首页> 外文期刊>Mutation Research: International Journal on Mutagenesis, Chromosome Breakage and Related Subjects >X-ray induction of microsatellite instability at autosomal loci in human lymphoblastoid WTK1 cells
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X-ray induction of microsatellite instability at autosomal loci in human lymphoblastoid WTK1 cells

机译:X射线诱导人淋巴母细胞WTK1细胞中常染色体基因座的微卫星不稳定性

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Many models of carcinogenesis posit that multiple genetic events are required for a normal cell to become cancerous. As the mutation rate of a single gene is in the range of 10(-8) to 10(-5) per cell division, a central question remains, how does a single cell acquire multiple mutations? One hypothesis, originally articulated by Loeb [10], proposed that some mutations may not be isolated events, but are associated with a mutator phenotype that leads to the occurrence of additional mutations elsewhere in the cellular genome. To test this hypothesis, we utilized a human lymphoblastoid cell line (WTK1) that is known to be hypermutable at the autosomal thymidine kinase (TK) locus. We isolated 139 independent clones which were selected for new TK mutations that arose either spontaneously or as the result of a single X-ray exposure of 1.5 Gy. These clones were examined for second-site alterations in several microsatellite loci scattered throughout the genome using polymerase chain reaction (PCR) amplification followed by both denaturing gel electrophoresis and single-stranded conformational polymorphism (SSCP) analysis. Of these clones, 21 exhibited second-site mutations primarily involving loss of heterozygosity, 17 arose from irradiated cells whereas the remaining four arose from non-irradiated cells. We further examined the 17 clones which exhibited alterations specifically at the D16S265 locus; alterations at this site were associated with an enhanced frequency of mutations at other loci in the same region of chromosome 16q, but were not associated with additional mutations at other sites in the genome. Furthermore, new mutations arose in loci on 16q when these clones were propagated for 6 months in culture. Overall, these results support the hypothesis that radiation can induce a type of genetic instability which may facilitate the occurrence of multiple mutations throughout the genome in a small population of exposed cells. Furthermore, some cells may possess localized regions in the genome which are highly sensitive to the induction of instability. (C) 2001 Elsevier Science B.V. Ail rights reserved. [References: 38]
机译:许多致癌模型认为,正常细胞发生癌变需要多种遗传事件。由于每个细胞分裂中单个基因的突变率在10(-8)到10(-5)之间,一个中心问题仍然存在,即单个细胞如何获得多个突变? Loeb最初提出的一个假说[10]提出某些突变可能不是孤立的事件,而是与导致细胞基因组其他地方发生其他突变的突变体表型有关。为了验证这一假设,我们利用了已知在常染色体胸苷激酶(TK)基因座处高度可变的人类淋巴母细胞系(WTK1)。我们分离了139个独立克隆,这些克隆被选择用于新的TK突变,这些突变是自发产生的,或者是由于1.5 Gy的单次X射线暴露而产生的。使用聚合酶链反应(PCR)扩增,然后变性凝胶电泳和单链构象多态性(SSCP)分析,检查了这些克隆在分散在整个基因组中的几个微卫星基因座中的第二位点改变。在这些克隆中,有21个显示出第二位突变,主要涉及杂合性的丧失,其中17个来自辐照细胞,而其余四个则来自非辐照细胞。我们进一步检查了17个克隆,它们在D16S265基因座处表现出特异性的改变。该位点的改变与染色体16q相同区域中其他基因座的突变频率增加有关,但与基因组其他位点的其他突变无关。此外,当这些克隆在培养物中繁殖6个月时,在16q处基因座中出现了新的突变。总体而言,这些结果支持以下假设:辐射可诱发某种类型的遗传不稳定性,这可能会促进在少数暴露细胞中整个基因组中发生多个突变。此外,一些细胞可能在基因组中具有对诱导不稳定性高度敏感的局部区域。 (C)2001 Elsevier Science B.V. Ail版权所有。 [参考:38]

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