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转基因小鼠体细胞和生殖细胞组织中自发lacZ基因突变的序列谱。

Sequence spectra of spontaneous lacZ gene mutations in transgenic mouse somatic and germline tissues.

作者信息

Douglas G R, Gingerich J D, Gossen J A, Bartlett S A

机构信息

Harvard Medical School, Beth Israel Hospital, Boston, MA 02215.

出版信息

Mutagenesis. 1994 Sep;9(5):451-8. doi: 10.1093/mutage/9.5.451.

Abstract

As a critical step in determining whether transgenic mouse gene mutation systems are suitable models for the detection and quantification of induced gene mutations in vivo, spontaneous mutant frequencies and mutation spectra have been characterized for liver, bone marrow, and male germ cells of the lacZ transgenic mouse strain 40.6. The lacZ transgene is carried on a recombinant bacteriophage lambda shuttle vector that is recovered from mouse genomic DNA, and analysed in vitro for mutations that occurred in the mouse tissues. Mutations are detected visually as clear or pale blue plaques when X-gal is the substrate for beta-galactosidase; whereas, the wild-type plaques are dark blue. There was no statistical difference in the mutant frequency among the three tissues studied, the pooled mutant frequency being 2.23 +/- 0.41 per 10(5) pfu. The predominant type of mutation was GC-->AT transitions, with most occurring in 5'-CpG dinucleotides, suggesting that the deamination of 5-methylcytosine is the main mechanism of mutagenesis. There was, however, a statistically significant difference in the base pair substitution mutation spectrum for the liver and bone marrow when mutations were grouped according to GC or AT base-pairs. The proportion of transition versus transversion mutations was also statistically different among the three tissues, resulting mainly from the fact that germ cells were different from both bone marrow and liver. A lower number of spontaneous transitions in male germ cells was accompanied by an increase in transversions, with the proportion of GC-->AT transitions in 5'-CpG sites also declining.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

作为确定转基因小鼠基因突变系统是否适合用于体内诱导基因突变检测和定量的关键步骤,已对lacZ转基因小鼠品系40.6的肝脏、骨髓和雄性生殖细胞的自发突变频率及突变谱进行了表征。lacZ转基因携带在一种重组噬菌体λ穿梭载体上,该载体从小鼠基因组DNA中回收,并在体外分析小鼠组织中发生的突变。当以X-gal作为β-半乳糖苷酶的底物时,突变可通过肉眼检测为清晰或淡蓝色噬菌斑;而野生型噬菌斑为深蓝色。在所研究的三种组织中,突变频率无统计学差异,合并突变频率为每10(5)个噬菌斑形成单位2.23±0.41。主要的突变类型是GC→AT转换,大多数发生在5'-CpG二核苷酸中,这表明5-甲基胞嘧啶的脱氨基是诱变的主要机制。然而,当根据GC或AT碱基对将突变分组时,肝脏和骨髓的碱基对替换突变谱存在统计学显著差异。三种组织中转换突变与颠换突变的比例也存在统计学差异,这主要是因为生殖细胞与骨髓和肝脏均不同。雄性生殖细胞中自发转换的数量较少,同时颠换增加,5'-CpG位点中GC→AT转换的比例也下降。(摘要截短于250字)

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