Institut de Pharmacologie et de Biologie Structurale, Université de Toulouse, CNRS, Université Paul Sabatier (UPS), 31077 Toulouse, France.
CNRS UMR 7276, 87025 Limoges, France.
Proc Natl Acad Sci U S A. 2017 Jun 6;114(23):6092-6097. doi: 10.1073/pnas.1701631114. Epub 2017 May 22.
Class switch recombination (CSR) plays an important role in adaptive immune response by enabling mature B cells to switch from IgM expression to the expression of downstream isotypes. CSR is preceded by inducible germline (GL) transcription of the constant genes and is controlled by the 3' regulatory region (3'RR) in a stimulus-dependent manner. Why the 3'RR-mediated up-regulation of GL transcription is delayed to the mature B-cell stage is presently unknown. Here we show that mice devoid of an inducible CTCF binding element, located in the constant gene, display a marked isotype-specific increase of GL transcription in developing and resting splenic B cells and altered CSR in activated B cells. Moreover, insertion of a GL promoter downstream of the CTCF insulator led to premature activation of the ectopic promoter. This study provides functional evidence that the 3'RR has a developmentally controlled potential to constitutively activate GL promoters but that this activity is delayed, at least in part, by the CTCF insulator, which borders a transcriptionally active domain established by the 3'RR in developing B cells.
类别转换重组(CSR)在适应性免疫反应中起着重要作用,使成熟 B 细胞能够从 IgM 表达转换为下游同种型的表达。CSR 以前是可诱导的种系(GL)恒定基因的转录,并以刺激依赖性的方式受 3'调控区(3'RR)的控制。目前尚不清楚为什么 3'RR 介导的 GL 转录的上调会延迟到成熟 B 细胞阶段。在这里,我们发现缺乏位于恒定基因中的可诱导 CTCF 结合元件的小鼠在发育中和静止的脾 B 细胞中表现出明显的同种型特异性 GL 转录增加,并改变了活化 B 细胞中的 CSR。此外,将 GL 启动子插入 CTCF 绝缘子的下游会导致异位启动子的过早激活。这项研究提供了功能证据,表明 3'RR 具有在发育上控制 GL 启动子的潜在能力,但这种活性至少部分被 CTCF 绝缘子延迟,该绝缘子位于 3'RR 在发育中的 B 细胞中建立的转录活性区域的边界处。