Proctor C J, Lydall D A, Boys R J, Gillespie C S, Shanley D P, Wilkinson D J, Kirkwood T B L
Institute for Ageing and Health, and School of Clinical Medical Sciences-Gerontology, Centre for Integrated Systems Biology of Ageing and Nutrition, Newcastle University, Newcastle upon Tyne NE4 6BE, UK.
J R Soc Interface. 2007 Feb 22;4(12):73-90. doi: 10.1098/rsif.2006.0148.
One of the DNA damage-response mechanisms in budding yeast is temporary cell-cycle arrest while DNA repair takes place. The DNA damage response requires the coordinated interaction between DNA repair and checkpoint pathways. Telomeres of budding yeast are capped by the Cdc13 complex. In the temperature-sensitive cdc13-1 strain, telomeres are unprotected over a specific temperature range leading to activation of the DNA damage response and subsequently cell-cycle arrest. Inactivation of cdc13-1 results in the generation of long regions of single-stranded DNA (ssDNA) and is affected by the activity of various checkpoint proteins and nucleases. This paper describes a mathematical model of how uncapped telomeres in budding yeast initiate the checkpoint pathway leading to cell-cycle arrest. The model was encoded in the Systems Biology Markup Language (SBML) and simulated using the stochastic simulation system Biology of Ageing e-Science Integration and Simulation (BASIS). Each simulation follows the time course of one mother cell keeping track of the number of cell divisions, the level of activity of each of the checkpoint proteins, the activity of nucleases and the amount of ssDNA generated. The model can be used to carry out a variety of in silico experiments in which different genes are knocked out and the results of simulation are compared to experimental data. Possible extensions to the model are also discussed.
出芽酵母中的一种DNA损伤应答机制是在进行DNA修复时使细胞周期暂时停滞。DNA损伤应答需要DNA修复和检查点途径之间的协同相互作用。出芽酵母的端粒由Cdc13复合体封端。在温度敏感型cdc13 - 1菌株中,端粒在特定温度范围内未受到保护,导致DNA损伤应答激活,随后细胞周期停滞。cdc13 - 1的失活会导致单链DNA(ssDNA)长区域的产生,并受各种检查点蛋白和核酸酶活性的影响。本文描述了一个数学模型,该模型阐述了出芽酵母中未封端的端粒如何启动导致细胞周期停滞的检查点途径。该模型用系统生物学标记语言(SBML)编码,并使用随机模拟系统衰老生物学电子科学整合与模拟(BASIS)进行模拟。每次模拟都跟踪一个母细胞的时间进程,记录细胞分裂次数、每个检查点蛋白的活性水平、核酸酶的活性以及产生的ssDNA量。该模型可用于进行各种计算机模拟实验,其中敲除不同基因,并将模拟结果与实验数据进行比较。还讨论了该模型可能的扩展。