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免疫球蛋白基因间体细胞突变频率的比较。

Comparison of somatic mutation frequency among immunoglobulin genes.

作者信息

Motoyama N, Miwa T, Suzuki Y, Okada H, Azuma T

机构信息

Department of Molecular Biology, Nagoya City University School of Medicine, Japan.

出版信息

J Exp Med. 1994 Feb 1;179(2):395-403. doi: 10.1084/jem.179.2.395.

Abstract

We analyzed the frequency of somatic mutation in immunoglobulin genes from hybridomas that secrete anti-(4-hydroxy-3-nitrophenyl)acetyl (NP) monoclonal antibodies. A high frequency of mutation (3.3-4.4%) was observed in both the rearranged VH186.2 and V lambda 1 genes, indicating that somatic mutation occurs with similar frequency in these genes in spite of the absence of an intron enhancer in lambda 1 chain genes. In contrast to the high frequency in J-C introns, only two nucleotide substitutions occurred at positions -462 and -555 in the 5' noncoding region in one of the lambda 1-chain genes and in none of the other three so far studied. Since a similar low frequency of somatic mutation was observed in the 5' noncoding region of inactive lambda 2-chain genes rendered inactive because of incorrect rearrangement, this region may not be a target or alternatively, may be protected from the mutator system. We observed a low frequency of nucleotide substitution in unrearranged V lambda 1 genes (approximately 1/15 that of rearranged genes). Together with previous results (Azuma T., N. Motoyama, L. Fields, and D. Loh, 1993. Int. Immunol. 5:121), these findings suggest that the 5' noncoding region, which contains the promoter element, provides a signal for the somatic mutator system and that rearrangement, which brings the promoter into close proximity to the enhancer element, should increase mutation efficiency.

摘要

我们分析了分泌抗(4-羟基-3-硝基苯基)乙酰(NP)单克隆抗体的杂交瘤中免疫球蛋白基因的体细胞突变频率。在重排的VH186.2和Vλ1基因中均观察到高频率的突变(3.3 - 4.4%),这表明尽管λ1链基因中不存在内含子增强子,但这些基因中的体细胞突变频率相似。与J-C内含子中的高频率相反,在一个λ1链基因的5'非编码区的-462和-555位点仅发生了两个核苷酸替换,而在目前研究的其他三个基因中均未发生。由于在因重排错误而失活的无活性λ2链基因的5'非编码区观察到类似的低体细胞突变频率,该区域可能不是靶点,或者可能受到突变系统的保护。我们在未重排的Vλ1基因中观察到低频率的核苷酸替换(约为重排基因的1/15)。结合先前的结果(Azuma T., N. Motoyama, L. Fields, and D. Loh, 1993. Int. Immunol. 5:121),这些发现表明包含启动子元件的5'非编码区为体细胞突变系统提供了信号,并且重排使启动子与增强子元件紧密相邻,应该会提高突变效率。

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