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Cell-Fate Determination from Embryo to Cancer Development: Genomic Mechanism Elucidated

机译:从胚胎到癌症发展的细胞命运测定:阐明了基因组机制

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摘要

Elucidation of the genomic mechanism that guides the cell-fate change is one of the fundamental issues of biology. We previously demonstrated that whole genome expression is coordinated by the emergence of a critical point at both the cell-population and single-cell levels through the physical principle of self-organized criticality. In this paper, we further examine the genomic mechanism that determines the cell-fate changes from embryo to cancer development. The state of the critical point, acting as the organizing center of the cell fate, determines whether the genome resides in a super- or sub-critical state. In the super-critical state, a specific stochastic perturbation can spread over the entire system through the “genome engine”, an autonomous critical-control genomic system, whereas in the sub-critical state, the perturbation remains at a local level. The cell-fate changes when the genome becomes super-critical. We provide a consistent framework to develop a time-evolutional transition theory for the biological regulation of the cell-fate change.
机译:阐明指导细胞命运变化的基因组机制是生物学的基本问题之一。我们先前证明,通过自组织临界的物理原理,整个基因组的表达都受到细胞群和单细胞水平上临界点的出现的协调。在本文中,我们进一步研究了决定从胚胎到癌症发展的细胞命运变化的基因组机制。临界点的状态,作为细胞命运的组织中心,决定了基因组是处于超临界状态还是亚临界状态。在超临界状态下,特定的随机扰动可以通过“基因组引擎”(一种自主的关键控制基因组系统)在整个系统中传播,而在次临界状态下,扰动则保持在局部级别。当基因组变得超临界时,细胞命运就会发生变化。我们提供了一个一致的框架来发展时间演化理论来对细胞命运的变化进行生物调控。

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