Jung David, Bassing Craig H, Fugmann Sebastian D, Cheng Hwei-Ling, Schatz David G, Alt Frederick W
Howard Hughes Medical Institute, The Children's Hospital, Harvard Medical School, Boston, MA, USA.
Immunity. 2003 Jan;18(1):65-74. doi: 10.1016/s1074-7613(02)00507-1.
V(D)J recombination occurs efficiently only between gene segments flanked by recombination signals (RSs) containing 12 and 23 base pair spacers (the 12/23 rule). A further limitation "beyond the 12/23 rule" (B12/23) exists at the TCRbeta locus and ensures Dbeta usage. Herein, we show that extrachromosomal V(D)J recombination substrates recapitulate B12/23 restriction in nonlymphoid cells. We further demonstrate that the Vbeta coding flank, the 12-RS heptamer/nonamer, and the 23-RS spacer each can significantly influence B12/23 restriction. Finally, purified core RAG1 and RAG2 proteins (together with HMG2) also reproduce B12/23 restriction in a cell-free system. Our findings indicate that B12/23 restriction of V(D)J recombination is cemented at the level of interactions between the RAG proteins and TCRbeta RS sequences.
V(D)J重排仅在由含12和23个碱基对间隔序列的重组信号(RSs)侧翼的基因片段之间高效发生(12/23规则)。在TCRβ基因座存在“超越12/23规则”(B12/23)的进一步限制,并确保Dβ的使用。在此,我们表明染色体外V(D)J重排底物在非淋巴细胞中重现了B12/23限制。我们进一步证明Vβ编码侧翼、12-RS七聚体/九聚体和23-RS间隔序列各自均可显著影响B12/23限制。最后,纯化的核心RAG1和RAG2蛋白(连同HMG2)在无细胞系统中也重现了B12/23限制。我们的研究结果表明,V(D)J重排的B12/23限制在RAG蛋白与TCRβ RS序列之间相互作用的水平上得以确立。