Sakano H, Hüppi K, Heinrich G, Tonegawa S
Nature. 1979 Jul 26;280(5720):288-94. doi: 10.1038/280288a0.
The entire nucleotide sequence of a 1.7-kilobase embryonic DNA fragment containing five joining (J) DNA segments for mouse immunoglobulin kappa chain gene has been determined. Each J DNA segment can encode amino acid residues 96--108. Comparison of one of the five J DNA sequences with those of an embryonic variable (V) gene and a complete kappa chain gene permitted localisation of a precise recombination site. The 5'-flanking regions of J DNA segments could form an inverted stem structure with the 3'-non-coding region of embryonic V genes. This hypothetical structure and gel-blotting analysis of total embryo and myeloma DNA suggest that the somatic recombination may be accompanied by excision of an entire DNA segment between a V gene and a J DNA segment. Antibody diversity may in part be generated by modulation of the precise recombination sites.
已确定一个1.7千碱基的胚胎DNA片段的完整核苷酸序列,该片段包含小鼠免疫球蛋白κ链基因的五个连接(J)DNA片段。每个J DNA片段可编码氨基酸残基96 - 108。将五个J DNA序列之一与一个胚胎可变(V)基因和一个完整κ链基因的序列进行比较,确定了一个精确的重组位点。J DNA片段的5'侧翼区域可与胚胎V基因的3'非编码区域形成反向茎结构。这种假设结构以及对总胚胎和骨髓瘤DNA的凝胶印迹分析表明,体细胞重组可能伴随着V基因和J DNA片段之间整个DNA片段的切除。抗体多样性可能部分是由精确重组位点的调节产生的。