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核代谢与表观基因组的调控。

Nuclear metabolism and the regulation of the epigenome.

机构信息

Massachusetts General Hospital Cancer Center, Harvard Medical School, Boston, MA, USA.

The Broad Institute of Harvard and MIT, Cambridge, MA, USA.

出版信息

Nat Metab. 2020 Nov;2(11):1190-1203. doi: 10.1038/s42255-020-00285-4. Epub 2020 Oct 12.

Abstract

Cellular metabolism has emerged as a major biological node governing cellular behaviour. Metabolic pathways fuel cellular energy needs, providing basic chemical molecules to sustain cellular homeostasis, proliferation and function. Changes in nutrient consumption or availability therefore can result in complete reprogramming of cellular metabolism towards stabilizing core metabolite pools, such as ATP, S-adenosyl methionine, acetyl-CoA, NAD/NADP and α-ketoglutarate. Because these metabolites underlie a variety of essential metabolic reactions, metabolism has evolved to operate in separate subcellular compartments through diversification of metabolic enzyme complexes, oscillating metabolic activity and physical separation of metabolite pools. Given that these same core metabolites are also consumed by chromatin modifiers in the establishment of epigenetic signatures, metabolite consumption on and release from chromatin directly influence cellular metabolism and gene expression. In this Review, we highlight recent studies describing the mechanisms determining nuclear metabolism and governing the redistribution of metabolites between the nuclear and non-nuclear compartments.

摘要

细胞代谢已成为控制细胞行为的主要生物学节点。代谢途径为细胞的能量需求提供燃料,提供维持细胞内稳态、增殖和功能的基本化学分子。因此,营养物质的消耗或可利用性的变化会导致细胞代谢朝着稳定核心代谢物池(如 ATP、S-腺苷甲硫氨酸、乙酰-CoA、NAD/NADP 和 α-酮戊二酸)的完全重编程。由于这些代谢物是各种必需代谢反应的基础,因此代谢已经通过代谢酶复合物的多样化、代谢活性的波动以及代谢物池的物理分离来在不同的亚细胞区室中运作。鉴于这些相同的核心代谢物也被染色质修饰物用于建立表观遗传特征,染色质上代谢物的消耗和释放直接影响细胞代谢和基因表达。在这篇综述中,我们强调了最近描述决定核代谢的机制和调节代谢物在核和非核区室之间重新分布的研究。

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