CTCF as a boundary factor for cohesin-mediated loop extrusion: evidence for a multi-step mechanism.

Anders S Hansen
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引用次数: 45

Abstract

Mammalian genome structure is closely linked to function. At the scale of kilobases to megabases, CTCF and cohesin organize the genome into chromatin loops. Mechanistically, cohesin is proposed to extrude chromatin loops bidirectionally until it encounters occupied CTCF DNA-binding sites. Curiously, loops form predominantly between CTCF binding sites in a convergent orientation. How CTCF interacts with and blocks cohesin extrusion in an orientation-specific manner has remained a mechanistic mystery. Here, we review recent papers that have shed light on these processes and suggest a multi-step interaction between CTCF and cohesin. This interaction may first involve a pausing step, where CTCF halts cohesin extrusion, followed by a stabilization step of the CTCF-cohesin complex, resulting in a chromatin loop. Finally, we discuss our own recent studies on an internal RNA-Binding Region (RBRi) in CTCF to elucidate its role in regulating CTCF clustering, target search mechanisms and chromatin loop formation and future challenges.

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CTCF 作为凝聚素介导的环挤压的边界因子:多步骤机制的证据。
哺乳动物基因组结构与功能密切相关。在从千碱基到兆碱基的范围内,CTCF 和凝聚素将基因组组织成染色质环。从机理上讲,粘合素会双向挤出染色质环,直到遇到被占据的 CTCF DNA 结合位点。奇怪的是,染色质环主要是在 CTCF 结合位点之间以会聚方向形成的。CTCF 如何以特定方向的方式与凝聚素相互作用并阻止其挤出一直是一个机理之谜。在此,我们回顾了最近揭示这些过程的论文,并提出了 CTCF 与凝聚素之间的多步骤相互作用。这种相互作用可能首先涉及一个暂停步骤,即 CTCF 停止凝聚素的挤出,然后是 CTCF-凝聚素复合物的稳定步骤,最终形成染色质环。最后,我们讨论了自己最近对 CTCF 内部 RNA 结合区(RBRi)的研究,以阐明其在调控 CTCF 聚类、目标搜索机制和染色质环形成方面的作用以及未来的挑战。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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