Max F. Perutz Laboratories, University of Vienna, Vienna, Austria.
Cell Cycle. 2012 Apr 15;11(8):1626-33. doi: 10.4161/cc.20052.
To study meiosis, synchronous cultures are often indispensable, especially for physical analyses of DNA and proteins. A temperature-sensitive allele of the Pat1 protein kinase (pat1-114) has been widely used to induce synchronous meiosis in the fission yeast Schizosaccharomyces pombe, but pat1-114-induced meiosis differs from wild-type meiosis, and some of these abnormalities might be due to higher temperature needed to inactivate the Pat1 kinase. Here, we report an ATP analog-sensitive allele of Pat1 [Pat1(L95A), designated pat1-as2] that can be used to generate synchronous meiotic cultures at physiological temperature. In pat1-as2 meiosis, chromosomes segregate with higher fidelity, and spore viability is higher than in pat1-114 meiosis, although recombination is lower by a factor of 2-3 in these mutants than in starvation-induced pat1(+) meiosis. Addition of the mat-Pc gene improved chromosome segregation and spore viability to nearly the level of starvation-induced meiosis. We conclude that pat1-as2 mat-Pc cells offer synchronous meiosis with most tested properties similar to those of wild-type meiosis.
为了研究减数分裂,通常需要同步培养,特别是对于 DNA 和蛋白质的物理分析。Pat1 蛋白激酶(pat1-114)的一个温度敏感等位基因已被广泛用于诱导裂殖酵母 Schizosaccharomyces pombe 的同步减数分裂,但 pat1-114 诱导的减数分裂与野生型减数分裂不同,其中一些异常可能是由于需要更高的温度来使 Pat1 激酶失活。在这里,我们报告了 Pat1 的一个 ATP 类似物敏感等位基因 [Pat1(L95A),命名为 pat1-as2],它可用于在生理温度下产生同步减数分裂培养物。在 pat1-as2 减数分裂中,染色体的分离具有更高的保真度,孢子活力高于 pat1-114 减数分裂,尽管这些突变体中的重组比饥饿诱导的 pat1(+)减数分裂低 2-3 倍。添加 mat-Pc 基因可将染色体分离和孢子活力提高到接近饥饿诱导减数分裂的水平。我们得出结论,pat1-as2 mat-Pc 细胞提供了具有与野生型减数分裂相似的大多数特性的同步减数分裂。