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A Stochastic Model of Epigenetic Dynamics in Somatic Cell Reprogramming

机译:体细胞重编程中表观遗传动力学的随机模型

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摘要

Somatic cell reprogramming has dramatically changed stem cell research in recent years. The high pace of new findings in the field and an ever increasing amount of data from new high throughput techniques make it challenging to isolate core principles of the process. In order to analyze such mechanisms, we developed an abstract mechanistic model of a subset of the known regulatory processes during cell differentiation and production of induced pluripotent stem cells. This probabilistic Boolean network describes the interplay between gene expression, chromatin modifications, and DNA methylation. The model incorporates recent findings in epigenetics and partially reproduces experimentally observed reprogramming efficiencies and changes in methylation and chromatin remodeling. It enables us to investigate, how the temporal progression of the process is regulated. It also explicitly includes the transduction of factors using viral vectors and their silencing in reprogrammed cells, since this is still a standard procedure in somatic cell reprogramming. Based on the model we calculate an epigenetic landscape for probabilities of cell states. Simulation results show good reproduction of experimental observations during reprogramming, despite the simple structure of the model. An extensive analysis and introduced variations hint toward possible optimizations of the process that could push the technique closer to clinical applications. Faster changes in DNA methylation increase the speed of reprogramming at the expense of efficiency, while accelerated chromatin modifications moderately improve efficiency.
机译:近年来,体细胞重编程已极大地改变了干细胞的研究。该领域新发现的高速发展以及来自新的高通量技术的数据量不断增加,因此很难隔离该过程的核心原理。为了分析这种机制,我们在细胞分化和诱导多能干细胞生产过程中开发了已知调节过程的一个子集的抽象机制模型。这个概率布尔网络描述了基因表达,染色质修饰和DNA甲基化之间的相互作用。该模型结合了表观遗传学的最新发现,并部分复制了实验观察到的重编程效率以及甲基化和染色质重塑的变化。它使我们能够研究过程的时间进度是如何调节的。它还明确包括使用病毒载体进行因子转导及其在重编程细胞中的沉默,因为这仍然是体细胞重编程中的标准程序。基于该模型,我们为细胞状态的概率计算了一个表观遗传景观。尽管模型结构简单,但仿真结果显示在重新编程期间实验观察结果的良好再现。广泛的分析和引入的变化暗示可能对工艺进行优化,从而可能使该技术更接近于临床应用。 DNA甲基化的更快变化以效率为代价提高了重新编程的速度,而加速的染色质修饰则适度地提高了效率。

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