DIVISION-SITE SELECTION, CELL-SEPARATION, AND FORMATION OF ANUCLEATE MINICELLS IN SCHIZOSACCHAROMYCES-POMBE MUTANTS RESISTANT TO CELL-WALL LYTIC ENZYMES
A. Grallert et al., DIVISION-SITE SELECTION, CELL-SEPARATION, AND FORMATION OF ANUCLEATE MINICELLS IN SCHIZOSACCHAROMYCES-POMBE MUTANTS RESISTANT TO CELL-WALL LYTIC ENZYMES, Protoplasma, 198(3-4), 1997, pp. 218-229
In most eukaryotic organisms that have cell walls, cell separation or
cytokinesis is a degradative enzymatic process. Zn the fission yeast S
chizosaccharomyces pombe, it is a post-M-phase event that includes the
degradation of part of the cell wall and the primary septum. We descr
ibe the isolation of mutants partially defective in cytokinesis by enr
ichment of clones resistant to cell-wall lytic enzymes. The mutations
confer mycelial morphology (chains of nonseparated cells) and define f
our genes. Sep2-SA2 was subjected to detailed genetic and cytological
analysis. Its cells frequently form complex septa composed of multiple
layers, which appear as twin septa separated by anucleate minicells i
f the cell length is extended. This suggests that a polar signal-like
mechanism may also operate in S. pombe during division-site selection
and sep2(+) takes part in it. Sep2(+) seems to be involved in several
cell cycle functions because its mutation can transiently block cell-c
ycle progression after nuclear division and provoke a transition from
haploidy to diploidy in the double mutant sep2-SA2 cex1-SA2. Cex1-SA2
is another novel mutation which causes cell-length extension.