A IncRNA-SWI/SNF complex crosstalk controls transcriptional activation at specific promoter regions

被引:63
|
作者
Grossi, Elena [1 ,2 ]
Raimondi, Ivan [1 ,2 ]
Goni, Enrique [1 ,2 ]
Gonzalez, Jovanna [1 ,2 ]
Marchese, Francesco P. [1 ,2 ]
Chapaprieta, Vicente [3 ]
Martin-Subero, Jose, I [3 ,4 ,5 ,6 ]
Guo, Shuling [7 ]
Huarte, Maite [1 ,2 ]
机构
[1] Univ Navarra, Ctr Appl Med Res, Dept Gene Therapy & Regulat Gene Express, Pamplona 31008, Spain
[2] Inst Hlth Res Navarra IdiSNA, Pamplona, Spain
[3] Univ Barcelona, Fac Med, Dept Fonaments Clin, Barcelona, Spain
[4] Inst Invest Biomed August Pi i Sunyer IDIBAP, Barcelona, Spain
[5] Inst Catalana Recerca & Estudis Avancats ICREA, Barcelona, Spain
[6] Ctr Invest Biomed Red Canc CIBERONC, Madrid, Spain
[7] Ionis Pharmaceut, Dept Antisense Drug Discovery & Clin Dev, Carlsbad, CA USA
基金
欧洲研究理事会;
关键词
GENE-EXPRESSION; CHROMATIN; SENESCENCE; CANCER; P16(INK4A); MUTATIONS; ENHANCERS; DISCOVERY; SERVER; CELLS;
D O I
10.1038/s41467-020-14623-3
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
LncRNAs have been shown to be direct players in chromatin regulation, but little is known about their role at active genomic loci. We investigate the role of lncRNAs in gene activation by profiling the RNA interactome of SMARCB1-containing SWI/SNF complexes in proliferating and senescent conditions. The isolation of SMARCB1-associated transcripts, together with chromatin profiling, shows prevalent association to active regions where SMARCB1 differentially binds locally transcribed RNAs. We identify SWINGN, a IncRNA interacting with SMARCB1 exclusively in proliferating conditions, exerting a pro-oncogenic role in some tumor types. SWINGN is transcribed from an enhancer and modulates the activation of GAS6 oncogene as part of a topologically organized region, as well as a larger network of pro-oncogenic genes by favoring SMARCB1 binding. Our results indicate that SWINGN influences the ability of the SWI/SNF complexes to drive epigenetic activation of specific promoters, suggesting a SWI/SNF-RNA cooperation to achieve optimal transcriptional activation.
引用
收藏
页数:16
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