Cutting Edge: Developmental Stage-Specific Recruitment of Cohesin to CTCF Sites throughout Immunoglobulin Loci during B Lymphocyte Development

被引:127
作者
Degner, Stephanie C. [1 ]
Wong, Timothy P. [1 ]
Jankevicius, Gytis [1 ]
Feeney, Ann J. [1 ]
机构
[1] Scripps Res Inst, Dept Immunol & Microbial Sci, La Jolla, CA 92037 USA
基金
美国国家卫生研究院;
关键词
HEAVY-CHAIN LOCUS; HUMAN GENOME; CELL DEVELOPMENT; CHROMATIN; INSULATOR; GENE; IKAROS;
D O I
10.4049/jimmunol.182.1.44
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Contraction of the large Igh and Ig kappa loci brings all V genes, spanning > 2.5 Mb in each locus, in proximity to DJ(H) or J(kappa) genes. CCCTC-binding factor (CTCF) is a transcription factor that regulates gene expression by long-range chromosomal looping. We therefore hypothesized that CTCF may be crucial for the contraction of the Ig loci, but no CTCF sites have been described in any V loci. Using ChIP-chip, we demonstrated many CTCF sites in the V-H and V-kappa regions. However, CTCF enrichment in the Igh locus, but not the Ig kappa locus, was largely unchanged throughout differentiation, suggesting that CTCF binding alone cannot be responsible for stage-specific looping. Because cohesin can colocalize with CTCF, we performed chromatin immunoprecipitation for the cohesin subunit Rad21 and found lineage and stage-specific Rad21 recruitment to CTCF in all Ig loci. The differential binding of cohesin to CTCF sites may promote multiple loop formation and thus effective V(D)J recombination. The Journal of Immunology, 2009, 182: 44-48.
引用
收藏
页码:44 / 48
页数:5
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