4.6 Article

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

Journal

JOURNAL OF IMMUNOLOGY
Volume 182, Issue 1, Pages 44-48

Publisher

AMER ASSOC IMMUNOLOGISTS
DOI: 10.4049/jimmunol.182.1.44

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Funding

  1. National Institutes of Health [R01 A129672, R01 A152313]
  2. National Institutes of Health Training Grant [T32 HL07195]
  3. NATIONAL HEART, LUNG, AND BLOOD INSTITUTE [T32HL007195] Funding Source: NIH RePORTER
  4. NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES [R01AI029672, R01AI052313] Funding Source: NIH RePORTER

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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.

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