Hiramatsu R, Akagi K, Matsuoka M, Sakumi K, Nakamura H, Kingsbury L, David C, Hardy R R, Yamamura K, Sakano H
Department of Molecular and Cell Biology, University of California, Berkeley 94720-3200, USA.
Cell. 1995 Dec 29;83(7):1113-23. doi: 10.1016/0092-8674(95)90138-8.
Using transgenic substrates, we found that the immunoglobulin kappa gene 3' enhancer (E3') acts as a negative regulator in V kappa-J kappa joining. Although the E3' was originally identified as a transcriptional enhancer, it acts in a suppressive manner for recombinational regulation. Base substitution analysis has shown that the PU.1-binding site within the E3' regulates the B/T specificity of V kappa-J kappa joining. In a substrate with a mutated PU.1-binding site (GAGGAA to TCTTCG), V kappa-J kappa joining occurred not only in B cells, but also in T cells. The E3' region is also responsible for determining the pro-B/pre-B specificity of V kappa-J kappa joining. When the E3' region was deleted, kappa gene rearrangement actively occurred at the early pro-B stage of B cell development: nongermline (N) nucleotides were common at recombination junctions.
利用转基因底物,我们发现免疫球蛋白κ基因3'增强子(E3')在Vκ-Jκ连接中起负调控作用。尽管E3'最初被鉴定为转录增强子,但它在重组调控中以抑制方式起作用。碱基替换分析表明,E3'内的PU.1结合位点调节Vκ-Jκ连接的B/T特异性。在具有突变的PU.1结合位点(GAGGAA变为TCTTCG)的底物中,Vκ-Jκ连接不仅发生在B细胞中,也发生在T细胞中。E3'区域还负责决定Vκ-Jκ连接的前B细胞/前B细胞特异性。当E3'区域被删除时,κ基因重排在B细胞发育的早期前B细胞阶段活跃发生:重组连接处常见非种系(N)核苷酸。