Department of Immunobiology, Yale University School of Medicine, 300 Cedar Street, Box 208011, New Haven, CT 06520-8011, USA.
Cell. 2010 Apr 30;141(3):419-31. doi: 10.1016/j.cell.2010.03.010. Epub 2010 Apr 15.
The critical initial step in V(D)J recombination, binding of RAG1 and RAG2 to recombination signal sequences flanking antigen receptor V, D, and J gene segments, has not previously been characterized in vivo. Here, we demonstrate that RAG protein binding occurs in a highly focal manner to a small region of active chromatin encompassing Ig kappa and Tcr alpha J gene segments and Igh and Tcr beta J and J-proximal D gene segments. Formation of these small RAG-bound regions, which we refer to as recombination centers, occurs in a developmental stage- and lineage-specific manner. Each RAG protein is independently capable of specific binding within recombination centers. While RAG1 binding was detected only at regions containing recombination signal sequences, RAG2 binds at thousands of sites in the genome containing histone 3 trimethylated at lysine 4. We propose that recombination centers coordinate V(D)J recombination by providing discrete sites within which gene segments are captured for recombination.
V(D)J 重组的关键初始步骤是 RAG1 和 RAG2 与抗原受体 V、D 和 J 基因片段侧翼的重组信号序列结合,这在体内以前尚未得到描述。在这里,我们证明 RAG 蛋白以高度聚焦的方式结合到一个包含 Ig kappa 和 Tcr alpha J 基因片段以及 Igh 和 Tcr beta J 和 J 近端 D 基因片段的小活性染色质区域。这些我们称为重组中心的小 RAG 结合区域的形成以发育阶段和谱系特异性的方式发生。每个 RAG 蛋白都能够在重组中心内进行特异性结合。虽然仅在含有重组信号序列的区域检测到 RAG1 结合,但 RAG2 结合在基因组中数千个含有组蛋白 3 赖氨酸 4 三甲基化的位点上。我们提出重组中心通过提供离散的位点来协调 V(D)J 重组,在这些位点中捕获基因片段进行重组。