Rare mitochondrial lineages with relict distributions can sometimes be disproportionately informative about deep events in human prehistory. We have studied one such lineage, haplogroup R0a, which uniquely is most frequent in Arabia and the Horn of Africa, but is distributed much more widely, from Europe to India. We conclude that: (1) the lineage ancestral to R0a is more ancient than previously thought, with a relict distribution across the Mediterranean/Southwest Asia; (2) R0a has a much deeper presence in Arabia than previously thought, highlighting the role of at least one Pleistocene glacial refugium, perhaps on the Red Sea plains; (3) the main episode of dispersal into Eastern Africa, at least concerning maternal lineages, was at the end of the Late Glacial, due to major expansions from one or more refugia in Arabia; (4) there was likely a minor Late Glacial/early postglacial dispersal from Arabia through the Levant and into Europe, possibly alongside other lineages from a Levantine refugium; and (5) the presence of R0a in Southwest Arabia in the Holocene at the nexus of a trading network that developed after ~3 ka between Africa and the Indian Ocean led to some gene flow even further afield, into Iran, Pakistan and India.
Low-frequency mitochondrial (and Y-chromosome) lineages with a relict distribution can be disproportionately informative about deep events in human prehistory. Mitochondrial DNA (mtDNA) haplogroups N1a1a and X, which have both been recovered from prehistoric remains as well as from living people, are good examples1,2,3. Another such lineage, with a very different distribution, is mtDNA haplogroup R0a, although to date it has never been recovered from prehistoric remains so we are entirely reliant on the modern diversity to draw conclusions about its history. R0a is unique in reaching very high frequencies in the Arabian Peninsula and is also common on the far side of the Bab el-Mandeb strait (or “Gate of Tears”), in the Horn of Africa, along with several other haplogroups of Eurasian origin.
More generally, the Horn of Africa is exceptional in harbouring very high mtDNA haplogroup diversity4 and populations in the Horn have significant non-autochthonous African ancestry across the genome5,6,7,8,9,10. Recent studies of complete human genomes have concluded that this 30–50% of non-African legacy in Cushitic- and Semitic-speaking populations is the result of admixture from Arabia beginning ~3,000 years ago (3 ka)11,12, at a time when common cultural features developed across the Horn and southern Arabia13, suggesting a link with the origin of the Ethiosemitic languages14. However, others have argued that such autosomal dating needs to be treated with considerable caution10,15. Moreover, some have also proposed that the source for the Horn lineages was in the Levant rather than Arabia10,11, whilst others have provided further evidence in favour of Arabia15.
Analyses of the uniparental genetic systems, in particular mtDNA, have suggested much more ancient gene flow into the Horn, from both the Levant and Arabia, although the timing has not been very clearly defined. Haplogroup M1 is thought to have arrived from the Mediterranean some time since the Last Glacial Maximum (LGM)16. The North African haplogroup U6a is found at lower levels and with possibly a different trajectory16. Haplogroup N1a1a in the Horn also separated from Arabia in the Late Glacial3 and several African subclades of haplogroup R0a and of haplogroup HV1 have been dated to the mid-Holocene17,18. The Y-chromosome19,20,21 and several genome-wide studies10,15 have recently supplied further evidence supporting the scenario of ancient migrations from the Arabian Peninsula into the Horn of Africa, well before the spread of agriculture into that region. Fernandes et al.15 recently estimated the combined Near Eastern/Arabian genome-wide fraction in Ethiopia at almost 40%, closely matching the West Eurasian fraction of 37% in our Ethiopian mtDNA database.
The most prominent Eurasian mitochondrial lineage that is shared across the Horn and Arabia is R0a, which is found at very low frequencies across west Eurasia, but reaches levels of up to 35% in eastern Yemen and up to 15% in some parts of the Horn of Africa facing the Red Sea9,15,17,18,22,23,24,25,26,27. It has been thought to have originated in the Near East and to have spread into Arabia at the end of the Pleistocene, albeit with difficulties in defining a source27; others have hypothesized a more ancient ancestry within Arabia28. This question is of great interest because evidence in favour of deeper Arabian ancestry would imply the existence of refugial areas in Arabia spanning the Last Glacial Maximum, which have been hypothesized but never confirmed29. The timing and mode of its subsequent entry into Eastern Africa also remain to be clarified15,27, as well as its history in Europe30,31. Here we analyse 205 whole mitogenomes from R0a and its sister clade R0b, alongside 733 R0a and R0b control-region sequences, in order to address these issues.
Deep ancestry of R0a
R0a’b (of which R0a forms the major part: Fig. 1; Fig. S1), which dates to ~40 ka using ML, is the sole known sister clade to the major West Eurasian haplogroup HV, with the two together comprising haplogroup R0. R0 branches directly from macro-haplogroup R, which dates to ~59 ka15. Although haplogroup R predominates amongst West Eurasians, especially Europeans, continent-specific basal branches are also found amongst South Asians, East Asians, Southeast Asians and Oceanians32. Thus whilst haplogroup R is a global non-African founder clade, R0 is primarily West Eurasian.
R0a, dating to ~30 ka using ML (Table 1) falls into at least five major subclades, three (R0a1, R0a2’3 and R0a4) already known17,33 and two (R0a5 and R0a6) newly defined here (Fig. 1). Two further basal haplotypes (#201 and #202) are seen in Italy and Spain, respectively. Along with a third lineage basal to R0a1 known from control-region data to occur in Egypt (Fig. S1) and the distribution of the very rare R0b, these might suggest a pre-LGM Mediterranean/Near Eastern source for R0a and R0a1, 25–40 ka. Alternatively, they might represent relicts of Late Glacial or postglacial dispersals around the Mediterranean.
R0a4, R0a5 and R0a6 are all rare. A survey of the R0a5 HVS-I motif indicates a wide distribution across the Near East and Europe (Table S2) and a deep Glacial ancestry (36.9 ± 14.1 ka with HVS-I; the two mitogenomes diverge at 18.8 ± 6.6 ka). A similar assessment for haplogroup R0a6 is more difficult, because its only control-region mutation is the reversion of the 16126 transition, but its distribution appears to be mainly restricted to Pakistan (mainly but not exclusively Kalash), with Palestinian, Iranian and Italian singletons (see also Fig. S1). Given its prevalence in the Kalash, we may hope that future elucidation of this lineage may help shed light on the origins of the Kalash people.
In contrast, the frequency and distribution for R0a4 cannot be assessed from published datasets because it lacks any diagnostic control-region mutations. With this limitation in mind, Fig. 1 and Table S1 indicate that R0a4 encompasses mainly mitogenomes from Western Europe, Spain in particular, but also Iraq.
An Arabian source for the major R0a lineages
The great majority of R0a mitogenomes cluster within R0a1 and R0a2’3, dating to the LGM (~26 ka and 21 ka, respectively), each mainly represented by a single star-like subclade, R0a1a and R0a2. These subclades both coalesce to the Late Glacial: ~13 and 17 ka (Table 1). These are the two major expansion lineages in R0a, but although widespread, they are both overwhelmingly seen in Arabia, especially Yemen (Fig. 2). However, R0a1 also includes R0a1b, comprising mainly lineages from Arabia and several possibly related lineages including a Bedouin from Arabia and a Moroccan. Given that the former have an Arabian origin and the latter are also from Arab-speaking populations, that probably spread from Arabia during the Muslim conquests, the whole of R0a1 seems likely to have an Arabian origin, dating back to at least 26 ka and thus spanning the LGM. This implies that the several Iranian lineages and a single Syrian lineage within R0a1a were derived from an Arabian source. This is supported by the HVS-I network, in which Iranian lineages broadly represent a small subset of Arabian R0a1a diversity (Fig. S1). This is also the case for the few Syrian and Iraqi lineages and the single branch shared by two Druze individuals is very recently diverged. Moreover, an overall ρ estimate for Fertile Crescent lineages in the HVS-I network for R0a1a, as a simple, unbiased measure of diversity, is only 64.4% of that for Arabian lineages. Thus R0a1 most likely entered Arabia by 26 ka, with the few northern Near Eastern lineages due to recent gene flow from Arabia into the Fertile Crescent. We need to recall this when we consider the founder analysis, below.
Similarly, R0a2’3, at ~21 ka, most likely has an Arabian ancestry. R0a3 is a minor Late Glacial Arabian subclade that sits alongside a paraphyletic Iranian lineage (shared with an Egyptian in the HVS-I dataset). As with R0a1a, Iranian HVS-I lineages within the major R0a2 are broadly a subset of Arabian diversity, with a number of ancestral haplotypes at elevated frequencies (Fig. S1). This may be explained by sporadic gene flow across the Gulf, but some Iranian lineages (along with lineages found further east in Pakistan) may also represent gene flow along the maritime trading networks which intensified in the mid- to late Holocene34. There is also a subclade, R0a1a1a, dating to ~3.5 ka (part of a larger clade, R0a1a1, that is also largely restricted to Yemen, dating to 10.3 ka), associated with the settlement of the island of Socotra, which may also have been part of a wider process of increased maritime activity and exchange35.
Similarly to R0a1a, if we examine R0a2 lineages from the Levant as a potential source pool, although some are ambiguous, more than a third of the R0a Druze in the HVS-I network (Fig. S1) belong to a derived largely European subclade (R0a2r), dating to ~12 ka (younger than the Arabian expansions); one belongs to a European cluster; and several to Arabian clusters. Again, of four Syrian lineages in the database, one belongs to the European/Druze R0a2r, one to the diverse Arabian subclade R0a2f (which also includes more than a third of Iraqi lineages at its tip) and one to R0a1a7, the most frequent in Yemen according to the HVS-I network, with derived lineages in Pakistan and possibly also Oman (Fig. S1). This phylogeographic pattern is markedly distinct from that in R0a5, for example. A comparison of overall ρ in HVS-I for putative R0a2 lineages (although much less clearly distinguished in the network) shows that the ρ value for the Fertile Crescent is below (albeit closer: 95.6%) that of the Arabian lineages. Again, the best explanation is an Arabian source for the Levantine lineages, in some cases as a result of sporadic gene flow, but for the majority due to Late Glacial expansions through the Levant into Mediterranean Europe, as we discuss further below. This once again suggests a Glacial arrival in Arabia, by 26 ka, although in this case the existence of the Levantine/European R0a2r subclade may suggest that we should not completely rule out a source in a Levantine refugium and Later Glacial expansions into Arabia as an alternative possibility.
With this caveat, this overall pattern strongly suggests that R0a1 and R0a2’3 both entered Arabia before or around the LGM and that the R0a1b/R0a1* and R0a3/R0a2’3* lineages are relicts that were not caught up to the same extent in the Late Glacial expansions that followed the LGM. This conclusion is further supported by the Bayesian skyline plots (BSPs) and reciprocal founder analyses detailed below.
Expansions of R0a1 and R0a2’3 lineages
The conclusion is strengthened by the distribution of the remaining lineages within each subclade. R0a1a encompasses at least eight major subclades (R0a1a1–8; R0a1a5–8 newly reported) and many paraphyletic lineages. Levantine lineages belong mainly to Negev desert Bedouin and Palestinians. The Bedouin have an Arabian Peninsula ancestry and genome-wide PCA and ADMIXTURE analyses indicate that Palestinians too are more similar to Arabian populations than to other Levantine populations and likely have substantial Arabian ancestry36,37. There is a single small Ethiopian subclade, R0a1a2, dating to ~5 ka but diverging directly from the R0a1a root and several sporadic singleton Horn lineages, but the vast majority of African R0a lineages fall within R0a2.
The larger R0a2 dates to ~16 ka, with 18 derived subclades which coalesce mainly to the Late Glacial, ~13 and 15 ka (Table 1). The Bølling-Allerød interstadial began ~14.7 ka38 and is associated with de-glaciation in Europe and a wet phase in the Near East/Arabia, which might have facilitated movements of hunter-gatherers into previously arid areas39. There are two major Eastern African subclades, R0a2b and R0a2g, dating to ~13 and ~11 ka respectively and several minor ones, one of similar age and another of which dates to ~4 ka but again diverges basally from R0a2. There is also a major Late Glacial subclade, R0a2r, found in southern Europeans but with two basal Druze lineages (from Israel and Lebanon); and several very minor subclades pointing to dispersals into Eastern Europe and Iran/Pakistan.
The BSPs (Fig. 3) show that these coalescences correspond to two major phases of population growth amongst R0a lineages in both the Late Glacial – the Bølling-Allerød interstadial (R0a2) – and the immediate postglacial, after the Younger Dryas (R0a1a). The BSP for R0a as a whole points to a major episode of ~12-fold growth from ~16 ka until ~10 ka, with a more recent episode of ~20-fold growth at ~3 ka. The separate plots show that whilst the growth of R0a2 overlaps with R0a overall, R0a1a was involved in a subsequent population expansion, in the early postglacial warming period following the Younger Dryas glacial relapse, ~11.5 ka. The finding of distinct demographic histories for R0a1a and R0a2 suggests that they may at one time have characterized different populations, possibly even dispersing from separate glacial refugial areas.
BSPs based on geographic origin (Fig. S2) confirmed a primary Bølling-Allerød expansion, with an additional expansion restricted to the Arabian Peninsula ~3 ka (shadowed in Eastern Africa). The plots also suggest that the earliest major signal of Late Glacial expansion was in Arabia, beginning ~17 ka, rather than in the Fertile Crescent (~14 ka), once again supporting an Arabian source. There is no independent expansion signature in Eastern Africa.
Major dispersal episodes: founder analysis
In order to date and quantify the main dispersal episodes, we performed a founder analysis on the mitogenome data. This identifies “founder sequences” shared between two populations as potential evidence for gene flow between the two populations. In this case, however, this poses a problem, since we have seen above that we cannot uniquely identify a source population and that most if not all of the Levantine and Iranian lineages in the major subclades are likely due to subsequent gene flow. (This is almost certainly the case also for most of the Mediterranean and North African lineages within R0a1 and R0a2’3.) Nevertheless, we performed the analysis assuming a northern source, in order to provide the most conservative estimate for the age of Arabian lineages. Although this assumption almost certainly doesn’t hold for R0a1a and probably also for R0a2, the analysis can still provide a clear picture of the main expansion episodes, to complement the skyline plots.
We therefore assumed a source in the Fertile Crescent, including the Levant and Iraq, both with and without Iran, in order to explore further the pattern in Arabia and to quantify and date subsequent dispersals into the Horn of Africa, Europe and South Asia, including Arabia in the source when assessing dispersals into Eastern Africa (Tables S3–S9, Fig. 4). We included Levantine Bedouin and Palestinian lineages as part of the Arabian sample, as discussed above.
First, we show Eastern Africa alone as the sink (Fig. 4A and Table S3), with the whole of Southwest Asia as the source. Here there is no Late Glacial peak, but rather a clear signal right at the start of the Holocene with both criteria: 11.8 ka with f2 and 10.8 with f1. With f2, this is the sole signal, but with f1 there is a second, more recent peak at 2.8 ka. The difference occurs in R0a2b, which is classed as a single African founder by the f2 criterion, whereas R0a2b2 is classed as a distinct founder dating to 2.9 ka with f1. This lineage has been elevated to high frequency (10.3–12.5%, the most frequent lineage) in Ethiopian Jews against a genome-wide background that is almost identical to other Ethiopians and it is not seen in Yemeni Jews, where an Arabian lineage within R0a2c is seen at even higher frequency22,40 instead. Because of this, despite the superficial confirmation of the ~3 ka migration inferred from autosomal studies, we should be cautious of taking the f1 result at face value. It may be that this population has subsequently experienced gene flow back towards the Levant and that this is the reason for identifying the migration with f1 that is screened out with the more stringent f2. However, given the inferences of substantial later northwards gene flow discussed above, we consider f2 the more plausible criterion for this dataset, at least regarding the settlement of Arabia. Nevertheless, some gene flow ~3 ka is possible, especially given the strong growth signal around this time in the Arabian BSP and may also be indicated by mtDNA haplogroup HV1 (see Discussion).
We next show the results when Eastern Africa and Arabia are combined into a single sink population (Fig. 4B and Table S4). The f2 criterion indicates a single Late Glacial expansion at ~15.4 ka, involving all R0a lineages. The f1 criterion distinguishes an additional more recent, postglacial expansion for R0a1a, ~11.0 ka, but the above discussion has explained why an additional migration is an unlikely scenario in practice. It does highlight, however, that further expansion, involving R0a1a in particular, took place in the postglacial, as also shown in the skyline plots. There is no sign under either criterion of the more recent dispersal at ~3 ka, confirming that, if it occurred at all (and involved R0a), its source was within Arabia and not in the Fertile Crescent.
We next show the results with Arabia alone as the sink, with the Fertile Crescent (excluding Iran) as the source (Fig. 4C and Table S5). Here again we see the major dispersal with the f2, ~15.6 ka. This represents our best estimate for the timing of the Late Glacial expansion of R0a. With f1 we see again both an even earlier Late Glacial peak at 17.6 ka and an additional episode at ~10.0 ka.
The reciprocal founder analysis, assuming Arabia as source and the Fertile Crescent as sink, including the Levant, Iraq and Iran (Fig. 4D and Table S6), shows a very slight early Holocene peak in f2 and major peaks towards the present for both f1 and f2. The picture is similar whether or not Palestinians are included within the Arabian source (not shown). Since the peaks are much more recent when Arabia is the source, this implies that any dispersals from Arabia towards the Fertile Crescent must have been much more recent than dispersals in the opposite direction. An analysis that excludes Iran (Fig. 4E and Table S7) differs in detail, yet retains the general features of more recent Holocene peaks especially towards the present for both f1 and f2. These results re-emphasise that the Fertile Crescent R0a variation seen today cannot be the main source for much of the diversity in Arabia, again confirming that Arabia is the most ancient reservoir of R0a variation. This in turn supports the arguments given above that the founder estimates for Arabia are in fact most likely expansion times within the Peninsula rather than dispersals from a Levantine refugium in the north.
Finally, we tested the migrations to South Asia (Fig. 4F and Table S8) and Europe (Fig. 4G and Table S9). As for the Horn of Africa and unlike for Arabia, we can safely interpret these results straightforwardly in terms of dispersals from an Arabian source. The results of the former shows a small peak ~7.8 ka with both f1 and f2 criteria, based on very few sequences and a stronger signal ~2 ka with f1, corresponding to R0a6. The mitogenomes yielding the ~2 ka signal mostly belong to the Kalash community, which is very isolated and carry low diversity of a number of mtDNA lineages of west Eurasian origin41. The 2 ka signal transposes to ~30 ka with f2, but examination of the tree shows clearly that this is an artefact: the lack of additional lineages deriving from the f2 founder candidate in South Asia, the low diversity within the Kalash and the presence of a Palestinian lineage in the clade, all point to the more recent introduction of the rare R0a6, suggesting that it may have been insufficiently sampled in Southwest Asia.
The results for Europe also suggest a primary dispersal into Southeast and Mediterranean Europe at the end of the Pleistocene/early Holocene, mainly involving R0a2r, with the signal a little earlier with f2 than f1. This may have been via a Levantine refugium, given the presence of basal Druze lineages in the cluster (and a Syrian in the HVS-I data). It recalls the patterns detected in a much larger fraction of haplogroup J and T lineages that dispersed from an inferred Levantine refugium along the Mediterranean after the LGM42. Some lineages may have dispersed later in the Holocene, but this is unclear given the small sample size (R0a occurs amongst Europeans at a rate of only 0.8%).
Evidence for glacial refugia in Arabia
The earliest settlement of Arabia by modern humans and its role in modern human dispersals out of Africa remain controversial43, although the consensus genetic estimate for the timing remains ~50–60 ka. We have argued for a “southern-route” dispersal out of Africa via Arabia at this time, since a Levantine source for all non-Africans would imply that basal non-African mtDNA diversity should be highest in the Near East, whereas the highest diversity is rather seen in South Asia30,44,45. A model of this kind – albeit, inevitably, with further complexity – is supported by the high productivity of ancient coastlines46,47,48. Autosomal dating has been used to suggest an earlier date49 and both qualitative arguments50 and simulations51 have been used to propose that the age of non-African mitogenomes might be older than the ~50–60 ka usually estimated52. However, these assertions are based on lines of reasoning that draw their estimates from inappropriately old population splits or ignore the phylogenetic and phylogeographic structure of mtDNA, where inferences are made from a hierarchy of nesting relationships, analogous to a stratigraphy, rather than simple haplogroup ages as often assumed by critics45,53,54. The model of a southern-route dispersal at ~50–60 ka has recently received strong support from an analysis of 104 complete genomes from Arabia55. These results are congruent with the most comprehensive mitogenome analyses that also stress the complexity of Arabian demographic history15,56 and with recent ancient DNA analyses57,58, although contrary to one rather idiosyncratic reanalysis of mitogenome data that minimises the role of Arabia59. Potential earlier dispersals identified from archaeological evidence51 therefore seem unlikely to have contributed substantially to the extant gene pool of the region. However, this is a topic that clearly requires much greater discussion, beyond the scope of the present article.
The earliest non-African ancestor of R0a, the root of haplogroup R, dates to ~59 ka and may (in line with the arguments summarised in the preceding paragraph) have originated in the Gulf Oasis soon after the dispersal of modern humans from Eastern Africa3. Its more immediate ancestor, R0a’b, dates to ~40 ka and its earliest branches have a relict distribution around the Mediterranean/Near East. We have identified several new minor sister subclades to the main R0a branches and these too have a similar distribution.
Nevertheless, multiple lines of evidence suggest that the major R0a subclades had entered Arabia and begun diversifying before the Last Glacial Maximum. This is in accord with evidence from rock art in Northern Arabia that the Neolithic pastoral economy was adopted by hunter–gatherers, rather than introduced by dispersing agriculturalists from the Near East60. However, there is little archaeological evidence for the presence of human populations in Arabia across the LGM, when environmental conditions were extremely poor61,62, suggesting that they survived, if at all, in glacial refugia. Rose29 proposed three potential “oases” in Arabia. Most attention has been given to the Gulf Oasis in the east which, as mentioned above, may have incubated early modern humans shortly after their initial move out of Africa. However, there are two further candidates – the South Arabian refugium in the Dhofar highlands and eastern Yemen-Oman coastal zone and the Red Sea coastal plain29. It seems likely that one or both of these were refugia for early Arabian hunter-gatherer groups carrying predominantly R0a1 and R0a2’3 and from which R0a1a and R0a2, in particular, expanded after the LGM. It is tempting to speculate that R0a2’3 may have sheltered in the Red Sea refugium, given the very early postglacial dispersals of R0a2 subclades both into the Horn of Africa and into southern Europe, likely via the Levant. Further work should enable us to test this hypothesis more precisely.
R0a1a began its dramatic expansions ~12 ka and is now seen mainly in the southern part of the Arabian Peninsula, such as Yemen and the island of Socotra, where it displays a more recent frequency peak approaching 40%35. However, the first major expansions in Arabia were earlier, in the early Late Glacial period and involved R0a2. Intriguingly, both expansions predate the early Holocene onset of pluvial conditions in the Peninsula63 and perhaps involved coastal regions now under water. Furthermore, R0a2 lineages expanded much further afield, across the Red Sea and into the Horn of Africa, in the immediate postglacial warming period, so that the present-day R0a frequency in parts of the Horn approaches 20%. This supports the pre-agricultural gene flow recently inferred from genome-wide data10 and may be linked to the establishment of obsidian exchange networks across the Red Sea in the early Holocene64,65. Both sets of analyses contrast with the previously established scenario that most of the non-African ancestry in the Horn is the result of admixture ~3 ka11,12. However, Hodgson et al.10 argue cogently that genome-wide dating methods based on linkage disequilibrium are strongly biased in favour of recent admixture events (see also15) and propose a deep Pleistocene ancestry for the Eurasian admixture, dating back as much as 23 ka. On the other hand, they and others11 also propose that the Eurasian admixture in the Horn came from the northeast, rather than from Arabia.
However, the limitations to current genome-wide analyses extend beyond the timing of dispersals to the identification of source populations, which can often be clarified on the basis of the phylogenetic nesting relationships identifiable with the non-recombining marker systems. In fact, the mtDNA evidence clearly indicates that Eurasian admixture in the Horn indeed occurred several times and from several distinct sources. In addition to R0a, there are four other potentially Eurasian ancient mtDNA clades in Eastern Africa: M1a, U6a, HV1 and N1a1a, which together with R0a make up 30% of Ethiopian lineages in our control-region database (n = 169). There is also a smattering of “accidental” lineages (7%) that most likely arrived within the last few centuries, so about 81% of the Eurasian lineages in Ethiopia are potentially ancient.
However, aside from R0a, only one other haplogroup is likely to indicate a Pleistocene dispersal from Arabia: N1a1a3. N1a1a3 dates to ~15.2 ka and N1a1a4 to only 850 years, but both diverge directly from the N1a1a root, which dates to ~25 ka, with the only closely related lineages seen in Arabia – a clearly similar pattern to R0a. HV1b1 in the Horn also has a Yemen source and dates to ~8.2 ka, leading to the suggestion of an early Holocene movement18, but it is interleaved with Yemeni lineages in the tree, suggesting that it may have arrived more recently. A very approximate founder age estimate suggests an arrival ~5 ka.
More frequent even than R0a in the Horn is M1a, thought to have arrived during the Late Glacial16. There are few lineages from which to estimate an arrival time, but M1a1c’d dates to ~12.0 ka. However, M1a probably arrived via Egypt rather than Yemen44. Another North African/Mediterranean lineage, haplogroup U6a, again has a likely source in Egypt/Near East44,66, but U6a2a1 in the Horn dates to ~4.0 ka.
In summary there were several late Pleistocene arrivals, from both North Africa/Levant and from Arabia and similarly there seem likely to have been several mid-Holocene arrivals, again from both sources. Overall, about 62% of the Eurasian lineages probably arrived in Ethiopia during the Pleistocene (~33% from Arabia and ~29% from the north), with ~19% in the mid-Holocene (but half from Arabia and half from the north), with the remaining ~19% likely very recent. Potentially, all of these different ages are conflated into the autosomal admixture estimate of 3 ka.
Our results do indicate population growth within Arabia at ~3 ka, which may be implicated in a late Holocene range expansion across the Arabian Sea involving perhaps HV1 and perhaps also of R0a1a1a lineages into the island of Socotra, where the age of the R0a1a1 lineages date to the same timeframe35. Populations survived along the southeast Arabian coast during the extreme aridity of the so-called “Dark Millennium” after 5.9 ka and may have prospered as climatic conditions improved again in the Arabian Bronze Age. Although there is less evidence from Yemen, this phase saw marked re-settlement of southeast Arabia during the Hafit phase of oasis agriculture after 5.1 ka67 and a similar trajectory seems likely to have taken place to the west.
The return to more pluvial conditions in Eastern Africa appears to have been later, ~4 ka68, matching estimates for the establishment of Ethiosemitic languages in the Horn14. It also coincides with the appearance of the poorly-known literate Daamat-Di’amat polity in northern Ethiopia/Eritrea, which extended from roughly 850–350 BC and has long been thought to show signs of Arabian influence69. However, some recent archaeological studies have downplayed the extent of Arabian influence and consider large-scale migration at this time unlikely, more in line with the evidence that we present here70. There may have been some minor gene flow due to the intensification of maritime trading networks that had begun around this time34,69, also indicated by the appearance of R0a lineage around the Indian Ocean as far as India. But the main episodes of Arabian settlement in the Horn occurred much earlier, at the end of the Ice Age.
Subjects and Methods
We identified candidate R0a mtDNAs by surveying control-region mutational motifs of ~10,000 subjects of various geographic origins (Africa, East and South Asia, the Near East, Caucasus and Europe) whose DNA was available in the laboratories participating in this study. For all subjects, we obtained appropriate written informed consent and the research was reviewed and approved by the Ethics Committee for Clinical Experimentation of the University of Pavia (Italy), board minutes of April 11th 2013. All experiments were performed in accordance with relevant guidelines and regulations.
We PCR-amplified 54 candidate R0a mtDNAs, selected on the basis of the presence of the diagnostic R0a control-region motif and completely sequenced them following a well-established Sanger protocol71. We aligned, assembled and compared them using Sequencher 5.0 (Gene Codes Corporation) relative to both the Revised Sapiens Reference Sequence (RSRS)33 and the revised Cambridge Reference Sequence (rCRS)72. We also identified and sequenced two candidate R0b mtDNAs, following the same approach.
We furthermore sequenced five additional candidate R0a mtDNAs (from the Csangos and Szekelys of Romania, see73 for sampling) using massively parallel sequencing. We enriched these mitogenomes in 62 midi-sized amplicons, purified them using AMPure XP beads (Beckman Coulter, Inc., Brea, CA, USA) and obtained MiSeq libraries using the Nextera XT DNA Sample preparation kit74. We performed MPS using the Illumina MiSeq benchtop sequencer (Illumina, San Diego, CA, USA) following the manufacturer’s recommendations. We analysed MiSeq-generated sequences using the NextGENe software (SoftGenetics, State College, PA, USA) and assessed them relative to both the internal MiSeq Reporter results and the corresponding control-region sequences73. We clarified remaining inconsistencies by Sanger sequencing to forensic quality standards75.
We analysed the 61 novel mitogenomes alongside 143 R0a (and one R0b) whole-mtDNA sequences already available in public databases. Geographic and/or ethnic affiliations of the 202 R0a mtDNAs, as well as their accession numbers are listed in Table S1, together with the two novel and one previously reported76 R0b mitogenomes. For the construction of the R0a phylogeny we employed a maximum parsimony approach with the aid of the mtPhyl software (http://eltsov.org/mtphyl.aspx), correcting the tree by hand with reference to PhyloTree (Build 17)77. A new haplogroup label was assigned following the established nomenclature only when the candidate haplogroup encompassed at least two haplotypes. We disregarded the unreliable np 60 when identifying clades.
We estimated coalescence times using both maximum likelihood (ML) and the ρ statistic (average distance of the haplotypes of a clade from the respective root haplotype)78 accompanied by a heuristic estimate of the standard error (σ) calculated from an estimate of the genealogy79. We used PAML 4.580 to obtain ML estimates, assuming the HKY85 mutation model (two parameters in the model of DNA evolution) with γ -distributed rates (approximated by a discrete distribution with 32 categories) and two partitions: coding region (from np 577 to np 16023) and control region (from np 16024 to np 576). We performed these calculations considering all substitutions except those at np 16519 and the 16182C and 16183C. We converted mutational distances into years using the substitution rate of about one mutation every 3,624 years for the entire mitogenome and correcting for purifying selection using the calculator provided by Soares et al.81.
We also obtained Bayesian skyline plots (BSPs)82 from BEAST 1.7.483 for haplogroup R0a and its most frequent subclades, using a strict molecular clock (lognormal distribution across branches and uncorrelated between them) and a HKY85-type model with γ-distributed rates. BSPs estimate effective population size through time from random sequences of a population. Haplogroups in general do not equate to population data, but the signal associated with a haplogroup might nevertheless signal demographic processes in the populations carrying it, as previously suggested52. To approximate the mutation rate to the one used in previous analyses, we used a U6 sequence (EF064317) as an outgroup44, setting the age of haplogroup R to ~59 ka (95% C.I: 49–69 ka), as an average of previously proposed estimates33,81; plus we considered the age obtained here for R0a as consistent internal calibration points52. Specifically, we ran 50,000,000 iterations, with samples drawn every 10,000 Markov chain Monte Carlo (MCMC) steps, after a discarded burn-in of 10,000,000 steps, as in Soares et al.52. We considered haplogroup R0a and its major subclades monophyletic in the analyses. We visualized the BSPs obtained in plots with Tracer v1.5 and Excel using a generation time of 25 years.
In order to estimate the times of migrations, we employed founder analysis30. This method assumes a strict division between assumed source and sink populations and two criteria (f1 and f2) for identifying founder sequences to allow as far as possible for homoplasy and back-migrations, by ensuring that sequence matches are not at the tips of the source phylogeny. We thus stipulate that founders must have at least one (f1) or two (f2) derived branches in the source population. We carried out the analysis for R0a using the whole mitogenomes – estimating the age of the migration of each founder using the ρ statistic. However, since the assumptions of the founder method do not allow the use of a time-dependent clock, as usually performed for whole mitogenomes81, we used an approximated linear rate. Given the relatively small difference between the mutation rate for time zero (average 2562 years for a mutation to happen) and the mutation rate for the oldest estimated founder (average 2667 years for a mutation to happen) we used the intermediate value between these (2651 years for a mutation to happen) as an estimate for the overall range, as previously15. We performed the founder analysis in several ways to estimate the arrival times of R0a lineages in different continents, in each case performing the analyses with Palestinians included either with Arabian populations, with Fertile Crescent populations or unassigned and also either including and excluding Iranian lineages from the Fertile Crescent source. We performed the following analyses: (1) from the Near East into Arabia/Eastern Africa; (2) Near East into Arabia; (3) Near East/Arabia into Eastern Africa; (4) Arabia into the Fertile Crescent (a “reciprocal” founder analysis to check the direction of dispersal: see84; (5) Near East/Arabia into South Asia; (6) Near East/Arabia into Europe. We scanned the distribution of founder ages for each region, defining equally spaced 200-year intervals for each migration from 0 to 50 ka.
We further assessed extant frequencies and geographical distributions of R0a and R0a1a by surveying published and unpublished datasets (more than 45,000 control-region sequences) for their diagnostic control-region mutational motifs. By searching our in-house database of unpublished sequences, the European DNA Profiling Group Mitochondrial Population Database (EMPOP)85,86 and published control-region sequences (mainly limited to HVS-I), we were able to evaluate a total of more than 100 populations (Table S2). We constructed spatial frequency distribution plots with the program Surfer 9 (Golden Software). We extended the search to members of two of the largest subclades restricted mainly to Eastern Africa, R0a2b1 and R0a2b2. Unfortunately, R0a2g, a third essentially African-specific subclade, does not harbour any diagnostic mutation in the control region, so that its geographic distribution could not be further evaluated. We also constructed a phylogenetic network of the HVS-I variation in R0a’b using the Network package (Fig. S1).
How to cite this article: Gandini, F. et al. Mapping human dispersals into the Horn of Africa from Arabian Ice Age refugia using mitogenomes. Sci. Rep. 6, 25472; doi: 10.1038/srep25472 (2016).
Haak, W. et al. Ancient DNA from the first European farmers in 7500-year-old Neolithic sites. Science 310, 1016–1018 (2005).
Perego, U. A. et al. Distinctive Paleo-Indian migration routes from Beringia marked by two rare mtDNA haplogroups. Curr Biol 19, 1–8 (2009).
Fernandes, V. et al. The Arabian cradle: mitochondrial relicts of the first steps along the southern route out of Africa. Am J Hum Genet 90, 347–355 (2012).
Gomes, V. et al. Mosaic maternal ancestry in the Great Lakes region of East Africa. Hum Genet 134, 1013–1027 (2015).
Levine, D. N. Greater Ethiopia: The Evolution of a Multiethnic Society. (University of Chicago Press, 2000).
Cavalli-Sforza, L. L., Menozzi, P. & Piazza, A. The history and geography of human genes. (Princeton University Press, 1994).
Passarino, G. et al. Different genetic components in the Ethiopian population, identified by mtDNA and Y-chromosome polymorphisms. Am J Hum Genet 62, 420–434 (1998).
Ehret, C. The civilizations of Africa: a history to 1800. (University of Virginia Press, 2002).
Non, A. L., Al-Meeri, A., Raaum, R. L., Sanchez, L. F. & Mulligan, C. J. Mitochondrial DNA reveals distinct evolutionary histories for Jewish populations in Yemen and Ethiopia. Am J Phys Anthropol 144, 1–10 (2011).
Hodgson, J. A., Mulligan, C. J., Al-Meeri, A. & Raaum, R. L. Early back-to-Africa migration into the Horn of Africa. PLoS Genet 10, e1004393 (2014).
Pagani, L. et al. Ethiopian genetic diversity reveals linguistic stratification and complex influences on the Ethiopian gene pool. Am J Hum Genet 91, 83–96 (2012).
Pickrell, J. K. et al. Ancient west Eurasian ancestry in southern and eastern Africa. Proc Natl Acad Sci USA 111, 2632–2637 (2014).
Phillipson, D. W. Ancient Ethiopia: Aksum, Its Predecessors and Successors. (British Museum Press, 1998).
Kitchen, A., Ehret, C., Assefa, S. & Mulligan, C. J. Bayesian phylogenetic analysis of Semitic languages identifies an Early Bronze Age origin of Semitic in the Near East. Proc Biol Sci 276, 2703–2710 (2009).
Fernandes, V. et al. Genetic stratigraphy of key demographic events in Arabia. PloS one 10, e0118625 (2015).
Pennarun, E. et al. Divorcing the Late Upper Palaeolithic demographic histories of mtDNA haplogroups M1 and U6 in Africa. BMC Evol Biol 12, 234 (2012).
Cerný, V. et al. Internal diversification of mitochondrial haplogroup R0a reveals post-last glacial maximum demographic expansions in South Arabia. Mol Biol Evol 28, 71–78 (2011).
Musilová, E. et al. Population history of the Red Sea–genetic exchanges between the Arabian Peninsula and East Africa signaled in the mitochondrial DNA HV1 haplogroup. Am J Phys Anthropol 145, 592–598 (2011).
Cruciani, F. et al. Tracing past human male movements in northern/eastern Africa and western Eurasia: new clues from Y-chromosomal haplogroups E-M78 and J-M12. Mol Biol Evol 24, 1300–1311 (2007).
Sanchez, J. J., Hallenberg, C., Børsting, C., Hernandez, A. & Morling, N. High frequencies of Y chromosome lineages characterized by E3b1, DYS19-11, DYS392-12 in Somali males. Eur J Hum Genet 13, 856–866 (2005).
Mendez, F. L. et al. Increased resolution of Y chromosome haplogroup T defines relationships among populations of the Near East, Europe and Africa. Hum Biol 83, 39–53 (2011).
Thomas, M. G. et al. Founding mothers of Jewish communities: geographically separated Jewish groups were independently founded by very few female ancestors. Am J Hum Genet 70, 1411–1420 (2002).
Kivisild, T. et al. Ethiopian mitochondrial DNA heritage: tracking gene flow across and around the gate of tears. Am J Hum Genet 75, 752–770 (2004).
Richards, M. et al. Extensive female-mediated gene flow from sub-Saharan Africa into near eastern Arab populations. Am J Hum Genet 72, 1058–1064 (2003).
Poloni, E. S. et al. Genetic evidence for complexity in ethnic differentiation and history in East Africa. Ann Hum Genet 73, 582–600 (2009).
Boattini, A. et al. mtDNA variation in East Africa unravels the history of Afro-Asiatic groups. Am J Phys Anthropol 150, 375–385 (2013).
Al-Abri, A. et al. Pleistocene-Holocene boundary in Southern Arabia from the perspective of human mtDNA variation. Am J Phys Anthropol 149, 291–298 (2012).
Rose, J. I. et al. Tabula rasa or refugia? Using genetic data to assess the peopling of Arabia. Arab Archaeol Epigr 24, 95–101 (2013).
Rose, J. I. New Light on Human Prehistory in the Arabo-Persian Gulf Oasis. Curr Anthropol 51, 849–883 (2010).
Richards, M. et al. Tracing European founder lineages in the Near Eastern mtDNA pool. Am J Hum Genet 67, 1251–1276 (2000).
Richards, M., Macaulay, V., Torroni, A. & Bandelt, H. J. In search of geographical patterns in European mitochondrial DNA. Am J Hum Genet 71, 1168–1174 (2002).
Torroni, A., Achilli, A., Macaulay, V., Richards, M. & Bandelt, H. J. Harvesting the fruit of the human mtDNA tree. Trends Genet 22, 339–345 (2006).
Behar, D. M. et al. A “Copernican” reassessment of the human mitochondrial DNA tree from its root. Am J Hum Genet 90, 675–684 (2012).
Boivin, N. & Fuller, D. Q. Shell Middens, Ships and Seeds: Exploring Coastal Subsistence, Maritime Trade and the Dispersal of Domesticates in and Around the Ancient Arabian Peninsula. J World Prehist 22, 113–180 (2009).
Cerný, V. et al. Out of Arabia-the settlement of island Soqotra as revealed by mitochondrial and Y chromosome genetic diversity. Am J Phys Anthropol 138, 439–447 (2009).
Haber, M. et al. Genome-wide diversity in the Levant reveals recent structuring by culture. PLoS Genetics 9, e1003316 (2013).
Pala, M., Chaubey, G., Soares, P. & Richards, M. B. The Archaeogenetics of European Ancestry. eLS. doi: 10.1002/9780470015902.a0024624 (2014).
Thiagarajan, N., Subhas, A. V., Southon, J. R., Eiler, J. M. & Adkins, J. F. Abrupt pre-Bølling-Allerød warming and circulation changes in the deep ocean. Nature 511, 75–78 (2014).
Parker, A. G. In The Evolution of Human Populations in Arabia Vertebrate Paleobiology and Paleoanthropology 39–49 (Springer: Netherlands,, 2010).
Behar, D. M. et al. Counting the founders: the matrilineal genetic ancestry of the Jewish Diaspora. PloS one 3, e2062 (2008).
Quintana-Murci, L. et al. Where west meets east: the complex mtDNA landscape of the southwest and Central Asian corridor. Am J Hum Genet 74, 827–845 (2004).
Pala, M. et al. Mitochondrial DNA signals of late glacial recolonization of Europe from near eastern refugia. Am J Hum Genet 90, 915–924 (2012).
Petraglia, M. D., Parton, A. & Groucutt, H. G. Green Arabia: Human prehistory at the Crossroads of Continents. Quaternary International 382, 1–7 (2015).
Olivieri, A. et al. The mtDNA legacy of the Levantine early Upper Palaeolithic in Africa. Science 314, 1767–1770 (2006).
Mellars, P., Gori, K. C., Carr, M., Soares, P. A. & Richards, M. B. Genetic and archaeological perspectives on the initial modern human colonization of southern Asia. Proc Natl Acad Sci USA 110, 10699–10704 (2013).
Bulbeck, D. Where River Meets Sea: A Parsimonious Model for Homo sapiens Colonization of the Indian Ocean Rim and Sahul. Curr Anthropol 48, 315–321 (2007).
Bailey, G. N. et al. Blue Arabia: Palaeolithic and underwater survey in SW Saudi Arabia and the role of coasts in Pleistocene dispersals. Quaternary International 382, 42–57 (2015).
Erlandson, J. M. & Braje, T. J. Coasting out of Africa: The potential of mangrove forests and marine habitats to facilitate human coastal expansion via the Southern Dispersal Route. Quaternary International 382, 31–41 (2015).
Scally, A. & Durbin, R. Revising the human mutation rate: implications for understanding human evolution. Nat Rev Genet 13, 745–753 (2012).
Boivin, N., Fuller, D. Q., Dennell, R., Allaby, R. & Petraglia, M. D. Human dispersal across diverse environments of Asia during the Upper Pleistocene. Quaternary International 300, 32–47 (2013).
Groucutt, H. S. et al. Rethinking the dispersal of Homo sapiens out of Africa. Evol Anthropol 24, 149–164 (2015).
Soares, P. et al. The Expansion of mtDNA Haplogroup L3 within and out of Africa. Mol Biol Evol 29, 915–927 (2012).
Macaulay, V. & Richards, M. B. Mitochondrial Genome Sequences and Their Phylogeographic Interpretation. eLS. doi: 10.1002/9780470015902.20843.pub2 (2013).
Pala, M., Soares, P., Chaubey, G. & Richards, M. B. In The Cambridge World History Volume 2. A World with Agriculture, 12,000 BCE–500 CE (eds G. Barker & C. Goucher ) 26–54 (Cambridge University Press, 2015).
Rodriguez-Flores, J. L. et al. Indigenous Arabs are descendants of the earliest split from ancient Eurasian populations. Genome Res 26, 151–162 (2016).
Cerný, V., Cizkova, M., Poloni, E. S., Al-Meeri, A. & Mulligan, C. J. Comprehensive view of the population history of Arabia as inferred by mtDNA variation. Am J Phys Anthropol 159, 607–616 (2015).
Posth, C. et al. Pleistocene Mitochondrial Genomes Suggest a Single Major Dispersal of Non-Africans and a Late Glacial Population Turnover in Europe. Curr Biol 26, 827–833 (2016).
Richards, M. B., Soares, P. & Torroni, A. Palaeogenomics: Mitogenomes and Migrations in Europe’s Past. Curr Biol 26, R243–R246 (2016).
Fregel, R., Cabrera, V., Larruga, J. M., Abu-Amero, K. K. & Gonzalez, A. M. Carriers of Mitochondrial DNA Macrohaplogroup N Lineages Reached Australia around 50,000 Years Ago following a Northern Asian Route. PloS one 10, e0129839 (2015).
Guagnin, M. et al. Hunters and herders: Exploring the Neolithic transition in the rock art of Shuwaymis, Saudi Arabia. Archaeological Research in Asia 4, 3–16 (2015).
Groucutt, H. S. & Petraglia, M. D. The prehistory of the Arabian peninsula: deserts, dispersals and demography. Evol Anthropol 21, 113–125 (2012).
Jennings, R. P. et al. The greening of Arabia: Multiple opportunities for human occupation of the Arabian Peninsula during the Late Pleistocene inferred from an ensemble of climate model simulations. Quaternary International 382, 181–199 (2015).
Preston, G. W. et al. A multi-proxy analysis of the Holocene humid phase from the United Arab Emirates and its implications for southeast Arabia’s Neolithic populations. Quaternary International 382, 277–292 (2015).
Khalidi, L. In The Evolution of Human Populations in Arabia (ed M. D. Petraglia, Rose, J. I. ) 279–291 (Springer: Netherlands,, 2010).
Khalidi, L. et al. Obsidian sources in highland Yemen and their relevance to archaeological research in the Red Sea region. J Archaeol Sci 37, 2332–2345 (2010).
Macaulay, V. et al. The emerging tree of West Eurasian mtDNAs: a synthesis of control-region sequences and RFLPs. Am J Hum Genet 64, 232–249 (1999).
Preston, G. W., PArker, A. G., Walkington, H., Leng, M. J. & Hodson, M. J. From nomadic herder-hunters to sedentary farmers: The relationship between climate change and ancient subsistence strategies in south-eastern Arabia. Journal of Arid Environments 86, 122–130 (2012).
Tierney, J. E. & deMenocal, P. B. Abrupt shifts in Horn of Africa hydroclimate since the Last Glacial Maximum. Science 342, 843–846 (2013).
Fattovich, R. The Development of Ancient States in the Northern Horn of Africa, c. 3. J World Prehist 23, 145–175 (2010).
Phillipson, L. Lithic Artefacts as a Source of Cultural, Social and Economic Information: the evidence from Aksum, Ethiopia. Afr Archaeol Rev 26, 45–58 (2009).
Torroni, A. et al. Do the four clades of the mtDNA haplogroup L2 evolve at different rates? Am J Hum Genet 69, 1348–1356 (2001).
Andrews, R. M. et al. Reanalysis and revision of the Cambridge reference sequence for human mitochondrial DNA. Nat Genet 23, 147 (1999).
Brandstätter, A. et al. Migration rates and genetic structure of two Hungarian ethnic groups in Transylvania, Romania. Ann Hum Genet 71, 791–803 (2007).
Parson, W. et al. Massively parallel sequencing of complete mitochondrial genomes from hair shaft samples. Forensic Sci Int Genet. 15, 8–15 (2015).
Fendt, L., Zimmermann, B., Daniaux, M. & Parson, W. Sequencing strategy for the whole mitochondrial genome resulting in high quality sequences. BMC Genomics 10, 139 (2009).
Achilli, A. et al. Mitochondrial DNA backgrounds might modulate diabetes complications rather than T2DM as a whole. PloS one 6, e21029 (2011).
van Oven, M. & Kayser, M. Updated comprehensive phylogenetic tree of global human mitochondrial DNA variation. Hum Mutat 30, E386–394 (2009).
Forster, P., Harding, R., Torroni, A. & Bandelt, H. J. Origin and evolution of Native American mtDNA variation: a reappraisal. Am J Hum Genet 59, 935–945 (1996).
Saillard, J., Forster, P., Lynnerup, N., Bandelt, H. J. & Nørby, S. mtDNA variation among Greenland Eskimos: the edge of the Beringian expansion. Am J Hum Genet 67, 718–726 (2000).
Yang, Z. PAML: a program package for phylogenetic analysis by maximum likelihood. Comput Appl Biosci. 13, 555–556 (1997).
Soares, P. et al. Correcting for purifying selection: an improved human mitochondrial molecular clock. Am J Hum Genet 84, 740–759 (2009).
Drummond, A. J., Rambaut, A., Shapiro, B. & Pybus, O. G. Bayesian coalescent inference of past population dynamics from molecular sequences. Mol Biol Evol 22, 1185–1192 (2005).
Drummond, A. J. & Rambaut, A. BEAST: Bayesian evolutionary analysis by sampling trees. BMC Evol Biol. 7, 214 (2007).
Soares, P. et al. Climate change and postglacial human dispersals in Southeast Asia. Mol Biol Evol 25, 1209–1218 (2008).
EMPOP. European DNA Profiling Group Mitochondrial Population Database. (2012) Available at: http://empop.online/. (Acessed: 15th October 2012).
Parson, W. & Dur, A. EMPOP–a forensic mtDNA database. Forensic Sci Int Genet. 1, 88–92 (2007).
The authors are grateful to all the donors for providing biological specimens. The authors want to thank Martina Dünser (Dep. of Visceral, Transplantation and Thoracic Surgery, Tirol Kliniken, Innsbruck) and Bettina Zelger (Dep. of Pathology, Medical University of Innsbruck) for retrieving information on a sample’s origin. This work was supported by the University of Pavia strategic theme “Towards a governance model for international migration: an interdisciplinary and diachronic perspective” (MIGRAT-IN-G), the Italian Ministry of Education, University and Research: Progetti Futuro in Ricerca 2012 (RBFR126B8I) (to A.A. and A.O.) and Progetti Ricerca Interesse Nazionale 2012 (to A.A., F.C., A.T. and O.S.), a Leverhulme Doctoral Scholarship award to M.B.R., a Newton International Fellowship to M.P., the intramural funding program of the Medical University Innsbruck for young scientists MUI-START, Project 2013042025 (to M.B.), an EMBO short-term fellowship (ASTF 70-2014/Award) and a University of Huddersfield University Research Fellowship award to F.G. P.S. is supported by FCT, European Social Fund, Programa Operacional Potencial Humano and the FCT Investigator Programme (IF/01641/2013) and acknowledges FCT I.P. for CBMA’s strategic funding UID/BIA/04050/2013.
The authors declare no competing financial interests.
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Gandini, F., Achilli, A., Pala, M. et al. Mapping human dispersals into the Horn of Africa from Arabian Ice Age refugia using mitogenomes. Sci Rep 6, 25472 (2016). https://doi.org/10.1038/srep25472
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