The dynamic properties of microtubules (MTs) are important for a wide varie
ty of cellular processes, including cell division and morphogenesis. MT ass
embly and disassembly in vivo are regulated by cellular factors that influe
nce specific parameters of MT dynamics. Here, we describe the characterizat
ion of a previously reported MT assembly inhibitor activity from Xenopus oo
cytes [Gard and Kirschner, 1987: J. Cell Biol. 105.2191-2201]. Video micros
copy measurements reveal that the inhibitor specifically decreases the plus
end growth rate of MTs and increases the critical concentration for tubuli
n. However, catastrophe frequency, rescue frequency, and shrinkage rates ar
e not affected by the activity. Chromatography on Mono Q and hydroxyapatite
columns has shown that the activity cofractionates with a subpopulation of
tubulin. This tubulin subpopulation and the MT assembly inhibitor activity
also co-migrate with a large S value (25-308) on sucrose gradients. The hi
gh molecular weight tubulin complex and the MT assembly inhibitor activity
are both developmentally regulated and disappear after oocyte maturation wi
th progesterone. Cell Motil. Cytoskeleton 45.51-57, 2000. (C) 2000 Wiley-Li
ss, Inc.