Bonnet Marie, Ferrier Pierre, Spicuglia Salvatore
Centre d'Immunologie de Marseille-Luminy, Université d'Aix Marseille, CNRS, UMR 6102, Inserm, U 631, Marseille, France.
Adv Exp Med Biol. 2009;650:116-32. doi: 10.1007/978-1-4419-0296-2_10.
The V(D)J recombination machinery assembles antigen receptor genes from germline V, D and J segments duringlymphocyte development. In alphabetaT cells, this leads to the production of the T-cell receptor (TCR) alpha and beta chains. Notably, V(D)J recombination at the Tcrb locus is tightly controlled at various levels, including cell-type and stage specificities, intralocus ordering and allelic exclusion. Although many of these controls are partly mediated at the level of genomic accessibility to the V(D)J recombinase, recent studies have uncovered novel mechanisms that are also likely to contribute to the developmental regulation of Tcrb gene rearrangement events. In this chapter, we summarize our current knowledge and highlight unanswered questions regarding the regulation of V(D)J recombination at the Tcrb locus, placing emphasis on mouse transgenesis and gene-targeting approaches.
V(D)J重组机制在淋巴细胞发育过程中,从种系V、D和J基因片段组装抗原受体基因。在αβT细胞中,这导致T细胞受体(TCR)α链和β链的产生。值得注意的是,Tcrb基因座处的V(D)J重组在多个水平上受到严格控制,包括细胞类型和阶段特异性、基因座内排序和等位基因排斥。尽管其中许多控制部分是在V(D)J重组酶的基因组可及性水平上介导的,但最近的研究发现了一些新机制,这些机制也可能有助于Tcrb基因重排事件的发育调控。在本章中,我们总结了我们目前的知识,并强调了关于Tcrb基因座处V(D)J重组调控的未解决问题,重点是小鼠转基因和基因靶向方法。