Transcription-induced mutations: increase in C to T mutations in the nontranscribed strand during transcription in Escherichia coli.

Cytosines in single-stranded DNA deaminate to uracils at 140 times the rate for cytosines in double-stranded DNA. If resulting uracils are not replaced with cytosine, C to T mutations occur. These facts suggest that cellular processes such as transcription that create single-stranded DNA should promote C to T mutations. We tested this hypothesis with the Escherichia coli tac promoter and found that induction of transcription causes approximately 4-fold increase in the frequency of C to U or 5-methylcytosine to T deaminations in the nontranscribed strand. Excess mutations caused by C to U deaminations were reduced, but not eliminated, by uracil-DNA glycosylase. Similarly, mutations caused by 5-methylcytosine to T deaminations were only partially reduced by the very short-patch repair process in E.coli. These effects are unlikely to be caused by differential repair of the two strands, and our results suggest that all actively transcribed genes in E. coli should acquire more C to T mutations in the nontranscribed strand.

[1]  T. Vartiainen,et al.  Genotoxic effects of the drinking water mutagen 3-chloro-4-(dichloromethyl)-5-hydroxy-2[5H]-furanone (MX) in mammalian cells in vitro and in rats in vivo. , 1991, Mutation research.

[2]  H. Hayatsu,et al.  Bisulfite modification of nucleic acids and their constituents. , 1976, Progress in nucleic acid research and molecular biology.

[3]  D. S. Hsu,et al.  Substrate spectrum of human excinuclease: repair of abasic sites, methylated bases, mismatches, and bulky adducts. , 1994, Proceedings of the National Academy of Sciences of the United States of America.

[4]  A. Bhagwat,et al.  A gene required for very short patch repair in Escherichia coli is adjacent to the DNA cytosine methylase gene , 1990, Journal of bacteriology.

[5]  C. Harris,et al.  Mutations in the p53 tumor suppressor gene: clues to cancer etiology and molecular pathogenesis. , 1994, Cancer research.

[6]  J. A. Halliday,et al.  Mechanisms of spontaneous mutation in DNA repair-proficient Escherichia coli. , 1991, Mutation research.

[7]  M. Lieb,et al.  Spontaneous mutation at a 5-methylcytosine hotspot is prevented by very short patch (VSP) mismatch repair. , 1991, Genetics.

[8]  B. Glickman,et al.  Sites of preferential induction of cyclobutane pyrimidine dimers in the nontranscribed strand of lacI correspond with sites of UV-induced mutation in Escherichia coli. , 1991, The Journal of biological chemistry.

[9]  M Lieb,et al.  Very short patch repair: reducing the cost of cytosine methylation , 1996, Molecular microbiology.

[10]  P. Jones,et al.  The rate of hydrolytic deamination of 5-methylcytosine in double-stranded DNA. , 1994, Nucleic acids research.

[11]  Keith C. Norris,et al.  DNA cytosine methylation and heat-induced deamination , 1986, Bioscience reports.

[12]  G. Douglas,et al.  Sequence spectra of spontaneous lacZ gene mutations in transgenic mouse somatic and germline tissues. , 1994, Mutagenesis.

[13]  W. Summers A simple method for extraction of RNA from E. coli utilizing diethyl pyrocarbonate. , 1970, Analytical biochemistry.

[14]  T. Kunkel,et al.  Activities and incision patterns of ABC excinuclease on modified DNA containing single-base mismatches and extrahelical bases. , 1986, The Journal of biological chemistry.

[15]  M. Dreyfus,et al.  Bacteriophage T7 RNA polymerase travels far ahead of ribosomes in vivo , 1992, Journal of bacteriology.

[16]  C. Hedgcoth,et al.  Determination of 5,6-dihydrouridine in ribonucleic acid. , 1970, Analytical biochemistry.

[17]  A. Skandalis,et al.  Strand bias in mutation involving 5-methylcytosine deamination in the human hprt gene. , 1994, Mutation research.

[18]  A. Bhagwat,et al.  A cytosine methyltransferase converts 5-methylcytosine in DNA to thymine. , 1995, Biochemistry.

[19]  B. Weiss,et al.  Specific mutator effects of ung (uracil-DNA glycosylase) mutations in Escherichia coli , 1982, Journal of bacteriology.

[20]  H. Fritz,et al.  The vsr gene product of E. coli K-12 is a strand- and sequence-specific DNA mismatch endonuclease , 1991, Nature.

[21]  M. Wyszynski,et al.  Cytosine deaminations catalyzed by DNA cytosine methyltransferases are unlikely to be the major cause of mutational hot spots at sites of cytosine methylation in Escherichia coli. , 1994, Proceedings of the National Academy of Sciences of the United States of America.

[22]  J. Gralla,et al.  Lac UV5 transcription in vitro. Rate limitation subsequent to formation of an RNA polymerase-DNA complex. , 1979, Biochemistry.

[23]  M. Borgerding,et al.  Inhibitory activity of cigarette-smoke condensate on the mutagenicity of heterocyclic amines. , 1994, Mutation research.

[24]  A. Bhagwat,et al.  Overproduction of DNA Cytosine Methyltransferases Causes Methylation and C T Mutations at Non-canonical Sites (*) , 1996, The Journal of Biological Chemistry.

[25]  P. D. de Jong,et al.  Spectrum of spontaneous mutation at the APRT locus of Chinese hamster ovary cells: an analysis at the DNA sequence level. , 1988, Proceedings of the National Academy of Sciences of the United States of America.

[26]  J. Brosius,et al.  Vectors bearing a hybrid trp-lac promoter useful for regulated expression of cloned genes in Escherichia coli. , 1983, Gene.

[27]  A. Datta,et al.  Association of increased spontaneous mutation rates with high levels of transcription in yeast. , 1995, Science.

[28]  T. Lindahl An N-glycosidase from Escherichia coli that releases free uracil from DNA containing deaminated cytosine residues. , 1974, Proceedings of the National Academy of Sciences of the United States of America.

[29]  H. Vrieling,et al.  DNA strand specificity for UV-induced mutations in mammalian cells , 1989, Molecular and cellular biology.

[30]  J. Roberts,et al.  Structure of transcription elongation complexes in vivo. , 1992, Science.

[31]  Philip J. Farabaugh,et al.  Molecular basis of base substitution hotspots in Escherichia coli , 1978, Nature.

[32]  T. Kunkel,et al.  A sensitive genetic assay for the detection of cytosine deamination: determination of rate constants and the activation energy. , 1990, Biochemistry.

[33]  P. Hanawalt,et al.  Repair of N-methylpurines in specific DNA sequences in Chinese hamster ovary cells: absence of strand specificity in the dihydrofolate reductase gene. , 1989, Proceedings of the National Academy of Sciences of the United States of America.

[34]  T. Kunkel,et al.  Cytosine deamination in mismatched base pairs. , 1993, Biochemistry.

[35]  P. Hanawalt,et al.  Selective removal of transcription-blocking DNA damage from the transcribed strand of the mammalian DHFR gene , 1987, Cell.

[36]  P. Hanawalt,et al.  Induction of the Escherichia coli lactose operon selectively increases repair of its transcribed DNA strand , 1989, Nature.

[37]  B. D. Davis,et al.  Transcriptional bias: a non-Lamarckian mechanism for substrate-induced mutations. , 1989, Proceedings of the National Academy of Sciences of the United States of America.

[38]  B Nyberg,et al.  Heat-induced deamination of cytosine residues in deoxyribonucleic acid. , 1974, Biochemistry.

[39]  H. Ochman,et al.  Asymmetries Generated by Transcription-Coupled Repair in Enterobacterial Genes , 1996, Science.

[40]  M. Wyszynski,et al.  HpaII methyltransferase is mutagenic in Escherichia coli , 1995, Journal of bacteriology.