CTCF-mediated chromatin looping provides a topological framework for the formation of phase-separated transcriptional condensates

CTCF 介导的染色质环化为相分离转录凝聚物的形成提供了拓扑框架

阅读:4
作者:Ryanggeun Lee, Moo-Koo Kang, Yong-Jin Kim, Bobae Yang, Hwanyong Shim, Sugyung Kim, Kyungwoo Kim, Chul Min Yang, Byeong-Gyu Min, Woong-Jae Jung, Eun-Chong Lee, Jung-Sik Joo, Gunhee Park, Won-Ki Cho, Hyoung-Pyo Kim

Abstract

CTCF is crucial to the organization of mammalian genomes into loop structures. According to recent studies, the transcription apparatus is compartmentalized and concentrated at super-enhancers to form phase-separated condensates and drive the expression of cell-identity genes. However, it remains unclear whether and how transcriptional condensates are coupled to higher-order chromatin organization. Here, we show that CTCF is essential for RNA polymerase II (Pol II)-mediated chromatin interactions, which occur as hyperconnected spatial clusters at super-enhancers. We also demonstrate that CTCF clustering, unlike Pol II clustering, is independent of liquid-liquid phase-separation and resistant to perturbation of transcription. Interestingly, clusters of Pol II, BRD4, and MED1 were found to dissolve upon CTCF depletion, but were reinstated upon restoration of CTCF, suggesting a potent instructive function for CTCF in the formation of transcriptional condensates. Overall, we provide evidence suggesting that CTCF-mediated chromatin looping acts as an architectural prerequisite for the assembly of phase-separated transcriptional condensates.

特别声明

1、本页面内容包含部分的内容是基于公开信息的合理引用;引用内容仅为补充信息,不代表本站立场。

2、若认为本页面引用内容涉及侵权,请及时与本站联系,我们将第一时间处理。

3、其他媒体/个人如需使用本页面原创内容,需注明“来源:[生知库]”并获得授权;使用引用内容的,需自行联系原作者获得许可。

4、投稿及合作请联系:info@biocloudy.com。