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Somatic hypermutation of the JC intron is markedly reduced in unrearranged kappa and H alleles and is unevenly distributed in rearranged alleles.

作者信息

Weber J S, Berry J, Litwin S, Claflin J L

机构信息

Department of Microbiology and Immunology, University of Michigan Medical School, Ann Arbor 48109.

出版信息

J Immunol. 1991 May 1;146(9):3218-26.

PMID:1901897
Abstract

Somatic hypermutation of the Ig genes occurs in rearranged V(D)J and its flanking sequences after Ag stimulation. Even though C regions and unrearranged V segments have been found to lack mutations, it is not known whether the mutational mechanism can be active in unrearranged J segments and their flanking regions. By polymerase chain reaction and direct sequencing of the 500 bp at the 5' end of the JC intron of hybridoma DNA derived from splenic B cells, we show that the frequency of mutations in unrearranged J regions of kappa and H chain genes is 0/7849 bp (upper 95% confidence interval, less than 0.00038) and 1/3209 bp (upper 95% confidence interval, less than 0.0015), respectively. The frequency (f) for the same region of rearranged kappa and H chain genes was 29/9380 bp (95% confidence, 0.0021 less than f less than 0.0044) and 16/2750 bp (95% confidence, 0.0033 less than f less than 0.0094), respectively. The significantly higher frequency of mutations in the rearranged alleles indicates that rearrangement is needed to effect full activation of the mutational mechanism. The data also show that mutations occur predominantly in the 5'-most 250 bp of the JC kappa intron. Statistical analysis of the distribution of mutations within the 5'-most 521 bp of the JC kappa intron reveals significant deviation (p = 0.000085) from a theoretically determined uniform distribution, indicating that mutations are not evenly distributed within this region.

摘要

相似文献

1
Somatic hypermutation of the JC intron is markedly reduced in unrearranged kappa and H alleles and is unevenly distributed in rearranged alleles.
J Immunol. 1991 May 1;146(9):3218-26.
2
Position of the rearranged V kappa and its 5' flanking sequences determines the location of somatic mutations in the J kappa locus.重排的Vκ及其5'侧翼序列的位置决定了Jκ基因座中体细胞突变的位置。
J Immunol. 1991 May 15;146(10):3652-5.
3
Mutations in Ig V(D)J genes are distributed asymmetrically and independently of the position of V(D)J.免疫球蛋白V(D)J基因中的突变呈不对称分布,且与V(D)J的位置无关。
J Immunol. 1994 Oct 15;153(8):3594-602.
4
The 5' boundary of somatic hypermutation in a V kappa gene is in the leader intron.Vκ基因中体细胞超突变的5'边界位于前导内含子中。
Eur J Immunol. 1994 Jun;24(6):1453-7. doi: 10.1002/eji.1830240632.
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Somatic hypermutation of an immunoglobulin transgene in kappa transgenic mice.κ转基因小鼠中免疫球蛋白转基因的体细胞超突变
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6
Ig heavy chain protein controls B cell development by regulating germ-line transcription and retargeting V(D)J recombination.免疫球蛋白重链蛋白通过调节种系转录和重新靶向V(D)J重组来控制B细胞发育。
J Immunol. 1994 Aug 15;153(4):1645-57.
7
V gene rearrangement is required to fully activate the hypermutation mechanism in B cells.V基因重排是B细胞中完全激活超突变机制所必需的。
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8
Clonal analysis of a human antibody response. III. Nucleotide sequences of monoclonal IgM, IgG, and IgA to rabies virus reveal restricted V kappa gene utilization, junctional V kappa J kappa and V lambda J lambda diversity, and somatic hypermutation.人类抗体应答的克隆分析。III. 针对狂犬病病毒的单克隆IgM、IgG和IgA的核苷酸序列揭示了受限的Vκ基因利用、连接区VκJκ和VλJλ多样性以及体细胞超突变。
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V kappa gene segments rearranged in chronic lymphocytic leukemia are distributed over a large portion of the V kappa locus and do not show somatic mutation.慢性淋巴细胞白血病中重排的Vκ基因片段分布在Vκ基因座的大部分区域,且未显示体细胞突变。
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J Immunol. 1998 Nov 1;161(9):4634-45.

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Complex regulation of somatic hypermutation by cis-acting sequences in the endogenous IgH gene in hybridoma cells.杂交瘤细胞内源性IgH基因中顺式作用序列对体细胞高频突变的复杂调控。
Proc Natl Acad Sci U S A. 2005 Aug 16;102(33):11829-34. doi: 10.1073/pnas.0505449102. Epub 2005 Aug 8.
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Somatic hypermutation introduces insertions and deletions into immunoglobulin V genes.
体细胞高频突变会在免疫球蛋白V基因中引入插入和缺失。
J Exp Med. 1998 Jan 5;187(1):59-70. doi: 10.1084/jem.187.1.59.
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New nucleotide sequence data on the EMBL File Server.欧洲分子生物学实验室文件服务器上的新核苷酸序列数据。
Nucleic Acids Res. 1991 Sep 11;19(17):4803-14. doi: 10.1093/nar/19.17.4803.
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Nucleic Acids Res. 1991 Aug 25;19(16):4577-89. doi: 10.1093/nar/19.16.4577.
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EMBO J. 1991 Dec;10(13):4331-41. doi: 10.1002/j.1460-2075.1991.tb05011.x.
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Immunology. 1992 Jan;75(1):3-9.
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