Migone N, Feder J, Cann H, van West B, Hwang J, Takahashi N, Honjo T, Piazza A, Cavalli-Sforza L L
Proc Natl Acad Sci U S A. 1983 Jan;80(2):467-71. doi: 10.1073/pnas.80.2.467.
DNA probes containing the switch region (S) associated with the human immunoglobulin heavy chain mu gene were used to investigate polymorphisms in the germ-line human DNA. Six polymorphisms, detected by a single restriction enzyme (Sst I) are described. Linkage studies in 29 families show that five of the six polymorphisms, although relatively unassociated in random individuals, segregate in complete linkage one to the other and to Gm allotypes (markers on the heavy chain of IgG), while the sixth segregates independently. Altogether, when one considers the DNA markers at the five closely linked loci and the IgG1 and IgG3 heavy chain allotypes, 33 different haplotypes have been described; of these, 28 are detected by the DNA polymorphism alone. Study of 158-187 random haplotypes showed strong linkage disequilibrium only between one DNA polymorphism (Sst A) and Gm. Of the polymorphic Sst I loci, one, Sst E [associated with 2.2- to 2.7-kilobase (kb) fragments], is included in the mu chain S region (S mu); another, Sst A (6.8-7.4 kb), must be very close to the gamma 1-gamma 3 chain gene cluster. Based on studies of an IgE human myeloma, a third polymorphism, Sst C (4.8-5.5 kb), should map 3' of the active epsilon chain gene. An Sst I restriction enzyme map of phage clones carrying the two alpha chain genes indicates that Sst A and Sst C loci probably overlap with the alpha 1 and alpha 2 S regions, respectively. Both deletion/duplications and point mutations were detected.
含有与人类免疫球蛋白重链μ基因相关的开关区(S)的DNA探针被用于研究人类种系DNA中的多态性。描述了通过单一限制酶(Sst I)检测到的六种多态性。对29个家族的连锁研究表明,六种多态性中的五种,尽管在随机个体中相对不相关,但彼此之间以及与Gm同种异型(IgG重链上的标记)完全连锁分离,而第六种则独立分离。总体而言,当考虑五个紧密连锁位点的DNA标记以及IgG1和IgG3重链同种异型时,已经描述了33种不同的单倍型;其中,仅通过DNA多态性检测到28种。对158 - 187个随机单倍型的研究表明,仅一种DNA多态性(Sst A)与Gm之间存在强连锁不平衡。在多态性Sst I位点中,一个位点Sst E [与2.2至2.7千碱基(kb)片段相关]包含在μ链S区域(Sμ)中;另一个位点Sst A(6.8 - 7.4 kb)必定非常接近γ1 - γ3链基因簇。基于对一种IgE人类骨髓瘤的研究,第三种多态性Sst C(4.8 - 5.5 kb)应该定位在活性ε链基因的3'端。携带两个α链基因的噬菌体克隆的Sst I限制酶图谱表明,Sst A和Sst C位点可能分别与α1和α2 S区域重叠。同时检测到了缺失/重复和点突变。