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首页> 外文期刊>The Journal of Biochemistry >DNA-based mutation assay GPMA (genome profiling-based mutation assay): reproducibility, parts-per-billion scale sensitivity, and introduction of a mammalian-cell-based approach
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DNA-based mutation assay GPMA (genome profiling-based mutation assay): reproducibility, parts-per-billion scale sensitivity, and introduction of a mammalian-cell-based approach

机译:基于DNA的突变检测GPMA(基于基于基于基于基于基于基于突变的突变测定):再现性,零件的规模敏感性,并引入哺乳动物 - 细胞的方法

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摘要

Genome profiling-based mutation assay (GPMA) is, to date, the only DNA sequence-based mutation assay that directly measures DNA alterations induced by mutagens. Here, the all-important congruence of mutagen assignment between DNA-based GPMA and the phenotype-based Ames test (the gold standard of mutagen assays) was confirmed qualitatively and semi-quantitatively by means of 94 chemical species (including previously examined 64). The high sensitivity (on the order of 10 ppb) and reproducibility of GPMA were also corroborated by the match between virtually independent experiments conducted in the distant past (10 years ago) and recently. Meanwhile, a standard experimental framework was established: the conditions of 100 parts per billion (ppb) concentration of a chemical and 15-generation culture of Escherichia coli. Moreover, a mammalian cell line (NIH 3T3) was shown to be suitable as a tester organism for the GPMA approach. Preliminary experimental results suggested that this approach can provide a qualitatively equivalent and quantitatively different mutagen assay results relative to the bacteria-based GPMA (renamed as bGPMA). This finding confirmed the effectiveness of the GPMA approach and indicates that mGPMA is a promising way to detect mammalian-cell mutagens.
机译:迄今为止,基因组分布的突变测定(GPMA)是唯一的基于DNA序列的突变测定,其直接测量由致诱变剂诱导的DNA改变。这里,通过94种化学物质(包括先前检查的64)定性和半定量确认基于DNA的GPMA和基于表型的AMES测试(包括先前检查64)的半定量证实了诱变基于DNA的GPMA和基于表型的AMES试验的全部重要组分通过在遥远过去(10年前)和最近的实际实验之间的几乎独立实验之间的匹配,高灵敏度(约10ppb阶)和GPMA的再现性也得到了证实。同时,建立了标准的实验框架:100亿百左右(PPB)浓度的大肠杆菌化学和15代培养物的条件。此外,显示哺乳动物细胞系(NIH 3T3)适合作为GPMA方法的测试器生物。初步实验结果表明,这种方法可以提供相对于基于细菌的GPMA(重命名为BGPMA)的定性等价和定量不同的诱变试验结果。这一发现证实了GPMA方法的有效性,并表明MGPMA是检测哺乳动物细胞诱变剂的有希望的方法。

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