Tsai Chia-Lun, Schatz David G
Department of Molecular Biophysics and Biochemistry, Howard Hughes Medical Institute, Yale University School of Medicine, New Haven, CT 06510, USA.
EMBO J. 2003 Apr 15;22(8):1922-30. doi: 10.1093/emboj/cdg185.
The RAG1 and RAG2 proteins perform critical DNA recognition and cleavage functions in V(D)J recombination, and also catalyze efficient DNA transposition in vitro. No transposition in vivo by the RAG proteins has been reported, suggesting regulation of the reaction by as yet unknown mechanisms. Here we report that RAG-mediated transposition is suppressed by physiological concentrations of the guanine nucleotide GTP, and by the full-length RAG2 protein. Both GTP and full-length RAG2 inhibit transposition by blocking the non-covalent 'capture' of target DNA, and both are capable of inhibiting RAG-mediated hybrid joint formation in vitro. We also observe that another intracellular signaling molecule, Ca(2+), stimulates RAG-mediated transposition and is capable of activating transposition even in reactions containing full-length RAG2 and GTP. RAG-mediated transposition has been proposed to contribute to the chromosomal translocations that underlie the development of lymphoid malignancies, and our findings highlight regulatory mechanisms that might prevent such occurrences, and circumstances in which these regulatory mechanisms could be overcome.
RAG1和RAG2蛋白在V(D)J重组中执行关键的DNA识别和切割功能,并且在体外也能催化高效的DNA转座。尚未有关于RAG蛋白在体内发生转座的报道,这表明该反应受到未知机制的调控。在此,我们报告鸟嘌呤核苷酸GTP的生理浓度以及全长RAG2蛋白可抑制RAG介导的转座。GTP和全长RAG2均通过阻断靶DNA的非共价“捕获”来抑制转座,并且二者都能够在体外抑制RAG介导的杂交接头形成。我们还观察到另一种细胞内信号分子Ca(2+)可刺激RAG介导的转座,甚至在含有全长RAG2和GTP的反应中也能够激活转座。RAG介导的转座被认为与淋巴恶性肿瘤发生所依赖的染色体易位有关,我们的研究结果突出了可能阻止此类事件发生的调控机制,以及这些调控机制可能被克服的情况。