TY - JOUR
T1 - Cortexillins, major determinants of cell shape and size, are actin- bundling proteins with a parallel coiled-coil tail
AU - Faix, Jan
AU - Steinmetz, Michel
AU - Boves, Heike
AU - Kammerer, Richard A.
AU - Lottspeich, Friedrich
AU - Mintert, Ursula
AU - Murphy, John
AU - Stock, Alexander
AU - Aebi, Ueli
AU - Gerisch, Günther
PY - 1996/8/23
Y1 - 1996/8/23
N2 - Cortexillins I and II of D. discoideum constitute a novel subfamily of proteins with actin-binding sites of the α-actinin/spectrin type. The C- terminal halves of these dimeric proteins contain a heptad repeat domain by which the two subunits are joined to form a two-stranded, parallel coiled coil, giving rise to a 19 nm tail. The N-terminal domains that encompass a consensus actin-binding sequence are folded into globular heads. Cortexillin- linked actin filaments form preferentially anti-parallel bundles that associate into meshworks. Both cortexillins are enriched in the cortex of locomoting cells, primarily at the anterior and posterior ends. Elimination of the two isoforms by gene disruption gives rise to large, flattened cells with rugged boundaries, portions of which are often connected by thin cytoplasmic bridges. The double-mutant cells are multinucleate owing to a severe impairment of cytokinesis.
AB - Cortexillins I and II of D. discoideum constitute a novel subfamily of proteins with actin-binding sites of the α-actinin/spectrin type. The C- terminal halves of these dimeric proteins contain a heptad repeat domain by which the two subunits are joined to form a two-stranded, parallel coiled coil, giving rise to a 19 nm tail. The N-terminal domains that encompass a consensus actin-binding sequence are folded into globular heads. Cortexillin- linked actin filaments form preferentially anti-parallel bundles that associate into meshworks. Both cortexillins are enriched in the cortex of locomoting cells, primarily at the anterior and posterior ends. Elimination of the two isoforms by gene disruption gives rise to large, flattened cells with rugged boundaries, portions of which are often connected by thin cytoplasmic bridges. The double-mutant cells are multinucleate owing to a severe impairment of cytokinesis.
U2 - 10.1016/S0092-8674(00)80136-1
DO - 10.1016/S0092-8674(00)80136-1
M3 - Article
C2 - 8752217
SN - 1097-4172
VL - 86
SP - 631
EP - 642
JO - Cell
JF - Cell
IS - 4
ER -