Department of Pulmonary Medicine, Erasmus MC Rotterdam, P.O. Box 2040, 3000 CA Rotterdam, The Netherlands.
Immunity. 2011 Oct 28;35(4):501-13. doi: 10.1016/j.immuni.2011.07.014.
Regulation of immunoglobulin (Ig) V(D)J gene rearrangement is dependent on higher-order chromatin organization. Here, we studied the in vivo function of the DNA-binding zinc-finger protein CTCF, which regulates interactions between enhancers and promoters. By conditional deletion of the Ctcf gene in the B cell lineage, we demonstrate that loss of CTCF allowed Ig heavy chain recombination, but pre-B cell proliferation and differentiation was severely impaired. In the absence of CTCF, the Igκ light chain locus showed increased proximal and reduced distal Vκ usage. This was associated with enhanced proximal Vκ and reduced Jκ germline transcription. Chromosome conformation capture experiments demonstrated that CTCF limits interactions of the Igκ enhancers with the proximal V(κ) gene region and prevents inappropriate interactions between these strong enhancers and elements outside the Igκ locus. Thus, although Ig gene recombination can occur in the absence of CTCF, it is a critical factor determining Vκ segment choice for recombination.
免疫球蛋白(Ig)V(D)J 基因重排的调节依赖于高级染色质组织。在这里,我们研究了 DNA 结合锌指蛋白 CTCF 的体内功能,该蛋白调节增强子和启动子之间的相互作用。通过条件性删除 B 细胞谱系中的 Ctcf 基因,我们证明 CTCF 的缺失允许 Ig 重链重组,但前 B 细胞增殖和分化受到严重损害。在没有 CTCF 的情况下,Igκ 轻链基因座显示出近端增加和远端 Vκ 使用减少。这与近端 Vκ 和减少 Jκ 生殖系转录增强有关。染色体构象捕获实验表明,CTCF 限制了 Igκ 增强子与近端 V(κ)基因区域的相互作用,并防止这些强增强子与 Igκ 基因座外的元件之间的不当相互作用。因此,尽管 Ig 基因重排可以在没有 CTCF 的情况下发生,但它是决定 Vκ 片段选择进行重排的关键因素。