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Transcriptionally active enhancers in human cancer cells.


ABSTRACT: The growth of human cancer cells is driven by aberrant enhancer and gene transcription activity. Here, we use transient transcriptome sequencing (TT-seq) to map thousands of transcriptionally active putative enhancers in fourteen human cancer cell lines covering seven types of cancer. These enhancers were associated with cell type-specific gene expression, enriched for genetic variants that predispose to cancer, and included functionally verified enhancers. Enhancer-promoter (E-P) pairing by correlation of transcription activity revealed ~ 40,000 putative E-P pairs, which were depleted for housekeeping genes and enriched for transcription factors, cancer-associated genes, and 3D conformational proximity. The cell type specificity and transcription activity of target genes increased with the number of paired putative enhancers. Our results represent a rich resource for future studies of gene regulation by enhancers and their role in driving cancerous cell growth.

SUBMITTER: Lidschreiber K 

PROVIDER: S-EPMC7838827 | biostudies-literature | 2021 Jan

REPOSITORIES: biostudies-literature

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Transcriptionally active enhancers in human cancer cells.

Lidschreiber Katja K   Jung Lisa A LA   von der Emde Henrik H   Dave Kashyap K   Taipale Jussi J   Cramer Patrick P   Lidschreiber Michael M  

Molecular systems biology 20210101 1


The growth of human cancer cells is driven by aberrant enhancer and gene transcription activity. Here, we use transient transcriptome sequencing (TT-seq) to map thousands of transcriptionally active putative enhancers in fourteen human cancer cell lines covering seven types of cancer. These enhancers were associated with cell type-specific gene expression, enriched for genetic variants that predispose to cancer, and included functionally verified enhancers. Enhancer-promoter (E-P) pairing by cor  ...[more]

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