配置代码:增强子-启动子排列和转录调控。

IF 4.5 2区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
Noel Buitrago, J Andres Vidal, Bomyi Lim
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引用次数: 0

摘要

增强子-启动子(E-P)相互作用对基因表达的精确时空调控是多细胞真核生物细胞分化和有机体发育的基本机制。尽管对增强子介导的基因调控进行了广泛的研究,但对特定E-P配置如何影响转录动力学的系统理解仍然不完整。实时成像、单细胞分析和染色质构象捕获技术的最新进展,通过提供时间分辨率和单细胞特异性,对这些动态调控过程进行了前所未有的深入研究,补充了传统的基于人群的方法。本文综述了最近关于E-P距离、增强子取向和定位、边界元素和多路相互作用如何共同影响基因表达的研究结果。关键的见解包括基因表达的非线性距离效应,增强子定位依赖的转录动力学,上下文依赖的边界元素功能,以及确保稳健发展计划的协同增强子合作。总之,这些构型依赖效应强调了E-P通讯在整个发育和进化过程中精确转录控制的复杂性和动态性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Configuring the Code: Enhancer-Promoter Arrangement and Transcriptional Regulation.

The precise spatial and temporal regulation of gene expression through enhancer-promoter (E-P) interactions represents a fundamental mechanism underlying cellular differentiation and organismal development in multicellular eukaryotes. Despite extensive studies on enhancer-mediated gene regulation, a systematic understanding of how specific E-P configurations affect transcriptional dynamics remains incomplete. Recent advances in live-imaging, single-cell assays, and chromatin conformation capture technologies have enabled unprecedented insights into these dynamic regulatory processes by providing temporal resolution and single-cell specificity that complement traditional population-based approaches. This review examines recent findings on how E-P distance, enhancer orientation and positioning, boundary elements, and multi-way interactions collectively influence gene expression. Key insights include non-linear distance effects on gene expression, enhancer positioning-dependent transcriptional kinetics, context-dependent boundary element function, and synergistic enhancer cooperation that ensures robust developmental programs. Together, these configuration-dependent effects underscore the intricate and dynamic nature of E-P communication in precise transcriptional control across development and evolution.

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来源期刊
Journal of Molecular Biology
Journal of Molecular Biology 生物-生化与分子生物学
CiteScore
11.30
自引率
1.80%
发文量
412
审稿时长
28 days
期刊介绍: Journal of Molecular Biology (JMB) provides high quality, comprehensive and broad coverage in all areas of molecular biology. The journal publishes original scientific research papers that provide mechanistic and functional insights and report a significant advance to the field. The journal encourages the submission of multidisciplinary studies that use complementary experimental and computational approaches to address challenging biological questions. Research areas include but are not limited to: Biomolecular interactions, signaling networks, systems biology; Cell cycle, cell growth, cell differentiation; Cell death, autophagy; Cell signaling and regulation; Chemical biology; Computational biology, in combination with experimental studies; DNA replication, repair, and recombination; Development, regenerative biology, mechanistic and functional studies of stem cells; Epigenetics, chromatin structure and function; Gene expression; Membrane processes, cell surface proteins and cell-cell interactions; Methodological advances, both experimental and theoretical, including databases; Microbiology, virology, and interactions with the host or environment; Microbiota mechanistic and functional studies; Nuclear organization; Post-translational modifications, proteomics; Processing and function of biologically important macromolecules and complexes; Molecular basis of disease; RNA processing, structure and functions of non-coding RNAs, transcription; Sorting, spatiotemporal organization, trafficking; Structural biology; Synthetic biology; Translation, protein folding, chaperones, protein degradation and quality control.
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