Foster S J, Dorner T, Lipsky P E
Department of Internal Medicine, Harold C. Simmons Arthritis Research Center, University of Texas Southwestern Medical Center, Dallas 75235-8884, USA.
Eur J Immunol. 1999 Oct;29(10):3122-32. doi: 10.1002/(SICI)1521-4141(199910)29:10<3122::AID-IMMU3122>3.0.CO;2-O.
The number and distribution of nucleotide substitutions in human VkappaJkappa genes were examined using a PCR technique that analyzed nonproductive and productive rearrangements amplified from genomic DNA of individual B cells. The results indicate that the mutational mechanism introduces replacement (R) mutations comparably throughout the length of the VkappaJkappa rearrangement, but tends to target specific triplets. Moreover, hotspots of mutational activity were identified in complementarity determining regions (CDR). A marked increase in the frequency of R mutations in CDR was noted when productive were compared to nonproductive rearrangements, indicating that these were selected into the expressed repertoire. Of note, amino acids encoded by codons adjacent to hotspots of mutation were also positively selected implying that similar regions were targeted for hypermutation and subsequent selection. In contrast to the distribution of CDR mutations, R mutations in the framework (FR) regions tended to be eliminated from productive VkappaJkappa rearrangements, implying that the somatic hypermutational machinery frequently introduced amino acid changes that were deleterious to the structural integrity of the kappa chain protein. The difference in the ratio of R to silent mutations in CDR and FR in the expressed repertoire, therefore, reflects the summation of positive selection of R mutations in the CDR and the elimination of R mutations in the FR. The data indicate that the balance between targeted mutation of VkappaJkappa rearrangements and subsequent selection and elimination governs the pattern of mutations manifest within the expressed kappa repertoire.
利用一种聚合酶链式反应(PCR)技术检测了人类VκJκ基因中核苷酸替换的数量和分布情况,该技术分析了从单个B细胞基因组DNA中扩增出的无功能和有功能重排。结果表明,突变机制在VκJκ重排的整个长度上相对均匀地引入替换(R)突变,但倾向于靶向特定的三联体。此外,在互补决定区(CDR)中鉴定出了突变活性热点。当将有功能重排与无功能重排进行比较时,发现CDR中R突变的频率显著增加,这表明这些突变被选入了表达库。值得注意的是,与突变热点相邻密码子编码的氨基酸也受到正向选择,这意味着相似区域是高突变和后续选择的目标。与CDR突变的分布相反,框架(FR)区域中的R突变倾向于从有功能的VκJκ重排中被消除,这意味着体细胞高突变机制经常引入对κ链蛋白结构完整性有害的氨基酸变化。因此,表达库中CDR和FR区域R突变与沉默突变比例的差异反映了CDR中R突变的正向选择和FR中R突变的消除的总和。数据表明,VκJκ重排的靶向突变与后续选择和消除之间的平衡决定了表达的κ链库中表现出的突变模式。