Study design

Based on our prior study [8], we performed whole-genome sequencing of hip skin cells as it would allow detection of versatile mutational processes, because it is mostly sun-shielded. UV-induced mutagenesis has lower contribution into overall mutation spectrum in this tissue which allows better detection of other types of mutagenesis. In this study, we analyzed somatic genome changes in single cell lineages from 34 fibroblasts obtained from skin biopsies taken from hips of a total of 21 donors, ages 25 to 79. Our dataset includes the hip fibroblasts from two donors sequenced previously [8]. In addition, we sequenced five genomes of clonal single melanocyte-derived lineages. Single skin fibroblasts were propagated in culture up to approximately 1,000,000 cells which provided sufficient high-quality genomic DNA for whole-genome sequencing and follow-up validation. The clonal single-melanocyte lineages were cultured in media up to 10,000 cells. DNA from these cells was whole-genome amplified and sequenced. In addition, we were able to grow one melanocyte clone up to 1,000,000 cells and performed whole-genome sequencing on this sample without whole-genome amplification. From each donor, we also sequenced whole blood DNA (Fig 1A).

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Fig 1. Schematics and total base substitutions identified per clonal lineage in this study.

(A) Schematics of the study design. From each donor, we obtained blood for whole-genome sequencing. In addition, we obtained skin biopsies from the hips of the donors from which fibroblasts and melanocyte clonal lineages were obtained. Fibroblasts were grown up to a million cells and their DNA was directly used for whole-genome sequencing, while melanocytes grew up to 10,000 cells and the DNA was whole-genome amplified and thereafter sequenced. (B) The total base substitutions in each clonal lineage versus the age of the donors. The pink filled circles denote melanocyte clones. The x-axis denotes the ages of the donors, while the y-axis denotes the number of base substitutions. The solid black line is the linear regression line for the samples, while the dotted black curves are the 95% confidence intervals. The source data for this figure is in S1 and S2 Tables.

https://doi.org/10.1371/journal.pgen.1009302.g001

The median sequencing depth for the samples was 78X with a minimum average coverage per site of 50X (S1 Table). The genome-wide changes detected in the clones were compared to blood samples from the same donors and only the variants unique to the clones were denoted as somatic changes in the clones. Stringent filtering criteria were applied to exclude changes that could have occurred during limited propagation of the clone. For this purpose, only base substitutions as well as indels calls within 45% and 55% (heterozygous alleles) or above 90% (homozygous alleles) allele frequencies were considered clonal and somatic in the initiating melanocyte or fibroblast cell. All other calls that did not conform to these allele frequencies were considered sub-clonal and were removed from the analysis as these most likely represented culture-induced artifacts. We also analyzed the allele frequencies of all somatic base substitutions in the clonal lineages. All fibroblast clonal lineages demonstrated a peak of mutation calls at the 45% to 55% allele frequencies, indicating that these samples were clonal (S1 Fig and S2 Table). We did not see such a peak in the whole-genome amplified melanocyte clones which could reflect uneven genome amplification and localized genome duplications during the whole-genome amplification step. Nonetheless, only analyzing heterozygous mutation calls within the 45% and 55% allele frequencies and homozygous mutation calls at >90% allele frequencies allows us to estimate the minimum number of somatic mutations in the founder cells. Mutations that accrue during culture and/or polymerase errors during whole genome amplification are expected to not be clonal and have allele frequencies <45%. For structural changes, clonal calls with variant junction reads representing at least 30% of the total junction reads, and no reads representing the variants in the blood genomes were identified as clonal somatic rearrangements present in the initiating fibroblast. Multiple samples sequenced from the same donors allowed intra-individual comparisons of somatic genome instability in humans.

UV-induced base substitutions and C➔T changes due to spontaneous cytosine deamination are prevalent in skin cells

We detected 402 to 14029 base substitutions in each clonal lineage sequenced and the mutations did not increase with the age of the donors (Fig 1B). Analysis of the mutation spectrum revealed that the predominant mutation in many samples was C➔T base substitution (S2 Fig and S2 Table). The number and types of base substitutions in melanocyte clones were similar to those seen in the fibroblasts (Figs 1B and S2 and S2–S4 Tables). To identify the predominant mutation signatures in our samples, we determined the cosine similarities of the 96 tri-nucleotide motif mutation profiles in our samples versus all the published mutation signatures derived from analysis of thousands of mutation catalogs from human tumors ([13], and https://cancer.sanger.ac.uk/cosmic/signatures). This allowed us to agnostically determine the mutation signatures previously identified in cancers that were also overrepresented in our samples. We saw that the SBS7b signature was overrepresented in many samples. These signatures comprise of C➔T changes at cC or tC motifs (S2 and S3 Figs). In addition, SBS1 was only weakly represented in our samples. We also found mutation signatures SBS2 and SBS11 present in the samples which also carry a strong SBS7b mutation signature. These are likely due to the overlap between the SBS2 and SBS11 mutation signatures with UV-induced mutations (S3 Table). We also used non-negative matrix factorization (NMF)-based deconvolution of mutation signatures as a parallel approach to agnostically determine the predominant signatures in our samples for single base substitutions and dinucleotide substitutions. We were able to detect SBS1, SBS5, and prominent UV mutation signatures (SBS7b and DBS1) in our cohort (S3 Table, S2 and S3 Figs). In 28 samples we also detected either SBS4 or SBS18 which are indicative of oxidative damage in the cells leading to G➔T (C➔A) changes (S2 and S3 Figs and S3 Table).

We then sought to determine if the most prominent components of mutational signatures identified above were statistically enriched in our samples. For this purpose, we used our previously described knowledge-based trinucleotide-motif-centered pipeline [8,14,15,35]. This pipeline calculates enrichment with mutations within pre-defined trinucleotide motifs. It also calculates the sample-specific p-values for enrichments and minimum estimate of mutation load assigned to a motif-specific mutagenic process after stringent statistical filtering. nCg➔nTg changes likely arise upon spontaneous deamination of methylated cytosines [15]. These mutations constitute the major component of SBS1 in COSMIC [12,13]. SBS1-associated mutation load has been shown to increase with age in cancers [36] and in healthy individuals [7,10,37,38]. Analysis of the nCg➔nTg changes in our donors demonstrated that this mutation type is statistically enriched in all the samples and was also found to linearly increase with the ages of the participants with an average increase of 0.4 mutations per year (Fig 2 and S4 Table). We also detected statistically significant enrichment with UV-associated C➔T changes in the tC or cC context (yCn➔yTn, major component of COSMIC SBS7b) in many of the sequenced samples as well as a prominent presence of CC➔TT changes (Fig 2 and S4 Table). The estimates of yCn➔yTn minimum mutation load correlate with direct counts of the less frequent CC➔TT and nTt➔nCt changes, which have previously been shown to be associated with UV-induced DNA damage in human cells [8,13] (S4 Fig). Altogether these three types of changes indicate the contribution of UV-induced changes in mutation load accumulated in skin. Interestingly, the UV-induced mutations did not correlate with the ages of the participants (Fig 2).

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Fig 2. Analysis of the motif-specific mutation signatures in the genomes of skin cells.

The minimum mutation load for the (A) nCg➔nTg mutation signature, (B) yCn➔yTn mutation signature and (C) the total mutation load for the CC➔TT dinucleotide changes are plotted against the ages of the participants. The solid pink circles denote the mutation load in melanocytes. The black solid line is the linear regression, and the dotted curves are the 95% confidence intervals for each dataset. The source data for this figure is S4 Table.

https://doi.org/10.1371/journal.pgen.1009302.g002

SBS1 mutations identified by SigProfilerExtractor (NMF-based deconvolution) and the minimum number of nCg➔nTg mutations analyzed by the knowledge-based pipeline correlate with each other. We saw a similar correlation between the mutations attributed to SBS7b by SigProfilerExtractor and the minimum number of yCn➔yTn mutations identified by the knowledge-based pipeline (S5 Fig). These data indicate that both methodologies perform similarly in the evaluation of mutation signatures.

Bulk exome sequencing reveals the presence of cancer drivers in the samples at less than 10% allele frequencies

Whole-exome sequencing up to 100X to 150X was also performed for bulk samples from which 14 fibroblast clones and four melanocyte clones, respectively (S1 Table). Analysis of single nucleotide variants (SNVs) in the bulk samples and comparisons with the clonal lineages derived from the bulk cells revealed the presence of overlapping SNVs in bulk and the corresponding clones. Interestingly, we did not see any overlapping SNVs between bulk samples and clonal lineages that were not derived from the same bulk sample, even if they were coming from the same donor (S5 Table). This observation validates our mutation calling pipeline and provides support for the presence of the mutations detected in the clonal lineages in the original skin biopsies.

The somatic mutations identified in the bulk samples were predominantly at or less than 10% allele frequencies (S5 Table and S6 Fig). This observation was also found to hold true for the allele frequencies of the overlapping SNVs in bulk samples and their corresponding clonal lineages (S7 Fig). The low allele frequency in the population demonstrates the large amount of heterogeneity in the dermal and the epidermal tissue.

We also annotated all the SNVs in all whole-genome sequenced clones and whole-exome sequenced bulk tissues for functional effects. All non-synonymous SNVs, stop gains, start or stop loss SNVs in the clones and bulk tissues were further analyzed using the Cancer Genome Interpreter [39] to determine if these were potentially cancer drivers. Of the 672 SNVs in the clones that had potentially functional impacts, 32 changes were in tumor driver genes and 13 changes were annotated as tumor drivers. One sample, DAG_H95, was found to have 3 tumor driver mutations, however the donor does not have any history of cancer (S2 Table). We also detected 3190 SNVs in the bulk tissues that could alter protein sequence, of which 390 were within tumor driver genes, and 62 of the mutations were annotated as driver mutations. Interestingly, these driver mutations were also present between 2 to 10% allele frequencies in the samples (S7 Fig). Overall, the results suggest that normal sun-shielded human skin carries a substantial proportion of cancer driver mutations, albeit at low allele frequencies.

Single base indels in homonucleotide repeats and deletions larger than 5 bases are ubiquitous in skin cells

We detected from 7 to 71 indels in the donors (Fig 3A and S6 Table). The insertions ranged from 1 base to 40 bases and deletions ranged from 1 to 171 bases (Fig 3B and S6 Table). The total number of indels per sample do not appear to increase statistically with the ages of the donors (Fig 3A). NMF-based deconvolution analysis of indel signatures or measuring the cosine similarities of indel patterns with the indel signatures currently annotated in cancers [13] demonstrated that two indel types were prevalent in our samples. The first was single base insertions or deletions in homopolymeric stretches associated in our samples with ID1, ID2 and ID7 (S8 Fig and S7 and S8 Tables). Since many samples had very low numbers of indels, it is possible that mathematical deconvolution of indel signatures may carry errors. Therefore, instead of the number of mutations within each signature, we used the total number of single base insertions or deletions in homopolymeric stretches for further downstream analyses. These types of indels were also found to increase linearly with the ages (0.22 mutations per year) of the donors consistent with the idea that they were associated with polymerase slippage at the homopolymeric repeats [40,41] during ongoing DNA replication in fibroblasts over the donors’ lifetime (Fig 3C). The second class of indels were deletions spanning five nucleotides or more, many of which have microhomology of one or more bases at the deletion junction (S8 Fig and S8 Table). Based on cosine similarities, these indels were highly similar to ID8 (S8 Table), the indel signature associated with double-strand break repair via non-homologous end joining [13]. Consistently, NMF-based deconvolution of indel signatures applied to our samples identified these deletions of five or more bases as part of novel signature which is a composite signature made up of ID8-like indels as well as indels in homopolymeric repeats (Signature A in S8 Fig and S8 Table). Such deletions spanning five or more nucleotides were identified in almost all samples and did not demonstrate a statistically significant increase with the ages of the donors. We also did not see any differences between the indel load or signatures in melanocytes versus the fibroblasts indicating that the processes yielding indels in both cell types are likely the same (Fig 3C).

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Fig 3. Analyses of indels in skin cells.

(A) The total number of indels identified in each sample plotted against the ages of the donors. The black dots denote fibroblast clones, while the pink dots denote the melanocyte clones. (B) The distribution of the lengths of the insertions and deletions detected in the clonal lineages. The source data for panels A and B is in S6 Table. (C) The number of insertions and deletions in homopolymeric repeats and the deletions spanning 5 bases or more plotted against the ages of the donors. The open circles denote fibroblast clones, while the filled in circles denote melanocyte clones. The source data for this figure are in S7 Table. (D) The number of insertions and deletions in homopolymeric repeats and the deletions spanning five bases or more plotted against the yCn➔yTn minimum mutation load in skin cells. The source data for this panel are in S4 and S6 Tables. In the graphs, the black solid line is the linear regression of the data, and the dotted black curves are the 95% confidence intervals.

https://doi.org/10.1371/journal.pgen.1009302.g003

The number of deletions spanning five or more nucleotides were found to also correlate in our samples with the UV-associated trinucleotide-centered yCn to yTn mutation signature. We did not see a positive correlation between the UV-associated mutation signatures and single base indels in homopolymeric repeats (Fig 3D). These data indicate that unlike indels at homopolymeric repeats, UV-induced DNA double strand breaks are the underlying etiology for deletions of five or more bases in human skin cells.

The majority of the insertions in skin cells are templated

The predominant insertions detected in our clonal lineages were templated single-base insertions (i.e. copied from the neighboring bases). Of the 186 single base insertions, 163 of the insertions were copied from the adjacent base (S9 Table). Such insertions most likely represent polymerase slippage events within homopolymeric runs of bases or erroneous Okazaki fragment maturation [40,41] and constitute the ID1, ID2 and ID3 indel signatures as mentioned above [13].

We also detected 28 instances of insertions larger than two bases in length. 18 of these larger insertions were a duplication of the neighboring residues. Three of these templated insertions carried small mismatches likely due to errors during copying of the neighboring residues (S9 Table). Such templated insertions along with deletions spanning five bases or more have been shown to be characteristic of non-homologous or microhomology-mediated end-joining of double-strand breaks [13,42,43]. As such, it is likely that repair of UV-induced double strand breaks also leads to insertions of two bases and more. However, the low numbers of such events do not allow statistical verification of this hypothesis.

UV-induced mutation load varies by race and is not impacted by the sex of the donors

Our cohort included five African American or Black donors and 16 White donors, thus allowing us to also determine if the accumulation of somatic genome changes is different between the two races. The total base substitutions in samples from the White donors (median 1824), were higher than in the skin fibroblasts and melanocytes obtained from African American or Black donors (median 715, p-value = 0.00002193, calculated by two-tailed Mann Whitney test). We reasoned that this lower mutation load in the African American donors might reflect the protective effect of melanin in skin. Consistently, we did see a prominent presence of UV-associated yCn➔yTn changes in skin cells from White donors (median for White donors = 209). However, we did not detect statistically significant enrichment with this mutation type in skin cells from Black donors (minimum estimate of mutation load = 0, Fig 4A and S10 Table). The number of nCg➔nTg mutations, which are not associated with UV-lesions did not vary across the two categories of donors (median for White donors = 48, median for African American donors = 40). In addition, although we did not see any difference in the total number of indels or the number of indels in homopolymeric repeats in skin cells obtained from donors of either race, we found increased numbers of deletions spanning five bases or more in skin cells obtained from White donors (median = 9) as compared to the skin cells obtained from African American or Black donors (median = 2, P-value = 0.0002781, calculated by two tailed Mann Whitney test) (Fig 4B and S10 Table). In order to avoid skewing of the data due to differences in sequencing methodologies used for melanocytes and fibroblasts in our samples, we also calculated P-values for each of the cohorts using a two tailed Mann-Whitney test after excluding the data from the melanocytes. Even in this data set, we were clearly able to detect an increase in UV-induced mutations in White donors as compared to African American or Black donors (S10 Table). Overall, our data can be explained by melanin in skin providing strong protection against UV-associated somatic mutations in the form of both UV-signature base substitutions as well as deletions of five bases or more.

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Fig 4. Base substitutions and indels in African American and White donors.

(A) The total number of base substitutions, the nCg➔nTg minimum mutation load and the yCn➔yTn minimum mutation load in African American and White donors. Melanocytes are depicted as filled black circles. (B) The total number of indels, single nucleotide indels in homopolymeric repeats and deletions spanning five bases or more in the African American and White donors. Melanocytes are depicted as filled black circles. A two-sided Mann-Whitney U-test was performed to compare the mutation load across the two cohorts. * denotes a Bonferroni corrected P-value < 0.05. The source data for this figure is in S10 Table.

https://doi.org/10.1371/journal.pgen.1009302.g004

Our cohort also consists of eight men and 13 women. Analysis of mutation load based on sex did not demonstrate any differences between the skin cells obtained from the men or the women (S9 Fig and S10 Table).

Structural variant hotspots colocalize with common fragile sites

Structural variants were only analyzed for the fibroblast clonal lineages and the single melanocyte clonally grown lineage for which we were able to obtain sufficient cells for WGS without whole-genome amplification, since the genome amplification process can result in many false rearrangement calls. There were 120 structural variants in the 35 sequenced clonal lineages (from 1 to 14 in each isolate) (Fig 5A and S11 Table). The structural variants included deletions, duplications, inversions ranging in size from 225 bp to 39 Mbp, as well as translocations. No age-dependent increase in structural variants was evident.

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Fig 5. The structural variants identified in the genomes of skin cells.

(A) The number of structural variants in each donor plotted against the ages of the donors. The black inclined line denotes the linear regression of the data, while the dotted curves denote the 95% confidence intervals. (B) The number of structural variants that were or were not within hotspots and common fragile sites. A Fisher’s exact test was performed to determine if structural variants in hotspots were also preferentially present within common fragile sites. (C) The types of structural variants that overlap and do not overlap common fragile sites. A Chi-square test was performed to determine if the structural variant types within common fragile sites were different from those that did not overlap common fragile sites. The source data for this figure are in S11 Table.

https://doi.org/10.1371/journal.pgen.1009302.g005

We identified genomic regions that are hotspots for chromosomal breakage and structural variation. Two or more rearrangements were denoted as part of a hotspot if they were less than or equal to 1Mbp apart and were present in different samples. Of the 120 structural variants identified, 55 rearrangements were within hotspots. Previously, we showed that structural variants identified in skin fibroblasts of two donors were often in the vicinities of common fragile sites (CFSs) [8]. To determine if the structural variants in this larger data set also often colocalize with CFSs, we identified those deletions, duplications and inversions that intersect common fragile sites within the HumCFS database [44]. We also identified those translocations as colocalizing with fragile sites, whose breakpoints were within 10kb of a CFS. 63 rearrangements were found to colocalize with CFSs. 18 of the rearrangements within CFSs were on chromosome 7, of which 14 rearrangements were within FRA7J, implying that this fragile site is expressed more prominently in fibroblasts than the other fragile sites, leading to higher levels of replication stalling and gross chromosomal breakage. Moreover, the majority of the rearrangements within hotspots also colocalized with CFSs, while the majority of rearrangements that were not within hotspots were scattered across the genome (Fig 5B and S11 Table). Interestingly, we did not see any difference in the types of structural variants that overlap and those that did not overlap CFSs (Fig 5C). Moreover, we determined the use of microhomology at the breakpoints to identify a role of microhomology mediated repair of DSBs at CFSs. Of the 120 rearrangements, only 15 rearrangements contained microhomology at the breakpoints (6 overlapping CFSs, and 9 not overlapping CFSs). These regions of microhomology were small and ranged from 2 to 3 bases. A Fisher’s exact test demonstrated no significant bias in the use of microhomology between the variants that overlapped CFSs versus those that do not (P-value 0.41) (S11 Table).

Overall, we hypothesize that replication-associated difficulties at CFSs are responsible for the generation of rearrangement hotspots in healthy human cells.

Ethics statement

Written consent was obtained from all participants in the Environmental Polymorphisms Registry (registered with ClinicalTrials.gov, NCT00341237, and approved by the NIH Institutional Review Board, protocol 04-E-0053). Each participant provided their age, sex and self-identified race.

Sample collection and processing

4 mm punch skin biopsies were collected from donors’ hips. Samples were collected from healthy cancer-free skin. After overnight incubation of the biopsies at 4°C in 2.66 units/ml dispase (Roche) and 50μg/ml gentamycin (Sigma Aldrich), the epidermis and dermis were separated. The epidermis was emulsified and plated in a six-well cell culture dish in the DermaLife Ma Melanocyte Medium Complete Kit (Lifeline Cell Technology) supplemented with 100μg/ml primocin (Invitrogen). Melanocytes were identified based on their dendritic shape and ability to grow adhered to the dish in serum-free media. The dermis from each biopsy was divided into six to eight pieces which were then allowed to adhere to a six-well cell culture dish and were grown in Dulbecco’s modified eagle’s medium (Gibco) supplemented with 1X non-essential amino acids (Hyclone), 10% Cosmic Calf Serum (Hyclone), 10% AmnioMax C-100 supplement (Gibco) and 100μg/ml primocin. Fibroblasts were identified as adherent cells elongated in shape that grew from the dermis pieces. All cultures were incubated at 37°C in a 5% carbon dioxide containing incubator. A portion of bulk cultures of both fibroblasts and melanocytes were harvested for genomic DNA, and another portion was diluted and plated to obtain single cell-derived clones. Fibroblast clones were expanded in culture for 5 to 6 additional passages (4–6 weeks) to obtain ~10⁶ cells, and genomic DNA was extracted. Genomic DNA extraction from all samples was performed with DNeasy Blood and Tissue kit (Qiagen). Melanocyte clones were expanded in culture for 2 to 3 passages to obtain 10,000 cells and genomic DNA was extracted. 1 to 2.5 ng of the melanocyte genomic DNA was treated with USER (NEB) to remove deaminated cytosines from genomic DNA that are an artifact of DNA extraction [62]. The DNA was amplified using the REPLI-g Mini Kit (Qiagen). 12 to 14 different primer sets were used for PCR across random loci at different chromosomal positions, ranging from 100bp to 500bp, from the amplified genomic DNA. Samples with 10 or more reactions with the correct amplification product were subsequently purified and used for whole-genome sequencing. This quality check allows us to only sequence the genomic DNA with uniform amplification. Venous blood was collected in three to five 8.5mL PAXgene blood DNA tubes (PreAnalytiX/Qiagen) and DNA was isolated from whole blood samples. For 38 DNA samples DNA libraries were prepared using Truseq DNA PCR-free 350bp insert kit (Illumina), and were subsequently sequenced using Illumina HiseqX. For the 30 remaining samples, libraries were prepared using the Nextera DNA Flex library Prep kit (Illumina) and sequenced using the NovaSeq 6000 system. All samples were sequenced as 150 base-paired reads to a depth of 50X to 132X. For a subset of donors, additional skin biopsies were obtained for establishing a second clonal fibroblast lineage.

We also analyzed whole-genome sequenced clonal hip fibroblasts (D1-L-H, D1-R-H1, D1-R-H2, D2-L-H and D2-R-H) from 2 donors that were obtained in a previous study [8].

Calling somatic genome changes in sequenced clones

The FASTQ reads for each clone and blood sample were aligned to the hg19 genome using the GATK best practices pipeline [63]. Three base substitution callers, SomaticSniper [64], VarScan2 [65,66] and Mutect2 [67] were used to identify the clone-specific mutation calls that were not present in blood of the same donors. Only base substitutions detected by all three callers were analyzed further. Any somatic mutations that were also present in the dbSNP138 database, or any SNVs that overlapped SimpleRepeats tract in the UCSC Genome Browser were removed. The final mutation calls were filtered based on allele frequencies, such that only heterozygous mutations with allele frequencies between 45% and 55% or homozygous mutations with allele frequencies greater than 90% were kept. This methodology of using three independent mutation callers and stringent filtering criteria were used previously for accurate measurements of somatic mutations in human fibroblasts and has demonstrated very high accuracy by orthogonal validations [8]. For bulk whole exome sequencing, Mutect2 was used to call mutations. SNVs that overlapped SimpleRepeats tract or were in the dbSNP138 database were removed. The mutation calls for both whole exome and whole-genome sequencing have been organized as MAF files in the TCGA format and have been submitted to dbGAP study phs001182.v2.p1. Somatic structural variants within 1Mb of each other in different donors were marked as being within a “hotspot”.

Delly was used to identify structural variants in the form of deletions, duplications, inversions and translocations [8,68]. Calls which were designated “LowQual” and/or “IMPRECISE” were removed. Clonality of structural variants was determined based on the allelic fraction of reads supporting the variants in the clone. Structural variants with 30% or more reads supporting the structural variant and the absence of any reads supporting the variants in blood were denoted as clonal somatic changes. Due to the low number of variants, we cannot rule out that some of the structural variants may have been generated due to a rearrangement in during the first few cell divisions of the founder cell in culture. However, we think this is unlikely as these cells were passaged less than 3 times before the generation of a clonal lineage. Moreover, the number and types of variants are similar to those detected in previous studies [69–71] indicating that the structural variants detected in our work were likely present in founder cells.

Indels were detected using the tool SV-ABA [72] and were filtered based on multiple criterion. Indel calls with a quality score less than 50 were removed and were only included if they occurred between 45%-55% allele frequency (heterozygous indel), or between 90%-100% allele frequency (homozygous indel). Indels that overlapped with the SimpleRepeats or the RepeatMasker tracts were removed as these calls were often found to be erroneous. A subset of the indels were visually verified by inspection of the alignments using the Integrative Genomics Viewer [73]. 46 indels were orthogonally verified via PCR amplification and Sanger Sequencing.

Analyzing base substitution and indel signatures in clones

We used the SigProfilerMatrixGenerator [74] to identify the different types of indels in our samples. SigProfilerExtractor [13] was used to deconvolute the single base substitution, dinucleotide base substitution and indel signatures in our samples. 9 processes with 10 iterations were used within SigProfilerExtractor for extraction of indel and base substitution signatures. MutationalPatterns [75] was used to both identify the cosine similarities between the mutation patterns in samples in this study and the signatures identified in COSMIC and to also identify the contributions of COSMIC signatures in our samples. For base substitutions, the function fit_to_signatures() within MutationalPatterns was used to identify the contributions of the COSMIC signatures on the mutation profile of each sample. For indels, the function fit_to_signatures() was modified to allow the matrix to have 83 rows instead of 96 so that the indels in our samples could be compared to the known ID signatures (83 channels) in COSMIC.

The enrichment of mutation signatures in each of the samples analyzed in this study was calculated as described in [8,14,35]. For this calculation, context is defined as the +/- 20 bases surrounding the mutated base. The mutated residue is capitalized in the annotation of the signature and the equation to calculate enrichment of a given mutation signature is provided below with the UV-mutation signature yCn➔yTn as an example.

For each motif, the reverse complement was also taken into account in the calculations. Mutations <10 bases apart, are excluded in this calculation as these are “complex” mutations that likely arise due to the activity of translesion polymerases and may confound the analysis of the mutation signatures. To determine if increased fold enrichments for the mutation signatures were statistically relevant a Fisher’s Exact test was performed wherein the ratio of the number of mutations within the trinucleotide motif (Mutations_yCn→yTn), and those that do not conform to the trinucleotide motif (Mutations_C→T), were compared to the number of unmutated bases in the context that either were in the trinucleotide motif (Context_ycn) versus those that were not in the context (Context_c). Multiple hypothesis testing was further accounted for by the correction of the P-values via the Benjamini-Hochberg method. For samples where enrichment > 1 and the corrected P-value < 0.05, the Minimum Mutation load was calculated for the enriched signature. The equation for calculating this is provided below for the yCn➔yTn mutation signature.

Analysis of bulk DNA samples

We also sequenced the exomes of 15 fibroblast bulk samples and 4 melanocyte bulk samples directly cultured from the biopsies. Bulk samples are defined as cells that were not propagated clonally. Libraries were prepared using the Nextera Flex for Enrichment library prep kit, Illumina Exome Panel (Illumina) and IDT for Illumina UD Indexes (Illumina). All samples were sequenced using the NovaSeq 6000 system up to approximately ~150X depth. Somatic mutations were called in the samples by using Mutect2. Whole-genome-sequenced blood samples from the donor corresponding to each bulk sample was used as a proxy for germline mutations. Only single nucleotide variants called by Mutect2 were further analyzed. Any mutations that were within the dbSNP138 database or in the SimpleRepeats tract were removed.

Annotation of SNVs

We used Annovar [76] to annotate SNVs for changes to protein sequence using the refGene track from UCSC Genome Browser. Nonsynonymous SNVs or SNVs affecting start or stop codons and splice sites were further annotated using the Cancer Genome Interpreter [39] as driver mutations or passenger mutations.