<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Liu Z</submitter><funding>NIAID NIH HHS</funding><funding>U.S. Department of Health &amp;amp; Human Services | NIH | National Institute of Allergy and Infectious Diseases</funding><funding>NCI NIH HHS</funding><funding>NIH HHS</funding><pagination>6943</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10628232</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>14(1)</volume><pubmed_abstract>Chromatin conformation reorganization is emerging as an important layer of regulation for gene expression and lineage specification. Yet, how lineage-specific transcription factors contribute to the establishment of cell type-specific 3D chromatin architecture in the immune cells remains unclear, especially for the late stages of T cell subset differentiation and maturation. Regulatory T cells (Treg) are mainly generated in the thymus as a subpopulation of T cells specializing in suppressing excessive immune responses. Here, by comprehensively mapping 3D chromatin organization during Treg cell differentiation, we show that Treg-specific chromatin structures were progressively established during its lineage specification, and highly associated with Treg signature gene expression. Additional</pubmed_abstract><journal>Nature communications</journal><pubmed_title>Foxp3 orchestrates reorganization of chromatin architecture to establish regulatory T cell identity.</pubmed_title><pmcid>PMC10628232</pmcid><funding_grant_id>R01 AI107027</funding_grant_id><funding_grant_id>R01-AI107027</funding_grant_id><funding_grant_id>R21 AI178938</funding_grant_id><funding_grant_id>P30 CA014195</funding_grant_id><funding_grant_id>DP5 OD023071</funding_grant_id><funding_grant_id>R21 AI154919</funding_grant_id><funding_grant_id>R21-AI178938</funding_grant_id><funding_grant_id>U01 CA260700</funding_grant_id><funding_grant_id>R01 AI151123</funding_grant_id><funding_grant_id>S10 OD023689</funding_grant_id><pubmed_authors>Liu Z</pubmed_authors><pubmed_authors>Zheng Y</pubmed_authors><pubmed_authors>Dixon JR</pubmed_authors><pubmed_authors>Liang Y</pubmed_authors><pubmed_authors>Lee DS</pubmed_authors></additional><is_claimable>false</is_claimable><name>Foxp3 orchestrates reorganization of chromatin architecture to establish regulatory T cell identity.</name><description>Chromatin conformation reorganization is emerging as an important layer of regulation for gene expression and lineage specification. Yet, how lineage-specific transcription factors contribute to the establishment of cell type-specific 3D chromatin architecture in the immune cells remains unclear, especially for the late stages of T cell subset differentiation and maturation. Regulatory T cells (Treg) are mainly generated in the thymus as a subpopulation of T cells specializing in suppressing excessive immune responses. Here, by comprehensively mapping 3D chromatin organization during Treg cell differentiation, we show that Treg-specific chromatin structures were progressively established during its lineage specification, and highly associated with Treg signature gene expression. Additional</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Nov</publication><modification>2026-07-14T22:40:45.493Z</modification><creation>2025-02-18T23:31:00.869Z</creation></dates><accession>S-EPMC10628232</accession><cross_references><pubmed>37932264</pubmed><doi>10.1038/s41467-023-42647-y</doi></cross_references></HashMap>