Center for Computational Natural Sciences and Bioinformatics, International Institute of Information Technology, Hyderabad, 500032, India.
Semmelweis University, Department of Medical Chemistry, Molecular Biology and Pathobiochemistry, Budapest, Hungary.
Sci Rep. 2018 Jan 9;8(1):180. doi: 10.1038/s41598-017-17478-9.
In response to developmental and environmental conditions, cells exit the mitotic cell cycle and enter the meiosis program to generate haploid gametes from diploid germ cells. Once cells decide to enter the meiosis program they become irreversibly committed to the completion of meiosis irrespective of the presence of cue signals. How meiotic entry and commitment occur due to the dynamics of the regulatory network is not well understood. Therefore, we constructed a mathematical model of the regulatory network that controls the transition from mitosis to meiosis in Schizosaccharomyces pombe. Upon nitrogen starvation, yeast cells exit mitosis and undergo conjugation and meiotic entry. The model includes the regulation of Mei2, an RNA binding protein required for conjugation and meiotic entry, by multiple feedback loops involving Pat1, a kinase that keeps cells in mitosis, and Ste11, a transcription activator required for the sexual differentiation. The model accounts for various experimental observations and demonstrates that the activation of Mei2 is bistable, which ensures the irreversible commitment to meiosis. Further, we show by integrating the meiosis-specific regulation with a cell cycle model, the dynamics of cell cycle exit, G1 arrest and entry into meiosis under nitrogen starvation.
为了适应发育和环境条件,细胞退出有丝分裂细胞周期,进入减数分裂程序,以从二倍体生殖细胞产生单倍体配子。一旦细胞决定进入减数分裂程序,它们就会不可逆地完成减数分裂,而不管 cue 信号的存在如何。由于调控网络的动态变化,减数分裂的进入和承诺是如何发生的还不是很清楚。因此,我们构建了一个控制 Schizosaccharomyces pombe 有丝分裂向减数分裂转变的调控网络的数学模型。在氮饥饿时,酵母细胞退出有丝分裂并经历接合和减数分裂进入。该模型包括由多个反馈回路调节 Mei2,Mei2 是一种 RNA 结合蛋白,对于接合和减数分裂进入是必需的,这些反馈回路涉及 Pat1,一种使细胞保持在有丝分裂中的激酶,以及 Ste11,一种性分化所必需的转录激活因子。该模型解释了各种实验观察,并表明 Mei2 的激活是双稳态的,这确保了对减数分裂的不可逆承诺。此外,我们通过将减数分裂特异性调控与细胞周期模型整合,展示了在氮饥饿下细胞周期退出、G1 期阻滞和进入减数分裂的动力学。