The plant actin cytoskeleton is characterized by a high diversity in regard
to gene families, isoforms, and degree of polymerization. In addition to t
he most abundant F-actin assemblies like filaments and their bundles, G-act
in obviously assembles in the form of actin oligomers composed of a few act
in molecules which can be extensively cross-linked into complex dynamic mes
hworks. The role of the actomyosin complex as a force generating system - b
ased on principles operating as in muscle cells - is clearly established fo
r long-range mass transport in large algal cells and specialized cell types
of higher plants. Extended F-actin networks, mainly composed of F-actin bu
ndles, are the structural basis for this cytoplasmic streaming of high velo
cities On the other hand, evidence is accumulating that delicate meshworks
built of short F-actin oligomers are critical for events occurring at the p
lasma membrane, e.g., actin interventions into activities of ion channels a
nd hormone carriers, signaling pathways based on phospholipids, and exo- an
d endocytotic processes. These unique F-actin arrays, constructed by polyme
rization-depolymerization processes propelled via synergistic actions of ac
tin-binding proteins such as profilin and actin depolymerizing factor (ADF)
/cofilin are supposed to be engaged in diverse aspects of plant morphogenes
is. Finally, rapid rearrangements of F-actin meshworks interconnecting endo
cellular membranes turn out to be especially important for perception-signa
ling purposes of plant cells, e.g., in association with guard cell movement
s, mechano- and gravity-sensing, plant host-pathogen interactions, and woun
d-healing. (C) 1999 Wiley-Liss, Inc.