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The hyperconnected 3D clique at the Ets1 locus is required for T cell function (ATAC-Seq)

ABSTRACT: The hyperconnected 3D clique at the Ets1 locus is required for T cell function (ATAC-Seq)

PROVIDER: PRJNA869316 | ENA |

REPOSITORIES: ENA

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			Action	DRS
	SRR21038470_1.fastq.gz	Fastqsanger.gz
	SRR21038470_2.fastq.gz	Fastqsanger.gz
	SRR21038471_1.fastq.gz	Fastqsanger.gz
	SRR21038471_2.fastq.gz	Fastqsanger.gz
	SRR21038472_1.fastq.gz	Fastqsanger.gz

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The hyperconnected 3D clique at the Ets1 locus is required for T cell function (RNA-Seq)

Project description:The spatiotemporal control of gene-expression programs relies on selection and nuclear organization of enhancers. Despite mounting evidence on the formation of multi-enhancer hubs with extensive spatial connectivity, the functional importance of these architectural units remains elusive. Here, we generated a new mouse model and genetically perturbed a genomic locus harboring the Ets1 gene which is hyperconnected in T cells and has strong association with immune-mediated diseases. Although T cell development was intact, competence towards CD4+ T helper 1 specialization was lost in vitro and in vivo after genetic perturbation of the Ets1 locus. Extensive high-resolution molecular mapping of 3D genome organization revealed that the hyperconnectivity of the Ets1 locus controlled the expression level of Ets1 which was required for the Th1-specific genome topology. Our work illustrates the functional relevance of multi-enhancer hub formation in T cells.

2023-06-20 | GSE211177 | GEO