Alexander's conquest of the Middle East would have taken Greek male lineages much further afield, perhaps as far as Afghanistan and Pakistan, although only at trace frequencies. It is known from a single carrier in Mali. Sectors in pie charts are coloured according to the haplogroup colour code to the left. Because of the separation of the two major waves around 3500 YBP and the subsequent isolation of many groups, modern Bantu languages can be divided into West and East Bantu.8, 9 Non-Bantu languages (that do not belong to the Niger-Congo phylum, eg, Khoisanid languages in the southwest of the continent and a few Cushitic and Nilo-Saharan tongues in the northeast6) have survived in areas that have not experienced extensive inward migration of Bantu speakers. (2002) states: "A possible explanation might be that haplotype 24 chromosomes [E-M2*] were already present across the Sudanese belt when the M191 mutation, which defines haplotype 22, arose in central western Africa. Populations in Northwest Africa, central Eastern Africa and Madagascar have tested at more moderate frequencies. E1b1a (L576) This population represents an East to West thrust in Africa, only E1b1a lineage able to survive crossing the A1b1 territories. The distribution and age of E-V13 clades in central and western Europe are consistent with a dispersal by Hallstatt and La Tne Celts, Italic tribes (including a Roman redistribution) and the later influx of Germanic tribes, particularly the Goths, who may have assimilated additional Proto-Slavic E-V13 lineages in East Germany, Poland and Ukraine before entering the Roman Empire. Within Africa, E-M2 displays a west-to-east as well as a south-to-north clinal distribution. Consequently, the haplogroup is often observed in the United States populations in men who self-identify as African Americans. The early development of agriculture triggered significant population growth, resulting in the expansion of early farming populations, along with the spread of language families in many parts of the world, including Africa.1 The many advantages of agricultural subsistence over foraging is a likely contributing factor to the rapid expansion of agriculturists and their languages during the holocene.2 A well-known example of this phenomenon in Africa is the expansion of the Bantu-speaking people (EBSP), which is thought, on the basis of linguistic evidence, to have started around 5000 years ago3 in the region on the border between modern day eastern Nigeria and Cameroon.4 It is widely accepted that there was an early split into eastern and western routes in which farmers first expanded east and also, within 1500 years, reached West-Central Africa. BMC Evol Biol 2010; 10: 92. E1B1A must be the standard for determining whether or not a male is a descendant of the Biblical Israelites. The frequency of E subclades has varied geographically over time due to founder effects in Neolithic, Bronze Age and Iron Age populations, i.e. Whilst E1b1a reaches its highest frequency of 81% in Senegal, only 1 of the 139 Senegalese that were tested showed M191/P86. Previously collected buccal-swab DNA samples from ethnic groups across sub-Saharan Africa were extracted by the standard phenol-chloroform method. In . Pakendorf et al7 identify and provide evidence of greater complexity in the process of the EBSP as suggested by Alves et al33 and Montano et al.34. even though his parent clade is not and brother E-M215 is not.
Something is wrong: Where do black people come from? "E3a" redirects here. Whilst E1b1a reaches its highest frequency of 81% in Senegal, only 1 of the 139 Senegalese that were tested showed M191/P86. For other uses, see. It has been hypothesized that E1b1a, including its subbranch E1b1a7 (defined by M191, and not tested in the present study), arose in west Central Africa and was later taken southward through a demic expansion ( Cruciani et al. This evidence suggests that at the end of the last glaciation 12,000 years ago, E1b1b men were present in the Levant, but not in other parts of the Near East. A single carrier was found in Mali. Slider with three articles shown per slide. E1b1a1a1f is defined by L485. The Goths settled over all the Italian peninsula. E1B1B1 is of Levant origin, E1B1A is East African. Z830, M310.1's . [16], At Deloraine Farm, in Nakuru County, Kenya, an iron metallurgist of the Iron Age carried haplogroups E1b1a1a1a1a/E-M58 and L5b1. Kayser M, Caglia A, Corach D et al. The merits of this hypothesis is that it would explain why M81 is so much more common in the Maghreb, and particularly in Tunisia, than in Italy today. E1b1a2 E1b1a2 is defined by the SNP mutation M329. [13] [14] Yes, I'm aware of Ramesses III belonging to Haplogroup E1b1a, but additional genetic testing suggest that the remains may indeed belong to y-dna haplogroup E1b1b[citation needed] which split from E1b1a about 40-50 thousand years ago, and tends to be common in the Levant, Northern Africa, and the Rift valley region in modern times.
Genetic history of the Middle East - Wikipedia Here, to test the hypothesis that . Pereira L, Gusmao L, Alves C et al. Holden CJ : Bantu language trees reflect the spread of farming across sub-Saharan Africa: a maximum-parsimony analysis. Cavalli-Sforza LL, Menozzi P, Piazza A : The History and Geography of Human Genes.
Hamitic origin of Haplogroup E | Forum - ProBoards [30] Three South Africans tested positive for this marker. The absence of E-V13 from Central Anatolia does not concord with a diffusion linked to Neolithic agriculture. Because the Bantu languages on the eastern route are more homogeneous than those on the western route,11 it is reasonable to speculate that later expansions occurred mainly on the eastern route. E1b1a and E1b1b are PN2 clade lineages. Brief thoughts on the likelihood of finding samples of E1b1a in the Levant._________SOURCES:[0:46] The relevant FaceBook thread:https://www.facebook.com/groups/israelitejews/permalink/724232359236083/[1:04] Past threads in which this was discussed:- https://www.facebook.com/groups/g49resource/posts/5410422012382894/- https://www.facebook.com/groups/thebiblicalrumbleroom/posts/1308376896600227[1:10] Scaled Innovations SNP tracker:http://scaledinnovation.com/gg/snpTracker.html[3:46] https://haplotree.info/maps/ancient_dna/slideshow_samples.php?searchcolumn=Country\u0026searchfor=Israel\u0026ybp=500000,0\u0026orderby=Y_Haplotree_Variant\u0026ascdesc=ASC[3:52] https://haplotree.info/maps/ancient_dna/slideshow_samples.php?searchcolumn=Country\u0026searchfor=Lebanon\u0026ybp=500000,0\u0026orderby=Y_Haplotree_Variant\u0026ascdesc=ASC [12] One Carioca from Rio de Janeiro, Brazil tested positive for the M58 SNP. [13][14], At Kindoki, in the Democratic Republic of Congo, there were three individuals, dated to the protohistoric period (230 BP, 150 BP, 230 BP); one carried haplogroups E1b1a1a1d1a2 (E-CTS99, E-CTS99) and L1c3a1b, another carried haplogroup E (E-M96, E-PF1620), and the last carried haplogroups R1b1 (R-P25 1, R-M415) and L0a1b1a1. Pakendorf B, Bostoen K, de Filippo C : Molecular perspectives on the Bantu expansion: a synthesis. Considering the Y haplogroup composition in our Dominican sample, we can note that the clades frequently observed in the Sahel are usually rare or absent. Google Scholar. Article Anthropology, archaeology, linguistics and, in recent decades, genetics have been used to elucidate some of the events and processes involved. Table 1 reports the frequencies of all observed haplogroups, including the component haplogroups of E1b1a. L791 and Z21466 have a mostly European distribution today and their ages point toward a Neolithic diffusion. Its main subclade E-M34 most probably emerged in the Levant about 15,000 years ago. Thank you for visiting nature.com. [25], Amid the Green Sahara, the mutation for sickle cell originated in the Sahara[26] or in the northwest forest region of western Central Africa (e.g., Cameroon)[26][27] by at least 7,300 years ago,[26][27] though possibly as early as 22,000 years ago. Although it is generally accepted that the EBSP has its origin in the so-called Bantu Homeland situated in the area of the border between Nigeria and the Grassfields of Cameroon, and that it followed both western and eastern routes, much less is known about the number and dates of those expansions, if more than one. In Europe, M81 is most common in Portugal (8%), Spain (4%), as well as in France (0-6%) and Italy (0-4%), where strong regional variations are observed. (2007), such population movements changed the pre-existing population Y chromosomal diversity in Central, Southern, and Southeastern Africa, replacing the previous haplogroup frequencies in these areas with the now dominant E1b1a1 lineages. Rare deep-rooting Y chromosome lineages in humans: lessons for phylogeography. In whichever scenario, it is clear that M81 benefited from a potent founder effect in the Maghreb, a region that was first dominated by the Carthaginian elite, but quickly became one of the favourite regions of residence for the Roman elite within the empire (along with Spain, France and Greece). Salas A, Richards M, De la FT et al. The major finding of these studies was that genetic distances (FST) among all EBSP groups are much less than the average FST among West-African and Nilo-Saharan groups, indicating a considerable level of homogeneity among EBSP groups. [15] Gad et al. Later, a group of citizen scientists with an interest in population genetics and genetic genealogy formed a working group to create an amateur tree aiming at being above all timely.
No Levantine ancestry for Ashkenazic Jews - The DNA Project M81 is especially common in western Iberia, notably Extremadura (15.5%), Andalusia (13.5%), southern Portugal (11%), the Canary Islands (11%), north-west Castille (10%) and Galicia (10%). Wood ET, Stover DA, Ehret C et al. Nucleic Acids Res 2001; 29: E88. Haplogroup E1b1b (formerly known as E3b) represents the last major direct migration from Africa into Europe. A few isolated occurrences of E-M2 have also been observed among populations in Southern Europe, such as Croatia, Malta, Spain and Portugal.[49][50][51][52]. The story of M81 is very unusual in that it is so young and diversified into a multitude of subclades within just a few centuries. These are to date the oldest known E1b1b individuals. NAP was supported by NERC-Case PhD studentship. View Profile View Forum Posts . Examples of founder effects include E-V12 in southern Egypt, E-V13 in the Balkans, E-V32 in Somalia, E-V65 on the Mediterranean coast of Africa, and E-M81 in Northwest Africa. Use the Previous and Next buttons to navigate the slides or the slide controller buttons at the end to navigate through each slide. The Etruscans, who may have come from western Anatolia, could have brought E-M34 to central Italy, which would then have been assimilated by the Romans. E1b1a, on the other hand, is said to have never left Africa but was reported in 6% of Natufian samples. By the time this paper was written ancient DNA data from the Levant and the Near East had surfaced. See Supplementary Table S4 for Guthrie classifications of all Bantu-speaking groups included in the analysis. Int J Legal Med 1997; 110: 125129. He is best remembered for being a strong defender of slavery. de Filippo C, Barbieri C, Whitten M et al.
Y-DNA Haplogroup E: E1b1b and E1b1a - Your DNA Guide Little genetic differentiation as assessed by uniparental markers in the presence of substantial language variation in peoples of the Cross River region of Nigeria. Montano et al. [17][18], At a San Jose de los Naturales Royal Hospital burial site, in Mexico City, Mexico, three enslaved West Africans of West African and Southern African ancestry, dated between 1453 CE and 1626 CE, 1450 CE and 1620 CE, and 1436 CE and 1472 CE, were found; one carried haplogroups E1b1a1a1c1b/E-M263.2 and L1b2a, another carried haplogroups E1b1a1a1d1/E-P278.1/E-M425 and L3d1a1a, and the last carried haplogroups E1b1a1a1c1a1c/E-CTS8030 and L3e1a1a. These branches split from one another around 47,500 years ago in the horn of Africa, followed by the emergence of prominent SNP mutation E-M2 which gained footing there. A good example is represented by some lineages internal to the E1b1a-M2 haplogroup, such as E1b1a-M10 and E1b1a-V5280, which are observed mainly in the Sahelian groups (D'Atanasio et al. The advantage of this hypothesis is that M81 is indeed found exclusively within the borders of the Roman Empire, and in a big part of the empire.
E1b1a | Rem N Kemi [25] Nana was of West African ancestry and carried haplogroup L2b3a. Nowadays, the highest genetic diversity of haplogroup E1b1b is observed in Northeast Africa, especially in Ethiopia and Somalia, which also have the monopoly of older and rarer branches like M281, V6 or V92. Each of these two lineages has a peculiar geographic distribution. Am J Hum Genet 2002; 71: 10821111. [59] It has also been observed in a number of populations in Mexico, the Caribbean, Central America, and South America among people of African descent. TMRCA for E1b1a as a whole was estimated at 61756588 YBP with the TMRCA for the youngest haplogroup (E1b1a8a1a) estimated at 11001638 YBP. [15] It was impossible to determine his cause of death. (2011) only found one out of 505 tested African subjects who was U175 positive but negative for U209. M310.1 itself dates from the Late Paleolithic and could have come to Italy via Anatolia and Greece any time between the Late Glacial period and the Iron Age, including with Neolithic farmers, the Minoans, or the Etruscans. Outside Europe, E1b1b is found at high frequencies in Morocco (over 80%), Somalia (80%), Ethiopia (40% to 80%), Tunisia (70%), Algeria (60%), Egypt (40%), Jordan (25%), Palestine (20%), and Lebanon (17.5%). However, since G2a is the only lineage that was consistently found in all Neolithic sites tested to date in Europe, the absence of Neolithic G2a lineages from Scandinavia and the Baltic implies that no Neolithic lineage survives there, and consequently E-V13 does not date from the Neolithic in the region. Eur J Hum Genet 21, 423429 (2013). That would mean that the M81 lineage only started to expand in Roman times, and continued to diffuse within all the borders of the Roman Republic/Empire - not just North Africa, but also Iberia, France, Italy, Greece, Turkey and the Levant. Attempts were made to identify genetic relationships among EBSP groups in the context of Africa as a whole10, 11 (also see Supplementary Figure S112). Only then would a later demic expansion have brought haplotype 22 chromosomes from central western to western Africa, giving rise to the opposite clinal distributions of haplotypes 22 and 24."[31]. (2018) tested the DNA of seven 15,000-year-old modern humans from Taforalt Cave in northeastern Morocco, and all of the six males belonged to haplogroup E-M78. E-M2 is primarily distributed within sub-Saharan Africa. By the definition of haplogroup A as "non-BT", it is almost completely restricted to Africa, though a very small handful of bearers have been reported in Europe and Western Asia. The first would be the Bronze Age Italic tribes from Central Europe, who in all logic would have possessed at least some E-V13 lineages before they invaded the Italian peninsula. Correspondence to The Bantu expansion revisited: a new analysis of Y chromosome variation in Central Western Africa. Mol Biol Evol 2011; 28: 12551269. In this study, haplogroup E1b1a8a1a, the haplogroup with the shortest TMRCA, was observed in all eastern data sets (three from Malawi, one from Mozambique (in both cases, all speakers of Guthrie classification Bantu languages N and P spoken on the eastern side of Africa) and one from Pretoria, n (samples)=18) but in none of the eight western groups (all speakers of Guthrie classification Bantu languages H, B and C spoken on the western side of Africa) (Fishers exact test: haplogroup present/absent in data set P=0.0008; haplogroup frequency P<0.0001). We thank all DNA donors and those assisting in sample collection and Professor Mark Thomas and Dr Krishna Veeramah for their support with typing and helpful comments and suggestions on the manuscript.
Ramesses III is not E1b1a - Ancient Egypt Hum Genet 2005; 117: 366375. Klopfstein S, Currat M, Excoffier L : The fate of mutations surfing on the wave of a range expansion. Almost immediately afterwards, CTS5856 split into six subclades, then branched off into even more subclades in the space of a few generations. E1b1a1 is defined by markers DYS271/M2/SY81, M291, P1/PN1, P189, P293, V43, and V95. Haplogroup E1b1a is an ancient brother to E1b1b, but has left a completely different fingerprint on the world today. Bellwood P : Early agriculturalist population diasporas? [25] Kuto was of western Central African ancestry and carried haplogroups E1b1a-CTS2198 and L2a1a2. The range and mean of sample sizes of the 43 groups are 25118 and 63, respectively. E1b1a (M58) Expansion between the Great Lakes & Midwest Africa like the Levant or the southern Arabian Peninsula could have served as an incubator for the early diversification of non-African uniparental haplogroup varieties like Y chromosome DE-YAP*, CF-P143* and mtDNA M and N . [25] Coosaw was of West African and Native American ancestry and carried haplogroups E2b1a-CTS2400 and A2.
Searching for the roots of the first free African American - Nature The second would be the ancient Greeks, who heavily colonized southern Italy from the 9th century BCE until the Roman conquest in the 3rd century BCE. The control region of the mtDNA sequence, due to its high mutation rate, has been extensively used in examining the impact of EBSP on the genetic landscape of sub-Saharan Africa.5, 17, 18, 19 It has been postulated that some mtDNA haplogroups (eg, L3b, L3e and L2a), based on their distribution in sub-Saharan Africa, are associated with the EBSP, whereas the presence of haplogroup L1c at high frequency in some populations on the western route is thought to be the result of assimilation of local female hunter gatherers.17 It has been suggested that because agriculturist men are more likely to marry local women rather than vice versa,15, 16 the maternal genetic profile of Bantu-speaking groups is marked by considerable diversity. A1b1b-M32 has a wide distribution including Khoisan speaking and East African populations, and scattered members on the Arabian Peninsula. In 2002 he was named among the 100 Greatest Britons following a UK-wide vote. He belonged to the subclade E-M34. Nat Genet 2000; 26: 358361. Buccal swabs were collected from males >18 years old unrelated at the paternal grandfather level but otherwise randomly selected from 43 groups across sub-Saharan Africa (Supplementary Table S1, samples from Ghana, Nigeria and Cameroon were included in Veeramah et al (2010)35 and from South Africa in Thomas et al (2000)36). Due to the scarcity of full genomic sequences available from the Balkans, it is not yet clear when E-V13 expanded in that region. Multiple origins of Ashkenazi Levites:Y chromosome evidence for both Near Eastern and European ancestries. around the Czech Republic). volume21,pages 423429 (2013)Cite this article. Ancient East, West and North Germanics had different Y-DNA lineages, Johnson/Johnston/Johnstone DNA Surname Project, E1b1b (Y-DNA). (=> see also the discussions Was E-V13 a major lineage of Hallstatt Celts and Italics? In this study, we analyse, as did Alves et al,33 both UEP and short tandem repeat (STR) (in this study restricted to NRY) to show that geographic frequency distributions and the time to the most recent common ancestors (TMRCAs) of haplogroups, comprising haplogroup E1b1a in 43 sub-Saharan African groups (n=2757) with diverse linguistic affiliations (Supplementary Figure S1), reveal multiple waves of expansion from West Africa, with a late expansion along the eastern route but not the western. [29] West Africans, bearing the Benin sickle cell haplotype, may have migrated into the northern region of Iraq (69.5%), Jordan (80%), Lebanon (73%), Oman (52.1%), and Egypt (80.8%). (adsbygoogle = window.adsbygoogle || []).push({}); Neparczki et al. PubMedGoogle Scholar. If that is the case, E-M78 or E-M123 could have come to southern Europe through North African cattle herders during the Neolithic, although this hypothesis remains purely conjectural. The low percentage of E-V13 is coastal Sardinia would be better explained by more recent settlements on the island by the Romans, or even the Goths, who also settled in Sardinia. But the history of the region is so complex that there might be many separate branches of E-V13 that each came with a different invasion (e.g. It would be unthinkable that over 1,500 years of Hellenisation and Byzantine rule in Anatolia and the Levant didn't leave any genetic trace. [2] E-M329 is also frequent in Southwestern Ethiopia, especially among Omotic -speaking populations. Luis JR, Rowold DJ, Regueiro M et al. The Levant versus the Horn of Africa: evidence for bidirectional corridors of human migrations. CAS Berniell-Lee G, Calafell F, Bosch E et al. [33] In other words, as one moves to West Africa from western Central Africa, the less subclade E1b1a1f is found. E1b1a1a1b is defined by M116.2, a private marker. The samples were classified into groups primarily by cultural identity, first language spoken and then by place of collection. Tanya M Simms 2011, The Peopling of the Bahamas: A Phylogeographical Of these lineages, the most common subclade is L2a, which is found in Africa the Levant and in the Americas.. Haplogroup L2 has been observed among specimens at the island cemetery in Kulubnarti, Sudan, which date from the Early Christian period (AD 550-800).. Haplogroup L2a. E1b1a1a1a is defined by marker M58. Genetic and demographic implications of the Bantu expansion: insights from human paternal lineages. Iranic tribes, La Tne Celts, Romans, Goths, Slavs). Research Department of Genetics, The Centre for Genetic Anthropology, Evolution and Environment, University College London, London, UK, Naser Ansari Pour,Christopher A Plaster&Neil Bradman, You can also search for this author in All haplogroups within E1b1a were observed in the Bantu Homeland, West-Central Africa, East Africa and Ghana, whereas haplogroup E1b1a8a1a, although present in the Bantu Homeland and East Africa, was not observed in either Ghana or West-Central Africa. The K257 and Y4970 branch emerged around 3000 BCE and is found in Iran, Armenia, Turkey, Russia, Greece, Italy and France, among others. This era, which ended in a large-scale civilization collapse across this region ( Cline, 2014 ), shaped later periods both demographically and culturally. Proto-Italics would have been a predominantly R1b-U152 tribe, but also carried a minority of E-V13, G2a-L140 (L13, L1264 and Z1816 subclades) and J2a1-L70 (PF5456 and Z2177 subclades). Combined use of biallelic and microsatellite Y-chromosome polymorphisms to infer affinities among African populations.
How many people in the world are estimated to have E1b1a DNA, a genetic mtDNA variability in two Bantu-speaking populations (Shona and Hutu) from Eastern Africa: implications for peopling and migration patterns in sub-Saharan Africa. Wairak people in Tanzania tested 4.6% (2/43) positive for E-M10. 3500-1150 BCE) was a formative period in the Southern Levant, a region that includes present-day Israel, Jordan, Lebanon, the Palestinian Authority, and southwest Syria.