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基因调控洞察:从调控基因组元件到 DNA-蛋白质和蛋白质-蛋白质相互作用。

Insights into gene regulation: From regulatory genomic elements to DNA-protein and protein-protein interactions.

机构信息

Research Institute of Molecular Pathology (IMP), Vienna BioCenter (VBC), Vienna, Austria.

Research Institute of Molecular Pathology (IMP), Vienna BioCenter (VBC), Vienna, Austria; Medical University of Vienna, Vienna BioCenter (VBC), Vienna, Austria.

出版信息

Curr Opin Cell Biol. 2021 Jun;70:58-66. doi: 10.1016/j.ceb.2020.11.009. Epub 2020 Dec 29.

DOI:10.1016/j.ceb.2020.11.009
PMID:33385708
Abstract

Transcription is orchestrated by non-coding regulatory elements embedded in chromatin, which exist within the larger context of chromosome topology. Here, we review recent insights into the functions of non-coding regulatory elements and their protein interactors during transcription control. A picture emerges in which the topological environment constraints enhancer-promoter interactions and specific enhancer-bound proteins with distinct promoter-compatibilities refine target promoter choice. Such compatibilities are encoded within the sequences of enhancers and promoters and realized by diverse transcription factors and cofactors with distinct biochemical activities. An emerging property of transcription factors and cofactors is the formation of nuclear microenvironments or membraneless compartments that can have properties of phase-separated liquids. These environments are able to selectively enrich certain proteins and small molecules over others. Further investigation into the interaction of transcriptional regulators with themselves and regulatory DNA elements will help reveal the complexities of gene regulation within the context of the nucleus.

摘要

转录是由染色质中嵌入的非编码调控元件协调的,这些元件存在于染色体拓扑结构的更大背景中。在这里,我们回顾了最近在转录调控过程中非编码调控元件及其蛋白相互作用体的功能的研究进展。一幅画面逐渐浮现,拓扑环境限制了增强子-启动子的相互作用,而具有不同启动子兼容性的特定增强子结合蛋白则可以精细地选择靶启动子。这种兼容性被编码在增强子和启动子的序列中,并由具有不同生化活性的多种转录因子和辅助因子来实现。转录因子和辅助因子的一个新兴特性是形成核微环境或无膜隔间,这些隔间可以具有相分离液体的性质。这些环境能够选择性地富集某些蛋白质和小分子,而排斥其他物质。进一步研究转录调节剂与自身和调节 DNA 元件的相互作用将有助于揭示细胞核内基因调控的复杂性。

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