Browse
Submit Data
Databases
API
Help

Dataset Information

0 Views

0 Connections

0 Citations

0 Reanalyses

0 Downloads

Omics score: 0

The subtype-specific transcriptional regulatory networks of intestinal innate lymphoid cells (ATAC-seq)

ABSTRACT: The subtype-specific transcriptional regulatory networks of intestinal innate lymphoid cells (ATAC-seq)

PROVIDER: PRJNA477001 | ENA |

REPOSITORIES: ENA

ACCESS DATA

Json Xml

Dataset's files

Source:

			Action	DRS
	SRR7405260_1.fastq.gz	Fastqsanger.gz
	SRR7405260_2.fastq.gz	Fastqsanger.gz
	SRR7405270_1.fastq.gz	Fastqsanger.gz
	SRR7405270_2.fastq.gz	Fastqsanger.gz
	SRR7405280_1.fastq.gz	Fastqsanger.gz

Items per page:

1 - 5 of 92

Similar Datasets

The subtype-specific transcriptional regulatory networks of intestinal innate lymphoid cells

Project description:The subtype-specific transcriptional regulatory networks of intestinal innate lymphoid cells

| PRJNA476998 | ENA

The subtype-specific transcriptional regulatory networks of intestinal innate lymphoid cells (RNA-seq)

Project description:The subtype-specific transcriptional regulatory networks of intestinal innate lymphoid cells (RNA-seq)

| PRJNA477002 | ENA

The subtype-specific transcriptional regulatory networks of intestinal innate lymphoid cells (ATAC-seq)

Project description:Innate lymphoid cells (ILCs) comprise a population of immune cells that promote tissue homeostasis, defense against infections, and inflammatory disease. Yet, the transcriptional control of these functions is not well understood. Here, we leverage an experimental-computational approach for transcriptional regulatory network (TRN) inference, recently validated in an in vitro context, to construct genome-scale TRNs for ILCs isolated ex vivo from the intestine of mice. Chromatin accessibility and gene expression are the key data for our TRN inference method. Thus, we generated ATAC-seq and RNA-seq datasets for ILCs of the small and large intestine to integrate with publicly available ILC genomics data. From our ILC TRN, we predict target genes for hundreds of transcription factors (TFs), recovering both known and novel TF regulators of ILC subtype-specific gene expression patterns. The identified TFs include both activators and repressors of lineage-specific genes. Using KO mice, we validated predictions for two such TFs, MAF and BCL6, as previously unknown regulators affecting the balance of ILC3-ILC1. We additionally demonstrate the utility of our ILC TRN to describe gene expression responses to Bcl6 KO in ILC1, NK and ILC3 and predict TF regulators in each subtype. The ILC TRN and “core” ILC subtype networks are publicly available through an interactive Jupyter-notebook web interface. We anticipate that these maps of ILC subtype-specific transcriptional regulation will serve as an important community resource and lead to the development of new strategies for the control of subtype-specific behaviors, especially in the context of disease.

2019-05-21 | GSE116091 | GEO

The subtype-specific transcriptional regulatory networks of intestinal innate lymphoid cells (RNA-seq)

2019-05-21 | GSE116092 | GEO

Regulatory innate lymphoid cells control innate intestinal inflammation

Project description:Regulatory innate lymphoid cells control innate intestinal inflammation

| PRJNA394222 | ENA

Intestinal fibroblastic reticular cell niches control innate lymphoid cell homeostasis and function - Innate lymphoid cells

Project description:Innate lymphoid cells (ILC) in the small intestine govern immune homeostasis and protect the host against gut pathogens. While distinct cell-intrinsic signals have been identified that determine ILC development and differentiation, it has remained unclear which cell population regulates ILC sustenance. Using unbiased single cell RNA transcriptomic analysis of intestinal fibroblasts, we have identified a specialized Ccl19-expressing fibroblastic reticular cell (FRC) population that underpins solitary intestinal lymphoid tissue (SILT) structures including cryptopatches and isolated lymphoid follicles. Conditional ablation of lymphotoxin-β receptor (LTβR) signalling in SILT FRC impeded the maturation of isolated lymphoid follicles and blocked ILC maintenance through the downregulation of IL-7, consequently resulting in the elevated susceptibility to bacterial infection. Moreover, specific Ltbr ablation in FRC during adulthood revealed that constant LTβR-dependent FRC-ILC interaction is required to maintain SILT structures and ILC populations. Taken together, our study unveils a critical intestinal FRC niche that secures protective gut immunity.

2022-02-12 | E-MTAB-10645 | biostudies-arrayexpress

Intestinal fibroblastic reticular cell niches control innate lymphoid cell homeostasis and function - Innate lymphoid cells

Project description:Intestinal fibroblastic reticular cell niches control innate lymphoid cell homeostasis and function - Innate lymphoid cells

| PRJEB46051 | ENA

Intestinal fibroblastic reticular cell niches control innate lymphoid cell homeostasis and function - Intestinal fibroblasts

2022-02-12 | E-MTAB-10638 | biostudies-arrayexpress

scRNA-seq of E18.5 small intestinal innate lymphoid cells

Project description:Embryonic innate lymphoid cells (ILCs) were isolated from small intestinal lamina propria to study their transcriptomic profile in the developing tissue.

2021-08-12 | GSE161441 | GEO

scRNA-seq of E18.5 small intestinal innate lymphoid cells

Project description:scRNA-seq of E18.5 small intestinal innate lymphoid cells

| PRJNA678307 | ENA