Willerford D M, Swat W, Alt F W
Howard Hughes Medical Institute, The Children's Hospital, Boston, Massachusetts 02115, USA.
Curr Opin Genet Dev. 1996 Oct;6(5):603-9. doi: 10.1016/s0959-437x(96)80090-6.
Recent insights into the mechanism of V(D)J recombination have clarified the direct role of the products of the recombination-activating genes Rag-1 and Rag-2 in site-specific DNA cleavage at recombination signal sequences and have identified components of the general DNA double-strand break repair pathway that participate in the rejoining of the Rag-1 and Rag-2-cut receptor gene segments. The V(D)J reaction is restricted to particular antigen receptor loci in a lineage-specific and stage-specific manner. This specificity appears to involve cis-regulatory elements, some of which also regulate transcription of the germline antigen receptor loci. Early developmental steps in the T and B lineages - including phenotypic differentiation, expansion of precursors, and selection processes - are effected in a stepwise fashion by signals generated, at least in part, by the products of the functionally rearranged antigen receptor genes themselves.
近期对V(D)J重组机制的深入了解,阐明了重组激活基因Rag-1和Rag-2的产物在重组信号序列处的位点特异性DNA切割中的直接作用,并确定了参与Rag-1和Rag-2切割的受体基因片段重新连接的一般DNA双链断裂修复途径的组成部分。V(D)J反应以谱系特异性和阶段特异性的方式局限于特定的抗原受体基因座。这种特异性似乎涉及顺式调节元件,其中一些元件也调节种系抗原受体基因座的转录。T和B谱系的早期发育步骤——包括表型分化、前体扩增和选择过程——至少部分地由功能重排的抗原受体基因自身的产物产生的信号逐步实现。