Department of Chemistry, Princeton University, Princeton, NJ, USA.
Department of Medicinal Chemistry, University of Utah, Salt Lake City, UT, USA.
Nat Chem Biol. 2020 Jun;16(6):620-629. doi: 10.1038/s41589-020-0517-x. Epub 2020 May 22.
In eukaryotes, chromatin remodeling and post-translational modifications (PTMs) shape the local chromatin landscape to establish permissive and repressive regions within the genome, orchestrating transcription, replication, and DNA repair in concert with other epigenetic mechanisms. Though cellular nutrient signaling encompasses a huge number of pathways, recent attention has turned to the hypothesis that the metabolic state of the cell is communicated to the genome through the type and concentration of metabolites in the nucleus that are cofactors for chromatin-modifying enzymes. Importantly, both epigenetic and metabolic dysregulation are hallmarks of a range of diseases, and this metabolism-chromatin axis may yield a well of new therapeutic targets. In this Perspective, we highlight emerging themes in the inter-regulation of the genome and metabolism via chromatin, including nonenzymatic histone modifications arising from chemically reactive metabolites, the expansion of PTM diversity from cofactor-promiscuous chromatin-modifying enzymes, and evidence for the existence and importance of subnucleocytoplasmic metabolite pools.
在真核生物中,染色质重塑和翻译后修饰(PTMs)塑造局部染色质景观,在基因组内建立允许和抑制区域,与其他表观遗传机制一起协调转录、复制和 DNA 修复。尽管细胞营养信号涵盖了大量的途径,但最近的注意力转向了这样一种假设,即细胞的代谢状态通过核内代谢物的类型和浓度传递给基因组,这些代谢物是染色质修饰酶的辅因子。重要的是,表观遗传和代谢失调都是一系列疾病的特征,这种代谢-染色质轴可能产生大量新的治疗靶点。在本观点中,我们强调了通过染色质调控基因组和代谢的新兴主题,包括来自化学活性代谢物的非酶促组蛋白修饰、辅因子混杂染色质修饰酶的 PTM 多样性的扩展,以及亚核细胞质代谢物池的存在和重要性的证据。