posted on 2010-12-13, 11:42authored byAndrew Chi-Ho Chan, Rhona H. Borts, Eva R. Hoffmann
Background: In many organisms, homologous chromosomes rely upon recombination-mediated linkages, termed
crossovers, to promote their accurate segregation at meiosis I. In budding yeast, the evolutionarily conserved mismatchrepair
paralogues, Msh4 and Msh5, promote crossover formation in conjunction with several other proteins, collectively
termed the Synapsis Initiation Complex (SIC) proteins or ‘ZMM’s (Zip1-Zip2-Zip3-Zip4-Spo16, Msh4-Msh5, Mer3). zmm
mutants show decreased levels of crossovers and increased chromosome missegregation, which is thought to cause
decreased spore viability.
Principal Findings: In contrast to other ZMM mutants, msh4 and msh5 mutants show improved spore viability and
chromosome segregation in response to elevated temperature (23°C versus 33°C). Crossover frequencies in the population
of viable spores in msh4 and msh5 mutants are similar at both temperatures, suggesting that temperature-mediated
chromosome segregation does not occur by increasing crossover frequencies. Furthermore, meiotic progression defects at
elevated temperature do not select for a subpopulation of cells with improved segregation. Instead, another ZMM protein,
Zip1, is important for the temperature-dependent improvement in spore viability.
Conclusions: Our data demonstrate interactions between genetic (zmm status) and environmental factors in determining
chromosome segregation.