首页> 美国卫生研究院文献>Environmental Health Perspectives >Mutations induced in the hypoxanthine phosphoribosyl transferase gene by three urban air pollutants: acetaldehyde benzoapyrene diolepoxide and ethylene oxide.
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Mutations induced in the hypoxanthine phosphoribosyl transferase gene by three urban air pollutants: acetaldehyde benzoapyrene diolepoxide and ethylene oxide.

机译:次黄嘌呤磷酸核糖基转移酶基因由三种城市空气污染物引起的突变:乙醛苯并a二醇环氧乙烷和环氧乙烷。

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摘要

Provisional mutational spectra at the hypoxanthine phosphoribosyl transferase (HPRT) locus in vitro have been worked out for acetaldehyde (AA) and benzo[a]pyrene diolepoxide (BPDE) in human (T)-lymphocytes and for ethylene oxide (EtO) in human diploid fibroblasts using Southern blotting and polymerase chain reaction (PCR)-based DNA sequencing techniques. The results indicate that large genomic deletions are the predominating hprt mutations caused by AA and EO, whereas BPDE induces point mutations that are mainly GC > TA transversions. The mutational spectra induced by the three agents are clearly different from the background spectrum in human T-cells. Thus, the hprt locus is a useful target for the study of chemical-specific mutational events that may help identify causes of background mutation in human cells in vivo.
机译:研究了次黄嘌呤磷酸核糖基转移酶(HPRT)基因座在体外的临时突变谱,用于人(T)淋巴细胞中的乙醛(AA)和苯并[a] py二醇环氧(BPDE)以及人二倍体中的环氧乙烷(EtO)。成纤维细胞使用Southern印迹和基于聚合酶链反应(PCR)的DNA测序技术。结果表明,大的基因组缺失是AA和EO引起的主要hprt突变,而BPDE诱导的点突变主要是GC> TA转化。这三种试剂诱导的突变谱与人T细胞的背景谱明显不同。因此,hprt基因座是研究化学特异性突变事件的有用靶点,该事件可能有助于确定体内人细胞背景突变的原因。

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