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CHARACTERIZATION OF A MUTATION IN YEAST CAUSING NONRANDOM CHROMOSOME LOSS DURING MITOSIS
Paloma Liras 1, John McCusker 1, Stephen Mascioli 1, and James E. Haber 1
1 Department of Biology and Rosenstiel Basic Medical Sciences
Research Center, Brandeis University, Waltham, Massachusetts 02154
Diploid strains of the yeast Saccharomyces cerevisiae homozygous
for a recessive chromosome loss mutation (chl) exhibit a high degree
of mitotic instability. Cells become monosomic for chromosome III at
a frequency of approximately one percent of all cell divisions. Chromosome
loss at this high frequency is also found for chromosome I, and at
lesser frequencies for chromosomes VIII and XVI. In contrast,
little or no chromosome loss is found for six other linkage groups tested
(II, V, VI, VII, XI and XVII). The chl mutation
also induces a ten-fold increase in both intergenic and intragenic mitotic
recombination on all ten linkage groups tested. The chl mutation
does not cause an increase in spontaneous mutations, nor are mutant strains
sensitive to UV or
irradiation. The effects of chl during
meiosis are observed primarily in reduced spore viability. A decrease in chromosome
III linkage relationships is also found.
Revised on December 5, 1977
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