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超越基因组编织:黏连蛋白环挤压之外CTCF的分子作用

Beyond genomic weaving: molecular roles for CTCF outside cohesin loop extrusion.

作者信息

Corin Aaron, Nora Elphège P, Ramani Vijay

机构信息

Tetrad Graduate Program, University of California, San Francisco, San Francisco, CA, USA; Gladstone Institute for Data Science and Biotechnology, Gladstone Institutes, San Francisco, CA, USA; Department of Biochemistry and Biophysics, University of California, San Francisco, San Francisco, CA, USA.

Department of Biochemistry and Biophysics, University of California, San Francisco, San Francisco, CA, USA; Cardiovascular Research Institute, University of California, San Francisco, San Francisco, CA, USA; Chan-Zuckerberg Biohub, San Francisco, CA, USA.

出版信息

Curr Opin Genet Dev. 2025 Feb;90:102298. doi: 10.1016/j.gde.2024.102298. Epub 2024 Dec 21.

DOI:10.1016/j.gde.2024.102298
PMID:39709822
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12058310/
Abstract

CCCTC-binding factor (CTCF) is a key regulator of 3D genome organization and transcriptional activity. Beyond its well-characterized role in facilitating cohesin-mediated loop extrusion, CTCF exhibits several cohesin-independent activities relevant to chromatin structure and various nuclear processes. These functions include patterning of nucleosome arrangement and chromatin accessibility through interactions with ATP-dependent chromatin remodelers. In addition to influencing transcription, DNA replication, and DNA repair in ways that are separable from its role in loop extrusion, CTCF also interacts with RNA and contributes to RNA splicing and condensation of transcriptional activators. Here, we review recent insight into cohesin-independent activities of CTCF, highlighting its multifaceted roles in chromatin biology and transcriptional regulation.

摘要

CCCTC结合因子(CTCF)是三维基因组组织和转录活性的关键调节因子。除了在促进黏连蛋白介导的环挤压中具有明确的作用外,CTCF还表现出几种与染色质结构和各种核过程相关的不依赖黏连蛋白的活性。这些功能包括通过与ATP依赖的染色质重塑因子相互作用来调控核小体排列模式和染色质可及性。除了以与其在环挤压中的作用可分离的方式影响转录、DNA复制和DNA修复外,CTCF还与RNA相互作用,并有助于RNA剪接和转录激活因子的凝聚。在这里,我们综述了对CTCF不依赖黏连蛋白活性的最新见解,强调了其在染色质生物学和转录调控中的多方面作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0a56/12058310/59c0bb274dd5/nihms-2067462-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0a56/12058310/59c0bb274dd5/nihms-2067462-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0a56/12058310/59c0bb274dd5/nihms-2067462-f0001.jpg

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本文引用的文献

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Nat Struct Mol Biol. 2025 Feb 21. doi: 10.1038/s41594-024-01465-6.
2
The single-molecule accessibility landscape of newly replicated mammalian chromatin.新复制的哺乳动物染色质的单分子可及性图谱。
Cell. 2025 Jan 9;188(1):237-252.e19. doi: 10.1016/j.cell.2024.10.039. Epub 2024 Nov 15.
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Genome access is transcription factor-specific and defined by nucleosome position.基因组的可及性是转录因子特异性的,并由核小体位置定义。
Mol Cell. 2024 Sep 19;84(18):3455-3468.e6. doi: 10.1016/j.molcel.2024.08.009. Epub 2024 Aug 28.
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Systematic assessment of ISWI subunits shows that NURF creates local accessibility for CTCF.对ISWI亚基的系统评估表明,NURF为CTCF创造了局部可及性。
Nat Genet. 2024 Jun;56(6):1203-1212. doi: 10.1038/s41588-024-01767-x. Epub 2024 May 30.
5
Single-molecule imaging reveals a direct role of CTCF's zinc fingers in SA interaction and cluster-dependent RNA recruitment.单分子成像揭示了 CTCF 的锌指在 SA 相互作用和簇依赖性 RNA 招募中的直接作用。
Nucleic Acids Res. 2024 Jun 24;52(11):6490-6506. doi: 10.1093/nar/gkae391.
6
Massively parallel dissection of RNA in RNA-protein interactions in vivo.在体内的 RNA-蛋白质相互作用中大规模平行分析 RNA。
Nucleic Acids Res. 2024 Jun 10;52(10):e48. doi: 10.1093/nar/gkae334.
7
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