David V, Folk N L, Maizels N
Department of Molecular Biophysics and Biochemistry, Yale University School of Medicine, New Haven, Connecticut 06510.
Genetics. 1992 Nov;132(3):799-811. doi: 10.1093/genetics/132.3.799.
We asked whether there are germ line immunoglobulin variable (V) segments that match sites of hypermutation in V regions encoding murine antibodies. Murine germ line DNA was probed with a panel of short deoxyoligonucleotides identical in sequence to segments of hypermutated V regions from hybridomas generated in the BALB/c response to the hapten 2-phenyloxazolone (Ox). Germ line sequences that match mutations in both heavy and kappa light chain V regions were identified, and clones of some of these germ line V segments were obtained. Comparison of these clones with hypermutated V regions revealed regions of identity ranging in size from 7 to over 50 nucleotides. In an effort to separate the effects of antigen selection from the mutagenic process, we also searched for matches to a panel of silent mutations in VH regions from germinal center B cells. Fourteen silent mutations occur among a collection of 36 hypermutated VH regions from two separate germinal centers of C57BL/6 mice stimulated with the hapten 4-hydroxy-3-nitrophenyl. Matches to nine of these silent mutations can be found among published sequences of C57BL/6 VH regions of the J558 family. Taken together, these data are consistent with the possibility that a template-dependent mutational process, like gene conversion, may contribute to somatic hypermutation.
我们探究了是否存在与编码鼠抗体的V区高突变位点相匹配的种系免疫球蛋白可变(V)区段。用一组短脱氧寡核苷酸探测鼠种系DNA,这些寡核苷酸的序列与BALB/c小鼠对半抗原2-苯基恶唑酮(Ox)产生反应时生成的杂交瘤中高突变V区的片段相同。鉴定出了与重链和κ轻链V区突变均相匹配的种系序列,并获得了其中一些种系V区段的克隆。将这些克隆与高突变V区进行比较,发现相同区域的大小在7至50多个核苷酸之间。为了将抗原选择的影响与诱变过程分开,我们还在生发中心B细胞的VH区寻找与一组沉默突变相匹配的序列。在用半抗原4-羟基-3-硝基苯基刺激的C57BL/6小鼠的两个独立生发中心的36个高突变VH区中,共出现了14个沉默突变。在已发表的J558家族C57BL/6 VH区序列中,可以找到与其中9个沉默突变相匹配的序列。综上所述,这些数据与如下可能性一致,即像基因转换这样的模板依赖性突变过程可能促成了体细胞高频突变。