Department of Biochemistry, University College of Science, Calcutta University, Kolkata 700019, West Bengal, India.
Free Radic Biol Med. 2012;52(11-12):2186-200. doi: 10.1016/j.freeradbiomed.2012.03.026. Epub 2012 Apr 17.
Nitric oxide (NO) acts as a signaling molecule in numerous physiological processes but excess production generates nitrosative stress in cells. The exact protective mechanism used by cells to combat nitrosative stress is unclear. In this study, the fission yeast Schizosaccharomyces pombe has been used as a model system to explore cell cycle regulation and stress responses under nitrosative stress. Exposure to an NO donor results in mitotic delay in cells through G2/M checkpoint activation and initiates rereplication. Western blot analysis of phosphorylated Cdc2 revealed that the G2/M block in the cell cycle was due to retention of its inactive phosphorylated form. Interestingly, nitrosative stress results in inactivation of Cdc25 through S-nitrosylation that actually leads to cell cycle delay. From differential display analysis, we identified plo1, spn4, and rga5, three cell cycle-related genes found to be differentially expressed under nitrosative stress. Exposure to nitrosative stress also results in abnormal septation and cytokinesis in S. pombe. In summary we propose a novel molecular mechanism of cell cycle control under nitrosative stress based on our experimental results and bioinformatics analysis.
一氧化氮 (NO) 在许多生理过程中充当信号分子,但过量产生会导致细胞中的硝化应激。细胞用于对抗硝化应激的确切保护机制尚不清楚。在这项研究中,裂殖酵母 Schizosaccharomyces pombe 被用作模型系统,以探索硝化应激下的细胞周期调控和应激反应。暴露于一氧化氮供体可通过 G2/M 检查点激活导致有丝分裂延迟,并引发重复复制。磷酸化 Cdc2 的 Western blot 分析表明,细胞周期中的 G2/M 阻滞是由于其非活性磷酸化形式的保留。有趣的是,硝化应激会导致 Cdc25 通过 S-亚硝化失活,从而导致细胞周期延迟。通过差异显示分析,我们鉴定了 plo1、spn4 和 rga5,这三个与细胞周期相关的基因在硝化应激下表达差异。暴露于硝化应激也会导致 S. pombe 中异常的分隔和胞质分裂。总之,根据我们的实验结果和生物信息学分析,我们提出了一种硝化应激下细胞周期控制的新分子机制。