CTCF公司
粘蛋白
机制(生物学)
挤压
循环(图论)
边界(拓扑)
细胞生物学
调节器
材料科学
转录因子
遗传学
生物
物理
冶金
染色质
DNA
基因
增强子
数学分析
组合数学
量子力学
数学
出处
期刊:Nucleus
[Informa]
日期:2020-01-01
卷期号:11 (1): 132-148
被引量:58
标识
DOI:10.1080/19491034.2020.1782024
摘要
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.
科研通智能强力驱动
Strongly Powered by AbleSci AI