Browse
Submit Data
Databases
API
Help

Dataset Information

0 Views

0 Connections

0 Citations

0 Reanalyses

0 Downloads

Omics score: 0

Complete loss of H3K9 methylation dissolves mouse heterochromatin organization [RNA-seq 2]

ABSTRACT: Establishment and characterization of mouse embryonic fibroblasts deficient for 6 H3K9 lysine methyltranswferases (KMT)

ORGANISM(S): Mus musculus

PROVIDER: GSE169636 | GEO | 2021/05/19

REPOSITORIES: GEO

ACCESS DATA

Json Xml

Dataset's files

Source:

			Action	DRS
		Other

Items per page:

1 - 1 of 1

Similar Datasets

Complete loss of H3K9 methylation dissolves mouse heterochromatin organization [ATAC-seq]

Project description:Establishment and charcterization of mouse embryonic fibroblasts deficient for 6 H3K9 lysine methyltranswferases (KMT)

2021-05-19 | GSE142104 | GEO

Complete loss of H3K9 methylation dissolves mouse heterochromatin organization [RNA-seq]

Project description:Establishment and charcterization of mouse embryonic fibroblasts deficient for 6 H3K9 lysine methyltranswferases (KMT)

2021-05-19 | GSE142103 | GEO

Complete loss of H3K9 methylation dissolves mouse heterochromatin organization [ChIP-seq]

Project description:Establishment and characterization of mouse embryonic fibroblasts deficient for 6 H3K9 lysine methyltransferases (KMT)

2021-05-19 | GSE169635 | GEO

Complete loss of H3K9 methylation dissolves mouse heterochromatin organization

Project description:Histone H3 lysine 9 (H3K9) methylation is a central epigenetic modification that defines heterochromatin from unicellular to multicellular organisms. In mammalian cells, H3K9 methylation can be catalyzed by at least six distinct SET domain enzymes: Suv39h1/Suv39h2, Eset1/Eset2 and G9a/Glp. We used mouse embryonic fibroblasts (MEFs) with a conditional mutation for Eset1 and introduced progressive deletions for the other SET domain genes by CRISPR/Cas9 technology. Compound mutant MEFs for all 6 SET domain methyltransferase (KMT) genes lack all H3K9 methylation states, derepress nearly all families of repeat elements and display genomic instabilities. Strikingly, the 6KO H3K9 KMT MEFs no longer maintain heterochromatin organization and have lost electron-dense heterochromatin. This is the first analysis of H3K9 methylation deficient mammalian chromatin and reveals a crucial function for H3K9 methylation in protecting heterochromatin organization and genome integrity.

2021-05-27 | PXD018175 | Pride

Complete loss of H3K9 methylation dissolves mouse heterochromatin organization.

Project description:Histone H3 lysine 9 (H3K9) methylation is a central epigenetic modification that defines heterochromatin from unicellular to multicellular organisms. In mammalian cells, H3K9 methylation can be catalyzed by at least six distinct SET domain enzymes: Suv39h1/Suv39h2, Eset1/Eset2 and G9a/Glp. We used mouse embryonic fibroblasts (MEFs) with a conditional mutation for Eset1 and introduced progressive deletions for the other SET domain genes by CRISPR/Cas9 technology. Compound mutant MEFs for all six SET domain lysine methyltransferase (KMT) genes lack all H3K9 methylation states, derepress nearly all families of repeat elements and display genomic instabilities. Strikingly, the 6KO H3K9 KMT MEF cells no longer maintain heterochromatin organization and have lost electron-dense heterochromatin. This is a compelling analysis of H3K9 methylation-deficient mammalian chromatin and reveals a definitive function for H3K9 methylation in protecting heterochromatin organization and genome integrity.

| S-EPMC8285382 | biostudies-literature

Complete loss of H3K9 methylation dissolves mouse heterochromatin organization

Project description:Complete loss of H3K9 methylation dissolves mouse heterochromatin organization

| PRJNA595914 | ENA

Complete loss of H3K9 methylation dissolves mouse heterochromatin organization

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

2021-05-19 | GSE142105 | GEO

Complete loss of H3K9 methylation dissolves mouse heterochromatin organization [ATAC-seq]

Project description:Complete loss of H3K9 methylation dissolves mouse heterochromatin organization [ATAC-seq]

| PRJNA595916 | ENA

Complete loss of H3K9 methylation dissolves mouse heterochromatin organization [RNA-seq]

Project description:Complete loss of H3K9 methylation dissolves mouse heterochromatin organization [RNA-seq]