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


ABSTRACT: 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 lncRNA 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.

SUBMITTER: Grossi E 

PROVIDER: S-EPMC7028943 | biostudies-literature | 2020 Feb

REPOSITORIES: biostudies-literature

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

Grossi Elena E   Raimondi Ivan I   Goñi Enrique E   González Jovanna J   Marchese Francesco P FP   Chapaprieta Vicente V   Martín-Subero José I JI   Guo Shuling S   Huarte Maite M  

Nature communications 20200218 1


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 ident  ...[more]

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