Doll Eveline, Molnar Monika, Cuanoud Gabriella, Octobre Guillaume, Latypov Vitaly, Ludin Katja, Kohli Jürg
Institute of Cell Biology, University of Berne, CH-3012 Berne, Switzerland.
Genetics. 2008 Oct;180(2):727-40. doi: 10.1534/genetics.108.092619. Epub 2008 Sep 9.
To determine whether recombination and/or sister-chromatid cohesion affect the timing of meiotic prophase events, the horsetail stage and S phase were analyzed in Schizosaccharomyces pombe strains carrying mutations in the cohesin genes rec8 or rec11, the linear element gene rec10, the pairing gene meu13, the double-strand-break formation genes rec6, rec7, rec12, rec14, rec15, and mde2, and the recombination gene dmc1. The double-mutant strains rec8 rec11 and rec8 rec12 were also assayed. Most of the single and both double mutants showed advancement of bulk DNA synthesis, start of nuclear movement (horsetail stage), and meiotic divisions by up to 2 hr. Only mde2 and dmc1 deletion strains showed wild-type timing. Contrasting behavior was observed for rec8 deletions (delayed by 1 hr) compared to a rec8 point mutation (advanced by 1 hr). An hypothesis for the role of cohesin and recombination proteins in the control of the G(1)-to-S transition is proposed. Finally, differences between azygotic meiosis and two other types of fission yeast meiosis (zygotic and pat1-114 meiosis) are discussed with respect to possible control steps in meiotic G(1).
为了确定重组和/或姐妹染色单体黏连是否影响减数分裂前期事件的时间安排,对粟酒裂殖酵母菌株的马尾藻期和S期进行了分析,这些菌株在黏连蛋白基因rec8或rec11、线性元件基因rec10、配对基因meu13、双链断裂形成基因rec6、rec7、rec12、rec14、rec15和mde2以及重组基因dmc1中携带突变。还检测了双突变菌株rec8 rec11和rec8 rec12。大多数单突变体和双突变体的大量DNA合成、核移动起始(马尾藻期)和减数分裂都提前了多达2小时。只有mde2和dmc1缺失菌株表现出野生型时间安排。与rec8点突变(提前1小时)相比,rec8缺失(延迟1小时)观察到相反的行为。提出了关于黏连蛋白和重组蛋白在控制G(1)到S期转变中作用的假说。最后,就减数分裂G(1)期可能的控制步骤,讨论了孤雌减数分裂与其他两种裂殖酵母减数分裂类型(合子减数分裂和pat1-114减数分裂)之间的差异。