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Effects of vitamin D on histone modification H3K4me3 in THP-1 cells

ABSTRACT: Effects of vitamin D on histone modification H3K4me3 in THP-1 cells

PROVIDER: PRJNA489509 | ENA |

REPOSITORIES: ENA

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			Action	DRS
	SRR7790700.fastq.gz	Fastqsanger.gz
	SRR7790701.fastq.gz	Fastqsanger.gz
	SRR7790702.fastq.gz	Fastqsanger.gz
	SRR7790693.fastq.gz	Fastqsanger.gz
	SRR7790703.fastq.gz	Fastqsanger.gz

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Effects of vitamin D on histone modification H3K4me3 in THP-1 cells

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Effects of vitamin D on histone modifications H3K27ac and H3K4me3 in THP-1 cells

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Genome wide map of H3K4me3 histone modification in C6 rat glioma cells [SOLiD]

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Genome wide maps of H3K4me3 and H3ac histone modifications in C6 rat glioma cells [Illumina]

Project description:We report maps of H3K4me3 and H3ac - activiting expression histone modifications in C6 rat glioma cells. The data was obtained using whole genome high throughput technology. The sequencing was performed on HiSeq Ilumina platform. Examination of H3K4me3 histone modification and H3ac histone modification in C6 rat glioma cell line

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Genome-wide mapping of the histone modification H3K4me3 in bovine early embryos [ChIP-seq]

Project description:Reprogramming of histone modification regulates gene expression and mammal preimplantation development. Trimethylation of lysine 4 on histone 3 (H3K4me3) has unique landscape in mouse oocytes and early embryos. However, the dynamics and function of H3K4me3 in livestock embryos remain unclear. To address how it is reprogrammed in domestic animals, we profiled changes of H3K4me3 during bovine early embryo development. Notably, the overall signal of H3K4me3 decreased during embryonic genome activation (EGA). By utilizing ultra-low-input native ChIP-seq (ULI-NChIP-seq) technology, we observed widespread broad H3K4me3 domains in oocytes and embryos. The signal of broad H3K4me3 began to decrease after fertilization and was lowest after EGA. Along with the removal of broad H3K4me3, deposition of H3K4me3 at promoter regions enhanced gradually. Besides, the transcriptional activity and signal of promoter H3K4me3 showed positive correlation after the erasure of broad H3K4me3 at 16-cell stage. Moreover, knocking down of demethylases KDM5A, KDM5B and KDM5C caused EGA delay and blastocyst formation failure. RNA-seq analysis revealed 47.8% down-regulated genes in knockdown embryos at 8/16-cell stage were EGA genes, and 63.1% of up-regulated genes were maternal transcripts. Particularly, the positive correlation between transcriptional activity and promoter H3K4me3 during EGA was restrained when knocking down of KDM5A, KDM5B and KDM5C. Overall, our work initiatively mapped the genomic reprogramming of H3K4me3 during bovine preimplantation development, and KDM5A/B/C played roles in modulating oocyte-to-embryonic transition (OET) through timely erasure of broad H3K4me3 domains far away from promoters.

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