| Literature DB >> 31875554 |
Kenta Shinoda1, Yaakov Maman2, Andres Canela3, David G Schatz4, Ferenc Livak5, André Nussenzweig6.
Abstract
During V(D)J recombination, RAG proteins introduce DNA double-strand breaks (DSBs) at recombination signal sequences (RSSs) that contain either 12- or 23-nt spacer regions. Coordinated 12/23 cleavage predicts that DSBs at variable (V) gene segments should equal the level of breakage at joining (J) segments. Contrary to this, here we report abundant RAG-dependent DSBs at multiple Vκ gene segments independent of V-J rearrangement. We find that a large fraction of Vκ gene segments are flanked not only by a bone-fide 12 spacer but also an overlapping, 23-spacer flipped RSS. These compatible pairs of RSSs mediate recombination and deletion inside the Vκ cluster even in the complete absence of Jκ gene segments and support a V(D)J recombination center (RC) independent of the conventional Jκ-centered RC. We propose an improved model of Vκ-Jκ repertoire formation by incorporating these surprisingly frequent, evolutionarily conserved intra-Vκ cluster recombination events.Entities:
Keywords: END-seq; HTGTS; RAG; VDJ recombination; ig kappa locus; ig repertoire; immunoglobulin; recombination center; recombination signal sequence; variable
Mesh:
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Year: 2019 PMID: 31875554 PMCID: PMC8214342 DOI: 10.1016/j.celrep.2019.11.088
Source DB: PubMed Journal: Cell Rep Impact factor: 9.423