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VκJκ重排的体细胞高频突变:DNA两条链上RGYW基序的靶向作用以及RGYW基序内突变密码子的优先选择

Somatic hypermutation of VkappaJkappa rearrangements: targeting of RGYW motifs on both DNA strands and preferential selection of mutated codons within RGYW motifs.

作者信息

Foster S J, Dörner T, Lipsky P E

机构信息

Department of Internal Medicine and Harold C. Simmons Arthritis Research Center, University of Texas Southwestern Medical Center, Dallas, TX 75235-8884, USA.

出版信息

Eur J Immunol. 1999 Dec;29(12):4011-21. doi: 10.1002/(SICI)1521-4141(199912)29:12<4011::AID-IMMU4011>3.0.CO;2-W.

Abstract

Productive and nonproductive VkappaJkappa gene rearrangements from individual peripheral blood B cells were analyzed for the pattern and distribution of mutations. The eight RGYW motifs and their inverse repeats, WRCY, were present in germ-line Vkappa genes significantly more often than anticipated by random chance (1.6-fold and 1.4-fold, respectively) and were also mutated in nonproductive rearrangements significantly more often than expected, with a frequency 1.96 fold greater than that of non-RGYW / WRCY motifs. As a result, 50 % of all mutations in nonproductive VkappaJkappa rearrangements occurred in RGYW / WRCY motifs. Each RGYW tetramer and its corresponding WRCY contained mutations at comparable frequencies. Furthermore, mutations of G and C were significantly more frequent in RGYW / WRCY but not in other tetranucleotides. Finally, mutations in codons contained within RGYW / WRCY were significantly more frequent in complementarity-determining regions but not framework regions of productive compared to nonproductive rearrangements and were increased by a factor that was significantly greater than for mutations in other motifs. These results indicate that the mutational machinery targets the overrepresented RGYW motifs in Vkappa genes on both DNA strands and that the resulting replacement mutations are preferentially selected into the productive repertoire.

摘要

分析了来自个体外周血B细胞的有功能和无功能的VκJκ基因重排的突变模式和分布。种系Vκ基因中八个RGYW基序及其反向重复序列WRCY出现的频率明显高于随机预期(分别为1.6倍和1.4倍),并且在无功能重排中的突变频率也明显高于预期,其频率比非RGYW / WRCY基序高1.96倍。因此,无功能VκJκ重排中所有突变的50%发生在RGYW / WRCY基序中。每个RGYW四聚体及其相应的WRCY以相当的频率发生突变。此外,RGYW / WRCY中G和C的突变明显更频繁,但在其他四核苷酸中并非如此。最后,与无功能重排相比,RGYW / WRCY内密码子的突变在有功能重排的互补决定区而非框架区明显更频繁,并且增加的倍数明显大于其他基序中的突变。这些结果表明,突变机制靶向DNA两条链上Vκ基因中过度存在的RGYW基序,并且由此产生的替换突变优先被选择进入有功能的库中。

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