richard A. Zuellig et al.
CITATION STYLE
Zuellig, R. A., Bornhauser, B. C., Amstutz, R., Constantin, B., & Schaub, M. C. (2011). Tissue expression and actin binding of a novel N-terminal utrophin isoform. Journal of Biomedicine and Biotechnology, 2011. https://doi.org/10.1155/2011/904547
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