Activation is required for gamete docking. Live, activated imp12
mt- mutants were mixed with fixed, SYTOX-labeled wild-type mt+
gametes and the percentage of docked cells was determined as described in
MATERIALS AND METHODS. Unactivated mt+ gametes were treated under the
following conditions before fixation: A, activated with dibutyryl cAMP and
papaverine; UnA→L, cell walls were removed with lysin; L→A, cells
treated with lysin followed by activation; and A→L, activation followed
by lysin treatment. Triplicate samples were counted for each experiment (bar,
SEM).