CTCF-binding elements mediate control of V(D)J recombination

被引:207
作者
Guo, Chunguang [1 ,2 ]
Yoon, Hye Suk [1 ,2 ]
Franklin, Andrew [1 ,2 ]
Jain, Suvi [1 ,2 ]
Ebert, Anja [3 ]
Cheng, Hwei-Ling [1 ,2 ]
Hansen, Erica [1 ,2 ]
Despo, Orion [1 ,2 ]
Bossen, Claudia [4 ]
Vettermann, Christian [5 ]
Bates, Jamie G. [5 ]
Richards, Nicholas [1 ,2 ]
Myers, Darienne [1 ,2 ]
Patel, Harin [1 ,2 ]
Gallagher, Michael [1 ,2 ]
Schlissel, Mark S. [5 ]
Murre, Cornelis [4 ]
Busslinger, Meinrad [3 ]
Giallourakis, Cosmas C. [1 ,2 ,6 ]
Alt, Frederick W. [1 ,2 ]
机构
[1] Childrens Hosp, Howard Hughes Med Inst, Immune Dis Inst, Boston, MA 02115 USA
[2] Harvard Univ, Sch Med, Dept Genet, Boston, MA 02115 USA
[3] Res Inst Mol Pathol, A-1030 Vienna, Austria
[4] Univ Calif San Diego, Div Biol Sci, La Jolla, CA 92093 USA
[5] Univ Calif Berkeley, Dept Mol & Cell Biol, Berkeley, CA 94720 USA
[6] Massachusetts Gen Hosp, Gastrointestinal Unit, Boston, MA 02114 USA
关键词
B-CELL DEVELOPMENT; HEAVY-CHAIN LOCUS; VH GENE SEGMENTS; IGH LOCUS; REGULATORY ELEMENTS; INTRONIC ENHANCER; ANTISENSE TRANSCRIPTION; LYMPHOCYTE DEVELOPMENT; NUCLEAR-ORGANIZATION; REGION;
D O I
10.1038/nature10495
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
Immunoglobulin heavy chain (IgH) variable region exons are assembled from V-H, D and J(H) gene segments in developing B lymphocytes. Within the 2.7-megabase mouse Igh locus, V(D)J recombination is regulated to ensure specific and diverse antibody repertoires. Here we report in mice a key Igh V(D)J recombination regulatory region, termed intergenic control region 1 (IGCR1), which lies between the V-H and D clusters. Functionally, IGCR1 uses CTCF looping/insulator factor-binding elements and, correspondingly, mediates Igh loops containing distant enhancers. IGCR1 promotes normal B-cell development and balances antibody repertoires by inhibiting transcription and rearrangement of D-H-proximal V-H gene segments and promoting rearrangement of distal V-H segments. IGCR1 maintains ordered and lineage-specific V-H(D)J(H) recombination by suppressing V-H joining to D segments not joined to J(H) segments, and V-H to DJ(H) joins in thymocytes, respectively. IGCR1 is also required for feedback regulation and allelic exclusion of proximal V-H-to-DJ(H) recombination. Our studies elucidate a long-sought Igh V(D) J recombination control region and indicate a new role for the generally expressed CTCF protein.
引用
收藏
页码:424 / U182
页数:8
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