Han S, Zheng B, Schatz D G, Spanopoulou E, Kelsoe G
Department of Microbiology and Immunology, University of Maryland School of Medicine, 655 West Baltimore Street, Baltimore, MD 21201, USA.
Science. 1996 Dec 20;274(5295):2094-7. doi: 10.1126/science.274.5295.2094.
The products of the Rag1 and Rag2 genes drive genomic V(D)J rearrangements that assemble functional immunoglobulin and T cell antigen receptor genes. Expression of the Rag genes has been thought to be limited to developmentally immature lymphocyte populations that in normal adult animals are primarily restricted to the bone marrow and thymus. Abundant RAG1 and RAG2 protein and messenger RNA was detected in the activated B cells that populate murine splenic and Peyer's patch germinal centers. Germinal center B cells thus share fundamental characteristics of immature lymphocytes, raising the possibility that antigen-dependent secondary V(D)J rearrangements modify the peripheral antibody repertoire.
Rag1和Rag2基因的产物驱动基因组V(D)J重排,从而组装功能性免疫球蛋白和T细胞抗原受体基因。Rag基因的表达一直被认为仅限于发育不成熟的淋巴细胞群体,在正常成年动物中主要局限于骨髓和胸腺。在构成小鼠脾脏和派尔集合淋巴结生发中心的活化B细胞中检测到大量RAG1和RAG2蛋白及信使RNA。生发中心B细胞因此具有未成熟淋巴细胞的基本特征,这增加了抗原依赖性继发性V(D)J重排修饰外周抗体库的可能性。