Guan Shanli, Tang Jiajia, Di Cuixia, Cheng Bo
School of Life Sciences, Lanzhou University, Lanzhou 730000, Gansu, P.R. China.
Bio-Medical Research Center, Institute of Modern Physics, Chinese Academy of Sciences, Lanzhou 730000, Gansu, P.R. China.
STAR Protoc. 2025 Mar 21;6(1):103597. doi: 10.1016/j.xpro.2025.103597. Epub 2025 Jan 28.
The detailed chromatin assembly processes for many epigenetic regulatory complexes are largely unknown. Here, we present a protocol utilizing heterochromatin-targeting module (HTM) module-mediated chromatin tethering followed by microscopy-based visualization to detect the recruitment priority between two components in Polycomb repressive complex 1 (PRC1). Moreover, we detail procedures for detecting the resultant histone-modifying activities of PRC1 using immunofluorescence (IF) analyses. This approach allows directly visualization of the on-chromatin assembly of the histone-modifying complexes of interest in live cells. For complete details on the use and execution of this protocol, please refer to Cheng et al..
许多表观遗传调控复合物的详细染色质组装过程在很大程度上尚不清楚。在这里,我们提出了一种方案,利用异染色质靶向模块(HTM)介导的染色质拴系,随后通过基于显微镜的可视化来检测多梳抑制复合物1(PRC1)中两个组分之间的招募优先级。此外,我们详细介绍了使用免疫荧光(IF)分析检测PRC1产生的组蛋白修饰活性的程序。这种方法可以直接在活细胞中可视化感兴趣的组蛋白修饰复合物的染色质组装情况。有关本方案使用和执行的完整详细信息,请参考Cheng等人的文章。