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Susceptibility loci for radiation lymphomagenesis in mice

机译:小鼠辐射淋巴瘤的敏感性基因座

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BALB/c and STS mice are susceptible and resistant, respectively, to radiation lymphomagenesis. Our previous study suggested that Prkdc encoding DNA-dependent protein kinase (DNA-PKcs) is a candidate for the lymphoma susceptibility locus on chromosome 16. The STS-derived segment with the wild-type Prkdc allele confers resistance in BALB/c, a variant defective in DNA-PKcs. The presence of a lymphoma susceptibility locus on chromosome 4 has also been suggested. To assess the effects of these loci on the susceptibility, we subjected chromosome 16 and chromosome 4 congenic lines by 4x 1.1 and/or 1.7 Gy of X-irradiation. In the chromosome 16 congenic lines carrying the wild-type STS allele at Prkdc, lymphoma resistance was prominent after 4x1.1 Gy of X-irradiation, but modest at 4 x 1.7 Gy. Mice with the proximal half of STS-derived chromosome 4 showed resistance to the induction of lymphomas by the 4 x 1,7 Gy X-irradiation procedure. Thus, lymphoma susceptibility is controlled by more than one gene with differenteffects.
机译:BALB / C和STS小鼠分别对放射性淋巴瘤进行敏感和抗性。我们以前的研究表明,PRKDC编码DNA依赖性蛋白激酶(DNA-PKC)是染色体16的淋巴瘤敏感性座位的候选者。与野生型PRKDC等位基因的STS衍生的区段赋予BALB / C的抗性,变体DNA-PKCS有缺陷。还提出了染色体4上的淋巴瘤敏感性座位的存在。为了评估这些基因座对易感性的影响,我们通过4×1.1和/或1.7Gy进行染色体16和染色体4个Congenic系的X辐射。在Prkdc携带野生型STS等位基因的染色体16系上,X-1 GY在X-辐射4×11g后突出,但适度为4 x 1.7 GY。具有近一半的STS衍生的染色体4的小鼠显示了4×1,7 Gy X-辐照程序的诱导淋巴瘤的抗性。因此,淋巴瘤易感性由具有不同效应的多种基因控制。

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