Browse
Submit Data
Databases
API
Help

Dataset Information

0 Views

0 Connections

0 Citations

0 Reanalyses

0 Downloads

Omics score: 0

Transient naive reprogramming corrects hiPS cells functionally and epigenetically [ONT DNA-seq]

ABSTRACT: Transient naive reprogramming corrects hiPS cells functionally and epigenetically [ONT DNA-seq]

PROVIDER: PRJNA999723 | ENA |

REPOSITORIES: ENA

ACCESS DATA

Json Xml

Dataset's files

Source:

			Action	DRS
	SRR25454127_1.fastq.gz	Fastqsanger.gz
	SRR25454128_1.fastq.gz	Fastqsanger.gz
	SRR25454129_1.fastq.gz	Fastqsanger.gz
	SRR25454130_1.fastq.gz	Fastqsanger.gz
	SRR25454131_1.fastq.gz	Fastqsanger.gz

Items per page:

1 - 5 of 11

Similar Datasets

Transient naive reprogramming corrects hiPS cells functionally and epigenetically

Project description:Transient naive reprogramming corrects hiPS cells functionally and epigenetically

| PRJNA668312 | ENA

Transient naive reprogramming corrects hiPS cells functionally and epigenetically [ONT DNA-seq]

Project description:Cells undergo a major epigenome reconfiguration when reprogrammed to human induced pluripotent stem cells (hiPS cells). However, the epigenomes of hiPS cells and human embryonic stem (hES) cells differ significantly, which affects hiPS cell function. These differences include epigenetic memory and aberrations that emerge during reprogramming, for which the mechanisms remain unknown. Here we characterized the persistence and emergence of these epigenetic differences by performing genome-wide DNA methylation profiling throughout primed and naive reprogramming of human somatic cells to hiPS cells. We found that reprogramming-induced epigenetic aberrations emerge midway through primed reprogramming, whereas DNA demethylation begins early in naive reprogramming. Using this knowledge, we developed a transient-naive-treatment (TNT) reprogramming strategy that emulates the embryonic epigenetic reset. We show that the epigenetic memory in hiPS cells is concentrated in cell of origin-dependent repressive chromatin marked by H3K9me3, lamin-B1 and aberrant CpH methylation. TNT reprogramming reconfigures these domains to a hES cell-like state and does not disrupt genomic imprinting. Using an isogenic system, we demonstrate that TNT reprogramming can correct the transposable element overexpression and differential gene expression seen in conventional hiPS cells, and that TNT-reprogrammed hiPS and hES cells show similar differentiation efficiencies. Moreover, TNT reprogramming enhances the differentiation of hiPS cells derived from multiple cell types. Thus, TNT reprogramming corrects epigenetic memory and aberrations, producing hiPS cells that are molecularly and functionally more similar to hES cells than conventional hiPS cells. We foresee TNT reprogramming becoming a new standard for biomedical and therapeutic applications and providing a novel system for studying epigenetic memory.

2023-08-11 | GSE239579 | GEO

Transient naive reprogramming corrects hiPS cells functionally and epigenetically [WGBS]

Project description:Transient naive reprogramming corrects hiPS cells functionally and epigenetically [WGBS]

| PRJNA668324 | ENA

Transient naive reprogramming corrects hiPS cells functionally and epigenetically [ChIP-seq]

Project description:Transient naive reprogramming corrects hiPS cells functionally and epigenetically [ChIP-seq]

| PRJNA670246 | ENA

Transient naive reprogramming corrects hiPS cells functionally and epigenetically [ATAC-seq]

Project description:Transient naive reprogramming corrects hiPS cells functionally and epigenetically [ATAC-seq]

| PRJNA740328 | ENA

Transient naive reprogramming corrects hiPS cells functionally and epigenetically [scRNA-Seq]

Project description:Transient naive reprogramming corrects hiPS cells functionally and epigenetically [scRNA-Seq]