Fission yeast cells tolerate the total absence of the cdc25 mitotic inducer
in two cases, either in cdc2-3w or in wee1 genetic backgrounds, In the cdc
2-3w cdc25 Delta double mutant, the rate-limiting step leading to mitosis i
s reaching a critical size. However, the size control of this mutant operat
es in late G(2), which is different from wild-type (WT) cells. This fact su
ggests that in WT the rate-limiting molecular process during the G(2) timer
is the Tyr15 dephosphorylation of cdc2, for which the cdc25 phosphatase (t
ogether with its back-up, pyp3) is dependent. In the wee1-50 cdc25 Delta mu
tant, the population splits into different clusters, all lacking mitotic si
ze control. This strain maintains size homeostasis by a novel method, which
is random movement of the cells from one cluster to another in the success
ive generations. These cells should normally have a 'minimal cycle', a 'tim
er' with short G(1) and G(2) phases, However, very often the cells abort mi
tosis, possibly at an early event and return back to early Gz, thus lengthe
ning their cycles. The inability of these cells to start anaphase might be
caused by the absence of the main mitotic regulators (wee1 and cdc25) and t
he improper regulation of their back-up copies (mik1 and pyp3, respectively
).