Berger Shelley L, Sassone-Corsi Paolo
Department of Cell & Developmental Biology, Department of Biology, and Department of Genetics, Epigenetics Program, University of Pennsylvania, Philadelphia, Pennsylvania 19104-6508.
Center for Epigenetics and Metabolism, Department of Biological Chemistry, University of California, Irvine, Irvine, California 92697-4049.
Cold Spring Harb Perspect Biol. 2016 Nov 1;8(11):a019463. doi: 10.1101/cshperspect.a019463.
There is a dynamic interplay between metabolic processes and gene regulation via the remodeling of chromatin. Most chromatin-modifying enzymes use cofactors, which are products of metabolic processes. This article explores the biosynthetic pathways of the cofactors nicotinamide adenine dinucleotide (NAD), acetyl coenzyme A (acetyl-CoA), S-adenosyl methionine (SAM), α-ketoglutarate, and flavin adenine dinucleotide (FAD), and their role in metabolically regulating chromatin processes. A more detailed look at the interaction between chromatin and the metabolic processes of circadian rhythms and aging is described as a paradigm for this emerging interdisciplinary field.
通过染色质重塑,代谢过程与基因调控之间存在动态相互作用。大多数染色质修饰酶使用辅助因子,这些辅助因子是代谢过程的产物。本文探讨了烟酰胺腺嘌呤二核苷酸(NAD)、乙酰辅酶A(acetyl-CoA)、S-腺苷甲硫氨酸(SAM)、α-酮戊二酸和黄素腺嘌呤二核苷酸(FAD)等辅助因子的生物合成途径,以及它们在代谢调控染色质过程中的作用。本文将更详细地探讨染色质与昼夜节律和衰老代谢过程之间的相互作用,以此作为这个新兴跨学科领域的一个范例。
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