Department of Biological Engineering, Massachusetts Institute of Technology , Cambridge, MA, USA.
Nucleus. 2020 Dec;11(1):132-148. doi: 10.1080/19491034.2020.1782024.
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.
哺乳动物基因组结构与其功能密切相关。在千碱基到兆碱基的尺度上,CTCF 和黏连蛋白将基因组组织成染色质环。从机制上讲,黏连蛋白被提议双向挤出染色质环,直到它遇到被占据的 CTCF DNA 结合位点。奇怪的是,环主要在会聚方向上形成于 CTCF 结合位点之间。CTCF 如何以特定的方向与黏连蛋白相互作用并阻止其挤出仍然是一个机制之谜。在这里,我们回顾了最近的一些论文,这些论文阐明了这些过程,并提出了 CTCF 和黏连蛋白之间的多步相互作用。这种相互作用可能首先涉及一个暂停步骤,其中 CTCF 停止黏连蛋白的挤出,然后是 CTCF-黏连蛋白复合物的稳定步骤,导致染色质环的形成。最后,我们讨论了我们自己最近关于 CTCF 内部 RNA 结合区 (RBRi) 的研究,以阐明其在调节 CTCF 聚类、靶标搜索机制以及染色质环形成中的作用,以及未来的挑战。