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营养表观遗传学:代谢如何通过表观遗传控制细胞生理学、基因表达和疾病。

Nutritional Epigenetics: How Metabolism Epigenetically Controls Cellular Physiology, Gene Expression and Disease.

机构信息

Infection and Epigenetics Group, School of Biotechnology, Kalinga Institute of Industrial Technology, Bhubaneswar, Odisha, India.

出版信息

Subcell Biochem. 2022;100:239-267. doi: 10.1007/978-3-031-07634-3_8.


DOI:10.1007/978-3-031-07634-3_8
PMID:36301497
Abstract

The regulation of gene expression is a dynamic process that is influenced by both internal and external factors. Alteration in the epigenetic profile is a key mechanism in the regulation process. Epigenetic regulators, such as enzymes and proteins involved in posttranslational modification (PTM), use different cofactors and substrates derived from dietary sources. For example, glucose metabolism provides acetyl CoA, S-adenosylmethionine (SAM), α- ketoglutarate, uridine diphosphate (UDP)-glucose, adenosine triphosphate (ATP), nicotinamide adenine dinucleotide (NAD), and fatty acid desaturase (FAD), which are utilized by chromatin-modifying enzymes in many intermediary metabolic pathways. Any alteration in the metabolic status of the cell results in the alteration of these metabolites, which causes dysregulation in the activity of chromatin regulators, resulting in the alteration of the epigenetic profile. Such long-term or repeated alteration of epigenetic profile can lead to several diseases, like cancer, insulin resistance and diabetes, cognitive impairment, neurodegenerative disease, and metabolic syndromes. Here we discuss the functions of key nutrients that contribute to epigenetic regulation and their role in pathophysiological conditions.

摘要

基因表达的调控是一个动态的过程,受到内部和外部因素的影响。表观遗传谱的改变是调控过程的一个关键机制。表观遗传调节剂,如参与翻译后修饰(PTM)的酶和蛋白质,使用不同的辅助因子和来源于饮食的底物。例如,葡萄糖代谢提供乙酰辅酶 A、S-腺苷甲硫氨酸(SAM)、α-酮戊二酸、尿苷二磷酸(UDP)-葡萄糖、三磷酸腺苷(ATP)、烟酰胺腺嘌呤二核苷酸(NAD)和脂肪酸去饱和酶(FAD),这些物质被染色质修饰酶用于许多中间代谢途径中。细胞代谢状态的任何改变都会导致这些代谢物的改变,从而导致染色质调节因子活性失调,导致表观遗传谱的改变。这种表观遗传谱的长期或反复改变可导致多种疾病,如癌症、胰岛素抵抗和糖尿病、认知障碍、神经退行性疾病和代谢综合征。在这里,我们讨论了有助于表观遗传调控的关键营养素的功能及其在病理生理条件下的作用。

相似文献

[1]
Nutritional Epigenetics: How Metabolism Epigenetically Controls Cellular Physiology, Gene Expression and Disease.

Subcell Biochem. 2022

[2]
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Mitochondria-Nuclear Crosstalk: Orchestrating mtDNA Maintenance.

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[2]
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[3]
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本文引用的文献

[1]
Epigenetic Mechanisms Link Maternal Diets and Gut Microbiome to Obesity in the Offspring.

Front Genet. 2018-8-27

[2]
Organ Co-Relationship in Tryptophan Metabolism and Factors That Govern the Biosynthesis of Nicotinamide from Tryptophan.

J Nutr Sci Vitaminol (Tokyo). 2018

[3]
METHIONINE ADENOSYLTRANSFERASE4 Mediates DNA and Histone Methylation.

Plant Physiol. 2018-3-23

[4]
Effect of nutrient deprivation on the expression and the epigenetic signature of sirtuin genes.

Nutr Metab Cardiovasc Dis. 2018-4

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Atherosclerotic Calcification: Wnt Is the Hint.

J Am Heart Assoc. 2018-2-8

[6]
Spatiotemporal Control of Acetyl-CoA Metabolism in Chromatin Regulation.

Trends Biochem Sci. 2017-11-23

[7]
Impact of polyunsaturated and saturated fat overfeeding on the DNA-methylation pattern in human adipose tissue: a randomized controlled trial.

Am J Clin Nutr. 2017-4

[8]
Genome-wide DNA promoter methylation and transcriptome analysis in human adipose tissue unravels novel candidate genes for obesity.

Mol Metab. 2016-11-16

[9]
2016 Russell Ross Memorial Lecture in Vascular Biology: Molecular-Cellular Mechanisms in the Progression of Atherosclerosis.

Arterioscler Thromb Vasc Biol. 2017-2

[10]
Variable Methylation Potential in Preterm Placenta: Implication for Epigenetic Programming of the Offspring.

Reprod Sci. 2017-6

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