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Dynamic Signatures of the Epigenome: Friend or Foe?

机译:表观基因组的动态特征:朋友还是敌人?

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摘要

Highly dynamic epigenetic signaling is influenced mainly by (micro)environmental stimuli and genetic factors. The exact mechanisms affecting particular epigenomic patterns differ dependently on the context. In the current review, we focus on the causes and effects of the dynamic signatures of the human epigenome as evaluated with the high-throughput profiling data and single-gene approaches. We will discuss three different aspects of phenotypic outcomes occurring as a consequence of epigenetics interplaying with genotype and environment. The first issue is related to the cases of environmental impacts on epigenetic profile, and its adverse and advantageous effects related to human health and evolutionary adaptation. The next topic will present a model of the interwoven co-evolution of genetic and epigenetic patterns exemplified with transposable elements (TEs) and their epigenetic repressors Krüppel-associated box zinc finger proteins (KRAB–ZNFs). The third aspect concentrates on the mitosis-based microevolution that takes place during carcinogenesis, leading to clonal diversity and expansion of tumor cells. The whole picture of epigenome plasticity and its role in distinct biological processes is still incomplete. However, accumulating data define epigenomic dynamics as an essential co-factor driving adaptation at the cellular and inter-species levels with a benefit or disadvantage to the host.
机译:高度动态的表观遗传信号主要受(微)环境刺激和遗传因素影响。影响特定表观基因组模式的确切机制取决于上下文。在当前的审查中,我们重点研究人类表观基因组动态特征的原因和影响,这些特征是通过高通量分析数据和单基因方法进行评估的。我们将讨论由于表观遗传学与基因型和环境相互作用而产生的表型结果的三个不同方面。第一个问题涉及环境对表观遗传概况的影响及其与人类健康和进化适应有关的不利影响。下一个主题将提供遗传和表观遗传模式交织共进化的模型,并以转座因子(TEs)及其表观遗传抑制因子Krüppel相关的盒锌指蛋白(KRAB–ZNFs)为例。第三方面集中于在癌变过程中发生的基于有丝分裂的微进化,从而导致克隆多样性和肿瘤细胞的扩增。表观基因组可塑性及其在不同生物学过程中的作用的整体情况仍然不完整。然而,积累的数据将表观基因组动力学定义为驱动细胞和种间水平适应的必要辅助因子,对宿主有利或不利。

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