Suppr超能文献

免疫球蛋白基因中的体细胞高频突变。I. 体细胞突变与重复序列之间的相关性。体细胞突变特性和克隆选择。

Somatic hypermutagenesis in immunoglobulin genes. I. Correlation between somatic mutations and repeats. Somatic mutation properties and clonal selection.

作者信息

Rogozin I B, Solovyov V V, Kolchanov N A

机构信息

Institute of Cytology and Genetics, USSR Academy of Sciences, Siberian Department, Novosibirsk.

出版信息

Biochim Biophys Acta. 1991 Jun 13;1089(2):175-82. doi: 10.1016/0167-4781(91)90005-7.

Abstract

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.

摘要

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。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验