An Igh distal enhancer modulates antigen receptor diversity by determining locus conformation

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作者
Khalid H. Bhat
Saurabh Priyadarshi
Sarah Naiyer
Xinyan Qu
Hammad Farooq
Eden Kleiman
Jeffery Xu
Xue Lei
Jose F. Cantillo
Robert Wuerffel
Nicole Baumgarth
Jie Liang
Ann J. Feeney
Amy L. Kenter
机构
[1] University of Illinois College of Medicine,Department of Microbiology and Immunology
[2] University of Illinois Colleges of Engineering and Medicine,Department of Bioengineering
[3] Scripps Research,Department of Immunology and Microbiology, IMM
[4] Johns Hopkins University,22
[5] Faculty of Agriculture,W. Harry Feinstone Dept. Molecular Microbiology and Immunology, Bloomberg School of Public Health
[6] Medpace,SKUAST Kashmir, Division of Basic Science and Humanities
[7] Crown Bioscience,undefined
[8] Brookwood Baptist Health General Surgery Residency,undefined
[9] Sanford Burnham Prebys Medical Discovery Institute,undefined
[10] Immunotek,undefined
[11] 10441 Circle Dr. Apt 47C,undefined
来源
Nature Communications | / 14卷
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摘要
The mouse Igh locus is organized into a developmentally regulated topologically associated domain (TAD) that is divided into subTADs. Here we identify a series of distal VH enhancers (EVHs) that collaborate to configure the locus. EVHs engage in a network of long-range interactions that interconnect the subTADs and the recombination center at the DHJH gene cluster. Deletion of EVH1 reduces V gene rearrangement in its vicinity and alters discrete chromatin loops and higher order locus conformation. Reduction in the rearrangement of the VH11 gene used in anti-PtC responses is a likely cause of the observed reduced splenic B1 B cell compartment. EVH1 appears to block long-range loop extrusion that in turn contributes to locus contraction and determines the proximity of distant VH genes to the recombination center. EVH1 is a critical architectural and regulatory element that coordinates chromatin conformational states that favor V(D)J rearrangement.
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