Epidermolysis bullosa simplex-type mutations alter the dynamics of the keratin cytoskeleton and reveal a contribution of actin to the transport of keratin subunits

NS Werner, R Windoffer, P Strnad… - Molecular biology of …, 2004 - Am Soc Cell Biol
NS Werner, R Windoffer, P Strnad, C Grund, RE Leube, TM Magin
Molecular biology of the cell, 2004Am Soc Cell Biol
Dominant keratin mutations cause epidermolysis bullosa simplex by transforming keratin (K)
filaments into aggregates. As a first step toward understanding the properties of mutant
keratins in vivo, we stably transfected epithelial cells with an enhanced yellow fluorescent
protein-tagged K14R125C mutant. K14R125C became localized as aggregates in the cell
periphery and incorporated into perinuclear keratin filaments. Unexpectedly, keratin
aggregates were in dynamic equilibrium with soluble subunits at a half-life time of< 15 min …
Dominant keratin mutations cause epidermolysis bullosa simplex by transforming keratin (K) filaments into aggregates. As a first step toward understanding the properties of mutant keratins in vivo, we stably transfected epithelial cells with an enhanced yellow fluorescent protein-tagged K14R125C mutant. K14R125C became localized as aggregates in the cell periphery and incorporated into perinuclear keratin filaments. Unexpectedly, keratin aggregates were in dynamic equilibrium with soluble subunits at a half-life time of <15 min, whereas filaments were extremely static. Therefore, this dominant-negative mutation acts by altering cytoskeletal dynamics and solubility. Unlike previously postulated, the dominance of mutations is limited and strictly depends on the ratio of mutant to wild-type protein. In support, K14R125C-specific RNA interference experiments resulted in a rapid disintegration of aggregates and restored normal filaments. Most importantly, live cell inhibitor studies revealed that the granules are transported from the cell periphery inwards in an actin-, but not microtubule-based manner. The peripheral granule zone may define a region in which keratin precursors are incorporated into existing filaments. Collectively, our data have uncovered the transient nature of keratin aggregates in cells and offer a rationale for the treatment of epidermolysis bullosa simplex by using short interfering RNAs.
Am Soc Cell Biol