Spontaneous germline mutations generate genetic diversity in populations of sexually reproductive organisms and are thus regarded as a driving force of evolution. However, the cause and mechanism remain unclear. 8-oxoguanine (8-oxoG) is a candidate molecule that causes germline mutations, because it makes DNA more prone to mutation and is constantly generated by reactive oxygen species in vivo. We show here that endogenous 8-oxoG caused de novo spontaneous and heritable G to T mutations in mice, which occurred at different stages in the germ cell lineage and were distributed throughout the chromosomes. Using exome analyses covering 40.9 Mb of mouse transcribed regions, we found increased frequencies of G to T mutations at a rate of 2 × 10−7 mutations/base/generation in offspring of Mth1/Ogg1/Mutyh triple knockout (TOY-KO) mice, which accumulate 8-oxoG in the nuclear DNA of gonadal cells. The roles of MTH1, OGG1 and MUTYH are specific for the prevention of 8-oxoG-induced mutation and 99% of the mutations observed in TOY-KO mice were G to T transversions caused by 8-oxoG; therefore, we concluded that 8-oxoG is a causative molecule for spontaneous and inheritable mutations of the germ lineage cells.
Evolution requires de novo germline mutations that are newly generated in germ lineage cells and inheritable to the offspring. It is evident that germline mutations occur, because sporadic and deleterious mutations that cannot be transmitted to offspring continuously appear in human populations1,2,3,4. The human de novo germline mutation rate is estimated to be 1.20 × 10−8/nucleotide/generation1. However, the cause and mechanism of mutations in the germ cell lineage remain unclear. We hypothesized that the cause of these mutations would be endogenously and spontaneously generated and remain in the germ cell lineage. 8-oxoG is one of the candidate molecules for causing germline mutation, because it is endogenously generated by reactive oxygen species (ROS) derived from cellular respiration, constitutively exists in DNA5 and is known to cause G to T and A to C transversion mutations by the ability to pair with A as well as C during DNA replication6,7,8.
Mammals possess three enzymes to avoid 8-oxoG-induced mutations. MTH1 (mutT homologue 1, NUDT1) degrades 8-oxodGTP in the nucleotide pool to prevent its incorporation into DNA9. OGG1 (8-oxoG DNA glycosylase) excises 8-oxoG from DNA10,11 and MUTYH (mutY homologue, adenine DNA glycosylase) removes adenine misincorporated opposite 8-oxoG in DNA12. We and other groups have reported that mice deficient in these enzymes are prone to developing cancer, indicating a mutator phenotype in somatic cells13,14,15,16. MUTYH is also responsible for MUTYH-associated polyposis in humans17.
To evaluate the contribution of 8-oxoG to de novo germline mutation, we established the Mth1/Ogg1/Mutyh triple knockout (TOY-KO) mice, in which unrepaired endogenous 8-oxoG accumulates in the genome DNA. In this paper, using the TOY-KO mice, we showed that 8-oxoG causes G to T mutations in germ lineage cells (Supplementary Fig. S1 online).
Spontaneous mutations increased in Mth1−/−/Ogg1−/−/Mutyh−/− (TOY-KO) mice
To evaluate the contribution of 8-oxoG to de novo germline mutation, we established the TOY-KO mouse in the C57BL/6J background (>N16). TOY-KO mice are viable and fertile, although increased amounts of 8-oxoG accumulated in various tissues, including the gonads (Fig. 1a). Moreover, TOY-KO mice had a shorter lifespan (Fig. 1b) and developed various types of tumors (Fig. 1c). We maintained the TOY-KO mouse line originating from one pair (G1) to the 8th generation (G8) by intragenerational mating (Supplementary Fig. S2 online). More than 35% of TOY-KO mice carried macroscopically distinguishable tumors (Supplementary Fig. S2 online). As the generations increased, it became difficult to obtain mice for breeding because of the decreased number of weaned mice (Fig. 1d). Several phenotypic variations were found among the progeny, such as hydrocephalus, belly white spot and anophthalmia (Supplementary Fig. S2 online). In cases of hydrocephalus and white spot, the traits were transmitted to the next generation in an autosomal dominant fashion with incomplete penetrance (Fig. 2, Supplementary Fig. S2 online). These features indicate that heritable mutations could arise in the TOY-KO mice.
To detect mutations that occur in the germ cell lineage and are transmitted across generations of TOY-KO mice, we performed whole exome sequencing analysis (Fig. 3a). We searched for different sequences between the C57BL/6J mouse reference genome (MGSCv37) and TOY-KO mice that belonged to the most advanced generation of each branch of the pedigree (TOY365F, TOY609F and TOY450F, shown in Fig. 3b). No sequencing reads corresponding to parts of the wild-type reference sequences of targeted Mutyh, Mth1 and Ogg1 loci were obtained in chromosomes 4, 5 and 6, respectively (Supplementary Fig. S3 online), which confirmed that the TOY-KO mouse was indeed deficient for the three genes and validated our exome analysis. By analyzing the exome covering 40.9 Mb of mouse transcribed sequences, which included 19,427 genes from 17 chromosomes, excluding chromosomes 4, 5 and 6 from the analysis to avoid ambiguity, we identified 262 base substitution mutations (Fig. 3c, Supplementary Table S1 online, Supplementary Data S1 online). No insertion/deletion mutations were detected in this analysis.
Identification of mutation origin mice
The 262 mutations detected in TOY365F, TOY609F and TOY450F had occurred in one of the mice in the 8-generations of the pedigree (Fig. 3b); therefore, we determined the mutation origin mouse that initially possessed the mutated allele in its tail DNA. We traced each mutation on the pedigree by determining the sequences of all mutated alleles in 35 TOY-KO mice shown in the pedigree (Fig. 3b), using MassArray or Sanger's sequencing and identified the origin of each de novo mutation. The results of the sequencing are summarized in Supplementary Data S1 online with annotations. Among them, we considered that 247 mutations found in G2–G8 mice had spontaneously occurred in the germ cell lineage of TOY-KO mice, because these mutated alleles were derived from gametes of their parent mice (G1–G7) or were generated during early development of the mice (G2–G8). The spectrum of germline mutation observed in TOY-KO mice indicated a distinct feature: 99% (244/247) of the mutations were G to T transversions (Table 1). G to T mutations had specifically increased in TOY-KO mice lacking the ability to avoid 8-oxoG-induced mutations; therefore, we concluded that 8-oxoG is a causative molecule for spontaneous G to T mutation in the mouse germ cell lineage. These mutations arose in all progeny of each generation and in all chromosomes that we analyzed (Figs. 4 and 5a). The mutations ranged from synonymous substitutions to harmful mutations, such as a gain of a stop codon in the Ttn gene responsible for human hypertrophic cardiomyopathy18 (Supplementary Data S1 online).
By analyzing the position of the mutated G in di- and tri-nucleotide sequences, we found that G to T mutations occurred more often at GpC sites than at CpG sites and tended to occur at tri-nucleotides, which are typical sequences found in triplet repeat expansion disorders (Fig. 5b, c), such as CAG (Huntington's disease), CTG (Myotonic dystrophy) and GAA (Friedreich ataxia)19. It is probable that uneven distribution of mutable 8-oxoG is reflected by the tendency for DNA oxidation, or by the site preference of DNA polymerases in incorporating 8-oxodGTP. We also detected two G to A and one A to G transition mutations that were classified as synonymous coding or intronic mutations (Table 1, Supplementary Data S1 online).
De novo germline mutation rate of TOY-KO mouse
The detected mutations accumulated in TOY365F, TOY450F and TOY609F contained parts of the mutations that had occurred in the germ cells of the ancestral mice, because only half of the chromosomes derived from the father and mother had transmitted to the offspring via gametogenesis and fertilization in each generation. The numbers of newly arisen mutations detected only in TOY365F, TOY450F and TOY609F were 13, 18 and 18, respectively (Fig. 3b). Therefore, the de novo germline mutation rate was calculated to be 2.0 × 10−7/base/generation (13 + 18 + 18/3/40.9 Mb × 2/generation). This mutation rate is 18-fold higher than the basal level, 1.1 × 10−8 mutations/base/generation, calculated from the specific locus test in mice20. For human trio analysis1, the germline mutation rate was calculated to be 1.2 × 10−8 mutation/base/generation and the G to T transversion mutation was observed in about 9% of all mutations. These results indicated that an approximately 200-fold increase in G to T transversion mutations occurred in the TOY-KO mice. No G to A transition mutations occurred in TOY365F, TOY450F and TOY609F (totaling 245.4 Mb); therefore, the background mutation level of the TOY-KO mouse was estimated to be less than 4.1 × 10−9 G to A transition mutation/base/generation. This background mutation level is not high compared with that in humans (4.9 × 10−9 G to A transition mutation/base/generation)1.
Fates of de novo germline mutations
By following up the mutated alleles in the pedigree, we observed the fates of the de novo mutations, in which some were fixed and others were eliminated in later generations. As shown in Fig. 6, for example, mutation #187 initially appeared in TOY108M (G3) as a heterozygous allele, indicating that the mutation probably occurred in the germ cell lineage of the parents, either TOY77M or TOY84F and was transmitted to the progeny. At G5, it became homozygous in TOY138M and TOY131F and thus fixed in the progeny. Conversely, in another branch, the mutant allele was not transmitted to the offspring and eventually disappeared. These behaviors of the mutated allele represent the appearance, transmission, fixation and disappearance of a spontaneous mutation, which are the typical fates of a novel mutation in the evolutionary process.
Little research has been performed to identify the causative molecule of spontaneous germline mutations because it is a rare event. We considered that the causative molecule must possess certain features that make DNA more prone to mutation, be generated endogenously and spontaneously and remain in the germ cell lineage. In 2006, we reported that endogenous 8-oxoG is distributed in the genome of human lymphocytes in the steady state5. We hypothesized that 8-oxoG also exists in the genome of germ lineage cells and is responsible for spontaneous de novo germline mutations, because 8-oxoG is endogenously generated by ROS derived from cellular respiration and is known to cause transversion mutations. By disruption of the 8-oxoG exclusion system in mice, we detected increased spontaneous accumulation of germline mutations during the generations. These mutations were distributed throughout the chromosomes and inheritable to offspring across the generations, leading to an expansion of genetic diversity as well as disease-associated mutations.
The effects of 8-oxoG on spontaneous germline mutations were apparent in the TOY-KO mice. However, the production of 8-oxoG is dependent on the oxidation of guanine nucleotides, which occurs even in the wild-type cells independently of MTH1, OGG1 and MUTYH activities. It is likely that 8-oxoG universally causes de novo G-T transversion mutations, including germline mutations, although most of these mutations are efficiently prevented by the MTH1, OGG1 and MUTYH enzyme system.
When did the germline mutations occur? It is difficult to determine the timing of the occurrence of a mutation in the germ cell lineage; however, some examples were obtained that allowed us to speculate on the timing of mutations in our experiment. De novo mutations occur either in the germ cell lineage of the previous generation or during the very early developmental stage of the mutant mouse (Fig. 7). In eleven cases among 247 mutations, the mutations had likely occurred in the germ cell lineage of the parents, because the original mutated allele was detected in multiple mice of the same generation (Fig. 3b). For three mutations on the X chromosome (Mutation ID #257, #261 and #262), which began in males with a heterozygous status (Supplementary Fig. S4 online), the mutation probably occurred in a cell at an early stage of embryonic development, resulting in mosaicism of tail tissue. These results showed that the germline mutations occurred at different developmental stages of the germ cell lineage. It is noteworthy that most germline mutations occurred during mitoses, because the germ cell lineage from fertilized egg to differentiated sperm or egg requires a large number of mitoses and only one meiosis. In the other cases (233/247) shown in Fig. 3b (G2–G8), the original mutated allele was found in a single mouse of each generation and we could not identify when the mutation occurred.
By analogy to the Escherichia coli system, we considered that 8-oxoG-induced G to T mutation is suppressed by OGG1, MUTYH and MTH1, whereas the A to C mutation is prevented by MTH1 in mammalian cells (Supplementary Fig. S5 online). However, in contrast to the E. colimutT, mutM, mutY triple mutant, in which both G to T and A to C mutations increased21, no A to C germline mutations were detected in the TOY-KO mouse. Thus, it is likely that different mechanisms, such as mismatch repair22 or proof reading by DNA polymerase, may function to avoid A to C mutations caused by 8-oxodGTP in the TOY-KO mouse, even in the absence of MTH1. It has been reported that 2-hydroxy-deoxyadenosine (2-OHdA), an oxidized form of deoxyadenosine, is recognized as a substrate by the MUTYH protein and possesses premutagenic features23,24. 2-OHdATP, a triphosphate form of 2-OHdA, is a substrate of the MTH1 protein25. The MutY and MutT proteins of E. coli cannot recognize 2-OHdA, in contrast to the mammalian enzymes24,26. At the present, we cannot evaluate the contribution of 2-OHdA to the increase of germline mutation observed in TOY-KO mice, because we have not yet confirmed the accumulation of 2-OHdA in the DNA. Thus, the significance of 2-OHdA for germline mutations remains to be elucidated.
The TOY-KO mouse strain spontaneously accumulates mutations in the homozygous status. For genome-wide screening of mutants, this mouse has unique features and has the potential to take a complementary role to ENU mutagenesis27,28. The mutation is specific for G to T transversions and occurs spontaneously and continuously in both male and female germ lineage cells of TOY-KO mice. The mutation rate of TOY-KO mice (0.2 mutation/Mb/generation, on average, in male and female) is lower than ENU-treated male gametes (1 mutation/0.42–1.82 Mb for male mouse27, 1 mutation/3.7 Mb in male rat28); however, the number of mutations carried by each TOY-KO mouse increased as the generations increased. Similar to ENU mutagenesis, phenotype-driven screening is available. Currently, the TOY-KO mouse is only available in the C57BL/6J genetic background; however, it would be a good system for large genome-wide screening of dominant mutations. Using such mutator mice with a well-controlled genetic background would permit the evaluation of the contribution of aging and the difference between spermatogenesis and oogenesis on the accumulation of germline mutations. This system also enables us to assess the genotoxic effects of chemical and environmental factors on mammalian germ lineage cells.
Although de novo germline mutations cause sporadic genetic diseases in humans, their occurrence is an important step for the evolution of species, as well as selection for survival. 8-oxoG, one of the causative molecules of these mutations, is endogenously produced by ROS generated from biological processes, such as oxygen respiration and inflammation and is widely present in the DNA of various organisms. It is likely that the oxidative environment expands the genetic diversity of species by increasing the mutation rate of the germ lineage cells to accelerate the evolutionary process. MTH1, OGG1 and MUTYH, which are well conserved among species, may have contributed coordinately to control the germline mutation rate to an appropriate level for each species during evolution by controlling the amount of 8-oxoG in the genome (Supplementary Fig. S1 online).
Mth1+/−, Ogg1+/− and Mutyh+/− mice were established13,14,16 and backcrossed to C57BL/6J:Jcl (Clear Japan, Tokyo, Japan) for more than 16 generations. By crossing the C57BL/6J-background Ogg1+/−, Mth1+/− and Mutyh+/− mice, we obtained Mth1+/−/Ogg1+/− mice and Ogg1+/−/Mutyh+/− mice. Mth1+/−/Ogg1+/− mice were then mated with Ogg1+/−/Mutyh+/− mice to obtain Mth1+/−/Ogg1−/−/Mutyh+/− mice. Finally, by crossing the Mth1+/−/Ogg1−/−/Mutyh+/− mice, we obtained a pair of Mth1−/−/Ogg1−/−/Mutyh−/− mice (TOY32M and TOY44F). All animals were maintained in a temperature-controlled (22 ± 2°C, 55 ± 5% humidity), specific pathogen-free room with a 12-h light-dark cycle. The care and use of all animals were performed in accordance with prescribed national guidelines and the Animal Care and Use Committee of Kyushu University granted ethical approval for the study.
Quantification of 8-oxo-dG by LC-MS/MS
To detect the level of nuclear 8-oxodG, C57BL/6J:Jcl and TOY-KO mice (12–14 weeks old) were euthanized by cervical dislocation and tissues were immediately removed and frozen in liquid nitrogen. DNA was extracted using a DNA Extractor TIS Kit (# 296-67701, Wako Pure Chemical Industries, Osaka, Japan), according to the manufacturer's instructions, with a slight modification: 10 mM 2, 2, 6, 6-tetramethylpiperidine-N-oxyl (Wako Pure Chemical Industries) was added to all reagents at all stages of manipulation29. Extracted DNA was hydrolyzed with 0.17 mg/ml nuclease P1 (Yamasa, Chiba, Japan) and 1.7 μM acid phosphatase (P-1435, Sigma-Aldrich Japan Inc., Tokyo, Japan) in 17 mM sodium acetate buffer (pH 4.5) at 37°C for 30 min, followed by filtration at 12,000 × g for 3 min (Ultrafree-MC probind 0.45 μm, Millipore, Billerica, MA). The digested samples (100 μl) were subjected to liquid chromatography-tandem mass spectrometry (LC-MS/MS) analysis using a Shimadzu VP-10 HPLC system connected to an API3000 MS/MS system (PE-SCIEX, SpectraLab Scientific Inc, Ontario, Canada).
Statistical analyses were conducted using JMP 9.02 (SAS Institute Japan, Tokyo, Japan).
Detection of germ line mutations by whole exome sequencing
Exome sequencing libraries for three TOY-KO mice (TOY365F, TOY450F and TOY609F) and five DBF1 (DBA/2J:Jcl × C57BL/6J:Jcl F1) mice as controls were prepared using a SureSelectXT Mouse All Exon Kit (Agilent Technologies Japan, Tokyo, Japan), according to the manufacturer's instructions. Briefly, 3 μg of genomic tail DNA was sonicated into 150–180 bp fragments using a Covaris S2 System (Covaris, Woburn, MA, USA). The adaptors were ligated to the sonicated DNA after blunting and ~200 bp fragments were extracted using a 2% E-Gel (Life Technologies Japan, Tokyo, Japan). The extracted fragments were amplified with 2.5 mM SureSelect Pre-Capture primers and Platinum PCR Amplification Mix (Life Technologies), under the following conditions: 72°C for 20 min and 95°C for 5 min; 12 cycles of 95°C for 15 sec, 54°C for 45 sec and 70°C for 1 min; and a final extension at 70°C for 5 min. The PCR products were purified with a PureLink column (Life Technologies Japan). Purified PCR products (500 ng) were hybridized for 36 h at 65°C with SureSelect baits, according to the manufacturer's protocol. The captured libraries were amplified with the SureSelect Barcoding primer (BC1-8) for SOLiD with Herculase II Fusion DNA Polymerase (Agilent Technologies Japan), under the following conditions: 95°C for 5 min; 8 cycles of 95°C for 15 sec, 54°C for 45 sec and 70°C for 1 min; final extension at 70°C for 5 min. The captured barcoding libraries were quantified with an Agilent QPCR NHS Library Quantification Kit (Agilent Technologies Japan) and pooled. The four pooled libraries (1 pM) were amplified and purified with an EZ bead system (Life Technologies Japan). Purified P2-enriched beads were sequenced on one full slide of a SOLiD4 system (Life Technologies Japan). About 130 million paired-end sequencing reads (50 bp and 35 bp) were obtained from each library. Bioscope1.3.1 (Life Technologies Japan) was used to map the SOLiD paired-end reads to the mm9 reference mouse genome sequence (MGSCv37) using default parameters for Targeted resequencing methods. BEDtools v2.16.2 were used to calculate the coverage depth statistics and target enrichment efficiency. Avadis-NGS v1.3 (Strand Scientific Intelligence Inc., Karnataka, India) was used to carry out single nucleotide variant (SNV) calling with eight BAM format files (three TOY-KO lines and five control samples). The cutoff parameters of the SNV call were as follows: filtered sequencing quality ≤20, filtered PCR duplications, consensus base quality ≤50, total coverage <10, variants read depth <3 and the Decibel Score by Avadis-NGS v1.3 <50. The Decibel Score, read depth of the SNV allele and SNV allele frequency were used to sort these candidates. The iterative genomic viewer was used to check the candidates sequentially to eliminate apparent false positives. Finally, MassARRAY was used to select 286 mutation candidates for validation experiments (Supplementary Table S1 online).
Confirmation of mutations by sequencing
A MassARRAY3 Analyzer (Sequenom Inc, San Diego, CA) with iPLEX Gold Genotyping Reagent (Sequenom Inc) was used to validate the 286 candidates, according to the manufacturer's instructions. Briefly, MassARRAY Typer4 Assay Designer (Sequenom Inc) designed the 286 PCR primer pairs and 286 iPLEX primers as single-base extension primers for each candidate. We used 37 genomic DNA samples, including 35 samples from the TOY-KO pedigree and two control samples, as well as C57BL/6J and the original ES cell DNA to determine the origin of the de novo mutations in the TOY-KO pedigree. Ten nanograms of genomic DNA were used in each multiplex PCR for the MassARRAY. After dephosphorylation, single-base extension with the iPLEX primer and desalting were performed. The reaction products were spotted onto a 384-format SpectroCHIP with a MassARRAY Nanodispenser (Sequenom Inc) and then subjected to a MassARRAY 3 analyzer (Sequenom Inc). MassARRAY Typer 4.0 software (Sequenom Inc) was used to analyze the mass spectrum data.
Determination of the site preference of G to T mutation in di- and trinucleotide sequences
To analyze site preference of G to T mutation caused by Mth1/Ogg1/Mutyh deficiency, the 239 data of G to T mutation detected in G2–G8 were subjected (C to A mutations were converted to G to T mutation). The reference exon sequences and the 101 nucleotides those containing each mutation site (shown in Supplementary Data S1 online) were used to determine the site preference of mutation. The ratio shown in Fig. 5b, c were calculated as follows (data were summarized in Supplementary Table S2 online).
The number of each di- or tri-nucleotides sequences in the reference exon sequence were counted by 1 nucleotide sliding.
The number of each di- or tri-nucleotides sequences that include mutated guanine site were counted.
The frequency of each di- or tri-nucleotides sequences was calculated as follows: (A) /number of total nucleotide in reference exon sequence.
Total number of di- or tri-nucleotides sequences that include mutated guanine site were 478 and 717, respectively.
The expected value for a random mutation for each di- or tri-nucleotides sequences were calculated as (C) × (D).
The ratio (observed mutation for the expected value for a random mutation) was calculated as (B)/(E).
Kong, A. et al. Rate of de novo mutations and the importance of father's age to disease risk. Nature 488, 471–475 (2012).
Keightley, P. D. Rates and Fitness Consequences of New Mutations in Humans. Genetics 190, 295–304 (2012).
Xue, Y. et al. Deleterious- and disease-allele prevalence in healthy individuals: insights from current predictions, mutation databases and population-scale resequencing. Am. J. Hum. Genet. 91, 1022–1032 (2012).
Casals, F. & Bertranpetit, J. Human genetic variation, shared and private. Science 337, 39–40 (2012).
Ohno, M. et al. A genome-wide distribution of 8-oxoguanine correlates with the preferred regions for recombination and single nucleotide polymorphism in the human genome. Genome Res. 16, 567–575 (2006).
Shibutani, S., Takeshita, M. & Grollman, A. P. Insertion of specific bases during DNA synthesis past the oxidation-damaged base 8-oxodG. Nature 349, 431–434 (1991).
Maki, H. & Sekiguchi, M. MutT protein specifically hydrolyses a potent mutagenic substrate for DNA synthesis. Nature 355, 273–275 (1992).
Michaels, M. L., Cruz, C., Grollman, A. P. & Miller, J. H. Evidence that MutY and MutM combine to prevent mutations by an oxidatively damaged form of guanine in DNA. Proc. Natl. Acad. Sci. U.S.A. 89, 7022–7025 (1992).
Sakumi, K. et al. Cloning and expression of cDNA for a human enzyme that hydrolyzes 8-oxo-dGTP, a mutagenic substrate for DNA synthesis. J. Biol. Chem. 268, 23524–23530 (1992).
Radicella, J. P., Dherin, C., Desmaze, C., Fox, M. S. & Boiteux, S. Cloning and characterization of hOGG1, a human homolog of the OGG1 gene of Saccharomyces cerevisiae. Proc. Natl. Acad. Sci. U.S.A. 94, 8010–8015 (1997).
Rosenquist, T. A., Zharkov, D. O. & Grollman, A. P. Cloning and characterization of a mammalian 8-oxoguanine DNA glycosylase. Proc. Natl. Acad. Sci. U.S.A. 94, 7429–7434 (1997).
McGoldrick, J. P., Yeh, Y. C., Solomon, M., Essigmann, J. M. & Lu, A. L. Characterization of a mammalian homolog of the Escherichia coli MutY mismatch repair protein. Mol. Cell Biol. 15, 989–996 (1995).
Tsuzuki, T. et al. Spontaneous tumorigenesis in mice defective in the MTH1 gene encoding 8-oxo-dGTPase. Proc. Natl. Acad. Sci. U.S.A. 98, 11456–11461 (2001).
Sakumi, K. et al. Ogg1 knockout-associated lung tumorigenesis and its suppression by Mth1 gene disruption. Cancer Res. 63, 902–905 (2003).
Xie, Y. et al. Deficiencies in mouse Myh and Ogg1 result in tumor predisposition and G to T mutations in codon 12 of the K-ras oncogene in lung tumors. Cancer Res. 64, 3096–3102 (2004).
Sakamoto, K. et al. MUTYH-null mice are susceptible to spontaneous and oxidative stress induced intestinal tumorigenesis. Cancer Res. 67, 6599–6604 (2007).
Al-Tassan, N. et al. Inherited variants of MYH associated with somatic G:C T:A mutations in colorectal tumors. Nat. Genet. 30, 227–232 (2002).
Satoh, M. et al. Structural analysis of the titin gene in hypertrophic cardiomyopathy: identification of a novel disease gene. Biochem. Biophys. Res. Commun. 262, 411–417 (1999).
Orr, H. T. & Zoghbi, H. Y. Trinucleotide repeat disorders. Annu. Rev. Neurosci. 30, 575–621 (2007).
Drake, J. W., Charlesworth, B., Charlesworth, D. & Crow, J. F. Rates of spontaneous mutation. Genetics 148, 1667–1686 (1998).
Tajiri, T., Maki, H. & Sekiguchi, M. Functional cooperation of MutT, MutM and MutY proteins in preventing mutations caused by spontaneous oxidation of guanine nucleotide in Escherichia coli. Mutat. Res. 336, 257–267 (1995).
Russo, M. T. et al. The oxidized deoxynucleoside triphosphate pool is a significant contributor to genetic instability in mismatch repair-deficient cells. Mol. Cell Biol. 24, 465–474 (2004).
Kamiya, H. Mutagenicities of 8-hydroxyguanine and 2-hydroxyadenine produced by reactive oxygen species. Biol. Pharm. Bull. 27, 475–479 (2004).
Ushijima, Y. et al. A functional analysis of the DNA glycosylase activity of mouse MUTYH protein excising 2-hydroxyadenine opposite guanine in DNA. Nucleic Acids Res. 33, 672–682 (2005).
Fujikawa, K. et al. The oxidized forms of dATP are substrates for the human MutT homologue, the hMTH1 protein. J. Biol. Chem. 274, 18201–18205 (1999).
Kamiya, H. & Kasai, H. 2-hydroxyadenine in DNA is a very poor substrate of the Escherichia coli MutY protein. J. Radiat. Res. 41, 349–354 (2000).
Keays, D. A., Clark, T. G. & Flint, J. Estimating the number of coding mutations in genotypic- and phenotypic-driven N-ethyl-N-nitrosourea (ENU) screens. Mammalian Genome 17, 230–238 (2006).
Mashimo, T. et al. An ENU-induced mutant archive for gene targeting in rats. Nature Genetics 40, 514–515 (2008).
Tsuruya, K. et al. Accumulation of 8-oxoguanine in the cellular DNA and the alteration of the OGG1 expression during ischemia-reperfusion injury in the rat kidney. DNA Repair 2, 211–229 (2003).
We thank N. Adachi for the LC-MS/MS analysis and A. Matsuyama, K. Nakabeppu, S. Kitamura, K. Asakawa and T. Kuwano for technical support. This work was supported by grants from the Japan Society for the Promotion of Science (JSPS KAKENHI numbers: 20012038, 21240043, 21657002, 22300144, 22221004 and 25241016) and a Grant-in-Aid for JSPS Fellows (JSPS KAKENHI number 24·9979). This work was partly performed in the Cooperative Research Project Program of the Medical Institute of Bioregulation, Kyushu University.
The authors declare no competing financial interests.
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Ohno, M., Sakumi, K., Fukumura, R. et al. 8-oxoguanine causes spontaneous de novo germline mutations in mice. Sci Rep 4, 4689 (2015) doi:10.1038/srep04689
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