A role for cohesin in T-cell-receptor rearrangement and thymocyte differentiation

被引:192
作者
Seitan, Vlad C. [1 ,2 ,3 ]
Hao, Bingtao [4 ]
Tachibana-Konwalski, Kikue [5 ]
Lavagnolli, Thais [1 ,3 ]
Mira-Bontenbal, Hegias [1 ,3 ]
Brown, Karen E. [1 ,3 ]
Teng, Grace [6 ]
Carroll, Tom [3 ]
Terry, Anna [1 ,3 ]
Horan, Katie [7 ]
Marks, Hendrik [8 ]
Adams, David J. [9 ]
Schatz, David G. [6 ,10 ]
Aragon, Luis [2 ,3 ]
Fisher, Amanda G. [1 ,3 ]
Krangel, Michael S. [4 ]
Nasmyth, Kim [5 ]
Merkenschlager, Matthias [1 ,3 ]
机构
[1] Univ London Imperial Coll Sci Technol & Med, MRC, Clin Sci Ctr, Lymphocyte Dev Grp, London W12 0NN, England
[2] Univ London Imperial Coll Sci Technol & Med, MRC, Clin Sci Ctr, Cell Cycle Grp, London W12 0NN, England
[3] Univ London Imperial Coll Sci Technol & Med, MRC, Clin Sci Ctr, Epigenet Sect, London W12 0NN, England
[4] Duke Univ, Med Ctr, Dept Immunol, Durham, NC 27710 USA
[5] Univ Oxford, Dept Biochem, Oxford OX1 3QU, England
[6] Yale Univ, Sch Med, Dept Immunobiol, New Haven, CT 06520 USA
[7] Univ London Imperial Coll Sci Technol & Med, Cent Biol Serv, London W12 0NN, England
[8] Nijmegen Ctr Mol Life Sci, Dept Mol Biol, NL-6500 HB Nijmegen, Netherlands
[9] Wellcome Trust Genome Campus, Wellcome Trust Sanger Inst, Cambridge CB10 1SA, England
[10] Yale Univ, Sch Med, Howard Hughes Med Inst, New Haven, CT 06520 USA
基金
美国国家卫生研究院; 英国医学研究理事会; 英国惠康基金;
关键词
ANTIGEN-RECEPTOR; CHROMATIN ARCHITECTURE; V(D)J RECOMBINATION; POSITIVE SELECTION; TRANSGENIC MICE; DAD1; GENES; TCR-ALPHA; ACCESSIBILITY; REGION; LOCUS;
D O I
10.1038/nature10312
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Cohesin enables post-replicative DNA repair and chromosome segregation by holding sister chromatids together from the time of DNA replication in S phase until mitosis(1). There is growing evidence that cohesin also forms long-range chromosomal cis-interactions(2-4) and may regulate gene expression(2-10) in association with CTCF8,9, mediator(4) or tissue-specific transcription factors(10). Human cohesinopathies such as Cornelia de Lange syndrome are thought to result from impaired non-canonical cohesin functions(7), but a clear distinction between the cell-division-related and cell-division-independent functions of cohesion-as exemplified in Drosophila(11-13)-has not been demonstrated in vertebrate systems. To address this, here we deleted the cohesin locus Rad21 in mouse thymocytes at a time in development when these cells stop cycling and rearrange their T-cell receptor (TCR) a locus (Tcra). Rad21-deficient thymocytes had a normal lifespan and retained the ability to differentiate, albeit with reduced efficiency. Loss of Rad21 led to defective chromatin architecture at the Tcra locus, where cohesion-binding sites flank the TEA promoter and the Ea enhancer, and demarcate Tcra from interspersed Tcrd elements and neighbouring housekeeping genes. Cohesin was required for long-range promoter-enhancer interactions, Tcra transcription, H3K4me3 histone modifications that recruit the recombination machinery(14,15) and Tcra rearrangement. Provision of pre-rearranged TCR transgenes largely rescued thymocyte differentiation, demonstrating that among thousands of potential target genes across the genome(4,8-10), defective Tcra rearrangement was limiting for the differentiation of cohesin-deficient thymocytes. These findings firmly establish a cell-division-independent role for cohesin in Tcra locus rearrangement and provide a comprehensive account of the mechanisms by which cohesin enables cellular differentiation in a well-characterized mammalian system.
引用
收藏
页码:467 / U126
页数:7
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