Department of Biomedical Engineering, University of Michigan, Ann Arbor, MI, 48109, USA.
Greenwood Genetics Center, Greenwood, SC, 29646, USA.
Genome Biol. 2019 Mar 1;20(1):49. doi: 10.1186/s13059-019-1661-z.
Histone acetylation plays a central role in gene regulation and is sensitive to the levels of metabolic intermediates. However, predicting the impact of metabolic alterations on acetylation in pathological conditions is a significant challenge. Here, we present a genome-scale network model that predicts the impact of nutritional environment and genetic alterations on histone acetylation. It identifies cell types that are sensitive to histone deacetylase inhibitors based on their metabolic state, and we validate metabolites that alter drug sensitivity. Our model provides a mechanistic framework for predicting how metabolic perturbations contribute to epigenetic changes and sensitivity to deacetylase inhibitors.
组蛋白乙酰化在基因调控中起着核心作用,并且对代谢中间产物的水平敏感。然而,预测代谢改变对病理条件下乙酰化的影响是一个重大的挑战。在这里,我们提出了一个基因组规模的网络模型,该模型可以预测营养环境和遗传改变对组蛋白乙酰化的影响。它根据代谢状态确定对组蛋白去乙酰化酶抑制剂敏感的细胞类型,并且验证了改变药物敏感性的代谢物。我们的模型为预测代谢扰动如何导致表观遗传变化和对去乙酰化酶抑制剂的敏感性提供了一个机制框架。