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BANP opens chromatin and activates CpG island regulated genes [SLAM-Seq]

ABSTRACT: BANP opens chromatin and activates CpG island regulated genes [SLAM-Seq]

PROVIDER: PRJNA650408 | ENA |

REPOSITORIES: ENA

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			Action	DRS
	SRR12374000.fastq.gz	Fastqsanger.gz
	SRR12374100.fastq.gz	Fastqsanger.gz
	SRR12374001.fastq.gz	Fastqsanger.gz
	SRR12374002.fastq.gz	Fastqsanger.gz
	SRR12374003.fastq.gz	Fastqsanger.gz

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BANP opens chromatin and activates CpG island regulated genes [SLAM-Seq]

Project description:In mammalian genomes, the vast majority of RNA polymerase II initiation events take place at CpG island promoters. Despite their relevance our understanding of their regulation remains limited. Here we identify Banp as the long sought-after TF that binds the orphan CGCG element in CpG islands by combining single-molecule footprinting with interaction proteomics. We show that Banp drives activity of CpG islands that control essential metabolic genes in the mouse and human genome. Banp binding is strongly repelled by DNA methylation of its motif in vitro and in vivo, which restricts most binding to CpG islands and accounts for its absence at aberrantly methylated CpG islands in cancer cells. Upon binding to an unmethylated motif, Banp opens chromatin and positions nucleosomes. These findings expand our understanding of CpG island gene regulation and put forth a model whereby CpG islands rely for their activity on methylation sensitive TFs capable of opening and organizing chromatin.

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BANP opens chromatin and activates CpG island regulated genes [RNA-Seq]

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BANP opens chromatin and activates CpG island regulated genes [ChIP-Seq]

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BANP opens chromatin and activates CpG island regulated genes [ATAC-Seq]

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BANP opens chromatin and activates CpG island regulated genes [MNase-seq]

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BANP is an essential transcription factor that opens chromatin and activates CpG island regulated genes

Project description:While the majority of RNA polymerase II initiation events in mammalian genomes take place within CpG island (CGI) promoters, our understanding of their regulation remains limited. Here we combine single-molecule footprinting with interaction proteomics to identify BANP as a critical CGI regulator and the long sought-after TF that binds the orphan CGCG element in mouse and human. We show that BANP drives the activity of essential metabolic genes in the mouse genome in pluripotent and terminally differentiated cells. However, BANP binding is strongly repelled by DNA methylation of its motif in vitro and in vivo, which epigenetically restricts most binding to CGIs and accounts for its absence at aberrantly methylated CGIs in cancer cells. Upon binding to an unmethylated motif, BANP opens chromatin and phases nucleosomes. Our results establish Banp as a critical activator and put forth a model whereby CGI promoter activity relies on methylation-sensitive TFs capable of chromatin opening.

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BANP opens chromatin and activates CpG-island-regulated genes

Project description:BANP opens chromatin and activates CpG-island-regulated genes

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BANP opens chromatin and activates CpG island regulated genes [MNase-seq]

Project description:BANP opens chromatin and activates CpG island regulated genes [MNase-seq]

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BANP opens chromatin and activates CpG island regulated genes [ChIP-Seq]

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