Chromosomal Loop Domains Direct the Recombination of Antigen Receptor Genes

被引:123
作者
Hu, Jiazhi [1 ,2 ,3 ]
Zhang, Yu [1 ,2 ,3 ]
Zhao, Lijuan [1 ,2 ,3 ]
Frock, Richard L. [1 ,2 ,3 ]
Du, Zhou [1 ,2 ,3 ]
Meyers, Robin M. [1 ,2 ,3 ]
Meng, Fei-long [1 ,2 ,3 ]
Schatz, David G. [1 ,4 ]
Alt, Frederick W. [1 ,2 ,3 ]
机构
[1] Boston Childrens Hosp, Howard Hughes Med Inst, Boston, MA 02115 USA
[2] Boston Childrens Hosp, Program Cellular & Mol Med, Boston, MA 02115 USA
[3] Harvard Univ, Sch Med, Dept Genet, Boston, MA 02115 USA
[4] Yale Univ, Sch Med, Dept Immunobiol, New Haven, CT 06520 USA
关键词
ACUTE LYMPHOBLASTIC-LEUKEMIA; CELL IDENTITY GENES; V(D)J RECOMBINATION; TRANSCRIPTION FACTORS; DNA BREAKS; GENOME; CTCF; MECHANISMS; COMPLEXES; REVEALS;
D O I
10.1016/j.cell.2015.10.016
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
RAG initiates antibody V(D)J recombination in developing lymphocytes by generating "on-target'' DNA breaks at matched pairs of bona fide recombination signal sequences (RSSs). We employ bait RAG-generated breaks in endogenous or ectopically inserted RSS pairs to identify huge numbers of RAG "off-target'' breaks. Such breaks occur at the simple CAC motif that defines the RSS cleavage site and are largely confined within convergent CTCF-binding element (CBE)-flanked loop domains containing bait RSS pairs. Marked orientation dependence of RAG off-target activity within loops spanning up to 2 megabases implies involvement of linear tracking. In this regard, major RAG off-targets in chromosomal translocations occur as convergent RSS pairs at enhancers within a loop. Finally, deletion of a CBE-based IgH locus element disrupts V(D) J recombination domains and, correspondingly, alters RAG on-and off-target distributions within IgH. Our findings reveal how RAG activity is developmentally focused and implicate mechanisms by which chromatin domains harness biological processes within them.
引用
收藏
页码:947 / 959
页数:13
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