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与编码鼠抗半抗原抗体的基因中高突变序列相匹配的种系可变区。

Germ line variable regions that match hypermutated sequences in genes encoding murine anti-hapten antibodies.

作者信息

David V, Folk N L, Maizels N

机构信息

Department of Molecular Biophysics and Biochemistry, Yale University School of Medicine, New Haven, Connecticut 06510.

出版信息

Genetics. 1992 Nov;132(3):799-811. doi: 10.1093/genetics/132.3.799.

DOI:10.1093/genetics/132.3.799
PMID:1468632
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1205216/
Abstract

We asked whether there are germ line immunoglobulin variable (V) segments that match sites of hypermutation in V regions encoding murine antibodies. Murine germ line DNA was probed with a panel of short deoxyoligonucleotides identical in sequence to segments of hypermutated V regions from hybridomas generated in the BALB/c response to the hapten 2-phenyloxazolone (Ox). Germ line sequences that match mutations in both heavy and kappa light chain V regions were identified, and clones of some of these germ line V segments were obtained. Comparison of these clones with hypermutated V regions revealed regions of identity ranging in size from 7 to over 50 nucleotides. In an effort to separate the effects of antigen selection from the mutagenic process, we also searched for matches to a panel of silent mutations in VH regions from germinal center B cells. Fourteen silent mutations occur among a collection of 36 hypermutated VH regions from two separate germinal centers of C57BL/6 mice stimulated with the hapten 4-hydroxy-3-nitrophenyl. Matches to nine of these silent mutations can be found among published sequences of C57BL/6 VH regions of the J558 family. Taken together, these data are consistent with the possibility that a template-dependent mutational process, like gene conversion, may contribute to somatic hypermutation.

摘要

我们探究了是否存在与编码鼠抗体的V区高突变位点相匹配的种系免疫球蛋白可变(V)区段。用一组短脱氧寡核苷酸探测鼠种系DNA,这些寡核苷酸的序列与BALB/c小鼠对半抗原2-苯基恶唑酮(Ox)产生反应时生成的杂交瘤中高突变V区的片段相同。鉴定出了与重链和κ轻链V区突变均相匹配的种系序列,并获得了其中一些种系V区段的克隆。将这些克隆与高突变V区进行比较,发现相同区域的大小在7至50多个核苷酸之间。为了将抗原选择的影响与诱变过程分开,我们还在生发中心B细胞的VH区寻找与一组沉默突变相匹配的序列。在用半抗原4-羟基-3-硝基苯基刺激的C57BL/6小鼠的两个独立生发中心的36个高突变VH区中,共出现了14个沉默突变。在已发表的J558家族C57BL/6 VH区序列中,可以找到与其中9个沉默突变相匹配的序列。综上所述,这些数据与如下可能性一致,即像基因转换这样的模板依赖性突变过程可能促成了体细胞高频突变。

相似文献

1
Germ line variable regions that match hypermutated sequences in genes encoding murine anti-hapten antibodies.与编码鼠抗半抗原抗体的基因中高突变序列相匹配的种系可变区。
Genetics. 1992 Nov;132(3):799-811. doi: 10.1093/genetics/132.3.799.
2
V genes of the primary antibody response of C57BL/10 mice to the hapten phenyloxazolone.C57BL/10小鼠对半抗原苯恶唑酮的初次抗体应答的V基因
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3
Facultative role of germinal centers and T cells in the somatic diversification of IgVH genes.生发中心和T细胞在IgVH基因体细胞多样化中的兼性作用。
J Exp Med. 1995 Apr 1;181(4):1319-31. doi: 10.1084/jem.181.4.1319.
4
Early rearrangements of genes encoding murine immunoglobulin kappa chains, unlike genes encoding heavy chains, use variable gene segments dispersed throughout the locus.与编码重链的基因不同,编码小鼠免疫球蛋白κ链的基因早期重排使用分散在整个基因座中的可变基因片段。
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5
Analysis of patterns of DNA sequence variation in flanking and coding regions of murine germ-line immunoglobulin heavy-chain variable genes: evolutionary implications.小鼠种系免疫球蛋白重链可变基因侧翼和编码区DNA序列变异模式分析:进化意义
Proc Natl Acad Sci U S A. 1994 Dec 6;91(25):12163-7. doi: 10.1073/pnas.91.25.12163.
6
Light chain germ-line genes and the immune response to 2-phenyloxazolone.轻链种系基因与对2-苯基恶唑酮的免疫反应。
EMBO J. 1985 Dec 16;4(13A):3439-45. doi: 10.1002/j.1460-2075.1985.tb04102.x.
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Heavy chain variable region contribution to the NPb family of antibodies: somatic mutation evident in a gamma 2a variable region.重链可变区对NPb抗体家族的贡献:γ2a可变区中明显的体细胞突变。
Cell. 1981 Jun;24(3):625-37. doi: 10.1016/0092-8674(81)90089-1.
8
VH and V kappa segment structure of anti-insulin IgG autoantibodies in patients with insulin-dependent diabetes mellitus. Evidence for somatic selection.胰岛素依赖型糖尿病患者抗胰岛素IgG自身抗体的VH和Vκ片段结构。体细胞选择的证据。
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9
Nucleotide sequence of messenger RNA encoding VHDJH and VKJK of a highly conserved idiotype-defined primary response anti-hapten antibody.编码高度保守的独特型定义的初级反应抗半抗原抗体的VHDJH和VKJK的信使核糖核酸的核苷酸序列。
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10
Several V genes participate in the early phenyloxazolone response in various combinations.几个V基因以各种组合参与早期苯恶唑酮反应。
Eur J Immunol. 1986 Jan;16(1):98-105. doi: 10.1002/eji.1830160119.

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Gene conversion in human rearranged immunoglobulin genes.人类重排免疫球蛋白基因中的基因转换。
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Cis-acting regulatory sequences promote high-frequency gene conversion between repeated sequences in mammalian cells.顺式作用调控序列促进哺乳动物细胞中重复序列之间的高频基因转换。
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5
Co-existence of somatic hypermutation and gene conversion in hypervariable regions of single Igkappa clones.单个Igκ克隆高变区中体细胞高频突变与基因转换的共存。
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Altering the antibody repertoire via transgene homologous recombination: evidence for global and clone-autonomous regulation of antigen-driven B cell differentiation.通过转基因同源重组改变抗体库:抗原驱动的B细胞分化的全局和克隆自主调节的证据。
J Exp Med. 1995 Jan 1;181(1):271-81. doi: 10.1084/jem.181.1.271.

本文引用的文献

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