A Shuttle Vector System for Studying Ionizing Radiation-Induced Mutagenesis in Mammalian Cells.
نویسندگان
چکیده
منابع مشابه
Rearrangement and mutagenesis of a shuttle vector plasmid after passage in mammalian cells.
A shuttle vector plasmid that contains sequences from simian virus 40, pBR322, and a bacterial marker gene, galactokinase, has been constructed. After replication in cells permissive for virus progeny, plasmid DNA was introduced into a galactokinase-deficient bacterial strain and the relative frequency of colonies with plasmids but without galactokinase activity was determined. This assay showe...
متن کاملHeteroduplex-induced mutagenesis in mammalian cells.
We have shown previously that heteroduplexes containing single-stranded loops are repaired efficiently in monkey cells, but not always correctly: 2% of the repair products acquired mutations within a 350 base-pair target (Weiss, U. and Wilson, J.H., Proc. Natl. Acad. Sci. USA 87:1123-1126, 1987). The structures of the mutant genomes, which are described here, are consistent with an error-prone ...
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Background: Quercetin has been reported to modulate cell proliferation and apoptosis. The present study aimed at identifying whether treatment of ionizing radiation (IR) combined with quercetin induces apoptosis in HepG2 cells. Materials and Methods: HepG2 cells were plated at an appropriate density according to each experimental scale and irradiated with 1, 5 and 10 Gy gamma-rays from a 60Co s...
متن کاملChemically induced mutagenesis in a shuttle vector with a low-background mutant frequency.
We have developed a recombinant DNA shuttle vector that permits the molecular analysis of mutations induced in human cells by chemical or physical mutagens. The vector is able to replicate as a plasmid in Escherichia coli and in Epstein-Barr virus (EBV)-transformed human lymphoblastoid cell lines and contains the herpes simplex virus type 1 thymidine kinase gene (HSV tk) as the target for mutag...
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ژورنال
عنوان ژورنال: Journal of Radiation Research
سال: 1993
ISSN: 0449-3060,1349-9157
DOI: 10.1269/jrr.34.148