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重症联合免疫缺陷(SCID)突变对小鼠Pc-1(Ms6-hm)种系突变发生的影响。

Effect of SCID mutation on the occurrence of mouse Pc-1 (Ms6-hm) germline mutations.

作者信息

Yamauchi Masatake, Nishimura Mayumi, Tsuji Satsuki, Terada Minako, Sasanuma Motoe, Shimada Yoshiya

机构信息

Radiation Safety Research Centre, National Institute of Radiological Sciences 4-9-1 Anagawa, Inage, Chiba 263-8555, Japan.

出版信息

Mutat Res. 2002 Jun 19;503(1-2):43-9. doi: 10.1016/s0027-5107(02)00069-6.

Abstract

Mouse Pc-1 (Ms6-hm) is a hypervariable minisatellite locus that is unstable during intergenerational transmission. This hyper-instability of Pc-1 is useful for detecting germline mutation using a small number of experimental animals, although its molecular mechanism has not yet been elucidated. We examined the effect of severe combined immune deficiency (SCID) mutation on the spontaneous germline mutation at the Pc-1 locus using the CB17 mouse strain. Our results showed that the frequency of spontaneous germline mutation at Pc-1 in the offspring of wild-type parents was 9.7%. In F1 between SCID male and wild-type female, however, the frequency of germline mutation was drastically increased to 42.3%. When SCID female mice were mated with wild-type male, the frequency of germline mutation in F1 was slightly increased to 13.6%. These results suggest that DNA protein kinase catalytic subunit (DNA-PKcs), deficiency of which causes SCID mutation, plays an important role in the stable transmission of a genome containing hypervariable tandem repeats to progeny in male germ cells.

摘要

小鼠Pc-1(Ms6-hm)是一个高度可变的小卫星位点,在代际传递过程中不稳定。Pc-1的这种高度不稳定性有助于使用少量实验动物检测种系突变,尽管其分子机制尚未阐明。我们使用CB17小鼠品系研究了严重联合免疫缺陷(SCID)突变对Pc-1位点自发种系突变的影响。我们的结果表明,野生型亲本后代中Pc-1的自发种系突变频率为9.7%。然而,在SCID雄性与野生型雌性的F1代中,种系突变频率急剧增加至42.3%。当SCID雌性小鼠与野生型雄性交配时,F1代中的种系突变频率略有增加至13.6%。这些结果表明,DNA蛋白激酶催化亚基(DNA-PKcs)的缺乏会导致SCID突变,它在雄性生殖细胞中将含有高度可变串联重复序列的基因组稳定传递给后代的过程中起着重要作用。

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