CTCF-binding elements mediate accessibility of RAG substrates during chromatin scanning

• Suvi Jain ^[1] ; Zhaoqing Ba ^[1] ; Yu Zhang ^[1]
  1. [1] Howard Hughes Medical Institute

     Howard Hughes Medical Institute

     Estados Unidos

     
• Localización: Cell, ISSN 0092-8674, Vol. 174, Nº. 1, 2018, págs. 102-116
• Idioma: inglés
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• Resumen

  • RAG endonuclease initiates antibody heavy chain variable region exon assembly from V, D, and J segments within a chromosomal V(D)J recombination center (RC) by cleaving between paired gene segments and flanking recombination signal sequences (RSSs). The IGCR1 control region promotes DJ H intermediate formation by isolating Ds, J Hs, and RCs from upstream V Hs in a chromatin loop anchored by CTCF-binding elements (CBEs). How V Hs access the DJ HRC for V H to DJ H rearrangement was unknown. We report that CBEs immediately downstream of frequently rearranged V H-RSSs increase recombination potential of their associated V H far beyond that provided by RSSs alone. This CBE activity becomes particularly striking upon IGCR1 inactivation, which allows RAG, likely via loop extrusion, to linearly scan chromatin far upstream. V H-associated CBEs stabilize interactions of D-proximal V Hs first encountered by the DJ HRC during linear RAG scanning and thereby promote dominant rearrangement of these V Hs by an unanticipated chromatin accessibility-enhancing CBE function.