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Plasmid mediated mutagenesis of a cellular gene in transfected eukaryotic cells

机译:质粒介导的转染真核细胞中细胞基因的诱变

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摘要

NIH3T3 cells are widely used in transformation assays and readily take up transfected DNA. A system has been devised using NIH3T3 cells to measure the mutagenic effect of transfected DNA on recipient cell genes. NIH3T3 cells can be mutated to 6-thioguanine resistance at a frequency which suggests that at least a portion of the cells have only one functional copy of the HGPRT gene. They have a low spontaneous background mutation frequency (≈1×10?7). Transfection of three different plasmids into NIH3T3 cells induced 6-thioguanine resistant mutants at frequencies ranging from 3 to 11 fold above background. The mutant phenotype is stable and reversion frequencies of several mutants are ≤1×10?7. Southern blot analysis of the HGPRT gene in several mutants showed that 4 of 26 mutants (15.4%) had detectable alterations in the structure of the HGPRT gene. Interestingly 3 of the 4 mutants showing rearrangements were obtained by transfection of the HSV-2 morphological transforming region.
机译:NIH3T3细胞被广泛用于转化分析,并易于吸收转染的DNA。已经设计出使用NIH3T3细胞的系统,以测量转染的DNA对受体细胞基因的诱变作用。 NIH3T3细胞可以某种频率突变成对6-硫鸟嘌呤的抗性,这表明至少一部分细胞仅具有HGPRT基因的一个功能拷贝。它们具有较低的自发背景突变频率(≈1×10 ?7 )。将三种不同质粒转染到NIH3T3细胞中,诱导的6硫代鸟嘌呤抗性突变体的频率比背景高3到11倍。突变体表型稳定,几个突变体的回复频率≤1×10 ?7 。对几个突变体中的HGPRT基因进行Southern印迹分析表明,在26个突变体中有4个(占15.4%)在HGPRT基因的结构中具有可检测的变化。有趣的是,通过转染HSV-2形态转化区获得了显示重排的4个突变体中的3个。

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