Origins and functional consequences of somatic mitochondrial DNA mutations in human cancer

1All cancers result from somatic mutations in their genomes. Beyond the ∼3200 Mb of nuclear genomic DNA, human cells have hundreds to thousands of mitochondria present in every cell, each carrying one or a few copies of the 16,569 bp circular mitochondrial genomes. In addition to their role in cellular energy balance through oxidative phosphorylation, mitochondria are involved in many essential cellular functions including modulation of oxidation–reduction status, contribution to cytosolic biosynthetic precursors, and initiation of apoptosis. Mitochondria in eukaryotic cells evolved by endosymbiosis from a free-living α-proteobacterium. Over 2 billion years of co-evolution, many ancestral mitochondrial genes have transferred to the nucleus. What remains in the mitochondrial genome is distinctive for the striking asymmetry between the two complementary mtDNA strands in terms of nucleotide content and gene distribution. The heavy (H) strand is guanine-rich (C/G = 0.4) and is the template from which most mitochondrial proteins (12 out of 13) are transcribed, whereas only one protein-coding gene, MT-ND6, is transcribed from the correspondingly cytosine-rich light (L) strand.

2Mutations in the mitochondrial genome cause inherited disease, with a maternal inheritance pattern because only eggs contribute mitochondria to the zygote. The penetrance of inherited mitochondrial disease is determined stochastically by both the random assortment of mutated vs wild-type mitochondrial genomes during meiosis and random drift during the early cell divisions after fertilization. In cancer, the role of somatically acquired mtDNA mutations is controversial. Although cancer-specific mutations have been previously reported, the limited sample size or poor sensitivity of capillary sequencing for heteroplasmic mutations has not allowed a comprehensive analysis of the mutational signatures of mitochondrial mutations nor their likely functional significance. It has long been proposed that mitochondria might contribute to cancer development given their fundamental importance to cellular biology. Previous reports suggested that mitochondrial somatic mutations might be under positive selection and thus contribute to cancer development, but the small number of reported mutations renders this conclusion uncertain. Nonetheless, the hypothesis of functionally relevant mitochondrial mutations is an appealing one because cancer cells have greatly increased energy demands over normal cells and demonstrate a switch from aerobic glycolysis in mitochondria to lactic acid fermentation in the cytosol (the Warburg effect).

3In each cell cycle, the replicating genome is at risk of de novo mutations, which can promote the development of cancer. These mutations may be generated by intrinsic cellular errors during DNA replication or repair or through exposure to mutagens, such as reactive oxygen species, tobacco smoke, and ultraviolet light. Recently, >20 mutational signatures operative in cancers have been identified in the nuclear genome. Whether any of these mutational processes also affect the mitochondrial genome has not been studied. Furthermore, whether there are mtDNA-specific mutational processes in somatic cells remain unclear, although the many unique features of mtDNA replication and repair, coupled with the high concentration of reactive oxygen species generated by the electron transport chain, could be associated with distinctive mutation signatures.

4In this study, we compare 1675 cancer and paired normal mtDNA sequences across 31 tumor types using massively parallel DNA sequencing technologies to obtain a systematic and unbiased catalog of somatic mitochondrial mutations. We find that mtDNA mutations are almost exclusively the product of a mutational process that is specific to mitochondria and probably linked to the unique mechanism of genome replication these organelles employ. We find no evidence for positive selection of mitochondrial mutations during oncogenesis, suggesting that they confer no clonal advantage on the nascent cancer cells.

5We extracted the mtDNA sequences from 704 whole-genome and 971 whole-exome sequencing data generated on primary cancers and compared them with mtDNA sequences from their matched normal samples. Given the abundance of mtDNA per cancer cell, a standard coverage of 30–40× in the nuclear genome provides significantly greater coverage of the mitochondrial genome (average read depth = 7901.0×), enabling accurate identification of somatic mutations including rare heteroplasmic variants. We also assessed whether whole-exome sequencing could be used to identify mtDNA mutations from off-target reads derived from the mitochondrial genome. We found an average read depth of 92.1× across the mitochondrial genome in exome studies. From 139 samples in which we had both exome and whole-genome sequencing data, the overall read depths correlated strongly (R2 = 0.59, Figure 1—figure supplement 1) as did variant allele fractions for mtDNA somatic mutations (R2 = 0.97, Figure 1—figure supplement 2). Validation experiments suggested the sensitivity of whole-exome sequencing for detection of mtDNA somatic mutations to be 71.4% compared to whole-genome sequencing (Figure 1—figure supplement 3 and ‘Materials and Methods’, ‘Off-target mtDNA reads in whole-exome sequencing’ and ‘DNA cross-contamination’).

6To reduce potential false-positive calls of mtDNA somatic mutations, we only report variants called with an allele fraction of >3%. This eliminates the risk of miscalls due to mtDNA-derived pseudogenes in the nucleus (NuMTs) because mtDNA copy numbers are 100–1000 times higher than nuclear genomes in human somatic cells, and the sequence homology between mtDNA and NuMTs presented in the human reference genome is generally <95% (in 96 out of 101 NuMTs with length greater than 300 bp). Furthermore, pairwise comparison between cancer and matched normal mtDNAs from the same individual further minimizes the contamination of NuMTs in the mutation calling.

7In total, 1675 tumor–normal pairs across 31 tumor types were analyzed (Table 1 and Supplementary file 1). For 61 of these patients, we had sequencing data available from multiple sites of the primary cancer, several time points or matched primary cancers, and metastases (a total of 73 such cancer samples), allowing us to study the timing of mtDNA mutations in cancer evolution (Supplementary file 1). We identified 1907 somatic mtDNA substitutions (Figure 1 and Supplementary file 2). In contrast to inherited polymorphisms (n = 38,706, available at Supplementary file 2), which were almost always homoplasmic in both the cancer and counterpart normal, the variant allele fractions (VAFs) of these somatic substitutions were highly variable in the cancer, ranging from our detection threshold (3%) to homoplasmy (100%). Of these 1907 somatic substitutions, 1209 (63.4%) were not registered in the databases of mtDNA common polymorphism. In comparison, when we examined substitutions found in both the tumor and the normal samples from a patient, only 21 (0.05%) were not registered in the polymorphism databases, a significantly different fraction from the tumor-only variants (p < 10−10; Chi-squared test). We found 595 (31.2%) recurrent mutations that can be collapsed onto 246 mtDNA positions, which is a 6.9-fold higher level of recurrence than expected by chance (p < 10−10). This suggests that the generation or fixation of mtDNA mutations is not random, but influenced by factors such as the underlying mutational process or positive selection.

8Of the 1675 cancer samples, 976 (58.3%) harbored at least one somatic substitution and 521 (31.1%) had multiple substitutions, ranging from 2 to 7 (Figure 2A). In those with multiple substitutions, 72 pairs of mutations were sufficiently close to phase such that we could determine whether they were linked on the same mtDNA genome or were on different copies. We found that 45 (62.5%) pairs of mutations were linked on the same mtDNA genome (Supplementary file 3 and Figure 2—figure supplement 1). Furthermore, of these linked mutations, 33 showed a clear temporal order: that is, one mutation was demonstrably sub-clonal to the other. This is rather unexpected, since each somatic cell has 100–1000 copies of the mitochondrial genome, and we might anticipate that random mutations would, on average, affect different copies. That many pairs of mutations are phased on the same mtDNA genome and yet show a clear sub-clonal relationship suggests that they occur sufficiently separated in time to allow the mitochondrial genome carrying the earlier mutation to drift towards a substantial fraction of all genomes in that cell before the second mutation occurs, consistent with a previous report.

9The number of somatic mtDNA substitutions varied significantly according to tumor type (p = 4.4 × 10−52) after correcting for confounding variables such as sequencing coverage: gastric, hepatocellular, prostate, and colorectal cancers had the highest number of mtDNA substitutions (Figure 2B). In contrast, hematologic cancers (acute lymphoblastic leukemia, myeloproliferative disease, and myelodysplastic syndrome) had fewer mutations. Several possible explanations could underpin these differences across tumor types. It could be that the mutation rates differ across cell lineages; it could be that selection pressures shape the number of mutations; or the number of mtDNA genome generations could differ across cell lineages. Of these explanations, we believe that the second is unlikely because, as we shall see, positive selection is not a major component of mitochondrial mutations. Interestingly, we find a positive correlation between the number of mtDNA somatic mutations and age at diagnosis in breast cancers (p = 0.0004; Figure 2C), in keeping with the idea that the number of mitochondrial generations is linked to mutation burden. The mutational burden of an established cancer represents the accumulated variation acquired in the lineage of cell divisions from fertilized egg to transformed cell and will include events acquired in normal development and homeostasis as well as those acquired during tumorigenesis. Interestingly, mtDNA mutations have been found at high rates in normal colonic crypt cells. Given that we find high burdens of mutations in colonic tumors as well, the differences we see across tumor types may arise from pre- or post-transformation differences in mtDNA burden across tissues.

10With respect to signatures of somatic substitutions, C > T and T > C transitions constituted 90.9% of all the 1907 substitutions (Figure 1) among the six classes of possible base substitutions. To characterize this aggregated signature of mtDNA cancer specific mutations in more detail, we looked for the presence of mtDNA strand bias between the complementary H and L strands of mtDNA. The two main substitution classes showed an extreme level of mtDNA strand bias. 84.1% of the C > T transitions were on the H strand. This level of strand bias occurred despite the fact that cytosine is 2.4-fold less common on the H than the L strand, so the C > T substitution rate is 12.6-fold higher on the H strand. By contrast, 76.8% of the T > C transitions were on the L strand despite its lower thymine content (1.3-fold less than the H strand). This implies that the T > C mutation rate on the L strand is 4.2-fold higher than on the H strand.

11We then examined the sequence context in which these mutations occurred by examining the bases immediately 5′ and 3′ to the mutated bases. This generates 96 possible mutation classes (the 6 substitution classes multiplied by the 16 combinations of immediate 5′ and 3′ nucleotides). Both C > T and T > C mutations showed highly distinctive sequence contexts. CH > TH substitutions (i.e. C > T mutations on the H strand) were enriched for the NpCpG trinucleotide context (8- to 15-fold more frequent than expected by chance; Figure 3A). By contrast, TL > CL substitutions (i.e. T > C mutations on the L strand) showed 5- to 8-fold enrichment in NpTpC. This strand-asymmetric mutational signature is not similar to any of the 21 cancer-associated mutational signatures recently identified from the nuclear DNA of 30 different cancer types.

12Of the 18 tumor types that presented at least 25 mtDNA somatic substitutions in this study, the mutational signatures were broadly consistent across tumor types (Figure 3B), with the exception that multiple myeloma had a somewhat higher rate of TH > CH changes than other histologies (p = 8.1 × 10−6). Thus, in contrast to the mutational signatures found in nuclear genomes, where there is striking heterogeneity both across tumor types and across individuals within a tumor type, the mutational profile in the mitochondrial genome of somatic cells is remarkably homogeneous.

13The major known cause of mutational strand bias in nuclear DNA is transcription-coupled nucleotide excision repair, where DNA lesions on the transcribed (non-coding) strand are more frequently repaired. However, we find that the strand bias always favors CH > TH and TL > CL whether the gene is transcribed from the H strand or from the L strand (Figure 3—figure supplement 1). This is not compatible with transcription-coupled repair, for which the direction of strand bias is fundamentally dictated by which strand is transcribed.

14Instead, the mtDNA mutational strand bias reported here appears to be driven by differences in replication between the two strands. mtDNA replication harbors substantial strand asymmetry between the H and L strands: mtDNA replication initiates from an origin of replication (OH) in the D-loop, with the nascent H and the L strand replicating as leading and lagging strand, respectively. We observed that C > T substitutions were prevalent in the leading (heavy) strand, whereas T > C substitutions were found in the lagging (light) strand (Figure 1). Remarkably, this strand bias was reversed in the D-loop itself (Figures 1 and 3C), further suggesting that the mtDNA somatic mutations are replication-coupled: according to a recently proposed bidirectional model of mtDNA replication, mtDNA replication is also able to initiate from the so-called Ori-b site, typically located around genomic position 16,197 and proceeds on both strands away from the origin (Figure 1). Replication of the nascent H strand continues unimpeded like the traditional model, but the nascent L strand terminates at the so-called OH site, typically around mtDNA position 191 bp. Under this model, then, the leading and lagging strand are reversed in the few hundred base-pairs of the D-loop, which is consistent with the reversed mutational signature in this region (Figures 1 and 3C).

15It is not entirely straightforward to infer the mutational signatures operating on the mitochondrial genome in the germline. De novo mutations are generally rare and often discovered because they cause disease; distinguishing the ancestral base and the derived base is challenging for single nucleotide polymorphisms; and comparative mtDNA genomics across species extends over considerable evolutionary time. In contrast, because ancestral and derived states are defined for tumor–normal pairs, a much clearer picture emerges of the somatic mtDNA mutation signature. We therefore assessed whether the signature that emerges for somatic mitochondrial mutations could extend to explain sequence composition of the human mtDNA genome.

16It appears that the mutational mechanism which has generated the CH > TH and TL > CL signature in cancer mtDNA is equivalent to the one that has been operating during evolution of human germline mtDNA. This manifests as the depletion of certain codons in the reference human mtDNA sequence through the action of the CH > TH and TL > CL mutational process over time (Figure 4A). For example, the GCG triplet codon (Alanine) appears to have been replaced by its synonymous GCA codon (due to CH > TH (GL > AL)), with the former being 15.8-fold less frequently observed in the 12 mtDNA protein-coding genes that are transcribed from the H strand (and encoded on the L strand). All 32 synonymous codon pairs present the same tendency. Consistent with this interpretation, the gene transcribed from the L strand (MT-ND6) demonstrates the opposite direction of skew. Further analyses of mtDNA codon usage from seven animal species suggest that the CH > TH and TL > CL mutational pressure may be characteristic of vertebrates, and primates in particular (Figure 4—figure supplement 1).

17To quantify whether the somatic mutational signature we have defined can fully explain the trinucleotide frequency of human mtDNA, we performed evolutionary simulations. First, we simulated the evolution of a random DNA sequence under the mutational signature described here. By mutational pressure alone, the random sequence starts losing certain hypermutable trinucleotides until eventually reaching a stationary sequence composition. The actual sequence composition of the human mitochondrial genome strongly resembles this stationary distribution (Pearson's r = 0.83; p < 0.0001; Figure 4—figure supplement 2). In a second simulation, a random sequence encoding the exact amino acid sequence of the reference mitochondrial genome was evolved by synonymous mutations under the observed mtDNA signature until reaching a stationary sequence composition (mutation–selection equilibrium). These simulations also eventually approximate the observed human mitochondrial genome (Pearson's r = 0.96, p < 0.0001; Figure 4B). These analyses strongly suggest that the mitochondrial mutation signature observed in cancer cells closely reflects the mutation signature active in the germline, which has continuously shaped the mitochondrial genome during human evolution.

18Next, we assessed the functional impact of somatic mtDNA mutations. Of the 1907 substitutions, 1153 (60.5%) were in the 13 protein-coding genes. These include 63 nonsense, 4 stop-lost, 878 missense, and 208 silent substitutions (Supplementary file 2). In addition, out of 251 indels we observed, 110 occurred within protein-coding genes (Supplementary file 2). Of the missense substitutions, 245 (27.9%) were recurrent, affecting 107 distinct mtDNA sites. Although this very high level of mutation clustering could, at first sight, be interpreted as evidence for positive selection, we found that silent substitutions were also frequently recurrent (28 recurrent variants in 13 mtDNA sites), with no substantial difference in recurrence rates between silent and missense mutations (p = 0.19; Figure 5—figure supplement 1). We believe this recurrence to be the consequence of a high mtDNA mutation rate with restricted mutational signature (CH > TH and TL > CL). Independently recurring mutations in human germline mtDNA are well described across human evolution.

19The ratio of somatic missense to silent substitutions (Rms:s) is apparently higher (4.2, 878/208) than that observed for cancer-associated somatic mutations in nuclear DNA (generally around 2:1 to 3:1 across tumor types). At face value, this again could be interpreted as evidence for positive selection. However, as described above, the somatic mtDNA mutational signature shows extreme strand asymmetry and the same mutational signature has been operative in the germline over evolutionary time. Thus, the dominant mutational signature has already acted on potentially synonymous sites in the mitochondrial genome (Figure 4A), meaning that any new somatic changes are much less likely to be silent. In keeping with this, a dN/dS ratio (See ‘Materials and Methods’) calculated taking into account both the mutational signature and the mtDNA codon usage revealed that missense mutations accumulate at a frequency very close to that expected under neutrality (dN/dS = 1.21; 95% confidence interval, 1.015–1.434; p = 0.031). This indicates that despite the apparent high ratio of missense to silent mutations, the vast majority of mtDNA mutations are passengers with no convincing evidence suggesting the existence of driver mitochondrial DNA mutations. Additional gene-by-gene analysis further revealed that no single gene had a higher than expected rate of missense or nonsense mutations (Supplementary file 4).

20For nonsense substitutions and frameshift indels, we observe a somewhat different picture. Taking into account the mutation signature and amino acid composition of the mitochondrial genome, the overall ratio of nonsense mutations to silent mutations is exactly that expected by chance (dNonsense/dS = 1.004; 95% confidence interval, 0.699–1.443; p = 0.98). However, while missense and silent substitutions exhibited equivalent variant allele fractions (average VAFs; 40.1% and 40.9%, respectively; p = 0.8), nonsense substitutions presented significantly lower VAFs (average 26.4%; p = 6x10−5), as did frameshift indels (average 25.0%; p = 2 × 10−3; Figure 5A). Taken together, these data suggest that nonsense mutations occur at the expected rate given the underlying mutational process. However, while silent and missense substitutions frequently achieve high allele fractions in tumor cells due to the effects of random drift, there are significantly greater constraints on mitochondrial genomes carrying protein-inactivating mutations. The inference here is that cancer cells carrying such deleterious mutations at or near homoplasmy are at a selective disadvantage and hence do not contribute to clonal expansions, underlining the importance of functional mitochondria to cancer cells. The extent of such disadvantage may vary according to tumor type: for example colorectal cancers show less negative selection compared to breast cancers (p = 0.028; Figure 5—figure supplement 2).

21We found 171 mtDNA substitutions in mitochondrial tRNA sequences, which are very similar to the expected number (168.2, p = 0.82) from the mutational signature. Interestingly, none of the substitutions was located in the trinucleotide anticodon site of the tRNA (expected number = 7.6, p = 0.006). This suggests that mutations in tRNA anticodons confer a similar selective disadvantage as protein-truncating mutations, presumably because such mutations would lead to systematic erroneous aminoacylation of nascent proteins during translation of the relevant codon.

22Next, we assessed whether any specific somatic mutations showed evidence of positive selection. Out of the 1907 somatic substitutions, 16 (0.8%) overlapped with known disease-associated mtDNA mutations, such as mutations frequently detected in MELAS (Mitochondrial Encephalomyopathy, lactic acidosis, and stroke-like episodes) and LHON (Leber hereditary optic neuropathy) (Supplementary file 2). In addition, ten mutations within mitochondrial protein-coding, tRNA and rRNA genes showed significantly higher recurrent rate than expected from background mutational signature (Supplementary file 5). However, it remains unclear whether this high recurrence reflects positive selection, because any factors not included in our background model of the mutational process, such as local mutation hotspots, could also explain a mild excess of mutations at a given nucleotide.

23We investigated whether somatic mtDNA mutations are more likely to become homoplasmic later in tumor evolution by assessing paired cancer samples, either primary and metastasis (breast, colorectal, and prostate) or primary and relapse (myeloma) (Figure 5B and Supplementary file 1). As mentioned earlier, 73 late (metastasis or relapse) cancer samples were sequenced in addition to the primary tissues. Among the mtDNA mutations identified in either of the paired cancer samples, a number of different patterns were observed. There were mutations at high VAF in the primary not found in the metastasis (n = 49); mutations in the metastasis not found in the primary (n = 49); and shared mutations (n = 71) at high or low VAF, sometimes with evidence for drift (VAF difference >0.2) between the two samples (n = 25). These data, particularly the mutations found in the metastasis only, suggest that mitochondrial mutations can occur throughout the time course of tumor evolution, and still drift to homoplasmy with appreciable frequency, as suggested previously. To assess the plausibility of this conclusion, we modeled the dynamics of mtDNA mutations based on a few simplifying assumptions (See ‘Materials and Methods’, Evolutionary dynamics of neutral mitochondrial mutations). We find that the expected number of neutral mitochondrial mutations drifting to homoplasmy increases linearly with mutation rate and number of cell divisions. Based on a mutation rate of 10−7/base-pair/generation, this leads to an average ∼1 homoplasmic mutation for every 1000 cell generations.

24We also explored whether the mutational forces that are so critical to shaping the nuclear genome during tumor evolution could affect the mitochondrial genome. In cancers associated with exogenous mutagens, such as tobacco-associated lung cancer and ultraviolet light-associated melanomas, we found no evidence of the mutational signatures characteristic of these carcinogens among the mtDNA mutations (Figure 5C, Figure 5—figure supplement 3). Moreover, BRCA1 and BRCA2 mutations showed no evident influence on mitochondrial genomes in breast cancer (Figure 5C), in contrast to their effects on nuclear genomes exhibiting an even distribution of mutations across all trinucleotide contexts. Taken together, it appears that the primary mtDNA mutational process is endogenous to mitochondria and is very different to those operating in nuclear DNA. It is surprising that the endogenous mutational process has far greater impact than any external forces, as the physicochemical interactions of ultraviolet light or the chemicals in cigarette smoke with DNA should be similar in both genomes. The simulations described above suggest the major explanation to be that the endogenous mutation rate is several orders of magnitude greater than that expected for exogenous carcinogens, thus swamping any signal.

25In theory, there are two potential sources of the mtDNA variants we observed in cancer tissues: (1) somatically acquired, or de novo, mutations accumulated during the cancer clone's lineage of cell divisions from the fertilized egg or (2) low-level heteroplasmic mtDNA present in the oocyte (therefore maternally inherited) amplified in cancer but lost from normal tissue by random drift. We believe the majority of the variants we find are genuinely acquired somatically. First, of the 45 pairs of somatic mutations phased together on the same copy of the mtDNA genome, at least 33 (73.3%) showed a clear sub-clonal relationship and therefore their occurrence is separated in time, or apparently somatic. Secondly, 63.4% of our substitutions were not previously reported as germline polymorphisms. This is a much higher rate than reported for equivalent analyses on heteroplasmic variants in non-cancer samples (8/37; 21.6%), although methodological differences may somewhat contribute to this apparent difference. Thirdly, if the variants were due to inherited low-level heteroplasmy, we would not expect to see such variation across tissue types, since all tissue types derive from the fertilized egg. It is difficult to distinguish whether the variants we observe occur before or after the initiating driver mutations that herald tumorigenesis, but our analysis of paired samples does suggest that they can occur both early and late. Given the homogeneity of the mutational signature across tumor types and its inferred resemblance to the germline mtDNA mutational process, we would hypothesize that new mutations occur at a fairly constant and high rate per mitochondrial genome replication throughout all cell divisions.

26On the basis of the mutational signature observed here, somatic substitutions are unlikely to be attributable to reactive oxygen species (ROS), as previous reports have suggested. Guanine oxidation by ROS predominantly causes G:C > T:A transversion, which constitute only 4.0% of the mutations in our data (Figure 5C). Instead, we propose three replication-coupled mechanisms that can explain the strand asymmetric CH > TH and TL > CL mutational signature and define a model of the mtDNA mutational process (Figure 5D). First, the parent H strand, displaced and single-stranded during mtDNA replication, could be more prone to cytosine deamination (generating CH > TH) and/or adenine deamination (generating TL > CL). Secondly, endogenous mtDNA polymerase (POLG) replication errors (which show the pattern of C > T and A > G substitutions) could be preferentially generated on the leading strand. Thirdly, there may be differences between the efficiency of repair between the leading and lagging strand. Further, the mutation pattern reported here is consistent with the hypothesized bidirectional initiation of mtDNA genome replication.

27It appears that most of the mtDNA missense mutations we observe become fixed in tumor progenitor cells without distinct physiological advantage. All the statistical testing performed in this study—variant allele fraction comparison across different categories of somatic mutations, number of recurrent mutations, and dN/dS ratio—suggest that mtDNA somatic substitutions accumulate largely neutrally. This is not different from previous observations in nuclear genomes: of the thousands of somatic mutations found in a cancer genome, many fewer than a hundred are believed to confer a selective advantage to the cancer cell. In contrast, protein-truncating mutations showed evidence of negative selection, at the level of constraints on the allele fraction achieved. The implication of this is that the inactivating mutations occur at an appreciable rate, but the fraction of mitochondrial genomes per cell carrying these variants cannot increase beyond a certain limit without impairing the selective fitness of that cell. Having a sizable number of mitochondria with fully intact proteome remains critical to the fitness of a cancer cell.

28All the sequences were generated by Illumina platforms (either Genome Analyzer or HiSeq 2000). With respect to TCGA data, we downloaded aligned bam files through UCSC CGHub (http://cghub.ucsc.edu). Sequencing reads were aligned on the human reference genome build 37 (GRCh37) and human reference mtDNA sequence (revised Cambridge reference sequence, rCRS), mainly by BWA alignment tool. Samtools and Varscan2 were used for manipulating sequence reads and for calling somatic mutations, respectively. Sequence data have been deposited in the European Genome-phenome Archive (EGA; https://www.ebi.ac.uk/ega/home; study accession # EGAS00001000968; dataset accession numbers EGAD00001001014 for primary samples and EGAD00001001015 for metastatic samples). Sample accession numbers are available in the Supplementary file 6.

29Most of the currently available whole-exome capture kits, including Agilent Technologies SureSelect Human All Exon 50 Mb (Agilent Technologies Inc., Santa Clara, CA) used mostly in this study, do not target mtDNA genes. However, because of the abundance of mtDNA in human cells (100–100,000 copies per cell), it is expected that a number of mtDNA fragments could be off-target captured. We checked whether the amount of off-target mtDNA reads was sufficient for mtDNA variant detection. Whole-exome sequencing (normal samples) generated by CGP (n = 855), WUGSC (Washington University Genome Sequencing Center; n = 140), and BCM (Baylor College of Medicine; n = 85) contained ∼100 off-target mtDNA reads per 1M autosomal reads (Figure 1—figure supplement 4). We concluded that these could be sufficient for the downstream analyses, because ordinary 10 Gb whole-exome data would provide ∼60× read depth for mtDNA here. However, whole-exome data sequenced by BI (Broad Institute; n = 436) included far less, ∼3 off-target mtDNA per 1 M autosomal reads, which would show ∼2× mtDNA read depth per 10 Gb exome sequencing (Figure 1—figure supplement 4). It may be due to ‘improved’ exome-capture protocols by BI to increase the DNA-capture efficiency and on-target rate. Therefore, we did not include whole-exome data sequenced from BI for further analysis.

30139 samples were sequenced by both whole-genome and whole-exome sequencing. From these, we compared the amount of off-target mtDNA reads from whole-exome sequencing with that of whole-genome sequencing. It showed clear positive linear correlation (Figure 1—figure supplement 1).

31Given the abundance of mtDNA in the cancer cells, 1–214× coverage cancer whole nuclear genome sequencing provides extensive coverage of mtDNA (average read depth = 7901.0×; Supplementary file 2) enabling accurate identification of somatic mutations, even if heteroplasmic. Whole-exome sequencing data were also included because off-target reads provided sufficient coverage (average read depth = 92.1×) to analyze mtDNA mutations.

32This high coverage of mtDNA, especially from whole-genome sequencing, permitted us to identify heteroplasmic variants (our detection threshold was 3%; see ‘Variant calling’ for more details). However, because sample swaps and/or DNA cross-contaminations would definitely generate false-positive somatic variants, we filtered out suspicious DNA samples as described below.1. Major sample swapsA subset of tumor and normal sequencing pairs, of which the nuclear genotypes were not matching with each other, were removed from further analyses. We randomly selected 320 common single-nucleotide polymorphism sites on the 22 human autosomes, of which the minor allele frequency is ∼50% (45–55%) according to The 1000 Genomes Project. Of the 320 sites, homozygous positions in normal tissues (which showed >90% variant allele fraction (VAF) with bases Q score >20) were compared with the corresponding genotypes in the counterpart cancer. Sample pairs were removed if the genotype mismatch rate was greater than 0.1 (; Nhet, number of heterozygote positions; Nhom, number of homozygote positions; Nwt, number of wild-type positions) (Figure 1—figure supplement 5A). We note 0 is expected for the rate when genotyping is perfect and sample pairs are from the same individual. By contrast, 0.5 is expected when samples were from different individuals.2. Minor cross-contaminationWe estimated DNA cross-contamination levels with the VAF of autosomal homozygous SNPs genotyped from the common (population minor allele frequency ∼50%) SNP sites. Theoretically, if there is no sequencing (and mapping) error, all the homozygote SNP sites in pure samples should present 100% VAFs. However, when samples are contaminated, corresponding VAFs are reduced because the contaminant has only an ∼25% of chance of having homozygote SNPs on the same site. Therefore, minor contamination levels (C) of each cancer sequencing data were estimated as below:where RDhom is sequencing read depth, RCwt is read-count of wild-type alleles, and Ne is number of sequencing errors on each autosomal homozygote SNP site. For high accuracy, we only counted base with sufficient quality score (Q > 20). In order to estimate Ne, we assumed a conservative rate (sequencing error rate = 0.001). We considered sites covered by at least 10 reads and 90% VAF (Figure 1—figure supplement 5B). 95% confidence intervals of cross-contamination levels were calculated using binomial distribution.In order to clear somatic variants, here we made the very conservative assumption that somatic variants present in excess of 5-times of the 95% upper limit of C levels were true somatic rather than false-positives by low-level of cross-contamination.3. Germline polymorphisms and back mutationsWe further checked samples for contamination using known mtDNA polymorphisms. Because human mtDNA is small (16,569 bp) and extensively explored previously, most of germline mtDNA polymorphisms are already known. For example, 97.7% of the 39,036 inherited substitutions were known polymorphisms in the mtDB database. Therefore, when a tumor sample is contaminated by other samples, many somatic-like mtDNA substitutions by contaminants are likely to be overlapped with known mtDNA polymorphisms.At the same time, low-level contamination would generate excessive back mutations, which appeared to reverse germline common polymorphisms into wild-type alleles. Taken together, both the number of somatic substitutions known in mtDB and number of back mutations can be good indicators for mtDNA cross-contamination. Therefore, we filtered out tumor tissues with ≥3 known potentially somatic mutations or with ≥2 back mutations from the further analyses (Figure 1—figure supplement 5A and B).

331. Major sample swaps

34A subset of tumor and normal sequencing pairs, of which the nuclear genotypes were not matching with each other, were removed from further analyses. We randomly selected 320 common single-nucleotide polymorphism sites on the 22 human autosomes, of which the minor allele frequency is ∼50% (45–55%) according to The 1000 Genomes Project. Of the 320 sites, homozygous positions in normal tissues (which showed >90% variant allele fraction (VAF) with bases Q score >20) were compared with the corresponding genotypes in the counterpart cancer. Sample pairs were removed if the genotype mismatch rate was greater than 0.1 (; Nhet, number of heterozygote positions; Nhom, number of homozygote positions; Nwt, number of wild-type positions) (Figure 1—figure supplement 5A). We note 0 is expected for the rate when genotyping is perfect and sample pairs are from the same individual. By contrast, 0.5 is expected when samples were from different individuals.

352. Minor cross-contamination

36We estimated DNA cross-contamination levels with the VAF of autosomal homozygous SNPs genotyped from the common (population minor allele frequency ∼50%) SNP sites. Theoretically, if there is no sequencing (and mapping) error, all the homozygote SNP sites in pure samples should present 100% VAFs. However, when samples are contaminated, corresponding VAFs are reduced because the contaminant has only an ∼25% of chance of having homozygote SNPs on the same site. Therefore, minor contamination levels (C) of each cancer sequencing data were estimated as below:where RDhom is sequencing read depth, RCwt is read-count of wild-type alleles, and Ne is number of sequencing errors on each autosomal homozygote SNP site. For high accuracy, we only counted base with sufficient quality score (Q > 20). In order to estimate Ne, we assumed a conservative rate (sequencing error rate = 0.001). We considered sites covered by at least 10 reads and 90% VAF (Figure 1—figure supplement 5B). 95% confidence intervals of cross-contamination levels were calculated using binomial distribution.

37In order to clear somatic variants, here we made the very conservative assumption that somatic variants present in excess of 5-times of the 95% upper limit of C levels were true somatic rather than false-positives by low-level of cross-contamination.

383. Germline polymorphisms and back mutations

39We further checked samples for contamination using known mtDNA polymorphisms. Because human mtDNA is small (16,569 bp) and extensively explored previously, most of germline mtDNA polymorphisms are already known. For example, 97.7% of the 39,036 inherited substitutions were known polymorphisms in the mtDB database. Therefore, when a tumor sample is contaminated by other samples, many somatic-like mtDNA substitutions by contaminants are likely to be overlapped with known mtDNA polymorphisms.

40At the same time, low-level contamination would generate excessive back mutations, which appeared to reverse germline common polymorphisms into wild-type alleles. Taken together, both the number of somatic substitutions known in mtDB and number of back mutations can be good indicators for mtDNA cross-contamination. Therefore, we filtered out tumor tissues with ≥3 known potentially somatic mutations or with ≥2 back mutations from the further analyses (Figure 1—figure supplement 5A and B).

41We extracted mtDNA reads using Samtools. We used VarScan2 for initial variant calling with a few options (--strand-filter 1 (mismatches should be reported by both forward and reverse reads), --min-var-freq 0.03 (minimum VAF 3%), --min-avg-qual 20 (minimum base quality 20), --min-coverage 3 and --min-reads2 2). With respect to the --strand-filter, it generally removes variant when >90% of mismatches are reported from either of the H or the L mtDNA strand. However, where only reads with a specific orientation are could be aligned dominantly (i.e. in both extreme region of mitochondrial reference genome; only L strand reads could be aligned on the 5′ extreme of mtDNA), we compared strand bias between ‘perfect matches’ (# perfect matches from L strand reads / total # perfect matches) and mismatches (# mismatches from L strand reads / total # mismatches). If the difference between those two bias <0.1, the mutations were rescued. Of the 1907 mutations, 54 (2.8%) were rescued accordingly.

42Putative somatic variants called by VarScan2 were further filtered using criteria shown below.At least 4 unique reads supporting variants and all variant reads at least 20 phred scale sequencing quality score (Q 20 = 1% sequencing error rate) and at least 3% variant allele fractions (VAFs).A. Regardless of in WGS and in WES, the ≥4 mismatches and the ≥3% VAF criteria must be satisfied simultaneously.B. However, in WGS, the minimum number of reads (n = 4) criterion is not essential, because the ≥3% VAF criterion is much more stringent (3% VAF request at least 240 mismatches (>>4) given mtDNA coverage is ∼8000 for WGS).C. In WES, the ≥3% VAF criterion is relatively less important than in WGS, because the ≥4 mismatches criterion is more stringent. For example, 4 mismatches in 90x (WXS average) coverage region (VAF = 4.4%) automatically fulfill the ≥3% VAF criterion. For less covered regions (i.e. <40x coverage; n = 285 out of total 1907 substitutions), the VAF criterion becomes less important, because 4 mismatches would generate ≥10% VAF, much higher than the minimum threshold (i.e. 3%). As results, we are missing lower heteroplasmic variants (i.e. variants with 3–10% heteroplasmic levels) from low coverage samples (mostly by WXS). The lower sensitivity of WXS is also confirmed in our validation study (see “Validation of somatic variants” below).There is no minimum threshold for total coverage (# perfect matches + # mismatches).To increase sensitivity for detecting mutations, we rescued mutations with 3 unique variant reads (with at least 20 phred scale sequencing quality score) when VAFs is ≥ 20%. Of 1907 somatic substitutions, 32 (1.7%) were rescued accordingly.All somatic variants presenting with VAFs lower than our very conservative threshold for minor cross-contamination (5-times 95% upper limit of contamination levels for each tumor sample, see above “Minor cross-contamination of DNA samples”) were removed. When we could not estimate cross-contamination levels because of low sequencing depth of coverage (for nuclear genome), a conservative criterion (10% contamination level threshold) was explicitly used.Substitutions were further visually inspected using IGV. Thirteen frequent false-positive variants (shown below) by misalignment due to extensive level of homopolymers in rCRS and due to sequencing error in the reference mtDNA genome (3107N, see Mitomap (http://www.mitomap.org/bin/view.pl/MITOMAP/CambridgeReanalysis) for more information) were explicitly removed:1. Misalignment due to ACCCCCCCTCCCCC (rCRS 302-315)A302C, C309T, C311T, C312T, C313T, G316C2. Misalignment due to GCACACACACACC (rCRS 513-525)C514A, A515G, A523C, C524G3. Misalignment due to 3107N in rCRS (ACNTT, rCRS 3105-3109)C3106A, T3109C, C3110A

43At least 4 unique reads supporting variants and all variant reads at least 20 phred scale sequencing quality score (Q 20 = 1% sequencing error rate) and at least 3% variant allele fractions (VAFs).

44A. Regardless of in WGS and in WES, the ≥4 mismatches and the ≥3% VAF criteria must be satisfied simultaneously.

45B. However, in WGS, the minimum number of reads (n = 4) criterion is not essential, because the ≥3% VAF criterion is much more stringent (3% VAF request at least 240 mismatches (>>4) given mtDNA coverage is ∼8000 for WGS).

46C. In WES, the ≥3% VAF criterion is relatively less important than in WGS, because the ≥4 mismatches criterion is more stringent. For example, 4 mismatches in 90x (WXS average) coverage region (VAF = 4.4%) automatically fulfill the ≥3% VAF criterion. For less covered regions (i.e. <40x coverage; n = 285 out of total 1907 substitutions), the VAF criterion becomes less important, because 4 mismatches would generate ≥10% VAF, much higher than the minimum threshold (i.e. 3%). As results, we are missing lower heteroplasmic variants (i.e. variants with 3–10% heteroplasmic levels) from low coverage samples (mostly by WXS). The lower sensitivity of WXS is also confirmed in our validation study (see “Validation of somatic variants” below).

47There is no minimum threshold for total coverage (# perfect matches + # mismatches).

48To increase sensitivity for detecting mutations, we rescued mutations with 3 unique variant reads (with at least 20 phred scale sequencing quality score) when VAFs is ≥ 20%. Of 1907 somatic substitutions, 32 (1.7%) were rescued accordingly.

49All somatic variants presenting with VAFs lower than our very conservative threshold for minor cross-contamination (5-times 95% upper limit of contamination levels for each tumor sample, see above “Minor cross-contamination of DNA samples”) were removed. When we could not estimate cross-contamination levels because of low sequencing depth of coverage (for nuclear genome), a conservative criterion (10% contamination level threshold) was explicitly used.

50Substitutions were further visually inspected using IGV. Thirteen frequent false-positive variants (shown below) by misalignment due to extensive level of homopolymers in rCRS and due to sequencing error in the reference mtDNA genome (3107N, see Mitomap (http://www.mitomap.org/bin/view.pl/MITOMAP/CambridgeReanalysis) for more information) were explicitly removed:

511. Misalignment due to ACCCCCCCTCCCCC (rCRS 302-315)

52A302C, C309T, C311T, C312T, C313T, G316C

532. Misalignment due to GCACACACACACC (rCRS 513-525)

54C514A, A515G, A523C, C524G

553. Misalignment due to 3107N in rCRS (ACNTT, rCRS 3105-3109)

56C3106A, T3109C, C3110A

57We compared our variant calls with common inherited mtDNA polymorphisms deposited in the mtDB database as of 24th July 2013. Gene annotation of somatic variants was done using custom script based on human mtDNA gene information.

58To validate the sensitivity and specificity of variant calling in this study, 19 tumor and normal pairs (which were originally whole-genome sequenced) were whole-exome sequenced and mtDNA variants were assessed independently. Among the 28 somatic substitutions originally detected from the 19 tumor–normal whole-genome sequencing pairs, 20 (71.4%) were called as somatic (Figure 1—figure supplement 3). In addition, 5 (17.9%) presented evidence of variant reads in the validation set, although it was filtered out because of its low read depth of coverage in exome sequencings (showed 2–5 variant reads). Moreover, because 3 remaining sites were not sufficiently covered in the validation set to call somatic variants, these could not be evidence of the inaccuracy of whole-genome sequencing data, therefore not considered in the accuracy validation. Taken together, all the 25 somatic substitutions by whole-genome sequencing were highly likely to be true positives, therefore we concluded it provided ∼100% accuracy in the mtDNA somatic substitution assessment. Actually, the high accuracy of whole-genome sequencing is very likely and what we expect, because it provides extensive coverage of mtDNA (average read depth >7,500×), ∼3% heteroplasmic variants would present >200 variant reads.

59By contrast, the validation set (whole-exome sequencing) is called 21 somatic substitutions. Of these, 20 were common with whole-genome sequencing, and one was incorrectly called as somatic though it was actually germline substitutions in the whole-genome sequencing data. In addition, as mentioned above, the validation set missed 8 somatic substitutions called by whole-genome sequencing. Six out of eight undercalls (75%) were low heteroplasmic substitutions in whole-genome sequencing, ranging from 3.36% to 8.68%. Based on these data, we suggest 71.4% sensitivity (20/28) and 95.2% specificity (20/21) for exome-sequencing in detecting upto 3% heteroplasmic somatic mtDNA substitutions in cancer.

60We further checked the correlation of heteroplasmy level between the 20 mtDNA somatic mutations called both whole-genome and whole-exome sequencing. It showed great linear relationship (R2 = 0.97, Figure 1—figure supplement 2), further suggesting whole-exome sequencing data are appropriate for accurate detection of mtDNA somatic mutations.

61We phased 72 somatic substitution pairs, which arose in a single cancer sample and which located sufficiently close (from 10 bp to ∼500 bp), therefore both sites could be sequenced by same sequence fragments (Supplementary file 3 and Figure 2—figure supplement 1). We classified them as ‘different strand’, ‘co-clonal’, and ‘sub-clonal’ using criteria as follows:

62Different strand: the two somatic substitutions are obligate on different strands. Reads that report wild-type1(wt)-substitution2(subs) and subs1-wt2, but subs1-subs2, are observed.

63Co-clonal: reads reporting wt1-wt2 and subs1-subs2 are only observed.

64Sub-clonal: One substitution is sub-clonal to the other, but the two are definitely phased. Reads subs1-subs2 and either subs1-wt2 or wt1-subs2 are observed.

65To understand the relationship between tumor types and number of mtDNA mutations, Poisson regression and ANOVA were applied to our dataset using R software (http://www.r-project.org).where Nsub is number of mtDNA substitutions of each sample, CovT and CovN are coverage of tumor and normal mtDNA, respectively, (if Cov is >200, we replaced it by 200), t is tumor types.

66Poisson regression was applied to our breast cancer dataset.where Nsub is number of mtDNA substitutions of each sample, CovT and CovN are coverage of tumor and normal mtDNA, respectively, (if Cov is >200, we replaced it by 200), a is age at diagnosis. p-value in estimation of a was shown in the manuscript.

67Different mutational processes generate different combinations of mutation types, termed ‘signatures’. For example, ultraviolet (UV) light and tobacco smoking (polycyclic aromatic hydrocarbons) frequently generate C > T transitions and G > T transversions on non-transcribed (coding) strands in melanoma and lung cancers, respectively. To understand the mutational processes influencing cancer mtDNA, we correlated the 1907 mtDNA substitutions with 21 cancer specific mutational signatures in the nuclear DNA recently identified. However, none of the signature could explain the highly unique mtDNA substitutions.

68Mutational signature and strand bias were assessed as described in our previous reports. Briefly, the immediate 5′ and 3′ sequence context was extracted from rCRS. Substitution rate for each trinucleotide context was calculated with the number of substitution normalized by the frequency of the trinucleotide context observed in the rCRS, in the L and H strand, respectively. For analyses of substitutions falling in the mtDNA genes (13 protein-coding and 22 tRNA genes), transcribed/non-transcribed strand was also considered for comparison.

69In order to prove the strand bias is not transcription but replication-coupled, we checked strand biases of polymorphisms in the 12 L strand protein-coding genes, 1 H strand protein-coding gene (MT-ND6), and/or 22 tRNAs (Figure 3—figure supplement 1). For this specific purpose, we did not consider the sequence context (immediate 5′ and 3′ bases) because it over-classifies mutations (i.e. the number of mutation classes (n = 96) is larger than that of mutations). In other words, 12 classes of substitutions (six classes of possible base substitutions (C > A, C > G, C > T, T > A, T > C, T > G) × two strands (L and H strands)) were considered. Substitution rates are ratio between observed and expected numbers (H0 = same mutation rate for all substitution classes) for each substitution class. In order to understand which model (replicative or transcriptional strand) is appropriate to explain the strand-bias, Chi-square tests were used between the number of observed mutations for each class and expected ones under the background signature.

70We counted the codon frequencies in 13 mtDNA protein-coding genes. Because 12 L strand protein-coding genes and 1 H strand gene (MT-ND6) are under opposite mutational pressure (T > C and G > A for L strand genes; A > G and C > T for MT-ND6), we separated L and H strand genes for this analysis. T > C skew and G > A skew were calculated as shown below, to understand the TL > CL and CH > TH (equivalent to GL > AL) substitutions during the evolution of human mtDNA:where NA, NC, NG, and NT are number of A, C, G, and T base in the 3rd position of triplet codons in mtDNA genes, respectively.

71For the assessment of mtDNA codon usage of other animal species, we analyzed the mtDNA sequence of Caenorhabditis elegans (accession# NC_001328), Drosophila melanogaster (accession# NC_001709), D. rerio (accession# NC_002333), Xenopus laevis (accession# NC_001573), Mus musculus (accession# EU450583), Gallus domesticus (accession # NC_235570), and Pan troglodytes (NC_001643). We considered only L strand mtDNA genes in the cross-species analysis.

72To compare the number of recurrent substitutions between silent and missense substitutions, we randomly selected 100 substitutions each from 198 silent substitutions in the third base of triplet codons, 440 missense substitutions in the first base of triplet codons, and 405 missense substitutions in the second base of triplet codons. We counted the number of recurrent substitutions in each group. This was iterated 300 times independently. ANOVA testing was applied to determine the difference between the three groups (Figure 5—figure supplement 1).

73To estimate dN/dS values for missense mutations (wmis), we used an adaptation of the method described previously. Briefly, the rate of mutations is modeled as a Poisson process, with a rate given by a product of the mutation rate and the impact of selection. To obtain accurate estimates of dN/dS, we used two separate models, one using 12 single-nucleotide substitution rates and a more complex one accounting for any context dependence effect by 1-nucleotide upstream and downstream using 192 substitution rates. For example in the 12-rate model, the expected number of A > C mutations (λA>C) would be modeled as follows:where Lsyn,A>C and Lmis,A>C are the number of sites that can suffer a synonymous and missense A > C mutation, respectively, which are calculated for any particular sequence. The likelihood of observing the number of missense A > C mutations (Nmis,A>C) given the expected λmis,A>C is then calculated as:and the likelihood of the entire model is the product of all individual likelihoods. Wmis is fixed to be equal in all 12 (or 192) equations describing each substitution type, and a hill-climbing algorithm is used to find the maximum likelihood estimates for all rate and selection parameters. Likelihood Ratio Tests are then used to test deviations from neutrality (wmis = 1). The dN/dS ratio reported in the main text corresponds to the full context dependent model with 192 substitution rates. This method allows quantifying the strength of selection avoiding the confounding effect of gene length, sequence composition, different rates of each substitution type, and context-dependent mutagenesis.

74Along with the 1907 somatic mtDNA substitutions, we identified 109 and 142 somatic short insertions and deletions, respectively, from the 1675 cancer mtDNA sequences using Varscan2 (Supplementary file 2).

75We model the evolutionary dynamics of mitochondrial mutations under random drift and derive a simple equation for the expected number of homoplasmic mutations. There exist multiple levels at which mitochondrial mutations evolve: within mitochondria, in the cytoplasm, and on the cellular level. In this study, we focus on the dynamics in a single cell, which represents the founder of the last clonal expansion in the tumor cell population. The cellular dynamics during a clonal expansion is difficult to describe analytically, but it is important to realize that mutations of a clonal expansion preserves the allele frequencies of neutral variants and that mutations that occur after the expansion are unlikely to contribute to measurable allele frequencies, as the population becomes large.

76We model the evolutionary dynamics of mitochondrial mutations in the cytoplasm of a single cell by a Wright–Fisher process, in which the number of mitochondria in a subsequent generation is a binomial sample of the mitochondria in the previous generation. The number of mitochondria M is kept fixed. The marginal allele frequency X of a single site has two absorbing boundaries, X = 0 and X = M (homoplasmy), and the probability of fixation of an allele at frequency X by neutral drift is ρ = X/M. Note that this process leads, on the population level, to a dichotomization of heteroplasmic variants to either go extinct or become homoplasmic and fixate in a cell.

77Mutations on any of L (= 16,569 nt) sites in the mitochondrial genome are assumed to occur at a uniform rate μ per nucleotide per cell division, which is of order 10−7, based on a human inter-generational comparison. Hence the rate of neutral evolution is simply μLM/M = μL. Lastly, the expected time to fixation in the Wright–Fisher process is t = 2M. Putting these things together, the expected number of mutant alleles N in a cell initially without any mitochondrial mutations after T generation is

78This equation predicts a linear accumulation of neutral mutations over time, with a delay imposed by number of mitochondrial copies. A similar behavior has been reported using numerical simulations. When also considering heteroplasmic mutations, the expected number of alterations may be slightly higher.

79To check whether our model yields the correct behavior, we use the following numbers: the observed order of magnitude of mitochondrial mutations per patient was N = 1. The sequencing coverage on the mitochondrial genome indicates that there were of order M = 100 mitochondrial genome copies present per cancer cell. The expected number of mutations per cell division is μL = 1.6 × 10−3, it therefore requires around 1000 cell generations T to accumulate on average one homoplasmic mutation. This number of generations appears realistic for regenerating tissues. As expected, epithelial cancers had among the highest observed number of mitochondrial mutations, while hematopoietic cancers typically had lower numbers.

80Statistical testing was performed using R software. All p-values were calculated by two-tailed testing. Figures were generated using R and Microsoft Excel software.