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Vol. 11, Issue 10, 3525-3537, October 2000
Molecular, Cellular, and Developmental-Biology, Porter
Biosciences, University of Colorado, Boulder, Colorado 80309
Sporulation in yeast requires that a modified form of chromosome
segregation be coupled to the development of a specialized cell type, a
process akin to gametogenesis. Mps1p is a dual-specificity protein
kinase essential for spindle pole body (SPB) duplication and required
for the spindle assembly checkpoint in mitotically dividing
cells. Four conditional mutant alleles of MPS1
disrupt sporulation, producing two distinct phenotypic classes. Class I
alleles of mps1 prevent SPB duplication at the
restrictive temperature without affecting premeiotic DNA synthesis and
recombination. Class II MPS1 alleles progress through
both meiotic divisions in 30-50% of the population, but the asci are
incapable of forming mature spores. Although mutations in many other
genes block spore wall formation, the cells produce viable haploid
progeny, whereas mps1 class II spores are unable to
germinate. We have used fluorescently marked chromosomes to demonstrate
that mps1 mutant cells have a dramatically increased
frequency of chromosome missegregation, suggesting that loss of
viability is due to a defect in spindle function. Overall, our
cytological data suggest that MPS1 is required for
meiotic SPB duplication, chromosome segregation, and spore wall formation.
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