Recio L, Bond J A, Pluta L J, Sisk S C
Chemical Industry Institute of Toxicology, Research Triangle Park, NC.
IARC Sci Publ. 1993(127):235-43.
We have examined the mutagenicity of 1,3-butadiene in vivo in transgenic mice constructed with lambda phage shuttle vectors that contain either lacZ or lacI as transgenes. Thus far, we have shown that butadiene is mutagenic to the lung of lacZ mice (CD2F1, 625 ppm butadiene, 6 h/day, 5 days) and to the bone marrow of lacI mice (B6C3F1, 62.5, 625, 1250 ppm butadiene, 6 h/day, 5 days/week, 4 weeks) exposed by inhalation to the same concentrations used previously in bioassays of the carcinogenicity of butadiene. Analysis of the DNA sequences of lacI mutants from the bone marrow of lacI mice demonstrated a shift in the spectrum of mutation from G:C base pairs in the control group to mutation at A:T base pairs in the exposed group. In addition, analysis of DNA sequences of mutations in three animals exposed to butadiene showed evidence of mutant clonal expansion in vivo. These results indicate that butadiene induces mutation in mouse tissues. Analysis of mutations at the level of DNA sequences is useful for examining the relationship between mutation and mutant frequencies in vivo and the spectrum of mutation in transgenic animals after exposures to carcinogens.
我们已经在用含有lacZ或lacI作为转基因的λ噬菌体穿梭载体构建的转基因小鼠体内检测了1,3 - 丁二烯的致突变性。到目前为止,我们已经表明,丁二烯对lacZ小鼠的肺(CD2F1,625 ppm丁二烯,每天6小时,共5天)以及对lacI小鼠的骨髓(B6C3F1,62.5、625、1250 ppm丁二烯,每天6小时,每周5天,共4周)具有致突变性,这些小鼠通过吸入暴露于先前丁二烯致癌性生物测定中使用的相同浓度。对来自lacI小鼠骨髓的lacI突变体的DNA序列分析表明,突变谱从对照组中的G:C碱基对转变为暴露组中的A:T碱基对。此外,对三只暴露于丁二烯的动物的突变DNA序列分析显示了体内突变克隆扩增的证据。这些结果表明丁二烯可在小鼠组织中诱导突变。在DNA序列水平上分析突变对于研究体内突变与突变频率之间的关系以及暴露于致癌物后转基因动物的突变谱是有用的。