代谢驱动的染色质动力学:分子原理和技术进步

IF 14.5 1区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
Varun Sahu, Chao Lu
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引用次数: 0

摘要

细胞将代谢信息整合到转录等核心分子过程中,以适应环境变化。染色质作为真核生物基因组的生理模板,已成为细胞内代谢物波动的传感器和调节器。在这篇综述中,我们将重点介绍越来越多的染色质相关代谢物,这些代谢物的来源多种多样。我们讨论了在理解代谢酶活动塑造染色质结构和修饰的机制方面的最新进展、代谢酶看似广泛的作用如何产生特异性以及促进表观基因组-代谢组相互作用研究的技术。认识到代谢物是染色质调控网络的内在组成部分,对表观基因组的进化、功能和靶向治疗具有重要意义。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Metabolism-driven chromatin dynamics: Molecular principles and technological advances
Cells integrate metabolic information into core molecular processes such as transcription to adapt to environmental changes. Chromatin, the physiological template of the eukaryotic genome, has emerged as a sensor and rheostat for fluctuating intracellular metabolites. In this review, we highlight the growing list of chromatin-associated metabolites that are derived from diverse sources. We discuss recent advances in our understanding of the mechanisms by which metabolic enzyme activities shape the chromatin structure and modifications, how specificity may emerge from their seemingly broad effects, and technologies that facilitate the study of epigenome-metabolome interplay. The recognition that metabolites are immanent components of the chromatin regulatory network has significant implications for the evolution, function, and therapeutic targeting of the epigenome.
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来源期刊
Molecular Cell
Molecular Cell 生物-生化与分子生物学
CiteScore
26.00
自引率
3.80%
发文量
389
审稿时长
1 months
期刊介绍: Molecular Cell is a companion to Cell, the leading journal of biology and the highest-impact journal in the world. Launched in December 1997 and published monthly. Molecular Cell is dedicated to publishing cutting-edge research in molecular biology, focusing on fundamental cellular processes. The journal encompasses a wide range of topics, including DNA replication, recombination, and repair; Chromatin biology and genome organization; Transcription; RNA processing and decay; Non-coding RNA function; Translation; Protein folding, modification, and quality control; Signal transduction pathways; Cell cycle and checkpoints; Cell death; Autophagy; Metabolism.
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