Tsai Chia-Lun, Chatterji Monalisa, Schatz David G
Department of Molecular Biophysics and Biochemistry, Section of Immunobiology, Howard Hughes Medical Institute, Yale University School of Medicine, New Haven, CT 06510, USA.
Nucleic Acids Res. 2003 Nov 1;31(21):6180-90. doi: 10.1093/nar/gkg819.
In addition to their essential role in V(D)J recombination, the RAG proteins function as a transposase capable of inserting the V(D)J recombination intermediate, the signal end DNA fragment, into target DNA. RAG-mediated transposition has been suggested to contribute to genome instability and the development of lymphoid malignancies. Previous studies suggested that the RAG transposase exhibits a target site preference for GC rich sequences and hairpin structures. Here we demonstrate that a transposition hot spot (5'-GCCGCCGGGCC-3'), smaller portions of this hot spot and other GC rich motifs are able to target RAG-mediated transposition. Tracks of GC base pairs have been shown to have an unusually high rate of base pair breathing. Intriguingly, we find that DNA mismatches can efficiently target RAG-mediated transposition and suppress the use of other target sites. Hairpins, however, are not generally preferred targets. Our results indicate that target DNA melting may be a crucial step during RAG-mediated transposition, and that target site selection by the RAG transposase may be intimately linked to mutagenic and metabolic processes that transiently present favorable DNA structures to the transposition machinery.
除了在V(D)J重组中发挥重要作用外,RAG蛋白还作为一种转座酶发挥功能,能够将V(D)J重组中间体(信号末端DNA片段)插入到目标DNA中。RAG介导的转座作用被认为与基因组不稳定以及淋巴恶性肿瘤的发生发展有关。先前的研究表明,RAG转座酶对富含GC的序列和发夹结构表现出靶位点偏好。在此我们证明,一个转座热点(5'-GCCGCCGGGCC-3')、该热点的较小部分以及其他富含GC的基序能够靶向RAG介导的转座作用。已显示GC碱基对的序列具有异常高的碱基对呼吸频率。有趣的是,我们发现DNA错配能够有效地靶向RAG介导的转座作用,并抑制其他靶位点的使用。然而,发夹结构通常不是优先选择的靶标。我们的结果表明,靶DNA解链可能是RAG介导的转座过程中的关键步骤,并且RAG转座酶的靶位点选择可能与诱变和代谢过程密切相关,这些过程会短暂地向转座机制呈现有利的DNA结构。