首页> 外文期刊>Mutation Research: International Journal on Mutagenesis, Chromosome Breakage and Related Subjects >DNA fingerprint analysis in chemically mutagenized Chinese hamster lung cells.
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DNA fingerprint analysis in chemically mutagenized Chinese hamster lung cells.

机译:化学诱变的中国仓鼠肺细胞的DNA指纹分析。

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摘要

Using a multi-locus minisatellite Per-6 DNA probe, we performed DNA fingerprint analysis. Chinese hamster lung (CHL) cells were treated with six model chemicals: N-methyl-N'-nitro-N-nitrosoguanidine, mitomycin C, methyl methanesulfonate, furylfuramide, 2-acetylamino-fluorene, and cyclophosphamide, with or without S9 mix. 771 hypoxanthine phosphoribosyltransferase deficient clones (749 from mutagen-treated cells and 22 from untreated cells) and 90 unselected clones from untreated cells were isolated and analyzed. The spontaneous mutation frequency at CHL cell minisatellite loci was 0.31-0.63%. All the chemicals increased mutation frequencies. Almost all mutations localized to the three specific minisatellite loci corresponding to 4.2, 3.8, and 2.4 kb bands, suggesting that these regions are more unstable and susceptible to mutation. DNA fingerprint analysis is a promising technique for detecting mutations at neutral DNA regions, especially recombinational mutations, and may be useful for surveying genetic instability related to heritable defects or aging.
机译:使用多位点微型卫星Per-6 DNA探针,我们进行了DNA指纹分析。用六种模型化学物质处理中国仓鼠肺(CHL)细胞:N-甲基-N'-硝基-N-亚硝基胍,丝裂霉素C,甲磺酸甲酯,呋喃基呋喃酰胺,2-乙酰氨基芴和环磷酰胺,有或没有S9混合物。分离并分析了771个次黄嘌呤磷酸核糖基转移酶缺陷克隆(来自诱变处理细胞的749个和未处理细胞的22个)和90个未处理细胞的未选择克隆。 CHL细胞小卫星基因座的自发突变频率为0.31-0.63%。所有化学物质均增加了突变频率。几乎所有的突变都位于对应于4.2、3.8和2.4 kb波段的三个特定的小卫星基因座上,这表明这些区域更加不稳定并且易于突变。 DNA指纹分析是一种用于检测中性DNA区域的突变,特别是重组突变的有前途的技术,对于调查与遗传缺陷或衰老有关的遗传不稳定性可能很有用。

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