RNA transcribed from enhancers, i.e., eRNA, has been suggested to directly activate transcription by recruiting transcription factors and co-activators. Although there have been specific examples of eRNA functioning in this way, it is not clear how general this may be. We find that the AT-hook of SWI/SNF preferentially binds RNA and, as part of the esBAF complex, associates with eRNA transcribed from intronic and intergenic regions. Our data suggest that SWI/SNF is globally recruited in cis by eRNA to cell-type-specific enhancers, representative of two distinct stages that mimic early mammalian development, and not at enhancers that are shared between the two stages. In this manner, SWI/SNF facilitates recruitment and/or activation of MLL3/4, p300/CBP, and Mediator to stage-specific enhancers and super-enhancers that regulate the transcription of metabolic and cell lineage priming-related genes. These findings highlight a connection between ATP-dependent chromatin remodeling and eRNA in cell identity and typical- and super-enhancer activation.
Enhancer switching in cell lineage priming is linked to eRNA, Brg1's AT-hook, and SWI/SNF recruitment.
细胞谱系启动中的增强子转换与 eRNA、Brg1 的 AT 钩以及 SWI/SNF 募集有关
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作者:Saha Dhurjhoti, Animireddy Srinivas, Lee Junwoo, Thommen Anna, Murvin McKenzie M, Lu Yue, Calabrese J Mauro, Bartholomew Blaine
| 期刊: | Molecular Cell | 影响因子: | 16.600 |
| 时间: | 2024 | 起止号: | 2024 May 16; 84(10):1855-1869 |
| doi: | 10.1016/j.molcel.2024.03.013 | 研究方向: | 细胞生物学 |
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