Reversible contraction by looping of the Tcra and Tcrb loci in rearranging thymocytes

被引:119
作者
Skok, Jane A.
Gisler, Ramiro
Novatchkova, Maria
Farmer, Deborah
de Laat, Wouter
Busslinger, Meinrad
机构
[1] Res Inst Mol Pathol, Vienna Bioctr, A-1030 Vienna, Austria
[2] UCL, Dept Immunol & Mol Pathol, Div Infect & Immun, London W1T 4JF, England
[3] Erasmus MC, Dept Cell Biol & Genet, NL-3000 CA Rotterdam, Netherlands
基金
英国惠康基金;
关键词
D O I
10.1038/ni1448
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Reversible contraction of immunoglobulin loci juxtaposes the variable ( V) genes next to the ( diversity)-joining-constant (( D) JC) gene domain, thus facilitating V-( D)J recombination. Here we show that the T cell receptor beta ( Tcrb) and T cell receptor alpha delta ( Tcra-Tcrd) loci also underwent long-range interactions by looping in double-negative and double-positive thymocytes, respectively. Contraction of the Tcrb and Tcra loci occurred in rearranging thymocytes and was reversed at the next developmental stage. Decontraction of the Tcrb locus probably prevented further V-beta-DJ(beta) rearrangements in double- positive thymocytes by separating the V-beta genes from the DJC(beta) domain. In most double-negative cells, one Tcrb allele was recruited to pericentromeric heterochromatin. Such allelic positioning may facilitate asynchronous V-beta-DJ(beta) recombination. Hence, pericentromeric recruitment and locus 'decontraction' seem to contribute to the initiation and maintenance of allelic exclusion at the Tcrb locus.
引用
收藏
页码:378 / 387
页数:10
相关论文
共 60 条
[1]   The mechanism and regulation of chromosomal V(D)J recombination [J].
Bassing, CH ;
Swat, W ;
Alt, FW .
CELL, 2002, 109 :S45-S55
[2]   Critical functions for c-Myb at three checkpoints during thymocyte development [J].
Bender, TP ;
Kremer, CS ;
Kraus, M ;
Buch, T ;
Rajewsky, K .
NATURE IMMUNOLOGY, 2004, 5 (07) :721-729
[3]   Antisense intergenic transcription in V(D)J recombination [J].
Bolland, DJ ;
Wood, AL ;
Johnston, CM ;
Bunting, SF ;
Morgan, G ;
Chakalova, L ;
Fraser, PJ ;
Corcoran, AE .
NATURE IMMUNOLOGY, 2004, 5 (06) :630-637
[4]   Gene-targeted deletion and replacement mutations of the T-cell receptor beta-chain enhancer: The role of enhancer elements in controlling V(D)J recombination accessibility [J].
Bories, JC ;
Demengeot, J ;
Davidson, L ;
Alt, FW .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (15) :7871-7876
[5]   The mouse (Mus musculus) T cell receptor beta variable (TRBV), diversity (TRBD) and joining (TRBJ) genes [J].
Bosc, N ;
Lefranc, MP .
EXPERIMENTAL AND CLINICAL IMMUNOGENETICS, 2000, 17 (04) :216-228
[6]   The mouse (Mus musculus) T cell receptor alpha (TRA) and delta (TRD) variable genes [J].
Bosc, N ;
Lefranc, MP .
DEVELOPMENTAL AND COMPARATIVE IMMUNOLOGY, 2003, 27 (6-7) :465-497
[7]   Transient IL-7/IL-7R signaling provides a mechanism for feedback inhibition of immunoglobulin heavy chain gene rearrangements [J].
Chowdhury, D ;
Sen, R .
IMMUNITY, 2003, 18 (02) :229-241
[8]   Stepwise activation of the immunoglobulin μ heavy chain gene locus [J].
Chowdhury, D ;
Sen, R .
EMBO JOURNAL, 2001, 20 (22) :6394-6403
[9]   Capturing chromosome conformation [J].
Dekker, J ;
Rippe, K ;
Dekker, M ;
Kleckner, N .
SCIENCE, 2002, 295 (5558) :1306-1311
[10]   Chromatin compaction by a polycomb group protein complex [J].
Francis, NJ ;
Kingston, RE ;
Woodcock, CL .
SCIENCE, 2004, 306 (5701) :1574-1577