Absence of DNA polymerase θ results in decreased somatic hypermutation frequency and altered mutation patterns in Ig

被引:35
作者
Masuda, Keiji
Ouchida, Rika
Hikida, Masaki
Nakayama, Manabu
Ohara, Osamu
Kurosaki, Tomohiro
O-Wang, Jiyanq [1 ]
机构
[1] RIKEN, Yokohama Inst, Res Ctr Allergy & Immunol, Lab Antigen Receptor Divers, Yokohama, Kanagawa 2300045, Japan
[2] RIKEN, Yokohama Inst, Res Ctr Allergy & Immunol, Lab Lymphocyte Differentiat, Yokohama, Kanagawa 2300045, Japan
[3] Kazusa DNA Res Inst, Dept Human Gene Res, Chiba 2920818, Japan
[4] RIKEN, Yokohama Inst, Res Ctr Allergy & Immunol, Lab Immunogenom, Yokohama, Kanagawa 2300045, Japan
关键词
low fidelity DNA polymerase; immunoglobulin gene; somatic hypermutation; class switch recombination;
D O I
10.1016/j.dnarep.2006.06.006
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Multiple DNA polymerases participate in somatic hypermutation of immunoglobulin (Ig) genes. Mutations at A/T are largely dependent on DNA polymerase eta (POLH) whereas mutations at C/G appear to be generated by several DNA polymerases. We have previously shown that mice expressing a catalytically inactive POLQ (Polq-inactive) have a reduction in C/G mutations. Here we have generated mice that completely lack Polq expression (Polq-null). Polq-null mice have no obvious abnormality in B or T cell differentiation, and their splenic B cells responded normally to various activation signals and underwent normal Ig gene class switching. The mutant mice mounted relatively normal immune responses against a T-dependent antigen although there was a slight decrease in antigen specific antibodies. Polq-null mice exhibited a mild reduction in the overall mutation frequency, however, in contrast to Polq-inactive mice where the reduction mostly affected mutations at C/G, Polq-null mice showed a reduction of both C/G and A/T mutations and there was a significant increase of G to C transversions. These results confirm a role for POLQ in somatic hypermutation and suggest that in the complete absence of POLQ other polymerases may functionally substitute, resulting in a mutation pattern different from that found in Polq-inactive mice. (c) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:1384 / 1391
页数:8
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