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Polycomb- and Methylation-Independent Roles of EZH2 as a Transcription Activator [RNA-seq]

ABSTRACT: Polycomb- and Methylation-Independent Roles of EZH2 as a Transcription Activator [RNA-seq]

PROVIDER: PRJNA421358 | ENA |

REPOSITORIES: ENA

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			Action	DRS
	SRR6355942.fastq.gz	Fastqsanger.gz
	SRR6355943.fastq.gz	Fastqsanger.gz
	SRR6355944.fastq.gz	Fastqsanger.gz
	SRR6355945.fastq.gz	Fastqsanger.gz
	SRR6355946.fastq.gz	Fastqsanger.gz

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Polycomb- and Methylation-Independent Roles of EZH2 as a Transcription Activator

Project description:Polycomb- and Methylation-Independent Roles of EZH2 as a Transcription Activator

| PRJNA421353 | ENA

Polycomb- and Methylation-Independent Roles of EZH2 as a Transcription Activator [microarray]

Project description:Polycomb- and Methylation-Independent Roles of EZH2 as a Transcription Activator [microarray]

| PRJNA421357 | ENA

Polycomb- and Methylation-Independent Roles of EZH2 as a Transcription Activator [ChIP-seq]

Project description:Polycomb- and Methylation-Independent Roles of EZH2 as a Transcription Activator [ChIP-seq]

| PRJNA421359 | ENA

Polycomb- and Methylation-Independent Roles of EZH2 as a Transcription Activator [microarray]

Project description:EZH2 induces active transcription of the AR gene, thereby increasing AR level and promoting AR signaling. Importantly, EZH2-mediated activation of AR requires EZH2 protein occupancy at the AR gene promoter, but is independent of PRC2 as well as its histone methyltransferase activity

2018-12-01 | GSE107779 | GEO

Polycomb- and Methylation-Independent Roles of EZH2 as a Transcription Activator [RNA-seq]

2018-12-01 | GSE107781 | GEO

Polycomb- and Methylation-Independent Roles of EZH2 as a Transcription Activator [ChIP-seq]

2018-12-01 | GSE107780 | GEO

Polycomb- and Methylation-Independent Roles of EZH2 as a Transcription Activator.

Project description:Enhancer of Zeste 2 (EZH2) is the enzymatic subunit of Polycomb Repressive Complex 2 (PRC2), which catalyzes histone H3 lysine 27 trimethylation (H3K27me3) at target promoters for gene silencing. Here, we report that EZH2 activates androgen receptor (AR) gene transcription through direct occupancy at its promoter. Importantly, this activating role of EZH2 is independent of PRC2 and its methyltransferase activities. Genome-wide assays revealed extensive EZH2 occupancy at promoters marked by either H3K27ac or H3K27me3, leading to gene activation or repression, respectively. Last, we demonstrate enhanced efficacy of enzymatic EZH2 inhibitors when used in combination with AR antagonists in blocking the dual roles of EZH2 and suppressing prostate cancer progression in vitro and in vivo. Taken together, our study reports EZH2 as a transcriptional activator, a key target of which is AR, and suggests a drug-combinatory approach to treat advanced prostate cancer.

| S-EPMC6342284 | biostudies-literature

Polycomb- and Methylation-Independent Roles of EZH2 as a Transcription Activator

Project description:This SuperSeries is composed of the SubSeries listed below.

2018-12-01 | GSE107782 | GEO

Dual and separable roles for Ezh2 in neurogenic astroglia

Project description:The epigenetic mechanisms that enable specialized astrocytes to retain neurogenic competence throughout adult life are still poorly understood. Here we show that astrocytes that serve as neural stem cells (NSCs) in the adult mouse subventricular zone (SVZ) express the histone methyltransferase EZH2. This Polycomb repressive factor is required for neurogenesis independent of its role in SVZ NSC proliferation, as Ink4a/Arf-deficiency in Ezh2-deleted SVZ NSCs rescues cell proliferation, but neurogenesis remains defective. Olig2 is a direct target of EZH2, and repression of this bHLH transcription factor is critical for neuronal differentiation. Furthermore, Ezh2 prevents the inappropriate activation of genes that specify non-SVZ neuronal subtypes. In the human brain, SVZ cells including local astroglia also express EZH2, correlating with postnatal neurogenesis. Thus, EZH2 is an epigenetic regulator that distinguishes neurogenic SVZ astrocytes, orchestrating distinct and separable aspects of adult stem cell biology, which has important implications for regenerative medicine and oncogenesis. Examination of histone modifications (H3K27me3 and H3K4me3) in subventricular zone neural stem cells

2014-05-02 | E-GEOD-56394 | biostudies-arrayexpress

Affinify Purification of EZH2 and phosphodeficient EZH2 identifies phosphorylation dependent interactions of EZH2

Project description:Overexpression of EZH2 in estrogen receptor negative (ER-) breast cancer promotes metastasis. EZH2 has been mainly studied as the catalytic component of the Polycomb Repressive Complex 2 (PRC2) that mediates gene repression by trimethylating histone H3 at lysine 27 (H3K27me3). However, how EZH2 drives metastasis despite the low H3K27me3 levels observed in ER- breast cancer is unknown. We have shown that in human invasive carcinomas and distant metastases, cytoplasmic EZH2 phosphorylated at T367 is significantly associated with ER- disease and low H3K27me3 levels. Here, we explore the interactome of EZH2 and of a phosphodeficient mutant EZH2_T367A. We identified novel interactors of EZH2, and identified interactions that are dependent on the phosphorylation and cellular localization of EZH2 that may play a role in EZH2 dependent metastatic progression.

2018-07-03 | PXD010073 | Pride

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