瑞士/瑞士法郎
染色质重塑
转录因子
生物
染色质
SMARCA4型
染色质结构重塑复合物
抄写(语言学)
细胞生物学
染色质免疫沉淀
SMARCB1型
转录调控
癌症研究
核小体
组蛋白
发起人
RNA聚合酶Ⅱ
基因
增强子
分子生物学
基因表达调控
遗传学
基因表达
哲学
语言学
作者
Chase M Woodley,Alexander S. Romer,Jing Wang,Alissa D. Guarnaccia,David L. Elion,Jack N. Maxwell,Kiana Guerrazzi,Tyler McCann,Tessa M. Popay,Brittany K. Matlock,David K. Flaherty,Shelly L. Lorey,Qi Liu,William P. Tansey,April M. Weissmiller
出处
期刊:Oncogene
[Springer Nature]
日期:2021-04-30
卷期号:40 (20): 3593-3609
被引量:12
标识
DOI:10.1038/s41388-021-01804-7
摘要
The SNF5 subunit of the SWI/SNF chromatin remodeling complex has been shown to act as a tumor suppressor through multiple mechanisms, including impairing the ability of the oncoprotein transcription factor MYC to bind chromatin. Beyond SNF5, however, it is unknown to what extent MYC can access additional SWI/SNF subunits or how these interactions affect the ability of MYC to drive transcription, particularly in SNF5-null cancers. Here, we report that MYC interacts with multiple SWI/SNF components independent of SNF5. We show that MYC binds the pan-SWI/SNF subunit BAF155 through the BAF155 SWIRM domain, an interaction that is inhibited by the presence of SNF5. In SNF5-null cells, MYC binds with remaining SWI/SNF components to essential genes, although for a purpose that is distinct from chromatin remodeling. Analysis of MYC-SWI/SNF target genes in SNF5-null cells reveals that they are associated with core biological functions of MYC linked to protein synthesis. These data reveal that MYC can bind SWI/SNF in an SNF5-independent manner and that SNF5 modulates access of MYC to core SWI/SNF complexes. This work provides a framework in which to interrogate the influence of SWI/SNF on MYC function in cancers in which SWI/SNF or MYC are altered.
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