Department of Immunology and Genomic Medicine, Graduate School of Medicine, Kyoto University, Yoshida Sakyo-ku, Kyoto 606-8501, Japan.
Proc Natl Acad Sci U S A. 2009 Dec 29;106(52):22375-80. doi: 10.1073/pnas.0911879106. Epub 2009 Dec 11.
To initiate class switch recombination (CSR) activation-induced cytidine deaminase (AID) induces staggered nick cleavage in the S region, which lies 5' to each Ig constant region gene and is rich in palindromic sequences. Topoisomerase 1 (Top1) controls the supercoiling of DNA by nicking, rotating, and religating one strand of DNA. Curiously, Top1 reduction or AID overexpression causes the genomic instability. Here, we report that the inactivation of Top1 by its specific inhibitor camptothecin drastically blocked both the S region cleavage and CSR, indicating that Top1 is responsible for the S region cleavage in CSR. Surprisingly, AID expression suppressed Top1 mRNA translation and reduced its protein level. In addition, the decrease in the Top1 protein by RNA-mediated knockdown augmented the AID-dependent S region cleavage, as well as CSR. Furthermore, Top1 reduction altered DNA structure of the Smu region. Taken together, AID-induced Top1 reduction alters S region DNA structure probably to non-B form, on which Top1 can introduce nicks but cannot religate, resulting in S region cleavage.
为了启动类别转换重组 (CSR),激活诱导的胞嘧啶脱氨酶 (AID) 在 S 区诱导交错的切口断裂,S 区位于每个 Ig 恒定区基因的 5'端,富含回文序列。拓扑异构酶 1 (Top1) 通过切口、旋转和重新连接一条 DNA 链来控制 DNA 的超螺旋。奇怪的是,Top1 的减少或 AID 的过表达导致基因组不稳定。在这里,我们报告说,其特异性抑制剂喜树碱使 Top1 失活,可大大阻断 S 区的切割和 CSR,表明 Top1 负责 CSR 中的 S 区切割。令人惊讶的是,AID 的表达抑制了 Top1 mRNA 的翻译并降低了其蛋白水平。此外,通过 RNA 介导的敲低减少 Top1 蛋白会增加 AID 依赖性 S 区切割和 CSR。此外,Top1 的减少改变了 Smu 区域的 DNA 结构。总之,AID 诱导的 Top1 减少改变了 S 区 DNA 结构,可能是非 B 形式,Top1 可以在其上引入切口但不能重新连接,导致 S 区切割。