SIN3复合物代谢和表观遗传学调控之间的串扰协调。

Q3 Biochemistry, Genetics and Molecular Biology
Enzymes Pub Date : 2023-01-01 Epub Date: 2023-07-28 DOI:10.1016/bs.enz.2023.06.001
Imad Soukar, Anjalie Amarasinghe, Lori A Pile
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引用次数: 0

摘要

组蛋白的翻译后修饰控制基因的表达。来自中央和单碳代谢的代谢产物作为供体部分来修饰组蛋白并调节基因表达。因此,组蛋白修饰和基因调控与细胞的代谢状态有关。组蛋白修饰物,如SIN3复合物,调节参与增殖和代谢的基因。SIN3复合物含有组蛋白脱乙酰酶和组蛋白脱甲基酶,它们调节染色质景观和基因表达。在本章中,我们回顾了产生供体部分的代谢途径与调节增殖和代谢基因的表观遗传复合物之间的串扰。基因调节和代谢之间的这种串扰受到严格控制,这种串扰的破坏会导致代谢性疾病。我们讨论了有前景的治疗方法,这些方法可以直接调节组蛋白修饰物,并可以影响细胞的代谢状态,缓解一些代谢性疾病。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Coordination of cross-talk between metabolism and epigenetic regulation by the SIN3 complex.

Post-translational modifications of histone proteins control the expression of genes. Metabolites from central and one-carbon metabolism act as donor moieties to modify histones and regulate gene expression. Thus, histone modification and gene regulation are connected to the metabolite status of the cell. Histone modifiers, such as the SIN3 complex, regulate genes involved in proliferation and metabolism. The SIN3 complex contains a histone deacetylase and a histone demethylase, which regulate the chromatin landscape and gene expression. In this chapter, we review the cross-talk between metabolic pathways that produce donor moieties, and epigenetic complexes regulating proliferation and metabolic genes. This cross-talk between gene regulation and metabolism is tightly controlled, and disruption of this cross-talk leads to metabolic diseases. We discuss promising therapeutics that directly regulate histone modifiers, and can affect the metabolic status of the cell, alleviating some metabolic diseases.

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来源期刊
Enzymes
Enzymes Biochemistry, Genetics and Molecular Biology-Biotechnology
CiteScore
4.30
自引率
0.00%
发文量
10
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