Cutting Edge: CTNNBL1 Is Dispensable for Ig Class Switch Recombination

被引:22
作者
Han, Li [1 ]
Masani, Shahnaz [1 ]
Yu, Kefei [1 ]
机构
[1] Michigan State Univ, Dept Microbiol & Mol Genet, E Lansing, MI 48824 USA
基金
美国国家卫生研究院;
关键词
CYTIDINE DEAMINASE AID; SOMATIC HYPERMUTATION; B-CELLS; ANTIBODY DIVERSIFICATION; GENE CONVERSION; DNA DEAMINATION; ENZYME; TRANSCRIPTS; EXPRESSION; MECHANISM;
D O I
10.4049/jimmunol.1001643
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Ig class switch recombination (CSR) and somatic hypermutation require activation-induced cytidine deaminase (AID). The search for AID-interaction factors has been a major research effort in the field, as the mechanism of preferential targeting of AID to Ig loci remains elusive. CTNNBL1 is one of the few identified AID-interacting factors and has been shown to affect AID-mediated mutation and gene conversion in chicken DT40 cells. CTNNBL1 was also implicated in mammalian CSR by the fact that an AID mutant that fails to interact with CTNNBL1 also fails to support CSR in AID-deficient mouse B cells. To directly assess the role of CTNNBL1 in CSR, we disrupted the CTNNBL1 gene on both alleles in mouse CH12F3 cells by gene targeting. We found normal levels of CSR in CTNNBL1-deficient cells, indicating that CTNNBL1 is dispensable for CSR. The Journal of Immunology, 2010, 185: 1379-1381.
引用
收藏
页码:1379 / 1381
页数:3
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