Li Wenbo, Hu Yiren, Oh Soohwan, Ma Qi, Merkurjev Daria, Song Xiaoyuan, Zhou Xiang, Liu Zhijie, Tanasa Bogdan, He Xin, Chen Aaron Yun, Ohgi Kenny, Zhang Jie, Liu Wen, Rosenfeld Michael G
Howard Hughes Medical Institute, Department of Medicine, School of Medicine, University of California, San Diego, La Jolla, CA 92093, USA.
Howard Hughes Medical Institute, Department of Medicine, School of Medicine, University of California, San Diego, La Jolla, CA 92093, USA; Biological Sciences Graduate Program, University of California, San Diego, La Jolla, CA 92093, USA.
Mol Cell. 2015 Jul 16;59(2):188-202. doi: 10.1016/j.molcel.2015.06.002. Epub 2015 Jul 9.
Enhancers instruct spatio-temporally specific gene expression in a manner tightly linked to higher-order chromatin architecture. Critical chromatin architectural regulators condensin I and condensin II play non-redundant roles controlling mitotic chromosomes. But the chromosomal locations of condensins and their functional roles in interphase are poorly understood. Here we report that both condensin complexes exhibit an unexpected, dramatic estrogen-induced recruitment to estrogen receptor α (ER-α)-bound eRNA(+) active enhancers in interphase breast cancer cells, exhibiting non-canonical interaction with ER-α via its DNA-binding domain (DBD). Condensins positively regulate ligand-dependent enhancer activation at least in part by recruiting an E3 ubiquitin ligase, HECTD1, to modulate the binding of enhancer-associated coactivators/corepressors, including p300 and RIP140, permitting full eRNA transcription, formation of enhancer:promoter looping, and the resultant coding gene activation. Collectively, our results reveal an important, unanticipated transcriptional role of interphase condensins in modulating estrogen-regulated enhancer activation and coding gene transcriptional program.
增强子以一种与高阶染色质结构紧密相关的方式指导时空特异性基因表达。关键的染色质结构调节因子凝聚素I和凝聚素II在控制有丝分裂染色体方面发挥非冗余作用。但是凝聚素在染色体上的位置及其在间期的功能作用却知之甚少。在此,我们报告,在间期乳腺癌细胞中,两种凝聚素复合物均表现出意想不到的、由雌激素显著诱导的向与雌激素受体α(ER-α)结合的eRNA(+)活性增强子的募集,通过其DNA结合结构域(DBD)与ER-α表现出非经典相互作用。凝聚素至少部分通过招募E3泛素连接酶HECTD1来正向调节配体依赖性增强子激活,以调节增强子相关共激活因子/共抑制因子(包括p300和RIP140)的结合,从而实现完整的eRNA转录、增强子:启动子环化的形成以及由此产生的编码基因激活。总体而言,我们的结果揭示了间期凝聚素在调节雌激素调控的增强子激活和编码基因转录程序中一个重要的、意想不到的转录作用。