Chromosomal Loop Domains Direct the Recombination of Antigen Receptor Genes
Author(s) -
Jiazhi Hu,
Yu Zhang,
Lijuan Zhao,
Richard L. Frock,
Zhou Du,
Robin M. Meyers,
FeiLong Meng,
David G. Schatz,
Frederick W. Alt
Publication year - 2015
Publication title -
cell
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 26.304
H-Index - 776
eISSN - 1097-4172
pISSN - 0092-8674
DOI - 10.1016/j.cell.2015.10.016
Subject(s) - biology , recombination signal sequences , chromatin , v(d)j recombination , genetics , ctcf , recombination , pax5 , enhancer , gene , dna , locus (genetics) , microbiology and biotechnology , transcription factor , recombination activating gene
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.
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