Article
Sequence-dependent mutations in a shuttle vector plasmid replicated in a mismatch repair deficient human cell line.
Carcinogenesis - 1 Jul 1999
Tobi S E, Levy D D, Seidman1 M M, Kraemer1 K H
Abstract excerpt
We utilized a shuttle vector plasmid (pLSC) to assess the role of DNA sequence and mismatch repair on mutagenesis in human cells. pLSC contains an interrupted 29 bp mononucleotide poly(G) run within a bacterial suppressor tRNA gene, which acts as a highly sensitive mutagenic target for detection of base substitution and frameshift mutations. The frequency of spontaneous mutations in pLSC was found to be similar...
Topics
- Base Pair Mismatch
- Base Sequence
- Cell Line
- DNA Mutational Analysis
- DNA Repair
- DNA Replication
- Genes, Suppressor
- Genetic Vectors
- Humans
- Molecular Sequence Data
- Mutagenesis
- Mutation
- Plasmids
- RNA, Transfer
- Sequence Deletion
- Ultraviolet Rays
