Damla Kaptan’s research while affiliated with Middle East Technical University and other places

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Publications (18)


Unravelling Cultural and Genetic Interactions during the Aegean Neolithization
  • Conference Paper
  • Full-text available

November 2024

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58 Reads

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The emergence of Neolithic villages in Western Anatolia, particularly between 7000-6000 BCE, has caused debates regarding the driving forces behind this transition. While earlier hypotheses suggested demic diffusion from the Fertile Crescent, recent studies suggest more complex population dynamics. We address this question by combining material culture analyses with paleogenomic data to trace the Neolithic origins in the region. A single genome from the pre-7000 BCE period revealed a local population in Western Anatolia genetically linked to Epipaleolithic Central Anatolia, indicating continuity and adoption of farming by local hunter-gatherers. In the period 7000-6000 BCE, we found that some Neolithic populations still reflect a local genetic profile, while others show genetic affinity to Central Anatolia. This suggests significant population movement that accompanied cultural exchanges among regions, but also admixture between local populations and migrants from Central Anatolia, which we infer to have occurred at varying degrees in different settlements of Western Anatolia, with the highest rate observed in NW Anatolia. These admixed populations also appear to have migrated to the Western Aegean represented by N Greece here. However, when we compared material culture data with genetic data, we found no correlation between them. This suggests that cultural transmission might have occurred faster than genetic. Our analysis indicates that the Neolithization of the Aegean was a complex process involving genetic and cultural exchanges from Central Anatolia, along with admixture with local populations. These insights deepen our understanding of the intricate socio-cultural and genetic factors that influenced the development of Neolithic societies in the region.

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The Population History of Domestic Sheep Revealed by Paleogenomes

October 2024

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191 Reads

Molecular Biology and Evolution

Sheep was one of the first domesticated animals in Neolithic West Eurasia. The zooarchaeological record suggests that domestication first took place in Southwest Asia, although much remains unresolved about the precise location(s) and timing(s) of earliest domestication, or the post-domestication history of sheep. Here, we present 24 new partial sheep paleogenomes, including a 13,000-year-old Epipaleolithic Central Anatolian wild sheep, as well as 14 domestic sheep from Neolithic Anatolia, two from Neolithic Iran, two from Neolithic Iberia, three from Neolithic France, and one each from Late Neolithic/Bronze Age Baltic and South Russia, in addition to five present-day Central Anatolian Mouflons and two present-day Cyprian Mouflons. We find that Neolithic European, as well as domestic sheep breeds, are genetically closer to the Anatolian Epipaleolithic sheep and the present-day Anatolian and Cyprian Mouflon than to the Iranian Mouflon. This supports a Central Anatolian source for domestication, presenting strong evidence for a domestication event in SW Asia outside the Fertile Crescent, although we cannot rule out multiple domestication events also within the Neolithic Fertile Crescent. We further find evidence for multiple admixture and replacement events, including one that parallels the Pontic Steppe-related ancestry expansion in Europe, as well as a post-Bronze Age event that appears to have further spread Asia-related alleles across global sheep breeds. Our findings mark the dynamism of past domestic sheep populations in their potential for dispersal and admixture, sometimes being paralleled by their shepherds and in other cases not.


Ancient DNA analyses of two Early Chalcolithic Individuals from the West Mound

October 2024

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46 Reads

In this chapter, we investigate the genetics of two Early Chalcolithic Catalhoyuk individuals, U.18333 and U.16835, the only two burials yet recovered from the West Mound. These were two neonates buried within the same building. Using shotgun-sequenced partial genomes (0.06x and 0.02x coverage) we identify both as females. Despite being recovered from the same building, we find no close genetic kinship between them, in line with previously published kinship results from Catalhoyuk. We also find that the two West Mound neonates shared the same gene pool with Neolithic Catalhoyuk and other Central and West Anatolian Neolithic populations, and they did not carry the Caucasus-related U+201CeasternU+201D gene flow signature observed in later-coming Chalcolithic Anatolian genomes. This indicates no large-scale admixture between East and West Mound Catalhoyuk, and possibly that the post-Neolithic U+201CeasternU+201D gene flow event into Anatolia may have initiated only by the mid-6th millennium BCE.


Figure 1: Map of Aegean and Anatolian sites >6000 BCE with palaeogenomics data analysed in this study. Smaller fonts and symbols indicate sites where only published genomic data have been included, while bold fonts and large symbols indicate sites where new palaeogenomic data has been produced, with sample sizes shown in parentheses (see also Table 1, Figure S1, Tables S1-2). We also used published data of 453 individuals from U Mesopotamia, the Balkans, Zagros, Levant, Cyprus and from European sites in our analyses, not shown in this figure. To improve visualization, some of the locations were slightly shifted (the exact site coordinates can be found in Table S1-2).
Figure 4: The affinities of Epipalaeolithic Pınarbaşı, Girmeler and Aktopraklık genomes to C Anatolia versus W Anatolia/Greece analysed using f4-tests. The populations on the left side are C Anatolians post-7500 BCE (Çatalhöyük, Musular, Tepecik-Çiftlik) while those on the right side are Neolithic groups from W Anatolia or Greece. The boxplots show the distribution of the f4-statistics performed using groups of genomes per site; e.g. the top left comparison involves three comparisons of the form f4(Yoruba, Pınarbaşı/Girmeler/Aktopraklık; Çatalhöyük/Musular/Tepecik-Çiftlik, W Anatolia/Greece), one including Çatalhöyük, one Musular, and one Tepecik-Çiftlik. Colour coding indicates the proportion of nominally significant tests out of all comparisons (at |Z|>3). The "_HG" and "_N" suffixes indicate "hunter-gatherer" and "Neolithic"-related populations, respectively. The "CP" suffix stands for aDNA data produced using capture technologies (instead of shotgun).
Figure 5: IBD-sharing network across the Aegean showing distant genetic relatedness. The analysis was performed using imputed ancient genomes from the study region and includes ≥8 cM segments (the majority of these were 8-12 cM, and the only IBD-segments >16cM were found between Nea Nikeamedia-Revenia in Greece, and between Aktopraklık-Bahçelievler in NW Anatolia). The colours shown in the key indicate the strength of connections between pairs of genomes in any two sites. We calculate the strength given the number of comparisons and the maximum IBD sharing observed in the dataset. For example, if regions X and Y are represented by 3 and 5 genomes, if any two genomes share a maximum of 4 segments in the full dataset, and if across the 15 X-Y comparisons there are 7 segments in total shared, the X-Y connection strength is estimated as 7/(4x15) = 0.12 (see also Table S5 and Figure S22).
Figure 6: The influence of geographic proximity and genetic similarity on material culture similarities among 7 th millennium BCE sites across SW Asia and the Aegean. A: Presence/absence records of 58 material culture traits compiled from the literature for 16 SW Asian/Aegean sites covering 7000-5800 BCE and that have genetic data (see Table S6 for the full dataset). B-D: Correlations between pairwise distances among sites in material culture (Jaccard dissimilarity), geodesic distances (geographic shortest path estimates) and genetic distances (1-f3) across the 16 sites (Methods). E: Correlation between the residuals of sociocultural and genetic distances after each was regressed on geodesic distances using linear regression. The Spearman correlation coefficient and the Mantel test p-values are shown inside the panels. Partial Mantel tests between cultural and genetic distances controlling for the effect of geography were also non-significant (r=-0.03, p=0.56) (see also Figures S33-36).
Out-of-Anatolia: cultural and genetic interactions during the Neolithic expansion in the Aegean

June 2024

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614 Reads

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1 Citation

Western Anatolia has been a crucial yet elusive element in the Neolithic expansion from the Fertile Crescent to Europe. Using 30 new palaeogenomes from Anatolia c.8000-6000 BCE we describe the early Holocene genetic landscape of Western Anatolia, suggesting population continuity since the late Upper Pleistocene. Our findings indicate that the Neolithisation of Western Anatolia in the 7th millennium BCE was a multifaceted process, characterised by the assimilation of Neolithic practices by indigenous groups and the influx of populations from the east, their admixed descendants eventually laying the foundations of Neolithic Southeast Europe. Intriguingly, the observed diversity in material culture among Aegean Early Neolithic communities correlates with their geographical distances but not their genetic differences, signifying a decoupling between cultural developments and genetic admixture processes.


Figure 2: Characterising the Çatalhöyük East Mound gene pool and temporal change. A) 221 Multidimensional scaling (MDS) plot summarising outgroup f 3 -based genetic distances 222 among late Upper Pleistocene and early Holocene genomes from Southwest Asia, including 223 67 unrelated Çatalhöyük genomes. B) qpAdm modelling of ancestry sources (shown in 224 colours) 8th and 7th millennium Neolithic Anatolian genomes from Çatalhöyük (three 225 periods), Tepecik-Çiftlik, Musular, and Barcın. Each column indicates a feasible model, with 226 the y-axis showing admixture proportions. C) f 4 -statistics between groups of genomes from 227 the three Çatalhöyük periods. D) IBD-sharing with genetically sampled PPN and PN 228 settlements from Anatolia. The colour represents the relative strength of IBD-sharing 229 between two settlements, calculated as the total number of segments shared between all 230 pairwise comparisons divided by the total number of comparisons and the maximum sharing 231 between any pairs in the full sample. E) Mitochondrial DNA and Y chromosome haplogroup 232 diversity in Çatalhöyük and French Neolithic Gurgy (8), the latter representing a gene pool 233 shaped by patrilocal practices. The numbers of total pairs in each category is indicated on 234 the bars. The difference in chrY diversities between Gurgy and Çatalhöyük is significant as 235 measured by a random subsampling experiment (Figure S7). F) Comparison of the F ROH 236 values, the inbreeding coefficient estimated using runs of homozygosity (ROH) >4cM, 237 among different Neolithic sites in Anatolia. G) The distribution of mean F (inbreeding 238 coefficient) values in a sample of 16 individuals estimated using genealogy simulations 239
Figure 3: A network of genetic kin across Çatalhöyük buildings and the changing frequency 368 of genetic ties among co-burials. A) The figure shows genetic relatedness among intramural 369 burials with common SNPs >3000, shown as dots. The lines show close to more distant 370 relationships from dark to light colours. The coloured blocks show buildings, with building 371 numbers assigned by the excavation team indicated adjacent to the blocks. The height of the 372 blocks is proportional to the number of genetically represented burials in that building. North 373 and South refer to the two main excavation areas on the mound separated by ~200m. B) 374 The proportion of genetic kin (up to third-degree) identified between individuals buried in 375 different buildings in the three Çatalhöyük periods. C) The proportion of genetic kin (up to 376 third-degree) identified in co-burials within the same building, separated into three 377 Çatalhöyük periods. See also Figure S9 for the same proportion calculated for different sets 378 of relatives and age groups. The analysis involves 23 buildings. Percentages indicated on 379 the horizontal bars show the percentage of Monte Carlo simulations where the null 380 hypothesis of no difference between a pair of periods was rejected (p<0.05) out of 24 381 scenarios involving various assumptions/conditions. The overall rate of rejection among all 382 108 comparisons was 69% (see Figure S12 for details). D) The proportion of genetic kin 383 within co-burials in 15 buildings (only including buildings with a minimum of 2 burials). The 384 inset shows the Spearman correlation coefficient (p=0.03). 385 386 Co-burial of genetically unrelated individuals increases over time 387 388 Interestingly, we noticed a temporal change in the density of genetic connections among 389 burials in the same building. Specifically, co-buried pairs inside Early-period buildings were 390 frequently third-degree (e.g., cousin) or closer genetic kin (63%) (Figure 3), a pattern similar 391 to those of PPN Anatolian settlements such as Aşıklı, Boncuklu, and Çayönü(31, 42). In 392 contrast, genetic kin among co-buried pairs was only at 30% and 22% frequencies in the 393 Middle and Late periods, respectively (Figure 3, Figure S12). We also calculated the 394 correlation between co-burial genetic kin frequencies per building and the building ages and 395
Female lineages and changing kinship patterns in Neolithic Çatalhöyük

June 2024

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618 Reads

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1 Citation

Arguments have long suggested that the advent of early farming in the Near East and Anatolia was linked to a ‘Mother Goddess’ cult. However, evidence for a dominant female role in these societies has been scarce. We studied social organisation, mobility patterns and gendered practices in Neolithic Southwest Asia using 131 paleogenomes from Çatalhöyük East Mound (7100-5950 BCE), a major settlement in Central Anatolia with an uninterrupted occupation and an apparent egalitarian structure. In contrast to widespread genetic evidence for patrilocality in Neolithic Europe, the Çatalhöyük individuals revealed no indication of patrilocal mobility. Analysing genetic kin ties among individuals buried in the same house (co-burials) across 35 Çatalhöyük buildings, we identified close ties concentrated within buildings and among neighbours in Çatalhöyük’s Early period, akin to those in the preceding Pre-Pottery Neolithic in Southwest Asia. This pattern weakened over time: by the late 7th millennium BCE, subadults buried in the same building were rarely closely genetically related, despite sharing similar diets. Still, throughout the site’s occupation, genetic connections within Çatalhöyük buildings were much more frequently connected via the maternal than the paternal line. We also identified differential funerary treatment of female subadults compared to those of males, with a higher frequency of grave goods associated with females. Our results reveal how kinship practices changed while key female roles persisted over one thousand years in a large Neolithic community in western Eurasia.


Ancient Sheep Genomes Reveal Four Millennia of North European Short-Tailed Sheep in the Baltic Sea Region

May 2024

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185 Reads

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2 Citations

Genome Biology and Evolution

Sheep are among the earliest domesticated livestock species, with a wide variety of breeds present today. However, it remains unclear how far back this diversity goes, with formal documentation only dating back a few centuries. North European short-tailed (NEST) breeds are often assumed to be among the oldest domestic sheep populations, even thought to represent relicts of the earliest sheep expansions during the Neolithic period reaching Scandinavia less than 6000 years ago. This study sequenced the genomes (up to 11.6X) of five sheep remains from the Baltic islands of Gotland and Åland, dating from Late Neolithic (∼4100 calBP) to historical times (∼1600 CE). Our findings indicate that these ancient sheep largely possessed the genetic characteristics of modern NEST breeds, suggesting a substantial degree of long-term continuity of this sheep type in the Baltic Sea region. Despite the wide temporal spread, population genetic analyses show high levels of affinity between the ancient genomes and they also exhibit relatively high genetic diversity when compared to modern NEST breeds, implying a loss of diversity in most breeds during the last centuries associated with breed formation and recent bottlenecks. Our results shed light on the development of breeds in Northern Europe specifically as well as the development of genetic diversity in sheep breeds, and their expansion from the domestication center in general.


Population Genomic History of the Endangered Anatolian and Cyprian Mouflons in Relation to Worldwide Wild, Feral, and Domestic Sheep Lineages

April 2024

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197 Reads

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2 Citations

Genome Biology and Evolution

Once widespread in their homelands, the Anatolian mouflon (Ovis gmelini anatolica) and the Cyprian mouflon (Ovis gmelini ophion) were driven to near extinction during the 20th century and are currently listed as endangered populations by the IUCN. While the exact origins of these lineages remain unclear, they have been suggested to be close relatives of domestic sheep or remnants of proto-domestic sheep. Here, we study whole genome sequences of n = 5 Anatolian mouflons and n = 10 Cyprian mouflons in terms of population history and diversity, comparing them to eight other extant sheep lineages. We find reciprocal genetic affinity between Anatolian and Cyprian mouflons and domestic sheep, higher than all other studied wild sheep genomes, including the Iranian mouflon (Ovis gmelini). Studying diversity indices, we detect a considerable load of short runs of homozygosity (ROH) blocks (<2 Mb) in both Anatolian and Cyprian mouflons, reflecting small effective population size (Ne). Meanwhile, Ne as well as mutation load estimates are lower in Cyprian compared to Anatolian mouflons, suggesting the purging of recessive deleterious variants in Cyprian sheep under a small long-term Ne, possibly attributable to founder effects, island isolation, introgression from domestic lineages, or differences in their bottleneck dynamics. Expanding our analyses to worldwide wild and feral Ovis genomes, we observe varying viability metrics among different lineages, and a limited consistency between viability metrics and IUCN conservation status. Factors such as recent inbreeding, introgression, and unique population dynamics may have contributed to the observed disparities.


Figure 3. Heterozygosity and diversity estimates of the studied sheep lineages. (A) Genome-wide heterozygosity values estimated using genotype likelihoods. Only the high coverage individuals cym008 and oga018 from the ANM and CYM populations were included. (B) Within-population diversity values estimated using pairwise 1 -outgroup f 3 statistics per lineage. (C) Comparison of autosomal vs . X chromosome diversities, each estimated using pairwise 1 -outgroup f 3 statistics. The regression line was generated with the loess algorithm in the R stats package.
Figure 4. Runs of Homozygosity (ROH) analyses. (A) Number of ROH segments longer than 500 kb plotted against the total length of the segments found in each individual. The ANM and CYM populations are only represented by the high-coverage individuals oga018 and cym008, respectively. (B) Size distribution of ROH segments divided into four classes (0.5-1 Mb, 1-2 Mb, 2-3 Mb, 3-5 Mb). Inbreeding times corresponding to each size class was estimated assuming a generation time of 3 years and a recombination rate of 1.5 cM/Mb [38,39]. The x-axis is given in log scale. (C) Proportion of ROH segments longer than 500kb in each individual's genome.
Figure 5. Mutation load estimates using GERP scores. Relative mutation loads were calculated as average GERP scores weighted by the number of derived variants, only including variants found in conserved regions (GERP > 4) [41]. We used goat alleles to infer the derived
Figure 6. Co-evaluation of genetic viability metrics and IUCN status. (A) Correlations between viability metrics per individual compared across sheep lineages assessed by the IUCN. Regression lines were calculated using the method "loess" in the R stats package. (B) The IUCN status compared with the genetic viability metrics heterozygosity (π) , F ROH , and relative mutation load.
General information on the newly generated and published genomes.
Population genomic history of the endangered Anatolian and Cyprian mouflons in relation to worldwide wild, feral and domestic sheep lineages

November 2023

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270 Reads

Once widespread in their homelands, Anatolian mouflon (Ovis gmelini anatolica) and Cyprian mouflon (Ovis gmelini ophion) were driven to near extinction during the 20th century and are currently listed as endangered populations by the IUCN. While the exact origins of these lineages remain unclear, they have been suggested to be close relatives of domestic sheep or remnants of proto-domestic sheep groups. Here, we study whole genome sequences of n=5 Anatolian mouflons and n=10 Cyprian mouflons in terms of population history and diversity, relative to eight other extant sheep lineages. We find reciprocal genetic affinity between Anatolian and Cyprian mouflons and domestic sheep, higher than all other studied wild sheep genomes, including the Iranian mouflon (Ovis gmelini). Despite similar recent population dynamics, Anatolian and Cyprian mouflons exhibit disparate diversity levels, which can potentially be attributed to founder effects, island isolation, introgression from domestic lineages, or different bottleneck dynamics. The lower relative mutation load found in Cyprian compared to Anatolian mouflons suggests the purging of recessive deleterious variants in the former. This agrees with estimates of a long-term small effective population size in the Cyprian mouflon. Both subspecies harbor considerable numbers of runs of homozygosity (ROH) blocks <2 Mb, which reflects the effect of small population size. Expanding our analyses to worldwide wild and feral Ovis genomes, we observe varying viability metrics among different lineages, and a limited consistency between viability metrics and conservation status. Factors such as recent inbreeding, introgression, and unique population dynamics may contribute to the observed disparities.


Figure 1. Overview of the MTaxi pipeline. Flowchart and representations of the steps to determine the sample taxon. Here sheep and goat stand for the candidate species pair, but MTaxi can be applied to any pair of species where mitochondrial DNA reference sequences are available. Target sites represent mismatches (candidate substitutions) between the reference genomes, restricted to transversions. Blue coloured alleles represent transitions, red coloured alleles represent transversions. Reads are assigned to either taxon based on target sites. Purple coloured alleles represent sheep alleles, orange coloured alleles represent goat alleles. Reads may be assigned to the wrong taxon due to homoplastic mutations, technical error, or incomplete lineage sorting.
Figure 2. Distribution of target sites along reference mitochondrial genomes. The figure shows the position of target sites along (a) sheep and (b) goat (c) horse (d) donkey reference mitochondrial genomes. The sites represent transversion-type substitutions (n=197 for sheep and goat, and n=117 for horse and donkey). The figure was generated through CGview 39 .
MTaxi: A comparative tool for taxon identification of ultra low coverage ancient genomes

September 2023

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82 Reads

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2 Citations

A major challenge in zooarchaeology is to morphologically distinguish closely related species’ remains, especially using small bone fragments. Shotgun sequencing aDNA from archeological remains and comparative alignment to the candidate species’ reference genomes will only apply when reference nuclear genomes of comparable quality are available, and may still fail when coverages are low. Here, we propose an alternative method, MTaxi, that uses highly accessible mitochondrial DNA (mtDNA) to distinguish between pairs of closely related species from ancient DNA sequences. MTaxi utilises mtDNA transversion-type substitutions between pairs of candidate species, assigns reads to either species, and performs a binomial test to determine the sample taxon. We tested MTaxi on sheep/goat and horse/donkey data, between which zooarchaeological classification can be challenging in ways that epitomise our case. The method performed efficiently on simulated ancient genomes down to 0.3x mitochondrial coverage for both sheep/goat and horse/donkey, with no false positives. Trials on n=18 ancient sheep/goat samples and n=10 horse/donkey samples of known species identity also yielded 100% accuracy. Overall, MTaxi provides a straightforward approach to classify closely related species that are difficult to distinguish through zooarchaeological methods using low coverage aDNA data, especially when similar quality reference genomes are unavailable. MTaxi is freely available at https://github.com/goztag/MTaxi .


Figure 1. Overview of the MTaxi pipeline. Flowchart and representations of the steps to determine the sample taxon. Here sheep and goat stand for the candidate species pair, but MTaxi can be applied to any pair of species where mitochondrial DNA reference sequences are available. Target sites represent mismatches (candidate substitutions) between the reference genomes, restricted to transversions. Blue coloured alleles represent transitions, red coloured alleles represent transversions. Reads are assigned to either taxon based on target sites. Purple coloured alleles represent sheep alleles, orange coloured alleles represent goat alleles. Reads may be assigned to the wrong taxon due to homoplastic mutations, technical error, or incomplete lineage sorting.
Figure 2. Distribution of target sites along reference mitochondrial genomes. The figure shows the position of target sites along (a) sheep and (b) goat (c) horse (d) donkey reference mitochondrial genomes. The sites represent transversion-type substitutions (n=197 for sheep and goat, and n=117 for horse and donkey). The figure was generated through CGview 39 .
MTaxi: A comparative tool for taxon identification of ultra low coverage ancient genomes

July 2023

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87 Reads

A major challenge in zooarchaeology is to morphologically distinguish closely related species’ remains, especially using small bone fragments. Shotgun sequencing aDNA from archeological remains and comparative alignment to the candidate species’ reference genomes will only apply when reference nuclear genomes of comparable quality are available, and may still fail when coverages are low. Here, we propose an alternative method, MTaxi, that uses highly accessible mitochondrial DNA (mtDNA) to distinguish between pairs of closely related species from ancient DNA sequences. MTaxi utilises mtDNA transversion-type substitutions between pairs of candidate species, assigns reads to either species, and performs a binomial test to determine the sample taxon. We tested MTaxi on sheep/goat and horse/donkey data, between which zooarchaeological classification can be challenging in ways that epitomise our case. The method performed efficiently on simulated ancient genomes down to 0.3x mitochondrial coverage for both sheep/goat and horse/donkey, with no false positives. Trials on n=18 ancient sheep/goat samples and n=10 horse/donkey samples of known species identity also yielded 100% accuracy. Overall, MTaxi provides a straightforward approach to classify closely related species that are difficult to distinguish through zooarchaeological methods using low coverage aDNA data, especially when similar quality reference genomes are unavailable. MTaxi is freely available at https://github.com/goztag/MTaxi .


Citations (6)


... Contexts such as latrines that are less influenced by external factors and abundantly rich in organic remains are Likewise, sedaDNA may help to increase spatial coverage of historical distribution maps of wild species, as well as -on a more local scale-assessment of their presence in the surroundings of humans. A drawback of using sedaDNA for the detection of specific domesticated or wild variants of a taxon is that such variants may be hard to distinguish in case of low DNA yields from a certain taxon, quality or availability of references, postmortem damage (Atağ et al. 2022) and in some cases when samples have DNA from multiple closely related taxa. ...

Reference:

Archaeology meets environmental genomics: implementing sedaDNA in the study of the human past
MTaxi: A comparative tool for taxon identification of ultra low coverage ancient genomes

... Domestication has been the dominant and most enduring innovation of the transition from a hunter-gathering lifestyle to farming societies, representing the direct exploitation of genetic diversity of wild plants and animals for human benefit. Ancient DNA (aDNA) has proved crucial to understanding the domestication process and the interaction between domesticated species and their wild relatives both within domestication centers and throughout the regions that the domestics expanded into (1)(2)(3)(4)(5)(6)(7)(8)(9)(10)(11)(12)(13). The origins of the European domestic taurine, Bos taurus, are located in the Fertile Crescent (14,15) and unlike dogs, pigs and goats, where the wild forms are still extant, the wild cow (the aurochs) went extinct in 1627. ...

Ancient Sheep Genomes reveal four Millennia of North European Short-Tailed Sheep in the Baltic Sea region

... The genetic data were gathered from the following publications: Kılınç et al. (2016); Koptekin (2022); Koptekin et al. (2023;; Lazaridis et al. (2016;; Marchi et al. (2022); Mathieson et al. (2015;; Mattila et al. (2022); Narasimhan et al. (2019); Nikitin et al. (2024); Posth et al. (2023); Siska (2018); Skourtanioti et al. (2020); Wang et al. (2019;2023); Yaka et al. (2021). The information concerning the individuals from the Caucasus and those from neighbouring regions of the same periods is summarised in two tables, one presenting the characteristics (context, C14 dates, sex, mtDNA and Y haplogroups, references) of each of the individuals analysed (Supplementary Data 1), the other presenting the different names of the genetic groups to which these individuals are assigned (Supplementary Data 2). ...

Spatial and temporal heterogeneity in human mobility patterns in Holocene Southwest Asia and the East Mediterranean

Current Biology

... We split this inference into four phases with each phase targeting a simple inferential goal to prevent a number of technical problems such as high dimensionality and overparametrization. (B) the map shows details of Anatolia and surrounding regions with haplogroup frequencies by archeological site, except for neolithic southwestern Anatolia, where the grouping is at the regional scale (notice the tentacles out of the pie chart indicating the included locations, named below the map). text in red indicates data reported in previous studies (42,43), wherein haplogroups A to E were assigned using five diagnostic single-nucleotide polymorphism (SnP) markers of a 144-base pair (bp) control region fragment. Pie chart areas are proportional to their sample sizes (key, bottom left). ...

Archaeogenetic analysis of Neolithic sheep from Anatolia suggests a complex demographic history since domestication

Communications Biology

... The genetic data were gathered from the following publications: Kılınç et al. (2016); Koptekin (2022); Koptekin et al. (2023;; Lazaridis et al. (2016;; Marchi et al. (2022); Mathieson et al. (2015;; Mattila et al. (2022); Narasimhan et al. (2019); Nikitin et al. (2024); Posth et al. (2023); Siska (2018); Skourtanioti et al. (2020); Wang et al. (2019;2023); Yaka et al. (2021). The information concerning the individuals from the Caucasus and those from neighbouring regions of the same periods is summarised in two tables, one presenting the characteristics (context, C14 dates, sex, mtDNA and Y haplogroups, references) of each of the individuals analysed (Supplementary Data 1), the other presenting the different names of the genetic groups to which these individuals are assigned (Supplementary Data 2). ...

Variable kinship patterns in Neolithic Anatolia revealed by ancient genomes

Current Biology

... Studying natural selection on Anatolian human populations against the backdrop of lifestyle changes and admixture (Mathieson et al. 2015;Marchi et al. 2020), the study of domestic animal population dynamics as a proxy for human interaction and trade networks (Daly et al. 2018;Yurtman et al. 2020), and the study of ancient microbes from tooth samples and from dental calculus, including ancient pathogens and oral microbiomes (Key et al. 2020), are additional lines of study that we expect will attract increasing attention in the near future. ...

Archaeogenetic analysis of Neolithic sheep from Anatolia suggests a complex demographic history since domestication