Germline mutation rates at tandem repeat loci in DNA-repair deficient mice

被引:39
作者
Barber, RC
Miccoli, L
van Buul, PPW
Burr, KLA
van Duyn-Goedhart, A
Angulo, JF
Dubrova, YE
机构
[1] Univ Leicester, Dept Genet, Leicester LE1 7RH, Leics, England
[2] CEA, Lab Genet Radiosensibil, Dept Radiobiol & Radiopathol, Direct Sci Vivant, F-92265 Fontenay Aux Roses, France
[3] Leiden Univ, Ctr Med, Sylvius Lab, Dept Toxicogenet, NL-2333 Leiden, Netherlands
基金
英国惠康基金;
关键词
expanded simple tandem repeat loci; germline mutation; DNA repair; knock-out mouse; ionising radiation;
D O I
10.1016/j.mrfmmm.2004.05.003
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Mutation rates at two expanded simple tandem repeat (ESTR) loci were studied in the germline of non-exposed and irradiated severe combined immunodeficient (scid) and poly(ADP-ribose) polymerase (PARP-1(-/-)) deficient male mice. Non-exposed scid and PARP(-/-) male mice showed considerably elevated ESTR mutation rates, far higher than those in wild-type isogenic mice and other inbred strains. The irradiated scid and PARP-1(-/-) male mice did not show any detectable increases in their mutation rate, whereas significant ESTR mutation induction was observed in the irradiated wild-type isogenic males. ESTR mutation spectra in the scid and PARP-1(-/-) strains did not differ from those in the isogenic wild-type strains. Considering these data and the results of previous studies, we propose that a delay in repair of DNA damage in scid and PARP-1(-/-) mice could result in replication fork pausing which, in turn, may affect ESTR mutation rate in the non-irradiated males. The lack of mutation induction in irradiated scid and PARP-1(-/-) can be explained by the high cell killing effects of irradiation on the,germline of deficient mice. (C) 2004 Elsevier B.V. All rights reserved.
引用
收藏
页码:287 / 295
页数:9
相关论文
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