Reversion to nave human pluripotency creates a new methylation landscape devoid of blastocyst or germline memory
Transcriptomics Dataset
FAIR Metrics
0 evaluations
General Information
AccessionGSE76970
TitleReversion to nave human pluripotency creates a new methylation landscape devoid of blastocyst or germline memory
DescriptionHuman embryonic stem cells (hESCs) typically exhibit 'primed' pluripotency, analogous to stem cells derived from the mouse post-implantation epiblast. This has led to a search for growth conditions that support self-renewal of hESCs akin to hypomethylated nave epiblast cells in human pre-implantation embryos. We have discovered that reverting primed hESCs to a hypomethylated nave state or deriving a new hESC line under nave conditions results in the establishment of Stage Specific Embryonic Antigen 4 (SSEA4) negative hESC lines with a transcriptional program resembling the human pre-implantation epiblast. In contrast, we discovered that the methylome of nave hESCs in vitro is distinct from the human epiblast in vivo with loss of DNA methylation at primary imprints and a lost 'memory' of the methylation state of the human oocyte. This failure to recover the nave epiblast methylation landscape appears to be a consistent feature of self-renewing hypomethylated nave hESCs in vitro.
Landing Pagehttps://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE76970
RepositoryGene Expression Omnibus
Tools used to analyze the dataset

Dataset Accession

Clustergrammer
Published October 2017
Web-based tool for visualizing and analyzing high-dimensional data as interactive and shareable heatmaps
4645
ARCHS4
Published September 2017
ARCHS4 provides access to gene counts from HiSeq 2000 and HiSeq 2500 platforms for human and mouse experiments from GEO ...
4645
Canned Analyses generated with the dataset

Dataset Accession
Tool Name

Interactive heatmap visualization of RNA-seq dataset GSE76970
Highly interactive web-based heatmap visualization of the top 500 most variable genes in t...
FAIR Evaluation
Sorry, you must be signed in to evaluate this object.