Diatoms are a group of unicellular microalgae that are encased in a highly
ornamented siliceous cell wall, or frustule. Pennate diatoms haw: bilateral
symmetry and many genera possess an elongated slit in the frustule called
the raphe, a feature synonymous with their ability to adhere and glide over
a substratum, a process little understood. We have used cytoskeleton-disru
pting drugs to investigate the roles of actin, myosin, and microtubules in
diatom gliding or motility. No effect on diatom gliding was observed using
the cytochalasins, known actin inhibitors, or the microtubule-inhibitors or
yzalin and nocodiazole. The latrunculins are a new group of anti-actin drug
s, and we show here that they are potent inhibitors of diatom gliding, resu
lting in the complete disassociation of the raphe-associated actin cables.
The recovery of actin staining and motility following latrunculin treatment
was extremely fast. Cells exposed to latrunculin for 12 h recovered full f
unction and actin staining within 5 sec of the drug being removed, demonstr
ating that the molecular components required for this motility system are i
mmediately available. Butanedione monoxime (BDM), a known myosin inhibitor,
also reversibly inhibited diatom gliding in a manner similar to the latrun
culins. This work provides evidence that diatom gliding is based on an acti
n/myosin motility system. (C) 1999 Wiley-Liss, Inc.