Giblin William, Chatterji Monalisa, Westfield Gerwin, Masud Tehmina, Theisen Brian, Cheng Hwei-Ling, DeVido Jeffrey, Alt Frederick W, Ferguson David O, Schatz David G, Sekiguchi JoAnn
Department of Internal Medicine, University of Michigan, Ann Arbor, MI 48109, USA
Blood. 2009 Mar 26;113(13):2965-75. doi: 10.1182/blood-2008-07-165167. Epub 2009 Jan 6.
The RAG1/2 endonuclease initiates programmed DNA rearrangements in progenitor lymphocytes by generating double-strand breaks at specific recombination signal sequences. This process, known as V(D)J recombination, assembles the vastly diverse antigen receptor genes from numerous V, D, and J coding segments. In vitro biochemical and cellular transfection studies suggest that RAG1/2 may also play postcleavage roles by forming complexes with the recombining ends to facilitate DNA end processing and ligation. In the current study, we examine the in vivo consequences of a mutant form of RAG1, RAG1-S723C, that is proficient for DNA cleavage, yet exhibits defects in postcleavage complex formation and end joining in vitro. We generated a knockin mouse model harboring the RAG1-S723C hypomorphic mutation and examined the immune system in this fully in vivo setting. RAG1-S723C homozygous mice exhibit impaired lymphocyte development and decreased V(D)J rearrangements. Distinct from RAG nullizygosity, the RAG1-S723C hypomorph results in aberrant DNA double-strand breaks within rearranging loci. RAG1-S723C also predisposes to thymic lymphomas associated with chromosomal translocations in a p53 mutant background, and heterozygosity for the mutant allele accelerates age-associated immune system dysfunction. Thus, our study provides in vivo evidence that implicates aberrant RAG1/2 activity in lymphoid tumor development and premature immunosenescence.
RAG1/2核酸内切酶通过在特定重组信号序列处产生双链断裂,启动祖细胞淋巴细胞中的程序性DNA重排。这一过程称为V(D)J重组,它从众多V、D和J编码片段组装出极为多样的抗原受体基因。体外生化和细胞转染研究表明,RAG1/2也可能通过与重排末端形成复合物来发挥切割后作用,以促进DNA末端加工和连接。在本研究中,我们研究了一种RAG1突变形式RAG1-S723C在体内的影响,该突变体具有DNA切割能力,但在体外切割后复合物形成和末端连接方面存在缺陷。我们构建了一个携带RAG1-S723C低表达突变的基因敲入小鼠模型,并在这个完全体内环境中研究了免疫系统。RAG1-S723C纯合小鼠表现出淋巴细胞发育受损和V(D)J重排减少。与RAG基因完全缺失不同,RAG1-S723C低表达导致重排基因座内出现异常DNA双链断裂。在p53突变背景下,RAG1-S723C还易引发与染色体易位相关的胸腺淋巴瘤,突变等位基因的杂合性加速了与年龄相关的免疫系统功能障碍。因此,我们的研究提供了体内证据,表明RAG1/2异常活性与淋巴瘤发展和过早免疫衰老有关。