4WK8
FOXP3 forms a domain-swapped dimer to bridge DNA
4WK8 の概要
| エントリーDOI | 10.2210/pdb4wk8/pdb |
| 分子名称 | DNA (5'-D(*TP*TP*AP*GP*GP*AP*AP*AP*AP*TP*TP*TP*GP*TP*TP*TP*CP*AP*TP*AP*G)-3'), DNA (5'-D(*AP*AP*CP*TP*AP*TP*GP*AP*AP*AP*CP*AP*AP*AP*TP*TP*TP*TP*CP*CP*T)-3'), Forkhead box protein P3 (3 entities in total) |
| 機能のキーワード | foxp3, regulatory t cells, dna bridging, transcription regulation, transcription-dna complex, transcription/dna |
| 由来する生物種 | Homo sapiens (Human) 詳細 |
| タンパク質・核酸の鎖数 | 4 |
| 化学式量合計 | 33045.87 |
| 構造登録者 | |
| 主引用文献 | Chen, Y.,Chen, C.,Zhang, Z.,Liu, C.C.,Johnson, M.E.,Espinoza, C.A.,Edsall, L.E.,Ren, B.,Zhou, X.J.,Grant, S.F.,Wells, A.D.,Chen, L. DNA binding by FOXP3 domain-swapped dimer suggests mechanisms of long-range chromosomal interactions. Nucleic Acids Res., 43:1268-1282, 2015 Cited by PubMed Abstract: FOXP3 is a lineage-specific transcription factor that is required for regulatory T cell development and function. In this study, we determined the crystal structure of the FOXP3 forkhead domain bound to DNA. The structure reveals that FOXP3 can form a stable domain-swapped dimer to bridge DNA in the absence of cofactors, suggesting that FOXP3 may play a role in long-range gene interactions. To test this hypothesis, we used circular chromosome conformation capture coupled with high throughput sequencing (4C-seq) to analyze FOXP3-dependent genomic contacts around a known FOXP3-bound locus, Ptpn22. Our studies reveal that FOXP3 induces significant changes in the chromatin contacts between the Ptpn22 locus and other Foxp3-regulated genes, reflecting a mechanism by which FOXP3 reorganizes the genome architecture to coordinate the expression of its target genes. Our results suggest that FOXP3 mediates long-range chromatin interactions as part of its mechanisms to regulate specific gene expression in regulatory T cells. PubMed: 25567984DOI: 10.1093/nar/gku1373 主引用文献が同じPDBエントリー |
| 実験手法 | X-RAY DIFFRACTION (3.4006 Å) |
構造検証レポート
検証レポート(詳細版)
をダウンロード






