Reilly E B, Blomberg B, Imanishi-Kari T, Tonegawa S, Eisen H N
Proc Natl Acad Sci U S A. 1984 Apr;81(8):2484-8. doi: 10.1073/pnas.81.8.2484.
The frequencies of diverse rearrangements of variable (V)lambda to joining (J)lambda gene segments were examined by Southern blot hybridization in 30 murine B-cell lines, each producing an immunoglobulin lambda light chain of known subtype (lambda 1, lambda 2, or lambda 3). For 11 out of 12 lambda 1 chains, the rearrangement was V lambda 1----J lambda 1; for 9 out of 9 lambda 2 chains, it was V lambda 2----J lambda 2; and for 8 out of 9 lambda 3 chains, it was V lambda 1----J lambda 3. Similar results were obtained by considering the partial or complete sequences at the amino acid or cDNA level of 44 other lambda chains (24 previously described): for 43 of these chains the rearranged V-J gene segments were evidently V lambda 1-J lambda 1 for 28 lambda 1 chains, V lambda 2-J lambda 2 for 10 lambda 2 chains, and V lambda 1-J lambda 3 for 5 lambda 3 chains. Of the combined total of 74 chains there were 3 with unusual V lambda rearrangements, all involving the V lambda 2 gene segment: for 2 of these unusual chains, the encoding segments were V lambda 2-J lambda 1-C lambda 1 and for one they were V lambda 2-J lambda 3-C lambda 3. Thus, the results for all 74 lambda chains show that, in contrast to the apparently unrestricted V kappa----J kappa rearrangements for kappa chains, for each of the 3 murine lambda-chain subtypes V-J recombination is severely restricted: the V lambda gene segment expressed in lambda 1 and lambda 3 chains was nearly always V lambda 1 (95% and 93%, respectively), whereas in lambda 2 chains it was without exception V lambda 2 (19 out of 19 chains). Therefore V lambda-J lambda combinatorial variation is not a significant source of amino acid sequence diversity of lambda chains of inbred mice. If the order of the lambda gene segments is 5' V lambda 2-J lambda 2C lambda 2J lambda 4C lambda 4-V lambda 1-J lambda 3C lambda 3J lambda 1C lambda 1 3', as suggested previously and by the present findings, it appears that (i) when a V lambda gene segment rearranges in a developing B cell it ordinarily recombines with a J lambda gene segment in the nearest downstream (3') cluster of J lambda C lambda segments, and (ii) V lambda rearrangement to the upstream (5') cluster is very rare and possibly may not take place at all.
通过Southern印迹杂交法,在30个小鼠B细胞系中检测了可变(V)λ基因片段与连接(J)λ基因片段各种重排的频率,每个细胞系都产生已知亚型(λ1、λ2或λ3)的免疫球蛋白λ轻链。对于12条λ1链中的11条,重排为Vλ1----Jλ1;对于9条λ2链中的9条,重排为Vλ2----Jλ2;对于9条λ3链中的8条,重排为Vλ1----Jλ3。通过考虑另外44条λ链(24条先前已描述)的氨基酸或cDNA水平的部分或完整序列,也获得了类似结果:在这些链中的43条中,重排的V-J基因片段对于28条λ1链显然是Vλ1-Jλ1,对于10条λ2链是Vλ2-Jλ2,对于5条λ3链是Vλ1-Jλ3。在总共74条链中,有3条具有不寻常的Vλ重排,均涉及Vλ2基因片段:对于其中2条不寻常的链,编码片段是Vλ2-Jλ1-Cλ1,对于1条是Vλ2-Jλ3-Cλ3。因此,所有74条λ链的结果表明,与κ链明显不受限制的Vκ----Jκ重排相反,对于3种小鼠λ链亚型中的每一种,V-J重组都受到严格限制:在λ1和λ3链中表达的Vλ基因片段几乎总是Vλ1(分别为95%和93%),而在λ2链中无一例外是Vλ2(19条链中的19条)。因此,Vλ-Jλ组合变异不是近交系小鼠λ链氨基酸序列多样性的重要来源。如果λ基因片段的顺序如先前及本研究结果所提示的是5' Vλ2-Jλ2Cλ2Jλ4Cλ4-Vλ1-Jλ3Cλ3Jλ1Cλ1 3',那么似乎(i)当一个Vλ基因片段在发育中的B细胞中重排时,它通常与最靠近下游(3')的JλCλ片段簇中的一个Jλ基因片段重组,并且(ii)Vλ向上游(5')片段簇的重排非常罕见,甚至可能根本不会发生。