Department of Glycobiology, Institute of Chemistry, Slovak Academy of Sciences, Dubravska cesta 9, Bratislava, 845 38, Slovakia.
Department of Medical and Clinical Biophysics, Faculty of Medicine, Pavol Jozef Šafárik University in Košice, Trieda SNP 1, Košice, 040 11, Slovakia.
Sci Rep. 2024 Oct 4;14(1):23105. doi: 10.1038/s41598-024-74523-0.
In eukaryotes, chromosomal DNA is equally distributed to daughter cells during mitosis, whereas the number of chromosomes is halved during meiosis. Despite considerable progress in understanding the molecular mechanisms that regulate mitosis, there is currently a lack of complete understanding of the molecular mechanisms regulating meiosis. Here, we took advantage of the fission yeast Schizosaccharomyces pombe, for which highly synchronous meiosis can be induced, and performed quantitative proteomics and phosphoproteomics analyses to track changes in protein expression and phosphorylation during meiotic divisions. We compared the proteomes and phosphoproteomes of exponentially growing mitotic cells with cells harvested around meiosis I, or meiosis II in strains bearing either the temperature-sensitive pat1-114 allele or conditional ATP analog-sensitive pat1-as2 allele of the Pat1 kinase. Comparing pat1-114 with pat1-as2 also allowed us to investigate the impact of elevated temperature (25 °C versus 34 °C) on meiosis, an issue that sexually reproducing organisms face due to climate change. Using TMTpro 18plex labeling and phosphopeptide enrichment strategies, we performed quantification of a total of 4673 proteins and 7172 phosphosites in S. pombe. We found that the protein level of 2680 proteins and the rate of phosphorylation of 4005 phosphosites significantly changed during progression of S. pombe cells through meiosis. The proteins exhibiting changes in expression and phosphorylation during meiotic divisions were represented mainly by those involved in the meiotic cell cycle, meiotic recombination, meiotic nuclear division, meiosis I, centromere clustering, microtubule cytoskeleton organization, ascospore formation, organonitrogen compound biosynthetic process, carboxylic acid metabolic process, gene expression, and ncRNA processing, among others. In summary, our findings provide global overview of changes in the levels and phosphorylation of proteins during progression of S. pombe cells through meiosis at normal and elevated temperatures, laying the groundwork for further elucidation of the functions and importance of specific proteins and their phosphorylation in regulating meiotic divisions in this yeast.
在真核生物中,染色体 DNA 在有丝分裂过程中均等分配到子细胞中,而在减数分裂过程中染色体数目减半。尽管人们在理解调节有丝分裂的分子机制方面取得了相当大的进展,但目前仍缺乏对调节减数分裂的分子机制的全面理解。在这里,我们利用裂殖酵母 Schizosaccharomyces pombe,因为它可以高度同步地诱导减数分裂,并进行定量蛋白质组学和磷酸化蛋白质组学分析,以跟踪减数分裂过程中蛋白质表达和磷酸化的变化。我们将指数生长期有丝分裂细胞的蛋白质组和磷酸化蛋白质组与处于减数分裂 I 期或减数分裂 II 期的细胞进行比较,这些细胞分别携带 Pat1 激酶的温度敏感型 pat1-114 等位基因或条件性 ATP 类似物敏感型 pat1-as2 等位基因。比较 pat1-114 与 pat1-as2 还使我们能够研究高温(25°C 与 34°C)对减数分裂的影响,这是由于气候变化,有性繁殖生物面临的一个问题。使用 TMTpro 18plex 标记和磷酸肽富集策略,我们对 S. pombe 中的总共 4673 种蛋白质和 7172 个磷酸化位点进行了定量。我们发现,在 S. pombe 细胞通过减数分裂的过程中,有 2680 种蛋白质的蛋白水平和 4005 个磷酸化位点的磷酸化速率发生了显著变化。在减数分裂过程中表达和磷酸化发生变化的蛋白质主要代表那些参与减数细胞周期、减数重组、减数核分裂、减数分裂 I、着丝粒聚类、微管细胞骨架组织、子囊孢子形成、有机含氮化合物生物合成过程、羧酸代谢过程、基因表达和非编码 RNA 处理等的蛋白质。总之,我们的研究结果提供了在正常和高温条件下 S. pombe 细胞通过减数分裂时蛋白质水平和磷酸化变化的全局概述,为进一步阐明特定蛋白质及其磷酸化在调节该酵母减数分裂中的功能和重要性奠定了基础。