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通过Ig基因的体细胞高频突变过程,正常B细胞中的BCL-6基因突变。

Mutation of BCL-6 gene in normal B cells by the process of somatic hypermutation of Ig genes.

作者信息

Shen H M, Peters A, Baron B, Zhu X, Storb U

机构信息

Department of Molecular Genetics and Cell Biology, University of Chicago, Chicago, IL 60617, USA.

出版信息

Science. 1998 Jun 12;280(5370):1750-2. doi: 10.1126/science.280.5370.1750.

DOI:10.1126/science.280.5370.1750
PMID:9624052
Abstract

Immunoglobulin (Ig) genes are hypermutated in B lymphocytes that are the precursors to memory B cells. The mutations are linked to transcription initiation, but non-Ig promoters are permissible for the mutation process; thus, other genes expressed in mutating B cells may also be subject to somatic hypermutation. Significant mutations were not observed in c-MYC, S14, or alpha-fetoprotein (AFP) genes, but BCL-6 was highly mutated in a large proportion of memory B cells of normal individuals. The mutation pattern was similar to that of Ig genes.

摘要

免疫球蛋白(Ig)基因在作为记忆B细胞前体的B淋巴细胞中发生高度突变。这些突变与转录起始相关,但非Ig启动子在突变过程中也是允许的;因此,在发生突变的B细胞中表达的其他基因也可能发生体细胞超突变。在c-MYC、S14或甲胎蛋白(AFP)基因中未观察到显著突变,但在正常个体的大部分记忆B细胞中,BCL-6发生了高度突变。突变模式与Ig基因相似。

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