The Kets, an ethnic group in the Yenisei River basin, Russia, are considered the last nomadic hunter-gatherers of Siberia and Ket language has no transparent affiliation with any language family. We investigated connections between the Kets and Siberian and North American populations, with emphasis on the Mal’ta and Paleo-Eskimo ancient genomes, using original data from 46 unrelated samples of Kets and 42 samples of their neighboring ethnic groups (Uralic-speaking Nganasans, Enets and Selkups). We genotyped over 130,000 autosomal SNPs, identified mitochondrial and Y-chromosomal haplogroups and performed high-coverage genome sequencing of two Ket individuals. We established that Nganasans, Kets, Selkups and Yukaghirs form a cluster of populations most closely related to Paleo-Eskimos in Siberia (not considering indigenous populations of Chukotka and Kamchatka). Kets are closely related to modern Selkups and to some Bronze and Iron Age populations of the Altai region, with all these groups sharing a high degree of Mal’ta ancestry. Implications of these findings for the linguistic hypothesis uniting Ket and Na-Dene languages into a language macrofamily are discussed.
The Kets (an ethnic group in the Yenisei River basin, Russia) are among the least studied native Siberians. Ket language lacks apparent affiliation with any major language family and is clearly distinct from surrounding Uralic, Turkic and Tungusic languages1. Moreover, until their forced settlement in 1930s, Kets were considered the last nomadic hunter-gatherers of North Asia outside the Pacific Rim2.
Ket language, albeit almost extinct, is the only language of the Yeniseian family that survived into the 21st century. Most Yeniseian-speaking tribes (Arin, Assan, Baikot, Kott, Pumpokol, Yarin, Yastin) used to live south of the current Ket settlements. According to toponymic evidence, prior to the 17th century speakers of this language family occupied vast territories of Western and Central Siberia, from northern Mongolia in the south to the middle Yenisei River in the north and from the Irtysh River in the west to the Angara River in the east3,4. The Altai region was suggested as a homeland of the Yeniseian language family2 and ancestors of the Yeniseian people were tentatively associated5 with the Karasuk culture (3200-2700 YBP) of the upper Yenisei6. Yeniseian linguistic substrate is evident in many contemporary Turkic languages of this region (South Siberia): Altaian, Khakas, Shor, Tubalar, Tuvinian and in Mongolic Buryat language2. As these languages are spoken in river basins with Yeniseian river names1, the Yeniseian tribes were likely to have mixed with these ethnic groups (and with the Southern Samoyedic groups Kamasins and Mators, now extinct1) at different times. We expect to find genetic signatures of these events.
Over the centuries, Kets and other Yeniseian people suffered relocation, extinction and loss of language and culture. First, they were under a constant pressure from the reindeer herders to the north (Enets and Nenets) and east (Evenks) and the Turkic-speaking pastoralists to the south. Second, Russian conquest of Siberia, which started at the end of the 16th century, exposed the natives to new diseases, such as the 17th century smallpox epidemic7. Third, in the 20th century USSR resettled the Kets in Russian-style villages, thus interrupting their nomadic lifestyle2. Under the pressure of disease and conflict, the Kets have been gradually migrating north along the Yenisei River and now reside in several villages in the Turukhansk district (Krasnoyarsk region); around 1,200 people in total8. Until the 20th century, Kets, being nomadic hunters and fishers in a vast Siberian boreal forest, had little contact with other ethnic groups, which is manifested by the rarity of loanwords in Ket language2. However, since the collapse of the inter-Ket exogamous marriage system following the smallpox epidemics in the 17th and 18th centuries, Kets have been marrying Selkups, Uralic-speaking reindeer herders2,9. Moreover, during the 20th century, the settled Kets have been increasingly mixing with other native Siberian people and with the Russians, which resulted in irrevocable loss of Ket language, genotype and culture.
Recently, a tentative link was proposed between the Yeniseian language family and the Na-Dene family of Northwest North America (composed of Tlingit, Eyak and numerous Athabaskan languages), thus forming a Dene-Yeniseian macrofamily10,11,12. The Dene-Yeniseian-linkage is viewed by some as the first relatively reliable trans-Beringian language connection11, with important implications for timing of the alleged Dene-Yeniseian population split, the direction of the subsequent migration (from or to America), the possible language shifts and population admixture13,14,15.
So far, no large-scale population study was conducted with samples from each of the presently occupied Ket villages. Previously, six Ket individuals were genotyped16,17,18 and two of them sequenced19 These studies concluded that the Kets do not differ from surrounding Siberian populations, a rather surprising finding, given their unique language and ancient hunter-gatherer life-style. In order to clarify this issue, in 2013 and 2014 we collected 57 (46 unrelated) samples of Kets and 42 unrelated samples of their neighboring Uralic-speaking ethnic groups (Nganasans inhabiting the Taymyr Peninsula and Enets and Selkups living further south along Yenisei). We genotyped approximately 130,000 autosomal SNPs and determined mitochondrial and Y-chromosomal haplogroups with the GenoChip array20. We also performed high-coverage genome sequencing of two Ket individuals. Using these data, we investigated connections between Kets and modern and ancient Siberian and North American populations (including the Mal’ta and Saqqaq ancient genomes). In addition, we estimated Neanderthal contribution in Kets’ genome and in specific gene groups.
Mal’ta is a ~24,000 YBP old Siberian genome, recently described21 as a representative of ancient North Eurasians (ANE)22, a previously unknown northeastern branch of the Eurasian Paleolithic population. ANE contributed roughly 30–40% to the gene pool of Native Americans of the first settlement wave21 and about 50% to the Bronze Age Yamnaya culture in the Pontic-Caspian steppe6,23,24. Massive expansion of the Corded Ware culture around 5,000-4,000 YBP, originating from the Yamnaya source, introduced the ANE genetic pool into Central and Western Europe and thus reshaped its genetic landscape6,23. During the same period, the Afanasievo and Andronovo cultures, genetically similar to the Yamnaya culture, expanded into the Altai region (South Siberia) and later mixed with Siberian populations, giving rise to the Bronze Age Karasuk culture and later Iron Age cultures6.
A global maximum of ANE ancestry occurs in Native Americans, with lower levels in peoples of more recent Beringian origin, i.e. indigenous populations of Chukotka, Kamchatka, the Aleutian Islands and the American Arctic21,22,25. In modern Europe, ANE genetic contribution is the highest in the Baltic region, on the East European Plain and in the North Caucasus6,22,23. However, little is known about the distribution of ANE ancestry in its Siberian homeland. According to a single f4 statistic, the Kets had the third highest value of ANE genetic contribution among all Siberian ethnic groups, preceded only by Chukchi and Koryaks26. Thus, we suggest that the Kets might represent the peak of ANE ancestry in Siberia; the hypothesis we tested extensively in this study. We also investigated continuity between the modern Kets and Altaians and the ancient Bronze and Iron Age populations of the Altai region discussed above: the Karasuk culture samples dated to 3531-3261 YBP and Iron Age samples roughly dated to 2900-1100 YBP6.
The 4,000 YBP genome from Greenland16 represents the Saqqaq archeological culture (4,500-2,800 YBP). This culture formed a continuum with Dorset and Norton cultures (2,500-1,000 YBP), collectively termed Paleo-Eskimo25. Paleo-Eskimos were culturally and genetically distinct from modern Inuits and Eskimos13,25. The Saqqaq culture is a part of the wider Arctic Small Tool tradition (ASTt) that had rapidly spread across Beringia and the American Arctic coastal regions (but not the interior) after 4,800 YBP, bringing pottery, bow and arrow to the northern North America13,15,27. According to the archaeological data, the likely source of this spread was located in Siberia, namely in the Lena River basin (probably, in the Bel’kachi culture13). On genetic grounds, Paleo-Eskimos were also argued to represent a separate migration into America16,25,28. ASTt spread coincided with the arrival of mitochondrial haplogroup D2 into America and the spread of haplogroup D2a29; the Saqqaq individual bore haplogroup D2a130. The closest modern relatives of Saqqaq occur among Beringian populations (Chukchi, Koryaks, Inuits25) and Siberian Nganasans16. In addition, Saqqaq has been linked to Na-Dene-speaking Chipewyans (16% contribution to this population modeled with admixture graphs28). However, mitochondrial haplogroup data25,30,31 argues against the proximity of Paleo-Eskimos to contemporary Na-Dene people13,15, primarily due to the very high frequency of haplogroup A in the latter32. Archeological evidence seems to support this argument13.
There is no archaeological evidence of considerable trans-Beringian population movements between the inundation of the Bering Platform around 13,000-11,000 YBP and 4,800 YBP. Therefore, it is unlikely that the hypothetical Dene-Yeniseian language family has separated prior to 11,000 YBP, according to current concepts of time depth in language evolution13,15 and hence ASTt could be the vehicle spreading Dene-Yeniseian languages and genes from Siberia to Alaska and to the American Arctic13. However, as argued based on language phylogenetic trees33 in the framework of the Beringian standstill model29,34, the Dene-Yeniseian languages have originated in Beringia and spread in both directions. Irrespective of the migration direction and their relationship to contemporary Na-Dene groups, Paleo-Eskimos are the primary target for investigating genetic relationship with the Kets.
In this study, we found that: (1) Kets and Selkups constitute a clade closely related to Nganasans; (2) Nganasans, Kets, Selkups and Yukaghirs form a cluster of populations most closely related to Paleo-Eskimos in Siberia (not considering indigenous populations of Chukotka and Kamchatka); (3) unlike Nganasans, Kets derive roughly 30–40% of their ancestry from ancient North Eurasians; (4) Kets show genetic continuity with the hypothetical homeland of Yeniseian languages, as they are closely related to the ancient individuals of the Karasuk culture and to the later Iron Age individuals from the Altai.
Results and Discussion
Identification of a non-admixed Ket genotype
We compared the GenoChip SNP array data for the Ket, Selkup, Nganasan and Enets populations (Suppl. file S1) to the worldwide collection of populations35 based on 130 K ancestry-informative markers20.We applied GPS35 and reAdmix36 algorithms to infer provenance of the samples and confirm self-reported ethnic origin (see details in Suppl. Information, Section 4, Suppl. Figs. 4.2, 4.3, Suppl. Table 3). Combining the two algorithms, we identified a subset of non-admixed Kets among self-identified Ket individuals and nominated two individuals for whole-genome sequencing. ADMIXTURE37 revealed very similar profiles of components in individuals sequenced in this study and in two (Fig. 1A) or four (Suppl. Fig. 5.1) Kets from published sources. We note that proportion of the European component at K = 4 was slightly lower in the published Ket individuals (28% vs. 32% on average).
‘Ket-Uralic’ admixture component
Using the GenoChip SNP array20, we genotyped 130 K ancestry-informative markers in the Ket, Selkup, Nganasan and Enets populations (Suppl. file S1). Following the exclusion of first-, second- and third-degree relatives among the individuals genotyped in this study (Suppl. file S1, Suppl. Fig. 4.1), we merged the GenoChip array data with the published SNP array datasets to produce a worldwide dataset of 90 populations and 1,624 individuals, focused on Siberia and America (Suppl. Table 2). The intersection dataset, containing 32,189 SNPs (Suppl. Table 1), was analyzed with ADMIXTURE37 (Fig. 1). At K ≥ 11, ADMIXTURE identified a characteristic component for the Ket population (Suppl. Information Section 5). This component reached its global maximum of nearly 100% in Kets, closely followed by Selkups from this study (up to 81.5% at K = 19), the reference Selkups (up to 48.5%) and the Enets (up to 22.6%). The difference between the Selkups from this study and the reference Selkups21 can be attributed to a much closer geographic proximity of the former population to the settlements of Kets, with whom they have a long history of cohabitation and mixture2,10.
The ‘Ket’ component occurred at high levels (up to ~20%) in four Turkic-speaking populations of the Altai region: Shors, Khakases, Altaians and Teleuts. Notably, the Altai region was populated by Yeniseian-speaking people before they were forced to retreat north (Suppl. Information, Section 2). Lower levels of the ‘Ket’ component, from 5% to 15%, were observed in the following geographic regions (in decreasing order): the Volga-Ural region, Central and South Asia, East Siberia and Mongolia and North Caucasus. The ‘Ket’ component also occurred at a low level in Russians (up to 7.1%), Finns (up to 5.4%), and, remarkably, in the Saqqaq ancient genome from Greenland (7.2%, see below).
In order to verify and explain the geographic distribution of the ‘Ket’ admixture component, we have performed ADMIXTURE analysis on two additional datasets, different in population (Suppl. Table 2) and marker selection (Suppl. Table 1) (see Suppl. Information, Section 5). In summary, we suggest the existence of an admixture component with a peculiar geographic distribution, observed in some previous studies but not discussed there17,18. In addition to the Kets, this component is characteristic also for Samoyedic-speaking and Ugric-speaking people of the Uralic language family: Selkups, Enets, Nenets, Khanty, Mansi, with a notable exception of Samoyedic-speaking Nganasans. The proportion of the ‘Ket-Uralic’ admixture component correlated strongly with the worldwide frequency of mitochondrial haplogroup U4 (Pearson’s correlation coefficient up to 0.8 and a corresponding p-value of 7 × 10−8) and with the frequency of Y-chromosomal haplogroup Q in Eurasian populations (correlation coefficient up to 0.9 and p-value 2 × 10−7) (Suppl. Information, Section 10).
Kets in the context of Siberian populations
In order to study the relationship of Kets and other Siberian populations with the relevant ancient genomes, we have constructed three additional datasets: the dataset based on the Ket genome sequences and the HumanOrigins array SNP data22 and two datasets based on genome sequences only (Suppl. Tables 1 and 2). The Ket and Selkup populations were closely related according to multiple analyses (see the ADMIXTURE plot in Fig. 1, PCA plots in Suppl. Figs. 6.3, 6.6, TreeMix tree in Fig. 2 and outgroup f3 statistics38 in Suppl. Fig. 7.2). Nganasans appeared as the closest relatives of Kets according to statistics f3 (Yoruba; Ket, X): the statistic for Nganasans was significantly different from that of the second-best hit (Suppl. Fig. 7.2). In general, outgroup f3 statistics (Yoruba; Test, X) were tightly correlated between the Kets, the Selkups and the Nganasans, with Pearson’s correlation coefficients ranging from 0.96 to 0.999 (Suppl. Information, Section 7), suggesting that these populations form a closely related group. In line with these results, Nganasans, Kets, Selkups and Yukaghirs formed a clade in a maximum likelihood tree constructed with TreeMix on a HumanOrigins-based dataset of 194,750 SNPs (Fig. 2).
In our ADMIXTURE analyses (Fig. 1A, Suppl. Fig. 5.4), the Saqqaq Paleo-Eskimo individual featured the following components: Beringian, Siberian and South-East Asian. Thus, Saqqaq Paleo-Eskimo has mostly Beringian ancestry (similar to modern Eskimo, Inuits, Aleutians, Koryaks, etc.): see outgroup f3 statistics and associated Zdiff scores in Suppl. Figs. 7.17–7.19, migration edges modelled with TreeMix in Fig. 3 and the ADMIXTURE results in the original study16. Beringian ancestry in Saqqaq is combined with considerable Siberian ancestry: 32% or 28% as a sum of Siberian ADMIXTURE components in this study (Fig. 1A, Suppl. Fig. 5.4); ~25% according to ADMIXTURE analysis in the original study (Rasmussen et al. 2010)16; from 31% to 57% according to f4 statistic ratios calculated with various outgroups (Suppl. Information, Section 8, Suppl. Table 6). This ‘core Siberian’ component in Saqqaq is apparently most closely related to modern Nganasans16 (Suppl. Fig. 7.17) and to the Nganasan-related clade in general (see a TreeMix tree in Fig. 2). The Kets are the only representatives of this clade in the genome-based datasets in this study. According to the pairwise correlation between outgroup f3 statistics (the method used in Allentoft et al.6), Kets are closer to Saqqaq as compared to Nivkhs, Altaians, Buryats and Yakuts (Suppl. file S2). According to Euclidean distances in the ten-dimensional space of principal components on the HumanOrigins dataset, Kets were a closer population to Saqqaq than Nganasans, Selkups, Yukaghirs and the other populations (Fig. 4). However, the outgroup f3 statistics (Yoruba; Saqqaq, Ket) in many cases were not significantly different from f3 (Yoruba; Saqqaq, other Siberian population): e.g., see |Zdiff| scores < 3 for f3 (Yoruba; Saqqaq, Nivkh) (Suppl. Figs. 7.18, 7.19). The same result was produced with f4 (Saqqaq, Yoruba; Nivkh, Ket): an absolute Z-score was lower than 2 (Suppl. Fig. 8.18A,B).
Allentoft et al.6 have shown that in the early Bronze Age the Altai region was inhabited by a genetically West Eurasian population of the Afanasievo archaeological culture, most similar to the Yamnaya culture with about 50% of ANE ancestry6 and to the modern Avars (Suppl. file S2, Fig. 3, Suppl. Figs. 9.4, 9.5). In the late Bronze Age this population apparently had being gradually admixed with Siberians, giving rise to the Karasuk culture and the later cultures of the Iron Age6. The ancient genome ‘Iron Age Russia’, carbon-dated to 721–889 AD6, is most closely related to the typical modern Siberians: Nganasans according to the outgroup f3 statistic in the original study6 and Altaians or Koryaks according to the outgroup f3 statistics and their pairwise correlations on our datasets lacking Nganasans (Suppl. file S2). However, according to various analyses, the ‘Iron Age Altai’ (dated roughly to 2900-1500 YBP) and the Karasuk (carbon-dated to 3531-3261 YBP) populations of two and six genomes, respectively, are most closely related to each other and to Kets (Suppl. files S2, S3, Suppl. Figs. 7.5, 7.6, 8.17A, 9.1). The outgroup f3 statistics (Yoruba; Karasuk, X) on both genome-based datasets selected Kets as the best hit for Karasuk (Suppl. files S2, S3, Suppl. Fig. 7.5), although statistics for Mayans, Greenlanders, Mixe, Saqqaq, Mal’ta, Iron Age Russia and Aleutian were not significantly different (|Zdiff| score < 3). Similarly, Native American, Beringian populations and Selkups were the best hits for Iron Age Altai and Karasuk according to the outgroup f3 statistics in the original study (Kets were lacking in the dataset, see Allentoft, et al.6). Importantly, the Karasuk culture has been tentatively associated with the Yeniseian-speaking people based on the toponymic evidence5 and the Altai region is considered to be the homeland of the Yeniseian language family2. As another piece to this puzzle, we observed genetic continuity between the Kets and the ancient genomes from the Altai.
Mal’ta (ancient North Eurasian) ancestry in Kets
The outgroup statistic f3 (Yoruba; Mal’ta, Ket) (Raghavan et al. 2014)21 was higher than statistics for all other Siberian and most Beringian populations. However, the statistic values were not significantly different within a large group of North Eurasians, according to Zdiff scores (Suppl. Figs. 7.13–7.16). Zdiff score for f3 (Yoruba; Mal’ta, Ket) vs. f3 (Yoruba; Mal’ta, Nganasan) equaled 7.4, 7.0 vs. f3 (Yoruba; Mal’ta, Yukaghir) and only 2.7 vs. f3 (Yoruba; Mal’ta, Selkup) (Suppl. Fig. 7.13). Thus, we suggest that, unlike the other members of the Nganasan-related clade (Fig. 2), Kets and, to a lesser extent, Selkups have a high proportion of Mal’ta ancestry, alternatively referred to as the ANE ancestry22. The Mal’ta ancestry in Kets was further supported by the TreeMix39 analysis, specifically by a migration edge connecting Mal’ta to the Ket-Karasuk clade, with a weight of 43% (Suppl. Fig. 9.1, Suppl. Table 7). Taking into account the admixture coefficients for the two sequenced Ket individuals (Ket891 and Ket884, Fig. 1A), we selected Ket891 as an individual with lower values of the North European and Siberian admixture components (in the K = 19 dimensional space). In addition, Ket891 was identified as non-admixed by reAdmix analyses (Suppl. Table 3). Ket891 demonstrated a slightly closer genetic affinity to Mal’ta (compare Suppl. Figs. 7.13 and 7.14).
These results were consistent with calculations of f4 statistic in two configurations: (X, Chimp; Mal’ta, Stuttgart) or (X, Papuan; Sardinian, Mal’ta), reproducing the previously used statistics22,26 (Suppl. Figs. 8.1–8.6). f4 (X, Chimp; Mal’ta, Stuttgart) analysis tests whether the population X has more drift shared with Mal’ta or with Stuttgart (an early European farmer, EEF22). Sardinians were used as the closest modern proxy for EEF22 in f4 (X, Papuan; Sardinian, Mal’ta). All possible population pairs (X,Y) were tested by f4 (Mal’ta, Yoruba; Y, X) on the genome-based dataset, including both Ket individuals (Fig. 5A). Compared to Kets, Mal’ta was significantly closer to none of the populations including Native Americans.
Based on all analyses, we can tentatively model Kets as a two-way mixture of broadly defined East Asians and ANE. Therefore, ANE ancestry in Kets can be estimated, using various f4-ratios, at 27% to 43% (depending on reference populations and datasets), vs. 25–53% in various Native American groups (Suppl. Table 6, see details in Suppl. Information, Section 8). Given non-significant Zdiff scores and f4 statistics (Fig. 5A) discussed above, it is difficult to identify the exact Eurasian population west of Chukotka and Kamchatka with the highest degree of the Mal’ta ancestry, but Kets are a good candidate. We speculate that ANE component was acquired by ancestors of Kets in the Altai region, where the Bronze Age Okunevo culture was located, with a surprisingly close genetic proximity to Mal’ta6. Later, the Yeniseian-speaking people occupied this region until the 16th–18th centuries3,4.
Kets and Na-Dene speakers
In this study, Na-Dene-speaking people were represented by Athabaskans, Chipewyans, Tlingit, and, possibly, Haida. The latter language was originally included into the Na-Dene language family40, although this affiliation is now disputed10 Na-Dene-speaking people were suggested to be related, at least linguistically, to Yeniseian-speaking Kets10. ADMIXTURE, PCA, f3 and f4 statistics and TreeMix analyses failed to identify a link between Kets and Athabaskans, Chipewyans, or Tlingit (see Suppl. Information, Sections 7 and 8). TreeMix constructed trees where Athabaskans or Chipewyans formed a stable highly supported clade with other Native Americans (e.g., bootstrap support 99, Fig. 3A). This topology was supported by statistics f4 (Athabaskan, Yoruba; Ket, X), which demonstrated significantly negative Z-scores < −5, for Clovis, Greenlanders, Karitiana, Mayans and Mixe (Suppl. Fig. 8.19) on the genome-based dataset with or without transitions. Notably, the same topology was previously demonstrated for Athabaskans19.
Notably, the Arctic Small Tool tradition the Saqqaq culture belongs to, may reflect the Dene-Yeniseian movement over the Bering Strait13,15. According to the admixture graph analysis modeling relationships among Chipewyans, Saqqaq, Algonquin, Karitiana, Zapotec, Han and Yoruba28, only one topology fits these data. In this topology, the Chipewyans represent a mixture of 84% First Americans and 16% Saqqaq28. Our estimates using f4-ratios are roughly similar: 4–15% Saqqaq ancestry in Chipewyans and 0–9% in Athabaskans (Suppl. Table 6). Considering 57% as the highest proportion of Siberian ancestry in Saqqaq obtained in this study, we predict up to ~9.1% of Siberian ancestry in Chipewyans, i.e. 57 × 16% of Saqqaq ancestry in Chipewyans. Similarly, only 1.2% (noise level) of the Ket-Uralic admixture component is predicted in Chipewyans, with 7.2% as the highest percentage of this component found in Saqqaq (Fig. 1C). Given such low levels of expected genetic signal, we cannot reliably test the hypothetical genetic connection between Yeniseian and Na-Dene-speaking people, provided the employed methods and population samples. Moreover, considerable Beringian ancestry in Saqqaq makes the Saqqaq ancestry in Chipewyans difficult to distinguish from potential admixture with Eskimo and Inuits, representatives of the third settlement wave25,28. Hopefully, the question of the Dene-Yeniseian genetic relationship and its correlation with the linguistic relationship will be answered with a study of autosomal haplotypes and/or very rare allelic variants in relevant genomic data, which would test whether a relatively recent Siberian (Nganasan- and Ket-related) gene flow occurred into Chipewyans, for example and whether it was mediated by Paleo-Eskimos.
Based on previous studies16,25,28, the Saqqaq individual and the Paleo-Eskimos in general25 may represent a separate and relatively recent migration into America. The Paleo-Eskimos have large proportions of Beringian (i.e. Chukotko-Kamchatkan and Eskimo-Aleut), Siberian and South-East Asian ancestry. We have also shown that Kets and Selkups belong to a group of modern populations closest to an ancient source of Siberian ancestry in Saqqaq. This group also includes, but is probably not restricted to, Uralic-speaking Nganasans and Yukaghirs (the latter speak an isolated language). Unlike the other populations of this group, Kets, and, to a lesser degree Selkups, have a high proportion of Mal’ta (ancient North Eurasian) ancestry.
As shown previously28, Chipewyans, a modern Na-Dene-speaking population, have about 16% of Saqqaq ancestry. Thus, a gene flow dated at 5,000-6,000 YBP16 can be traced from the cluster of Siberian populations to Saqqaq and from Saqqaq to Na-Dene. However, the genetic signal in contemporary Na-Dene-speaking ethnic groups is substantially diluted. The genetic proximity of Kets to the source of Siberian ancestry in Saqqaq correlates with the hypothesis that Na-Dene languages of North America are specifically related to Yeniseian languages of Siberia, now represented by Ket language only10. However, this genetic link is indirect and requires further study of population movement and language shifts in Siberia.
In addition, we show that Kets represent a modern Siberian population closest to ancient individuals of the Karasuk culture, spanning a period from about 3400 YBP to 2900 YBP (the individuals analyzed were dated to 3531-3261 YBP) and to few investigated Iron Age individuals of the Altai region (2900-1100 YBP)6. This genetic continuity correlates with historical linguistic data suggesting that the homeland of Yeniseian languages was located in the Altai region2,5.
Saliva samples were collected and stored in the lysis buffer (50 mM Tris, 50 mM EDTA, 50 mM sucrose, 100 mM NaCl, 1% SDS, pH 8.0) according to the protocol of Quinque et al.41 The following cities and villages along the Yenisei River were visited (Suppl. Fig. 1.1): Dudinka (69.4°, 86.183°), Ust’-Avam (71.114°, 92.821°), Volochanka (70.976°, 94.542°), Potapovo (68.681°, 86.279°), Farkovo (65.720°, 86.976°), Turukhansk (administrative center of the Turukhanskiy district, 65.862°, 87.924°), Baklanikha (64.445°, 87.548°), Maduika (66.651°, 88.428°), Verkhneimbatsk (63.157°, 87.966°), Kellog (62.489°, 86.279°), Bakhta (68.841°, 96.144°), Bor (61.601°, 90.018°), Sulomai (61.613°, 91.180°). Volunteers rinsed their mouths with cold boiled water and then collected up to 2 mL of saliva into a tube filled with 3 mL of the buffer. Samples were stored at environmental temperature (ranging from 4 °C to 30 °C) for up to two weeks and DNA was isolated within one month after sample collection. Information about ethnicity, place of birth and about first-, second- and third-degree relatives was provided by the volunteers. The study was approved by the ethical committee of the Lomonosov Moscow State University (Russia) and the study methods were carried out in accordance with the approved guidelines and regulations. All volunteers have signed informed consent forms. The study was approved by local administrations of the Taymyr and Turukhansk districts and discussed with local committees of small Siberian nations for observance of their rights and traditions.
DNA extraction protocol was adapted from the high-salt DNA extraction method41. DNA extracted from saliva represents a mix of human and bacterial DNA and their ratio was checked by quantitative (q) PCR with 2 primer pairs (human: 1e1 5′-GTCCTCAGCGCTGCAGACTCCTGAC-3′, BG1R 5′-CTTCCGCATCTCCTTCTCAG-3′; bacterial: 8F 5′-AGAGTTTGATCCTGGCTCAG-3′, 519R 5′-GWATTACCGCGGKGCTG-3′). The PCR reaction mixture included: 13,2 μL of sterile water, 5 μL of qPCR master mix PK154S (Evrogen, Moscow, Russia), 0,4 μL of each primer and 1 μL of DNA sample. Amplification was performed with thermocycler StepOnePlus Applied BiosystemsTM (Life Technologies, USA) with the standard program. Most DNA samples had low levels of bacterial contamination and were used for further analysis: 22% of samples had the human/bacterial DNA ratio <1; 59% of samples had the ratio from 1 to 2, 19% of samples had the ratio >2.
GenoChip (the Genographic Project’s genotyping array)20 was used for genotyping 158 individuals (see details in Suppl. file S1). GenoChip includes ancestry-informative markers obtained for modern populations, the ancient Saqqaq genome and two archaic hominins (Neanderthal and Denisovan) and was designed to identify all known Y-chromosome and mitochondrial haplogroups. The chip allows genotyping about 12,000 Y-chromosomal and approximately 3,300 mitochondrial SNPs and over 130,000 autosomal and X-chromosomal SNPs. Genotyping was performed at the GenebyGene sequencing facility (TX, USA).
Control of Sex Assignment
In order to avoid mix-ups in sex assignment, we compared heterozygosity of X chromosome and missing rate among Y-chromosomal SNPs across the samples. All female samples had >62% Y-chromosomal SNPs missing and X chromosome heterozygosity >0.138, while male samples demonstrated values <1.2% and <0.007, respectively. Four wrong sex assignments were corrected based on these thresholds.
Genome sequencing and genotype calling
Genome sequencing has been performed for Ket individuals 884 (a male born in Baklanikha, mitochondrial haplogroup H, Y-chromosomal haplogroup Q1a2a1) and 891 (a female born in Surgutikha, mitochondrial haplogroup U5a1d). Prior to genome sequencing, we used NEBNext Microbiome DNA Enrichment Kit (New England Biolabs, USA) in order to enrich the samples for human DNA. This kit exploits the difference in methylation between eukaryotes and prokaryotes through selective binding of CpG-methylated (eukaryotic) DNA by the MBD2 protein. We took 500 ng of DNA from each sample and processed it according to manufacturer’s instructions. Success of the enrichment was estimated using qPCR with primers for human RPL30 and bacterial 16S rRNA genes. The resulting human-enriched fraction was used for library construction using the TruSeq DNA sample preparation kit (Illumina, USA). We made libraries also from non-enriched DNA in order to assess whether enrichment leads to biases in sequence coverage. Libraries from enriched and non-enriched DNA were sequenced using the HiSeq2000 instrument (Illumina, USA) with read length 101+101 bp, two lanes for each library. As both enriched and non-enriched libraries produced similar coverage profiles and similar SNP counts in test runs of the bcbio-nextgen genotype calling pipeline (data not shown), their reads were pooled for subsequent analyses. Resulting read libraries for samples 884 and 891 had a median insert size of 215 bp and 343 bp and coverage of 61x and 44x, respectively.
The bcbio-nextgen pipeline v. 0.7.9 (https://bcbio-nextgen.readthedocs.org/en/latest/) has been used with default settings for the whole read processing workflow: adapter trimming, quality filtering, read mapping on the reference genome hg19 with BWA, duplicate read removal with Picard, local realignment, SNP calling and recalibration with GATK v3.2-2 and annotation against dbSNP_138 with snpEff. Two alternative genotype calling modes have been tested in GATK: batch genotype calling for several samples, emitting only sites with at least one non-reference allele in at least one individual (GATK options –standard_min_confidence_threshold_for_calling 30.0 –standard_min_confidence_threshold_for_emitting 30.0, –emitRefConfidence at default); or calling genotypes for each sample separately, emitting all sites passing the coverage and quality filters (GATK options –standard_min_confidence_threshold_for_calling 30 –standard_min_confidence_threshold_for_emitting 30 –emitRefConfidence GVCF –variant_index_type LINEAR –variant_index_parameter 128000). The former approach maximized the output of dbSNP-annotated sites (7.36–7.62 million sites per individual vs. ~3.7 million sites for the latter approach) and therefore was used to generate calls subsequently merged with various SNP array and genomic datasets (Suppl. Table 1). To increase sensitivity of this approach, genotype calling has been performed with GATK HaplotypeCaller for six genomes in one run: Kets 884 and 891, two Yoruba and two Kinh (Vietnamese) individuals downloaded from the 1000 Genome Project database42. We chose Yoruba samples NA19238 and NA19239 and Vietnamese samples HG01873 and HG02522 as they had read coverage similar to the Ket samples.
Combined datasets generated in this study and their properties are listed in Suppl. Table 1. In all cases, datasets were designed to maximize population coverage in Russia (Siberia in particular), in Central Asia and in the Americas, while keeping only few reference populations in the Middle East, in South and South-East Asia, Africa, Australia and Oceania. Third-degree and closer relatives detected through questionnaires and pedigree analysis and individuals of mixed ethnicity were excluded from the Enets, Ket, Nganasan and Selkup population samples. Overall, 88 of 158 individuals remained (see supposed percentage of relatedness for each sample pair and a list of selected samples in Suppl. file S1 and hierarchical clustering of all samples based on genetic distance in Suppl. Fig. 4.1). All datasets underwent filtering using PLINK43 v. 1.9. Maximum missing rate per SNP thresholds of 0.03 or 0.05 were used (Suppl. Table 1), except for dataset ‘Ket genomes + reference genomes’, for which a more relaxed threshold of 0.11 was used to accommodate the Mari individual and ancient genomes with low coverage21 and to keep the high number of SNPs at the same time. Linkage disequilibrium (LD) filtering was applied to all datasets except for the GenoChip-based one since SNPs included into the GenoChip array underwent LD filtering with the r2 threshold of 0.4 as described in Elhaik et al.20. For the other datasets the following LD filtering settings were used: window size of 50 SNPs, window step of 5 SNPs, r2 threshold 0.5 (PLINK v. 1.9 option ‘–indep-pairwise 50 5 0.5’). Ancient genome data within the HumanOrigins dataset were provided as artificially haploid: one allele was selected randomly at each diploid site, since confident diploid calls were not possible for low-coverage ancient genomes (see further description of the approach in Lazaridis et al.22). We applied the same procedure to ancient genomes included into dataset ‘Ket genomes + reference genomes’. Other details pertaining to individual datasets are listed below and in Suppl. Table 1 and their population composition is shown in Suppl. Table 2.
GenoChip + Illumina arrays (alternative name ‘GenoChip-based’)
The dataset was constructed by merging selected populations genotyped with GenoChip35, genotyping data obtained with GenoChip in this study and SNP array data (various Illumina models) from the following sources: Behar et al.44; Cardona et al.45; Fedorova et al.17; Li et al.46; Kidd et al.47; Raghavan et al.21; Rasmussen et al.16; Reich et al.28; Silva-Zolezzi et al.48; Surakka et al.49; Yunusbayev et al.50. Three ancient genomes, La Braña51, Saqqaq16 and Clovis52, were also added (genotypes in VCF format were obtained from the respective publications). Only SNPs included into the GenoChip array were used and further filtered as described above. Maximum missing rate per individual was 50%, but three ancient genomes (Clovis, Saqqaq and La Braña) were exempt. After filtering, the dataset contained 1,624 individuals from 90 populations and 32,189 SNPs and included published data for two Ket individuals17.
Ket genomes + Illumina arrays
In order to include populations relevant for our analyses, e.g. Burusho, Khanty and Nenets, omitted from the previous dataset due to very low marker overlaps, full-genome SNP calls for two Ket individuals (see above) were merged with SNP array data (various Illumina models) from the following sources: HapMap353; Behar et al.44,54; Cardona et al.45; Fedorova et al.17; Li et al.46; Raghavan et al.21; Rasmussen et al.16; Reich et al.28; Silva-Zolezzi et al.48; Yunusbayev et al.50. The filtered dataset contained modern individuals only: 2,549 individuals from 105 populations and 103,495 SNPs and had low missing SNP rates (maximum missing rate per individual 0.04). The dataset included published data for four Ket individuals16,17 and was used for ADMIXTURE analysis only.
Ket genomes + HumanOrigins array (alternative name ‘HumanOrigins-based’)
For analyzing relevant ancient genomes alongside the Ket genomes in context of multiple modern populations genotyped with the HumanOrigins Affymetrix SNP array22,38, the full dataset of Lazaridis et al.22 was merged with Ket genome data and filtered (LD filtering with the r2 threshold of 0.5, maximum per SNP missing rate of 0.05). The resulting set contained 217 populations/genomes. In order to make the dataset more manageable computationally and more focused, 78 populations/genomes were removed, keeping the following ancient genomes with coverage >1x: Neanderthal and Denisovan genomes; La Braña 151, Loschbour22, Mal’ta/MA121 and Motala1222 (Eurasian hunter-gatherers); Stuttgart (a west European farmer of the LBK archaeological culture22) and Saqqaq16. The final dataset contained 1,786 individuals from 139 populations and 195,918 SNPs.
Ket genomes + HumanOrigins array + Verdu et al. 2014
The final version of the previous dataset ‘Ket genomes + HumanOrigins array’ was merged with Illumina 610-Quad SNP array genotyping data for six North American native populations (Haida, Nisga’a, Splatsin, Stswecem’c, Tlingit, Tsimshian55) and filtered (Suppl. Table 1). The major reason for constructing this dataset was the inclusion of Tlingit and Haida, Na-Dene-speaking populations not present in the other datasets and the dataset was used only for analyses focused on Na-Dene-speaking populations. The final dataset contained 1,867 individuals from 145 populations and 68,625 SNPs.
Ket genomes + reference genomes (alternative name ‘genome-based’)
The following 19 ancient genomes were included into the dataset: Clovis52, Late Dorset25 and Saqqaq16 Paleo-Eskimos, Mal’ta (an ANE representative21), Motala12 and Loschbour (WHG22), Stuttgart (EEF22) and 12 ancient genomes with coverage >1x were selected from archaeological cultures of the Altai region (labelled according to the original publication as Afanasievo, Andronovo, Iron Age Altai, Iron Age Russia and Karasuk)6. To ensure dataset uniformity, genotype calling for these ancient genomes was performed de novo in a batch run, instead of using published genotypes generated with different genotype calling protocols. Ancient DNA reads mapped on the reference genome hg19 (provided by their respective authors) were used for genotype calling with the ANGSD software v. 0.80056 with the following settings: SAMtools calling mode (option -GL 1); genotype likelihood output (option -doGlf 2); major allele specified according to the reference genome (-doMajorMinor 4); allele frequency obtained based on the genotype likelihoods (-doMaf 1); SNP p-value 10−6. The resulting genotype likelihood files were transformed into genotypes in the VCF format using BEAGLE utilities gprobs2beagle and beagle2vcf, with a minimum genotype likelihood cut-off of 0.6. Subsequently one allele was selected randomly at each diploid site, since confident diploid calls were not possible for low-coverage ancient genomes. Genotype data for ancient genomes were merged with the following modern samples using PLINK v. 1.9 (and subsequently filtered as described in Suppl. Table 1):(i) 7.36–7.62 million GATK genotype calls for two Kets, two Yoruba and two Vietnamese individuals; and (ii) one Aleutian, two Athabaskans, two Greenlanders, two Nivkhs25; one Avar, one Indian, one Mari, one Tajik21; one Australian aboriginal57, one Karitiana, one Mayan52; Simons Genome Diversity Project panels A58 and B59 containing 25 genomes of 13 populations. The final dataset contained 64 individuals from 36 populations and 398,163 SNPs.
Ket genomes + reference genomes without transitions
In order to mitigate the effect of ancient DNA deamination and the resulting C to T substitutions60, we constructed another version of the genome-based dataset, with all CT and AG SNPs excluded prior to the LD filtering step. The final dataset contained 64 individuals from 36 populations and 189,964 SNPs.
Ket genomes + Raghavan et al. 2015 with/without transitions
In order to include two additional Ket genomes, genomes of Altaians, Buryats, Yakuts, Koryaks and Eskimo (ten in total) and three genomes of Native Americans (Huichol, Mayan, Tsimshian) published by Raghavan et al.19, we merged these data with the genome-based dataset described above prior to linkage disequilibrium filtering and transition polymorphisms removal. Upon filtering, the resulting datasets contained 79 individuals from 43 populations, 225,010 SNPs in the original version and 104,727 SNPs with transitions excluded. These genome-based datasets were helpful due to an extended sampling of Siberian populations, but because of a relatively small number of markers they were used for few selected analyses only (Suppl. Table 1).
The principal component analysis (PCA) was carried out in the smartpca program included in the EIGENSOFT package61. We calculated 10 eigenvectors and ran the analysis without removing outliers. Then we computed the Euclidean distance in the space of ten principal components between all pairs of individuals and calculated mean distance between the Saqqaq individual and all modern populations.
The ADMIXTURE software implements a model-based Bayesian approach that uses block-relaxation algorithm in order to compute a matrix of ancestral population fractions in each individual (Q) and infer allele frequencies for each ancestral population (P)37. A given dataset is usually modeled using various numbers of ancestral populations (K). For each K from 2 to 25, 100 analysis iterations were generated with different random seeds. The best run was chosen according to the highest log likelihood. For each run 10-fold cross-validation (CV) was computed.
Maximum likelihood tree construction and admixture modelling was performed with the TreeMix v. 1.12 software39 on the genome-based dataset of 36 populations and 64 individuals: on its original version or the version with CT and AG SNPs excluded. Initially, SNP window length (k) was optimized by testing various values (k = 1, 5, 10, 20, 50, or 100) with 10 different random seeds and the k setting producing the highest percentage of variance explained by the model was selected. Final runs were performed with the following settings: SNP window length, 5; number of migration edges from 0 to 8; trees rooted with the San population; global tree rearrangements used (option ‘-global’); no sample size correction (option ‘-noss’); 100 iterations, selecting a tree with the highest likelihood (and with the highest percentage of explained variance among trees with identical likelihoods). No pre-defined migration events were incorporated. One hundred bootstrap replicates re-sampling blocks of 5 SNPs were calculated and respective trees were constructed for 6, 7 and 8 migration edges using TreeMix. Bootstrap support values for nodes were mapped on the original trees using RAxML. Bootstrap values for migration edges were interpreted as described in Suppl. Information, Section 9 and in the respective figure legends (Fig. 3).
f3 and f4, statistics
We used three and four population tests (f3 and f4) developed by Patterson, et al.38 and implemented in programs threepop and fourpop of the TreeMix39 package. The source code in C++ was modified to enable multithreading and computing the statistic for all population combinations containing a given population or population pair. SNP window length settings used for computing standard errors of f3 and f4 statistics are shown for each dataset in Suppl. Table 1. Statistic f3 (O; A, X1)38 measures relative amount of genetic drift shared between the test population A and a reference population X1, given an outgroup population O distant from both A and X1. Outgroup f3 statistic is always positive and its values can be interpreted only in the context of the reference dataset X. Statistic f4 (X, O; A, B)38 tests whether A and B are equidistant from X, given a sufficiently distant outgroup O: in that case the statistic is close to zero. Otherwise, the statistic shows whether X is more closely related to A or to B, hence f4 may be positive or negative. The statistical significance of f3 and f4 values is typically assessed using a Z-score: a statistic divided by its standard deviation. A threshold Z-score of 3 corresponds to a p-value of 0.00135 and is commonly used in case of multiple testing.
Plotting of various statistic values or sampling locations on the world map was performed using an open source software QGIS v.2.8 (http://qgis.org/en/site/) with open-source maps.
How to cite this article: Flegontov, P. et al. Genomic study of the Ket: a Paleo-Eskimo-related ethnic group with significant ancient North Eurasian ancestry. Sci. Rep. 6, 20768; doi: 10.1038/srep20768 (2016).
Vajda, E. J. Ket. Languages of the World/Materials Volume 204. Munich: Lincom Europa (2004).
Vajda, E. J. Loanwords in Ket. The Typology of Loanwords, ed. Haspelmath, M., Tadmoor, U. Oxford: Oxford University Press, 125–139 (2009).
Vajda, E. J. Yeniseian Peoples and Languages: a History of Their Study with an Annotated Bibliography and a Source Guide. Surrey, England: Curzon Press, 389 p. (2001).
Dul’zon, A. P. Ketskie toponimy Zapadnoy Sibiri [Ket toponyms of Western Siberia]. Uchenye Zapisky Tomskogo Gosudarstvennogo Pedagogicheskogo Instituta [Scholarly Proceedings of Tomsk State Pedagogical Institute] 18, 91–111 (1959).
Chlenova, N. L. Sootnoshenie kul’tur karasukskogo tipa i ketskikh toponimov na territorii Sibiri [The correlation between Karasuk-type cultures and Ket toponyms in Siberia]. Etnogenez i Etnicheskaya Istoriya Narodov Severa [Ethnogenesis and History of the Peoples of the North]. Moscow: Nauka, 223–230 (1975).
Allentoft, M. E. et al. Population genomics of Bronze Age Eurasia. Nature 522, 167–172 (2015).
Alekseenko, E. A. Kety: Etnograficheskie Ocherki [The Ket: Ethnographic Studies]. Leningrad: Nauka (1967).
Krivonogov, V. P. Kety: Desyat’ Let Spustya [The Ket: Ten Years Later]. Krasnoyarsk: RIO KGPU (2003).
Vajda, E. J. Siberian landscapes in Ket traditional culture. Landscape and Culture in Northern Eurasia, ed. Jordan, P. Walnut Creek, CA: Left Coast Press, 297–304 (2011).
Vajda, E. J. Siberian link with Na-Dene languages. The Dene-Yeniseian Connection, ed. Kari, J., Potter, B. A. Anthropological Papers of the University of Alaska: New Series 5, 33–99 (2010).
Comrie, B. The Dene-Yeniseian hypothesis: an introduction. The Dene-Yeniseian Connection, ed. Kari, J., Potter, B. A. Anthropological Papers of the University of Alaska: New Series 5, 25–32 (2010).
Ruhlen, M. The origin of the Na-Dene. Proc. Natl. Acad. Sci. USA 95, 13994–13996 (1998).
Potter, B. A. Archaeological patterning in Northeast Asia and Northwest North America: an examination of the Dene-Yeniseian hypothesis. The Dene-Yeniseian Connection, ed. Kari, J., Potter, B. A. Anthropological Papers of the University of Alaska: New Series 5, 138–167 (2010).
Scott, R. G. & O’Rourke, D. Genes across Beringia: a physical anthropological perspective on the Dene-Yeniseian hypothesis. The Dene-Yeniseian Connection, ed. Kari, J., Potter, B. A. Anthropological Papers of the University of Alaska: New Series 5, 119–137 (2010).
Ives, J. W. Dene-Yeniseian, migration and prehistory. The Dene-Yeniseian Connection, ed. Kari, J., Potter, B. A. Anthropological Papers of the University of Alaska: New Series 5, 324–334 (2010).
Rasmussen, M. et al. Ancient human genome sequence of an extinct Palaeo-Eskimo. Nature 463, 757–762 (2010).
Fedorova, S. a. et al. Autosomal and uniparental portraits of the native populations of Sakha (Yakutia): implications for the peopling of Northeast Eurasia. BMC Evol. Biol. 13, 127 (2013).
Yunusbayev, B. et al. The genetic legacy of the expansion of Turkic-speaking nomads across Eurasia. PLoS Genet. 11, e1005068 (2015).
Raghavan, M. et al. Genomic evidence for the Pleistocene and recent population history of Native Americans Science 349, 1–20 (2015).
Elhaik, E. et al. The GenoChip: a new tool for genetic anthropology. Genome Biol. Evol. 5, 1021–1031 (2013).
Raghavan, M. et al. Upper Palaeolithic Siberian genome reveals dual ancestry of Native Americans. Nature 505, 87–91 (2014).
Lazaridis, I. et al. Ancient human genomes suggest three ancestral populations for present-day Europeans. Nature 513, 409–413 (2014).
Haak, W. et al. Massive migration from the steppe was a source for Indo-European languages in Europe. Nature 522, 207–211 (2015).
Mathieson, I. et al. Genome-wide patterns of selection in 230 ancient Eurasians. Nature 528, 499-503 (2015).
Raghavan, M. et al. The genetic prehistory of the New World Arctic. Science 345, 1255832 (2014).
Seguin-Orlando, A. et al. Genomic structure in Europeans dating back at least 36,200 years. Science 346, 1113–1118 (2014).
McGhee, R. Ancient People of the Arctic. Vancouver: UBC Press (1996).
Reich, D. et al. Reconstructing Native American population history. Nature 488, 370–374 (2012).
Tamm, E. et al. Beringian standstill and spread of Native American founders. PLoS One 2, e829 (2007).
Gilbert, M. T. P. et al. Paleo-Eskimo mtDNA genome reveals matrilineal discontinuity in Greenland. Science 320, 1787–1789 (2008).
Hayes, M. G., Coltrain, J. B. & O’Rourke, D. H. Molecular archaeology of the Dorset, Thule and Sadlermiut: ancestor-descendent relationships in eastern North American arctic prehistory. The Dorset Culture: 75 Years after Jennes, ed. Sutherland, P. Hull: Canadian Museum of Civilization (2002).
Malhi, R. S. et al. Native American mtDNA prehistory in the American Southwest. Am. J. Phys. Anthropol. 120, 108–124 (2003).
Sicoli, M. A. & Holton, G. Linguistic phylogenies support back-migration from Beringia to Asia. PLoS One 9, e91722 (2014).
Pringle, H. Welcome to Beringia. Science 343, 961–963 (2014).
Elhaik, E. et al. Geographic population structure analysis of worldwide human populations infers their biogeographical origins. Nat. Commun. 5, 3513 (2014).
Kozlov, K. et al. Differential Evolution approach to detect recent admixture. BMC Genomics 16 Suppl 8, S9 (2015).
Alexander, D. H., Novembre, J. & Lange, K. Fast model-based estimation of ancestry in unrelated individuals. Genome Res. 19, 1655–1664 (2009).
Patterson, N. et al. Ancient admixture in human history. Genetics 192, 1065–1093 (2012).
Pickrell, J. K. & Pritchard, J. K. Inference of Population Splits and Mixtures from Genome-Wide Allele Frequency Data. PLoS Genet. 8, e1002967 (2012).
Dürr, M. & Renner, E. The history of the Na-Dene controversy: a sketch. Language and Culture in Native North America – Studies in Honor of Heinz-Jürgen Pinnow, ed. Dürr, M., Renner, E., Oleschinski, W. München and Newcastle: Lincom, 3–18 (1995).
Quinque, D., Kittler, R., Kayser, M., Stoneking, M. & Nasidze, I. Evaluation of saliva as a source of human DNA for population and association studies. Anal. Biochem. 353, 272–277 (2006).
Abecasis, G. R. et al. An integrated map of genetic variation from 1,092 human genomes. Nature 491, 56–65 (2012).
Purcell, S. et al. PLINK: a tool set for whole-genome association and population-based linkage analyses. Am. J. Hum. Genet. 81, 559–575 (2007).
Behar, D. M. et al. The genome-wide structure of the Jewish people. Nature 466, 238–242 (2010).
Cardona, A. et al. Genome-wide analysis of cold adaptation in indigenous Siberian populations. PLoS One 9, e98076 (2014).
Li, J. Z. et al. Worldwide human relationships inferred from genome-wide patterns of variation. Science 319, 1100–1104 (2008).
Kidd, J. R. et al. Single nucleotide polymorphisms and haplotypes in Native American populations. Am. J. Phys. Anthropol. 146, 495–502 (2011).
Silva-Zolezzi, I. et al. Analysis of genomic diversity in Mexican Mestizo populations to develop genomic medicine in Mexico. Proc. Natl. Acad. Sci. 106, 8611–8616 (2009).
Surakka, I. et al. Founder population-specific HapMap panel increases power in GWA studies through improved imputation accuracy and CNV tagging. Genome Res. 20, 1344–1351 (2010).
Yunusbayev, B. et al. The Caucasus as an Asymmetric Semipermeable Barrier to Ancient Human Migrations. Mol. Biol. Evol. 29, 359–365 (2011).
Olalde, I. et al. Derived immune and ancestral pigmentation alleles in a 7,000-year-old Mesolithic European. Nature 507, 225–228 (2014).
Rasmussen, M. et al. The genome of a Late Pleistocene human from a Clovis burial site in western Montana. Nature 506, 225–229 (2014).
Altshuler, D. M. et al. Integrating common and rare genetic variation in diverse human populations. Nature 467, 52–58 (2010).
Behar, D. M. et al. No Evidence from Genome-Wide Data of a Khazar Origin for the Ashkenazi Jews. Hum. Biol. 85, 859–900 (2013).
Verdu, P. et al. Patterns of Admixture and Population Structure in Native Populations of Northwest North America. PLoS Genet. 10, e1004530 (2014).
Korneliussen, T. S., Albrechtsen, A. & Nielsen, R. ANGSD: Analysis of Next Generation Sequencing Data. BMC Bioinformatics 15, 356 (2014).
Rasmussen, M. et al. An Aboriginal Australian genome reveals separate human dispersals into Asia. Science 334, 94–98 (2011).
Meyer, M. et al. A high-coverage genome sequence from an archaic Denisovan individual. Science 338, 222–226 (2012).
Prüfer, K. et al. The complete genome sequence of a Neanderthal from the Altai Mountains. Nature 505, 43–49 (2014).
Axelsson, E., Willerslev, E., Gilbert, M. T. P. & Nielsen, R. The Effect of Ancient DNA Damage on Inferences of Demographic Histories. Mol. Biol. Evol. 25, 2181–2187 (2008).
Patterson, N., Price, A. L. & Reich, D. Population structure and eigenanalysis. PLoS Genet. 2, e190 (2006).
We are grateful to all sample donors and to local community members for their help in sample collection. We thank Eske Willerslev, Simon Rasmussen, Maanasa Raghavan, Iñigo Olalde, Andrés Ruiz-Linares, David Reich, Noah Rosenberg and Ripan Malhi for sharing genotyping and sequencing data. We would like to thank National Genographic and Family Tree DNA for genotyping our samples, Shi Yan (Fudan University, Shanghai, China) and Horolma Pamjav (Institute of Forensic Medicine, Budapest, Hungary) for their help with compiling Y-chromosome haplogroup frequency tables. Special thanks go to Alexey S. Kondrashov for putting our team together. P.F., P.C. and A.Z. were supported by the Moravian-Silesian region projects MSK2013-DT1, MSK2013-DT2 and MSK2014-DT1 and by the Institution Development Program of the University of Ostrava. T.V.T. was supported by grants from The National Institute for General Medical Studies (GM068968), the Eunice Kennedy Shriver National Institute of Child Health and Human Development (HD070996) and National Science Foundation Division of Evolutionary Biology (1456634). Genome sequencing was supported by the Russian Science Foundation project no. 14-50-00150 and data analysis by the Russian Science Foundation project no. 14-24-00155.
The authors declare no competing financial interests.
About this article
Cite this article
Flegontov, P., Changmai, P., Zidkova, A. et al. Genomic study of the Ket: a Paleo-Eskimo-related ethnic group with significant ancient North Eurasian ancestry. Sci Rep 6, 20768 (2016). https://doi.org/10.1038/srep20768
Population genetic considerations for using biobanks as international resources in the pandemic era and beyond
BMC Genomics (2021)
The story of the lost twins: decoding the genetic identities of the Kumhar and Kurcha populations from the Indian subcontinent
BMC Genetics (2020)
BMC Bioinformatics (2019)
Application of the geographic population structure (GPS) algorithm for biogeographical analyses of wild and captive gorillas
BMC Bioinformatics (2019)
WhoGEM: an admixture-based prediction machine accurately predicts quantitative functional traits in plants
Genome Biology (2019)