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Deciphering the endogenous cistrome and transcriptome of estrogen receptor beta in ovary

ABSTRACT: Deciphering the endogenous cistrome and transcriptome of estrogen receptor beta in ovary

PROVIDER: PRJNA839733 | ENA |

REPOSITORIES: ENA

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			Action	DRS
	SRR19318036.fastq.gz	Fastqsanger.gz
	SRR19318037.fastq.gz	Fastqsanger.gz
	SRR19318038.fastq.gz	Fastqsanger.gz
	SRR19318039.fastq.gz	Fastqsanger.gz
	SRR19318040.fastq.gz	Fastqsanger.gz

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Deciphering the endogenous cistrome and transcriptome of estrogen receptor beta in ovary

Project description:ERβ is predominantly expressed in granulosa cells of the ovary, where its important for normal ovarian function and plays a vital role in folliculogenesis. However, the genome wide binding landscape of ERβ in the ovary was not determined and its interaction targets are unknown. To characterize the mechanism of ERβ, we performed ChIP-Seq using endogenous ERβ expression and mapped the cistrome of ERβ in the ovary using a validated antibody.

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Estrogen Receptor beta cistrome in mouse endometriotic tissue.

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Project description:The ESR1 Cistrome in human endometrial biopsies was characterized and compared to gene regulations between the proliferative and mid-secretory pahses to infer estrogen target genes. ESR1 and PGR cistromes and 3D-cjromatin structures in cultured endometrial biopsies were characterized and compared to gene regulations induced by estrogen or progesterone in comparison to the whole endometrium.

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The Estrogen receptor alpha cistrome defined by DamIP

Project description:We have developed a new method to study DNA-protein interaction in vivo called DamIP, which is based on fusing a protein of interest to a mutant form of DNA adenine methylatransferase (Dam) from E. coli. We showed previously that DamIP can efficiently identify in vivo binding sites of Dam-tethered human estrogen receptor alpha (hERα). In current study, we present the cistrome of hERα determined by DamIP and high throughput sequencing (DamIP-seq). The DamIP-seq defined hERα cistrome overlaps significantly with those determined by ChIP-chip or ChIP-seq, but identifies many new binding regions. As shown by conventional ChIP assay, many DamIP-seq unique hERα binding regions show relatively stable hERα binding, whereas DamIP-seq misses some regions with very transient hERα binding. The methyl-adenine modifications introduced by Dam are stable and do not decrease over 12 days. In summary, the current study provides both an alternate view of the hERα cistrome to further understand the mechanism of hERα mediated transcription, and a new tool to explore other transcriptional factors and cofactors. MCF7 cells were transfected with DamK9A or DamK9A-hERalpha. DamIP were performed from each sample and subjected to solexa sequencing

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Analysis of the Phosphorylated Estrogen Receptor-α Cistrome Reveals Association with Direct ER-DNA Binding and the Transcription Factor GRHL2

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