Rogozin I B, Solovyov V V, Kolchanov N A
Institute of Cytology and Genetics, USSR Academy of Sciences, Siberian Department, Novosibirsk.
Biochim Biophys Acta. 1991 Jun 13;1089(2):175-82. doi: 10.1016/0167-4781(91)90005-7.
Based on the analysis of some immunoglobulin V-gene sequences, somatic mutations are assumed to occur by correction of complementary violations in heteroduplexes formed by direct or inverted repeats. Correlation between somatic mutations and repeats is investigated by a statistical weights method in 323 somatic substitutions in 14 V-genes. Assuming absence of correlation, the probability of observing data in the sample would be very low (0.00004). This result supports the idea that somatic mutations may arise from heteroduplex repair. The high frequency of these mutations in complementarity-determining regions (CDRs) of V-genes may be due to a high concentration of repeats in these regions. Analysis of somatic substitutions has revealed that stabilizing selection seems to provide conservation of framework regions (FRs) (which leads to preservation of the protein's three-dimensional structure). Positive selection may be provided by B-lymphocyte proliferation with large changes in CDRs.
基于对一些免疫球蛋白V基因序列的分析,推测体细胞突变是通过纠正由正向或反向重复序列形成的异源双链体中的互补性错误而发生的。采用统计权重法研究了14个V基因中323个体细胞替换中体细胞突变与重复序列之间的相关性。假设不存在相关性,在样本中观察到数据的概率将非常低(0.00004)。这一结果支持了体细胞突变可能源于异源双链体修复的观点。V基因互补决定区(CDR)中这些突变的高频率可能是由于这些区域中重复序列的高浓度。体细胞替换分析表明,稳定选择似乎有助于框架区(FR)的保守(这导致蛋白质三维结构的保留)。正向选择可能由CDR发生大变化的B淋巴细胞增殖提供。