A structural hierarchy mediated by multiple nuclear factors establishes IgH locus conformation

被引:29
作者
Gerasimova, Tatiana [1 ]
Guo, Changying [1 ]
Ghosh, Amalendu [1 ]
Qiu, Xiang [1 ]
Montefiori, Lindsey [1 ]
Verma-Gaur, Jiyoti [2 ]
Choi, Nancy M. [2 ]
Feeney, Ann J. [2 ]
Sen, Ranjan [1 ]
机构
[1] NIA, Lab Mol Biol & Immunol, Baltimore, MD 21224 USA
[2] Scripps Res Inst, La Jolla, CA 92037 USA
基金
美国国家卫生研究院;
关键词
chromosome conformation; looping; architectural proteins; HEAVY-CHAIN LOCUS; CCCTC-BINDING FACTOR; INTRONIC ENHANCER; IMMUNOGLOBULIN LOCI; SEQUENCING REVEALS; CLASS SWITCH; 3D STRUCTURE; TRANSCRIPTION; RECOMBINATION; REGION;
D O I
10.1101/gad.263871.115
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Conformation of antigen receptor gene loci spatially juxtaposes rearranging gene segments in the appropriate cell lineage and developmental stage. We describe a three-step pathway that establishes the structure of the 2.8-Mb immunoglobulin heavy chain gene (IgH) locus in pro-B cells. Each step uses a different transcription factor and leads to increasing levels of structural organization. CTCF mediates one level of compaction that folds the locus into several 250- to 400-kb subdomains, and Pax5 further compacts the 2-Mb region that encodes variable (V-H) gene segments. The 5' and 3' domains are brought together by the transcription factor YY1 to establish the configuration within which gene recombination initiates. Such stepwise mechanisms may apply more generally to establish regulatory fine structure within megabase-sized topologically associated domains.
引用
收藏
页码:1683 / 1695
页数:13
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