Leder P, Max E E, Seidman J G, Kwan S P, Scharff M, Nau M, Norman B
Cold Spring Harb Symp Quant Biol. 1981;45 Pt 2:859-65. doi: 10.1101/sqb.1981.045.01.103.
Immunoglobulin kappa light-chain diversity arises, in large part, from an array of germ-line V-region genes that undergo somatic recombination with one of four active J-region segments. The diversity provided by this combinational system is increased by a recombination mechanism that allows variation of crossover points so as to generate additional diversity at a critical region of the light chain. The elaborate mechanism for generating diversity is accompanied not only by considerable waste, in terms of unused V and J regions in a given cell, but also by a range of aberrant recombinants that fail to produce active immunoglobulin genes.
免疫球蛋白κ轻链的多样性在很大程度上源于一系列种系V区基因,这些基因与四个活性J区片段之一进行体细胞重组。这种组合系统提供的多样性通过一种重组机制得以增加,该机制允许交叉点发生变化,从而在轻链的关键区域产生额外的多样性。产生多样性的精细机制不仅伴随着相当大的浪费,即在给定细胞中未使用的V区和J区,还伴随着一系列无法产生活性免疫球蛋白基因的异常重组体。