Myosin II is a major component of a contractile ring. To examine if myosin
II turns over in contractile rings, fluorescence of GFP-myosin II expressed
in Dictyostelium cells was bleached locally by laser illumination, and the
recovery was monitored. The fluorescence recovered with a half time of 7.0
1 +/- 2.62 s. This recovery was not caused by lateral movement of myosin II
from the nonbleached area, but by an exchange with endoplasmic myosin II.
Similar experiments were performed in cells expressing GFP-3ALA myosin II,
of which three phosphorylatable threonine residues were replaced with alani
ne residues. In this case, recovery was not detected within a comparable ti
me range. These results indicate that myosin II in the contractile ring per
forms dynamic turnover via its heavy chain phosphorylation. Because GFP-3AL
A myosin II did not show the recovery, it served as a useful marker of myos
in II movement, which enabled us to demonstrate cortical flow of myosin II
toward the equator for the first time. Thus, cortical flow accompanies the
dynamic exchange of myosin II during the formation of contractile rings.