Division of Cancer Pathobiology, Department of Pathology and Laboratory Medicine, Center for Childhood Cancer Research, Children's Hospital of Philadelphia, Abramson Family Cancer Research Institute, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, PA 19104.
J Immunol. 2014 Feb 15;192(4):1609-19. doi: 10.4049/jimmunol.1301599. Epub 2014 Jan 10.
The RAG proteins are comprised of core endonuclease domains and noncore regions that modulate endonuclease activity. Mutation or deletion of noncore RAG regions in humans causes immunodeficiency and altered TCR repertoire, and mice expressing core but not full-length Rag1 (Rag1(C/C)) or Rag2 (Rag2(C/C)) exhibit lymphopenia, reflecting impaired V(D)J recombination and lymphocyte development. Rag1(C/C) mice display reduced D-to-J and V-to-DJ rearrangements of TCRβ and IgH loci, whereas Rag2(C/C) mice show decreased V-to-DJ rearrangements and altered Vβ/VH repertoire. Because Vβs/VHs only recombine to DJ complexes, the Rag1(C/C) phenotype could reflect roles for noncore RAG1 regions in promoting recombination during only the D-to-J step or during both steps. In this study, we demonstrate that a preassembled TCRβ gene, but not a preassembled DβJβ complex or the prosurvival BCL2 protein, completely rescues αβ T cell development in Rag1(C/C) mice. We find that Rag1(C/C) mice exhibit altered Vβ utilization in Vβ-to-DJβ rearrangements, increased usage of 3'Jα gene segments in Vα-to-Jα rearrangements, and abnormal changes in Vβ repertoire during αβ TCR selection. Inefficient Vβ/VH recombination signal sequences (RSSs) have been hypothesized to cause impaired V-to-DJ recombination on the background of a defective recombinase as in core-Rag mice. We show that replacement of the Vβ14 RSS with a more efficient RSS increases Vβ14 recombination and rescues αβ T cell development in Rag1(C/C) mice. Our data indicate that noncore RAG1 regions establish a diverse TCR repertoire by overcoming Vβ RSS inefficiency to promote Vβ recombination and αβ T cell development, and by modulating TCRβ and TCRα gene segment utilization.
RAG 蛋白由核心内切酶结构域和非核心区域组成,这些区域调节内切酶活性。人类中非核心 RAG 区域的突变或缺失会导致免疫缺陷和 T 细胞受体(TCR)库改变,而表达核心但不表达全长 Rag1(Rag1(C/C))或 Rag2(Rag2(C/C))的小鼠则表现出淋巴细胞减少,反映了 V(D)J 重组和淋巴细胞发育受损。Rag1(C/C)小鼠显示 TCRβ和 IgH 基因座的 D 到 J 和 V 到 DJ 重排减少,而 Rag2(C/C)小鼠显示 V 到 DJ 重排减少和 Vβ/VH 库改变。由于 Vβs/VHs 仅与 DJ 复合物重组,因此 Rag1(C/C)表型可能反映了非核心 Rag1 区域在仅 D 到 J 步骤或两个步骤中促进重组的作用。在这项研究中,我们证明了一个预先组装的 TCRβ 基因,但不是预先组装的 DβJβ 复合物或生存的 BCL2 蛋白,完全挽救了 Rag1(C/C)小鼠中的αβ T 细胞发育。我们发现 Rag1(C/C)小鼠在 Vβ 到 DJβ 重排中表现出改变的 Vβ 利用,在 Vα 到 Jα 重排中增加了 3'Jα 基因片段的利用,以及在αβ TCR 选择过程中 Vβ 库的异常变化。在核心-Rag 小鼠等缺陷重组酶的背景下,假设低效的 Vβ/VH 重组信号序列(RSS)会导致 V 到 DJ 重组受损。我们表明,用更有效的 RSS 替换 Vβ14 RSS 会增加 Vβ14 重组并挽救 Rag1(C/C)小鼠中的αβ T 细胞发育。我们的数据表明,非核心 Rag1 区域通过克服 Vβ RSS 效率低下来促进 Vβ 重组和αβ T 细胞发育,并通过调节 TCRβ 和 TCRα 基因片段利用,建立了多样化的 TCR 库。