Egel R, Willer M, Kjaerulff S, Davey J, Nielsen O
Department of Genetics, University of Copenhagen, Denmark.
Yeast. 1994 Oct;10(10):1347-54. doi: 10.1002/yea.320101012.
We describe a rapid, sensitive and semi-quantitative plate assay for monitoring pheromone activity in the fission yeast Schizosaccharomyces pombe. It is based on the observation that meiosis requires stimulation by pheromone and exploits diploid strains that will only sporulate after addition of exogenous pheromone. The tester strains are heterozygous for mating type, are non-switching, and are mutated in one of the early subfunctions (either mat1-Mc or mat1-Pc), so that meiosis is only induced after exposure to exogenous pheromone (M-factor or P-factor, respectively). Pheromone activity is assessed as an iodine-positive halo of sporulation surrounding the pheromone source, and the width of the halo is related to the amount of pheromone being produced. The assay is sufficiently sensitive to monitor the low amount of M-factor produced by an M mam1 strain, and its sensitivity towards P-factor is greatly increased by using a hyper-sensitive tester strain lacking the Sxa2 protease that is believed to degrade this pheromone. We also demonstrate that the production of P-factor is very much stimulated by exposure of P cells to M-factor.
我们描述了一种用于监测裂殖酵母粟酒裂殖酵母中信息素活性的快速、灵敏且半定量的平板检测方法。该方法基于减数分裂需要信息素刺激这一观察结果,并利用了仅在添加外源信息素后才会形成孢子的二倍体菌株。测试菌株的交配型为杂合子,不发生转换,且在早期亚功能之一(mat1-Mc或mat1-Pc)中发生突变,因此只有在暴露于外源信息素(分别为M因子或P因子)后才会诱导减数分裂。信息素活性通过信息素源周围形成孢子的碘阳性晕圈来评估,晕圈的宽度与产生的信息素量相关。该检测方法足够灵敏,能够监测M mam1菌株产生的少量M因子,并且通过使用缺乏据信会降解该信息素的Sxa2蛋白酶的超灵敏测试菌株,其对P因子的敏感性大大提高。我们还证明,P细胞暴露于M因子会极大地刺激P因子的产生。