Using time-lapse video microscopy, we found that ooplasmic inclusions
in the fertilized medaka egg displayed two types of movement during oo
plasmic segregation. The first manifested itself as the movement of ma
ny inclusions (diameter = 1.5-11 mum) toward the animal pole at about
2.2 mum min-1; this type of movement appeared to be streaming. The sec
ond type of movement was faster (about 44 mum min-1) and saltatory; in
clusions displaying this type of movement were smaller (diameter less-
than-or-equal-to 1.0 mum) and moved toward the vegetal pole. The movem
ent of oil droplets toward the vegetal pole of the egg may represent a
third type of motion. All these movements began only after a strong c
ontraction of the ooplasm toward the animal pole, which at 25-degrees-
C began 10-12 min after fertilization and <3 min after formation of th
e second polar body. In eggs treated with microtubule poisons-colchici
ne, colcemid, or nocodazole-oil droplets did not move toward the veget
al pole, saltatory motion toward the vegetal pole was absent, and the
growth of the blastodisc was slowed. Eggs treated with beta-lumicolchi
cine, an inactive derivative of colchicine, showed normal movements. C
olchicine, while not inhibiting formation of the second polar body, di
d inhibit pronuclear migration. These results suggest that microtubule
s are involved in the movement of some ooplasmic inclusions, including
oil droplets, toward the vegetal pole; the movement of ooplasmic incl
usions toward the animal pole; and pronuclear migration.