Ibrahim Bashar
1 Bio System Analysis Group, Friedrich-Schiller-University Jena , and Jena Centre for Bioinformatics (JCB), Jena, Germany .
OMICS. 2015 May;19(5):294-305. doi: 10.1089/omi.2015.0027. Epub 2015 Apr 14.
Correct DNA segregation is a fundamental process that ensures the precise and reliable inheritance of genomic information for the propagation of cell life. Eukaryotic cells have evolved a conserved surveillance control mechanism for DNA segregation named the Spindle Assembly Checkpoint (SAC).The SAC ensures that the sister chromatids of the duplicated genome are not separated and distributed to the spindle poles before all chromosomes have been properly linked to the microtubules of the mitotic spindle. Biochemically, the SAC delays cell cycle progression by preventing activation of the anaphase-promoting complex (APC/C) or cyclosome whose activation by Cdc20 is required for sister-chromatid separation; this marks the transition into anaphase. In response to activation of the checkpoint, various species control the activity of both APC/C and Cdc20. However, the underlying regulatory pathways remain largely elusive. In this study, five possible model variants of APC/C regulation were constructed, namely BubR1, Mad2, MCC, MCF2, and an all-pathways model variant. These models were validated with experimental data from the literature. A wide range of parameter values has been tested to find the critical values of the APC/C binding rate. The results show that all variants are able to capture the wild-type behavior of the APC/C. However, only one model variant, which included both MCC as well as BubR1 as potent inhibitors of the APC/C, was able to reproduce both wild-type and mutant type behavior of APC/C regulation. In conclusion, the presented work informs the regulation of fundamental processes such as SAC and APC/C in cell biology and has successfully distinguished between five competing dynamical models using a systems biology approach. The results attest that systems-level approaches are vital for molecular and cell biology.
正确的DNA分离是一个确保基因组信息精确可靠遗传以维持细胞生命繁衍的基本过程。真核细胞进化出了一种保守的DNA分离监测控制机制,称为纺锤体组装检查点(SAC)。SAC确保在所有染色体都正确连接到有丝分裂纺锤体的微管之前,复制基因组的姐妹染色单体不会分离并分配到纺锤体两极。从生化角度来看,SAC通过阻止后期促进复合物(APC/C)或细胞周期体的激活来延迟细胞周期进程,而姐妹染色单体分离需要Cdc20激活APC/C;这标志着进入后期。作为对检查点激活的响应,不同物种会控制APC/C和Cdc20的活性。然而,潜在的调控途径在很大程度上仍然不清楚。在这项研究中,构建了APC/C调控的五种可能的模型变体,即BubR1、Mad2、MCC、MCF2和一个全途径模型变体。这些模型用文献中的实验数据进行了验证。测试了广泛的参数值以找到APC/C结合率的临界值。结果表明,所有变体都能够捕捉APC/C的野生型行为。然而,只有一个模型变体,即同时包含MCC和BubR1作为APC/C有效抑制剂的变体,能够重现APC/C调控的野生型和突变型行为。总之,本研究为细胞生物学中SAC和APC/C等基本过程的调控提供了信息,并成功地使用系统生物学方法区分了五个相互竞争的动力学模型。结果证明系统水平的方法对分子生物学和细胞生物学至关重要。