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整合在小鼠X染色体上的LacZ转基因自发突变的DNA序列分析。

DNA sequence analysis of spontaneous mutations at a LacZ transgene integrated on the mouse X chromosome.

作者信息

Gossen J A, de Leeuw W J, Bakker A Q, Vijg J

机构信息

Ingeny BV, Leiden, The Netherlands.

出版信息

Mutagenesis. 1993 May;8(3):243-7. doi: 10.1093/mutage/8.3.243.

Abstract

Transgenic mice with integrated shuttle vectors containing the LacZ mutational target gene were used to study spontaneous mutational events in vivo. The transgenic mouse strain used carries the LacZ transgene on the X chromosome and was previously found to be characterized by approximately 25-fold higher spontaneous mutation frequency in liver and brain compared with at least three other transgenic mouse strains. To determine the nature of in vivo spontaneous mutational events, 35 mutant LacZ genes isolated from liver and brain of mice from strain 35.5 were analyzed at the DNA sequence level. The results obtained indicate that single base-pair changes were predominant in both liver and brain. However, in liver the majority of mutations were transitions whereas in brain transversions were predominantly observed. Six mutants appeared to contain multiple dispersed mutations, separated by as much as 44 bp. Mutations were generally located within a 500 bp region encoding the active site of the beta-galactosidase protein. Our results indicate that spontaneous mutations at the LacZ transgene are tissue specific and dependent on the chromosomal position of the LacZ transgene.

摘要

利用携带含有LacZ突变靶基因的整合穿梭载体的转基因小鼠来研究体内自发突变事件。所使用的转基因小鼠品系在X染色体上携带LacZ转基因,先前发现与至少其他三种转基因小鼠品系相比,其肝脏和大脑中的自发突变频率高约25倍。为了确定体内自发突变事件的性质,对从35.5品系小鼠的肝脏和大脑中分离出的35个突变LacZ基因进行了DNA序列水平分析。获得的结果表明,单碱基对变化在肝脏和大脑中均占主导地位。然而,在肝脏中,大多数突变是转换,而在大脑中主要观察到颠换。六个突变体似乎包含多个分散的突变,相隔多达44个碱基对。突变通常位于编码β-半乳糖苷酶蛋白活性位点的500 bp区域内。我们的结果表明,LacZ转基因的自发突变具有组织特异性,并取决于LacZ转基因的染色体位置。

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