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Mus musculus

ABSTRACT: H3.3 deposition at endogenous retroviruses in embryonic stem cells

PROVIDER: PRJNA290025 | ENA |

REPOSITORIES: ENA

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			Action	DRS
	SRR2103630.fastq.gz	Fastqsanger.gz
	SRR2103621.fastq.gz	Fastqsanger.gz
	SRR2103631.fastq.gz	Fastqsanger.gz
	SRR2103622.fastq.gz	Fastqsanger.gz
	SRR2103632.fastq.gz	Fastqsanger.gz

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H3.3 deposition at endogenous retroviruses in embryonic stem cells

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Histone H3.3 is required for endogenous retroviral element silencing and genome stability [RNA-Seq]

Project description:Endogenous retroviruses (ERVs) have provided an evolutionary advantage in the diversification of transcript regulation and are thought to be involved in the establishment of extraembryonic tissues during development. However, silencing of these elements remains critical for the maintenance of genome stability. Here, we define a new chromatin state that is uniquely characterized by the combination of the histone variant H3.3 and H3K9me3, two chromatin ‘marks’ that have previously been considered to belong to fundamentally opposing chromatin states. H3.3/H3K9me3 heterochromatin is fundamentally distinct from ‘canonical’ H3K9me3 heterochromatin that has been under study for decades and this unique functional interplay of a histone variant and a repressive histone mark is crucial for silencing ERVs in ESCs. Our study solidifies the emerging notion that H3.3 is not a histone variant associated exclusively with “active” chromatin and further suggests that its incorporation at unique heterochromatic regions may be central to its function during development and the maintenance of genome stability. RNA-seq analysis of three embryonic stem cell lines WT, H3.3 KO1, and H3.3 KO2)

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Project description:A hyperdynamic H3.3 nucleosome marks promoter regions in pluripotent embryonic stem cells

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