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Haplogroup E-M35

E-M35, also known as E1b1b1-M35, is a human Y-chromosome DNA haplogroup. E-M35 has two basal branches, E-V68 and E-Z827. E-V68 and E-Z827 are primarily distributed in North Africa and the Horn of Africa, and occur at lower frequencies in the Middle East, Europe, and Southern Africa.

Origins
In June 2015, Trombetta et al. reported a previously unappreciated large difference in the age between haplogroup E-M215 (38.6 kya; 95% CI 31.4–45.9 kya) and its sub-haplogroup E-M35 (25.0 kya; 95% CI 20.0–30.0 kya) and estimated its origin to be in Horn of Africa, where the node separating the E-V38 and E-M215 branches occurs about 47,500 years ago (95% CI: 41.3–56.8 ka). E-M35 was dated by Batini in 2015 to between 15,400 and 20,500 years ago. All major sub-branches of E-M35 are thought to have originated in the same general area as the parent clade: in North Africa, the Horn of Africa, or nearby areas of the Near East. Some branches of E-M35 are assumed to have left Africa thousands of years ago, whereas others may have arrived from the Near East. For example, associates the spread of the haplogroup with the Neolithic Revolution, believing that the structure and regional pattern of E-M35 subclades potentially give "reagents with which to infer specific episodes of population histories associated with the Neolithic agricultural expansion". also estimate that E-M78 (called E1b1b1a1 in that paper) has been in Europe longer than 10,000 years. Accordingly, human remains excavated in a Spanish funeral cave dating from approximately 7,000 years ago were shown to be in this haplogroup. Two more E-M78 have been found in the Neolithic Sopot and Lengyel cultures too. Concerning E-M35 in Europe within this scheme, have remarked that E-M215 seems to represent a late-Pleistocene migration from North Africa to Europe over the Sinai Peninsula in Egypt. While this proposal remains uncontested, it has more recently been proposed by that there is also evidence for additional migration of E-M215 carrying men directly from North Africa to southwestern Europe, via a maritime route (see below.) ==Ancient DNA==
Ancient DNA
According to Lazaridis et al. (2016), Natufian skeletal remains from the ancient Levant predominantly carried the Y-DNA haplogroup E. Of the five Natufian specimens analysed for paternal lineages, one belonged to CT, one to E-M35, one to E-M215, one to E-Z830. Haplogroup E-M35 was also found the dominant marker among fossils from the ensuing Pre-Pottery Neolithic B culture, with the E-M78 and E-Z830 subclades observed in multiple PPNB specimens (~50%). Following Fregel et al. (2017), two Neolithic farmers from the North African site of Ifri n Ammar ou Moussa belonged to haplogroup E-L19. The majority of their genomes traced back to Natufian and PPN ancestry , indicating a recent intrusion into North Africa from the Levant. Their presence is likely linked to the spread of pastoral technologies from the Levant into North Africa. Loosdrecht et al. (2018) analysed genome-wide data from seven ancient Iberomaurusian individuals from the Grotte des Pigeons near Taforalt in eastern Morocco. The fossils were directly dated to between 15,100 and 13,900 calibrated years before present. The scientists found that five male specimens with sufficient nuclear DNA preservation all belonged to the E1b1b1a1 (M78) subclade, with one skeleton bearing the E1b1b1a1b1 parent lineage to E-V13. Martiniano et al. (2022) later reassigned all the Taforalt samples to haplogroup E-M78 and none to E-L618, the predecessor to E-V13. Haplogroup E-M35 has been identified among both Amorite and Akkadian remains, found in the sites of Megiddo, Ebla, and Alalakh. It is also attested among later Semitic populations, such as the Phoenicians who settled throughout the Mediterranean region, where it appears to have been the most prevalent lineage. Additionally, analyses of medieval Andalusian remains indicate that individuals examined for paternal DNA overwhelmingly belonged to the E-M81 subclade. In Egypt, haplogroup E-V1515 has been identified in the remains of an elite Egyptian individual from the site of Nuerat, dating to the Old Kingdom period, while haplogroup E-V22 has been detected in an ancient Egyptian mummy excavated at the Abusir el-Meleq archaeological site in Middle Egypt, dated to between the late New Kingdom and the Roman era. ==Distribution==
Distribution
E-M215 and E-M35 are quite common among Afroasiatic speakers. The linguistic group and carriers of E-M35 lineage have a high probability to have arisen and dispersed together from the Afroasiatic Urheimat. Amongst populations with an Afro-Asiatic speaking history, a significant proportion of Palestinians and Jewish male lineages are E-M35. Haplogroup E-M35, which accounts for approximately 18% to 20% of 18% of Palestinians and Ashkenazi and 8.6% to 30% The following table only includes sample populations with more than 1% E-M215 men with all known subclades as of June 2015. It contains the E-V1515 clade defined by Trombetta et al. 2015, and all the E1b1b subclades distributed below the Sahara (E-V42, E-M293, E-V92, E-V6), which were identified as E-M35 basal clades in a former phylogeny. At least some of these men, perhaps all, are known since early 2011 to be in a rare sibling clade to E-M35, known as E-V16 or E-M281. The discovery of M281 was announced by , who found it in two Ethiopian Oromo. found 5 more Ethiopian individuals and an equivalent SNP to M281, V16. It was in the 2011 paper that the family tree position (M215+/M35-) was discovered as described above. The E-M215 derivative, E-M35 is defined by the M35 SNP. 1 Turkmen individual from Jawzjan with a subclade defining mutation is referred to as E-M35*. As of June 2015, there is an increasingly complex tree structure which divides most men in E-M35 into two branches: E-V68 and E-Z827. The most frequently described subclades are E-M78, a part of E-V68, and E-M81, which is a branch of E-Z827. These two subclades represent the largest proportion of the modern E-M215 population. E-M78 is found over most of the range where E-M215 is found excluding Southern Africa. E-M81 is found mainly in North Africa. E-M123 is less common but widely scattered, with significant populations in specific parts of the Horn of Africa, the Levant, Arabia, Iberia, and Anatolia. A new clade (E-V1515) was defined by Trombetta et al. 2015, which originated about 12 kya (95% CI 8.6–16.4) in eastern Africa where it is currently mainly distributed. This clade includes the E-V42, E-M293, E-V92 and E-V6 subclades, which were identified as E-M35 basal clades in a previous phylogeny. TMRCA of the major nodes in E-M35 ==Subclades==
Subclades
E-V68 (E1b1b1a) E-V68, is dominated by its longer-known subclade E-M78. Three "E-V68*" individuals who are in E-V68 but not E-M78 have been reported in Sardinia, by , when announcing the discovery of V68. The authors noted that because E-V68* was not found in the Middle Eastern samples, this appears to be evidence of maritime migration from Africa to southwestern Europe. E-M78 is a commonly occurring subclade, widely distributed in North Africa, the Horn of Africa, West Asia, (the Middle East and Near East) "up to Southern Asia", The European distribution has a frequency peak centered in parts of the Balkans (up to almost 50% in some areas) and Sicily, and declining frequencies evident toward western, central, and northeastern Europe. Based on genetic STR variance data, suggests that E-M78 originated in the region of Egypt and Libya. about 18,600 years ago (17,300 – 20,000 years ago). describe Egypt as "a hub for the distribution of the various geographically localized M78-related subclades" and, based on archaeological data, they propose that the point of origin of E-M78 (as opposed to later dispersal from Egypt) may have been in a refugium which "existed on the border of present-day Sudan and Egypt, near Lake Nubia, until the onset of a humid phase around 8500 BC. The northward-moving rainfall belts during this period could have also spurred a rapid migration of Mesolithic foragers northwards in Africa, the Levant and ultimately onward to Asia Minor and Europe, where they each eventually differentiated into their regionally distinctive branches". Towards the south, also explain evidence that some subclades of E-M78, specifically E-V12 and E-V22, "might have been brought to Sudan from North Africa after the progressive desertification of the Sahara around 6,000–8,000 years ago". And similarly, propose that E-M78 in Ethiopia, Somalia and surrounding areas, back-migrated to this region from the direction of Egypt after acquiring the E-M78 mutation. Recently, E-M78 was dated by Trombetta et al. 2015. between 20,300 and 14,800 years ago. and a different young one in Armenia) makes a maritime movement from northern Africa to southern Europe the most plausible hypothesis so far to explain its distribution. Yfull lists 24 individuals, all of whom belong to a single branch that is 30% younger than their common ancestor with M81. E-M81 E-M81 is the most common subclade of haplogroup E-L19/V257. It is concentrated in the Maghreb, and is dominated by its E-M183 subclade. E-M183 is believed to have originated in the Northwest Africa and has an estimated age of 4700 ybp. This haplogroup reaches a mean frequency of 61% in the Maghreb and 51% in North Africa, decreasing in frequency from approximately 80% to 100% in Berber populations, including Saharawis, to approximately 29% to the east of this range in Egypt. Because of its young age and prevalence among these groups and also others such as Mozabite, Middle Atlas, Kabyle and other Berber groups, it is sometimes referred to as a genetic "Berber marker". report high levels amongst Tuareg in two Saharan populations – 77.8% near Gorom-Gorom, in Burkina Faso, and 81.8% from Gosi in Mali. There was a much lower frequency of 11.1% in the vicinity of Tanut in Niger. E-M81 is also quite common among Maghrebi Arabic-speaking groups. It is generally found at frequencies around 45% in coastal cities of Algeria and Tunisia (Jijel, Oran, Tizi Ouzou, Algiers, Tunis, Sousse). In this key area from Egypt to the Atlantic Ocean, report a M183-SM001 pattern of decreasing microsatellite haplotype variation (implying greater lineage age in the former areas) from the Reguibat tribe in Oran and they found M183* (not SM001) in Iberia, Libya and Morocco. however showed microsatellite variation decrease from East to West, accompanied by a substantial increasing frequency. At the eastern extreme of this core range, found M81 in 28.6% (10 out of 35 men) in el-Hayez in the Libyan Desert in Egypt. believe the pattern of distribution and variance to be consistent with the hypothesis of a "demic diffusion" from the East. There is no autochthonous presence of E-M81 in the Near East (there is one in Lebanon), indicating that M81 most likely emerged from its parent clade M35 either in North Africa, or possibly as far south as the Horn of Africa. In Europe, E-M81 is widespread but rare, in the Iberian Peninsula shows an average frequency of 4% (45/1140) in the Iberian Peninsula with frequencies reaching 3.5% in Galicia, 4% in Western Andalusia and Northwest Castile. However this study includes 153 individuals from Majorca, Minorca and Ibiza islands as well as 24 individuals from Gascony which are not in the Iberian Peninsula. Without these 177 individuals, average for Iberian Peninsula is 4.1% (40/963), it is found at comparable levels to E-M78, with an average frequency of around 5%. Its frequencies are higher in the western half of the peninsula with frequencies reaching 8% in Extremadura and southern Portugal, 4% to 5% in Galicia, 5% in western Andalusia and 4% in northwest Castile and 9% to 17% in Cantabria. to 41% (23/56). E-M81 is also found in France, 0,7% to 5,8% in Sardinia, approximately 2.12% overall in Sicily (but up to 7.14% in Piazza Armerina), and in very much lower frequency near Lucera (1.7%), in continental Italy, As a result of its old world distribution, this subclade is found throughout Brazil 5.4% in Brazil (Rio de Janeiro), and among Hispanic men from California and Hawaii 2.4%. In smaller numbers, E-M81 men can be found in areas in contact with North Africa, both around the Sahara, in places like Sudan, and around the Mediterranean in places like Lebanon, Turkey, and amongst Sephardi Jews. There are two recognized subclades of E-M81, although one is much more important than the other. The E-M81 subclade has been found in ancient Guanche (Bimbapes) fossils excavated in Punta Azul, El Hierro, Canary Islands, which are dated to the 10th century (~44%). E-M107 found one example of E-M107 in Mali. E-M183 E-M183 is extremely dominant (more than 99%) within E-M81. first described it as a subclade of E-M81. The known subclades of E-M183 include: • E-M165 found one example in Middle East. • E-L351 Found in two related participants in The E-M35 Phylogeny Project. E-Z830 (E1b1b1b2) This is a recently discovered subclade which has not yet been included in most haplogroup trees, E-Z830 includes the confirmed subclades of E-M123, E-V1515 (E-M293, E-V42, E-V6, E-V92), and E-Z830*, and is a sibling clade to E-L19. Currently, the E-M35 phylogeny project] recognizes four distinct clusters of Z830* carriers, two of which are exclusively Jewish in origin. The remaining two are significantly smaller, and include scattered individuals in Germany, Spain, Latin America, Egypt, and Ethiopia. E-PF2431 E-PF2431 is a minor subclade of E-L19 mostly found in Europe, with smaller but notable frequencies in the Middle East/North Africa and sub-Saharan Africa. This haplogroup has been identified among Phoenicians from Motya, ancient Romans from Pompeii, and Medieval Arabs. E-Z830 (E1b1b1b2) This is a recently discovered subclade which has not yet been included in most haplogroup trees, E-Z830 includes the confirmed subclades of E-M123, E-V1515 (E-M293, E-V42, E-V6, E-V92), and E-Z830*, and is a sibling clade to E-L19. Currently, the E-M35 phylogeny project] recognizes four distinct clusters of Z830* carriers, two of which are exclusively Jewish in origin. The remaining two are significantly smaller, and include scattered individuals in Germany, Spain, Latin America, Egypt, and Ethiopia. E-M123 E-M123 is mostly known for its major subclade E-M34, which dominates this clade. E-V1515 A new clade (E-V1515) was defined by Trombetta et al. 2015, which originated about 12 kya (95% CI 8.6–16.4) in eastern Africa where it is currently mainly distributed. This clade includes all the sub-Saharan haplogroups (E-V42, E-M293, E-V92, E-V6) reported as E-M35 basal clades in a previous phylogeny. E-V6 The E-V6 subclade of E-V1515 is defined by V6. identified a significant presence of these lineages in Ethiopia and also some in the neighboring Somalis. Among the Ethiopian and Somali samples, the highest were 14.7% among the Amhara and 16.7% among the Wolayta. To the south, identified one V6+ man in a sample of 35 Datooga of Tanzania. And further to the north, identified another 6 men in a sample of 93 from the Siwa Oasis, which is a Berber population E-V92 announced the discovery of E-V92 in two Amharas. Like E-V6 and E-V42 it possibly only exists in the area of Ethiopia. ==Phylogenetics==
Phylogenetics
Phylogenetic history Prior to 2002, there were in academic literature at least seven naming systems for the Y-Chromosome phylogenetic tree. This led to considerable confusion. In 2002, the major research groups came together and formed the Y-Chromosome Consortium (YCC). They published a joint paper that created a single new tree that all agreed to use. 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. The table below brings together all of these works at the point of the landmark 2002 YCC Tree. This allows a researcher reviewing older published literature to quickly move between nomenclatures. Research publications The following research teams per their publications were represented in the creation of the YCC Tree. Phylogenetic trees Cladogram with the main subclades: }} The following phylogenetic tree is based on the YCC 2008 tree and subsequent published research as summarized by ISOGG. It includes all known subclades as of June 2015 (Trombetta et al. 2015) • E-M215 (E1b1b) • E-M215*. Rare or non-existent. • E-M35 (E1b1b1) • E-V68 (E1b1b1a) • E-V2009. Found in individuals in Sardinia and Morocco. • E-M78 (E1b1b1a1). North Africa, Horn of Africa, West Asia, Sicily. (Formerly "E1b1b1a".) • E-M78*E-V1477. Found in Tunisian Jews. • E-V1083. • E-V1083*. Found only in Eritrea (1.1%) and Sardinia (0.3%). • E-V13E-V22E-V1129E-V12E-V12*E-V32E-V264E-V259. Found in North Cameroon. • E-V65 • E-CTS194 • E-Z827 (E1b1b1b) • E-V257/L19 (L19, V257) – E1b1b1b1 • E-PF2431E-M81 (M81) • E-PF2546 • E-PF2546* • E-CTS12227 • E-MZ11 • E-MZ12 • E-A929 • E-Z5009 • E-Z5009* • E-Z5010 • E-Z5013 • E-Z5013* • E-A1152 • E-A2227 • E-A428 • E-MZ16 • E-PF6794 • E-PF6794* • E-PF6789 • E-MZ21 • E-MZ23 • E-MZ80 • E-A930 • E-Z2198/E-MZ46 • E-A601 • E-L351 • E-Z830 (Z830) – E1b1b1b2 • E-M123 (M123) • E-M34 (M34) • E-M84 (M84) • E-M136 (M136) • E-M290 (M290) • E-V23 (V23) • E-L791 (L791,L792) • E-V1515. E-V1515 and its subclades are mainly restricted to eastern Africa. • E-V1515*E-V1486E-V1486*E-V2881E-V2881*E-V1792E-V92E-M293 (M293) • E-M293*E-P72 (P72) • E-V3065*E-V1700E-V42 (V42) • E-V1785E-V1785*E-V6 (V6) • E-V16/E-M281 (E1b1b2). Rare. Found in individuals in Ethiopia, Yemen and Saudi Arabia. ==See also==
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