Imbalanced deoxyribonucleoside triphosphate pools and spontaneous mutation rates determined during dCMP deaminase-defective bacteriophage T4 infections

• Published in: The Journal of biological chemistry Vol. 262; no. 12; pp. 5546 - 5553
• Main Authors: Sargent, R.G., Mathews, C.K.
• Format: Journal Article
• Language: English
• Published: Bethesda, MD Elsevier Inc 25-04-1987; American Society for Biochemistry and Molecular Biology
• Subjects: Base Sequence; Biological and medical sciences; DCMP Deaminase - genetics; Deoxyribonucleotides - metabolism; Escherichia coli - genetics; Escherichia coli - metabolism; Fundamental and applied biological sciences. Psychology; Genes; Genes, Viral; Microbiology; Mutation; Nucleotide Deaminases - genetics; phage T4; Replicative cycle, interference, host-virus relations, pathogenicity, miscellaneous strains; T-Phages - genetics; T-Phages - metabolism; Virology; Virus; DCMP deaminase; Mutagenesis; Spontaneous; Bactériophage T4; Nucleotide; Virus replication cycle; Pool; Mutation; Defectivity; Mechanism
• ISSN: 0021-9258; 1083-351X
• DOI: 10.1016/S0021-9258(18)45607-4

DNA precursor imbalances are known to be mutagenic in both eukaryotic and prokaryotic systems. Almost certainly, such mutagenesis involves competition between correctly and incorrectly base-paired precursors at replication sites. Since other factors may be involved, it is important to identify specific mutations induced by specific pool imbalances. Using bacteriophage T4, we have developed a system for such analysis. We prepare double mutants of T4; one mutation affects a phage-coded enzyme of deoxyribonucleoside triphosphate (dNTP) metabolism, while the second is an rII mutation known to revert along a specific pathway. We determine dNTP pools in infection by such a mutant and measure both the spontaneous reversion rate of the rII mutation and, in some cases, the nucleotide sequence at the mutant site. In this paper we analyze mutations induced by a deficiency of T4-encoded deoxycytidylate deaminase. This causes pools of 5-hydroxymethyl-dCTP to expand some 30-fold, while dTTP pools contract. This specifically stimulates AT-to-GC reversion. One of the four AT-to-GC reverters tested, rIIUV215, increases its reversion rate at least 1000-fold under these pool-imbalance conditions, while the other mutants tested show increases of only about 10-fold. Therefore, factors other than dNTP competition, including local DNA sequence environment, must be invoked to fully explain mechanisms of dNTP pool imbalance-induced mutagenesis. We discuss models for this, and we also report unexpected effects of the dCMP deaminase deficiency upon pools of ribonucleoside triphosphates.