| Haplogroup J-M267 | |
|---|---|
.PNG.webp) Interpolated geographical frequency distribution.[1] | |
| Possible time of origin | 17,000[2]–24,000 years before present (Di Giacomo 2004) |
| Possible place of origin | Western Asia[3][4] |
| Ancestor | J-P209 |
| Descendants | J-M62, J-M365.1, J-L136, J-Z1828 |
| Defining mutations | M267, L255, L321, L765, L814, L827, L1030 |
Haplogroup J-M267, also commonly known as Haplogroup J1, is a subclade (branch) of Y-DNA haplogroup J-P209 (commonly known as haplogroup J) along with its sibling clade haplogroup J-M172 (commonly known as haplogroup J2). (All these haplogroups have had other historical names listed below.[Phylogenetics 1][Phylogenetics 2])
Men from this lineage share a common paternal ancestor, which is demonstrated and defined by the presence of the single nucleotide polymorphism (SNP) mutation referred to as M267, which was announced in (Cinnioğlu 2004). This haplogroup is found today in significant frequencies in many areas in or near the Arabian Peninsula and Western Asia. Out of its native Asian Continent, it is found at very high frequencies in Sudan. It is also found at very high but lesser extent in parts of the Caucasus, Ethiopia and parts of North Africa and amongst most Levant peoples, incl. Jewish groups, especially those with Cohen surnames. It can also be found much less commonly, but still occasionally in significant amounts, in parts of southern Europe and as far east as Central Asia.
Origins
Since the discovery of haplogroup J-P209 it has generally been recognized that it shows signs of having evolved ~ 20,000 years ago somewhere in northwestern Iran, the Caucasus, the Armenian Highlands, and northern Mesopotamia.[5][6][3] The frequency and diversity of both its major branches, J-M267 and J-M172, in that region makes them candidates as genetic markers of the spread of farming technology during the Neolithic, which is proposed to have had a major impact upon human populations.
J-M267 has several recognized subclades, some of which were recognized before J-M267 itself was recognized, for example J-M62 Y Chromosome Consortium "YCC" 2002. With one notable exception, J-P58, most of these are not common (Tofanelli 2009). Because of the dominance of J-P58 in J-M267 populations in many areas, discussion of J-M267's origins require a discussion of J-P58 at the same time.
Distribution
Africa
North Africa and Horn of Africa
North Africa received Semitic migrations, according to some studies it may have been diffused in recent time by Arabs who, mainly from the 7th century A.D., expanded to northern Africa (Arredi 2004 and Semino 2004). However the Canary Islands is not known to have had any Semitic language. In North Africa J-M267 is dominated by J-P58, and dispersed in a very uneven manner according to studies so far, often but not always being lower among Berber and/or non-urban populations. In Ethiopia there are signs of older movements of J-M267 into Africa across the Red Sea, not only in the J-P58 form. This also appears to be associated with Semitic languages. According to a study in 2011, in Tunisia, J-M267 is significantly more abundant in the urban (31.3%) than in the rural total population (2.5%) (Ennafaa 2011).
| Population | Sample size | J*(xJ-M172) | total J-M267 | J-M267(xP58) | J-P58 | publication | previous research on same samples |
| Algeria (Arabs from Oran) | 102 | NA | 22.5% | NA | NA | Robino 2007 | |
| Algeria | 20 | NA | 35% | NA | NA | Semino 2004 | |
| Egypt | 147 | NA | 21.1% | 1.4% | 19.7% | Chiaroni 2009 | Luis 2004 |
| Egypt | 124 | NA | 19.8% | NA | NA | El-Sibai 2009 | |
| Egypt (Siwa, Western Desert) | 35 | NA | 31.4% | NA | NA | Kujanová 2009 | |
| Libya (Tuareg) | 47 | NA | 0% | NA | NA | Ottoni 2011 | |
| Libya (Benghazi) | 238 | NA | 39.5% | NA | NA | Alvarez 2014[7] | Elmrghni 2012 |
| Morocco (Arabs) | 87 | NA | 26.4% | NA | NA | Fadhlaoui-Zid 2013[8] | |
| Morocco (Arabs) | 49 | NA | 20.4% | NA | NA | Semino 2004 | |
| Morocco (Arabs) | 28 | NA | 60.7% | NA | NA | Underhill 2000[9] | |
| Morocco (Arabs) | 19 | NA | 31.5% | NA | NA | Francalacci 2008[10] | |
| Morocco (Berbers) | 64 | NA | 6.3% | NA | NA | Semino 2004 | |
| Morocco (Berbers) | 103 | NA | 10.7% | NA | NA | Semino 2004 | |
| Morocco (Rabat) | 267 | NA | 21.3% | NA | NA | Alvarez 2014 | Aboukhalid 2010 |
| Morocco (Casablanca) | 166 | NA | 15.7% | NA | NA | Alvarez 2014 | Laouina 2011 |
| Morocco (Figuig) | 96 | NA | 29.2% | NA | NA | Alvarez 2014 | Palet 2010 |
| Morocco (El Jadida) | 49 | NA | 8.2% | NA | NA | Alvarez 2014 | |
| Morocco (Fes) | 108 | NA | 16.7% | 0.0% | 16.7% | Regueiro 2015 | |
| Tunisia | 73 | NA | 34.2% | NA | NA | Semino 2004 | |
| Tunisia | 601 | Na | 16.64% | NA | NA | Pestano J, et al. (2013)[11] | |
| Tunisia (Sousse) | 220 | NA | 25.9% | 0.0% | 25.9% | Fadhlaoui-Zid 2015[12] | |
| Tunisia (Tunis) | 148 | NA | 32.4% | 1.3% | 31.1% | Grugni 2012 | Arredi 2004 |
| Tunisia | 52 | NA | 34.6% | NA | NA | Onofri 2008 | |
| Tunisia (Bou Omran Berbers) | 40 | NA | 0% | NA | NA | Ennafaa 2011 | |
| Tunisia (Bou Saad Berbers) | 40 | NA | 5% | 0% | 5% | Ennafaa 2011 | |
| Tunisia (Jerbian Arabs) | 46 | NA | 8.7% | NA | NA | Ennafaa 2011 | |
| Tunisia (Jerbian Berbers) | 47 | NA | 0% | NA | NA | Ennafaa 2011 | |
| Tunisia (Sened Berbers) | 35 | NA | 31.4% | 0% | 31.4% | Fadhlaoui-Zid 2011 | |
| Tunisia (Andalusi Zaghouan) | 32 | NA | 43.8% | 0% | 43.8% | Fadhlaoui-Zid 2011 | |
| Tunisia (Cosmopolitan Tunis) | 33 | NA | 24.2 | 0% | 24.2% | Fadhlaoui-Zid 2011 | |
| Tunisia (Sejenane) | 47 | NA | 34.0% | NA | NA | Alvarez 2014 | Frigi 2011 |
| Tunisia (Sfax) | 56 | NA | 25% | 0.0% | 25% | Regueiro 2015 | |
| Tunisia (Beja) | 72 | NA | 15.3% | 0.0% | 15.3% | Regueiro 2015 | |
| Canary Islands (pre-Hispanic) | 30 | NA | 16.7% | NA | NA | Fregel 2009 | |
| Canary Islands (17th-18th c) | 42 | NA | 11.9% | NA | NA | Fregel 2009 | |
| Canary Islands | 652 | NA | 3.5% | NA | NA | Fregel 2009 | |
| Sahrawis | 89 | NA | 20.2% | NA | NA | Fregel 2009 | Bosch 2001 and Flores 2001 |
| Sudan (Khartoum) | 35 | NA | 74.3% | 0.0% | 74.3% | Chiaroni 2009 | Tofanelli 2009 and Hassan 2008 |
| Sudan (Sudanese Arabs) | 35 | NA | 17.1% | 0.0% | 17.1% | Chiaroni 2009 | Hassan 2008 |
| Sudan (Nilo-Saharans) | 61 | NA | 4.9% | 3.3% | 1.6% | Chiaroni 2009 | Hassan 2008 |
| Ethiopia (Oromo) | 78 | NA | 2.6% | 2.6% | 0.0% | Chiaroni 2009 | Semino 2004 |
| Ethiopia (Amhara) | 48 | NA | 29.2% | 8.3% | 20.8% | Chiaroni 2009 | Semino 2004 |
| Ethiopia (Arsi) | 85 | 22% | NA | NA | NA | Moran 2004 | |
| Ethiopia | 95 | 21% | NA | NA | NA | Moran 2004 | |
| Somalis | 201 | 0.5% | 2.5% | NA | 2.5% | Sanchez 2005 | J-P58 might be 5% in upcoming study |
| Comoros | 293 | NA | 5.0% | NA | NA | Msaidie 2011 | |
| South Africa (Lemba) | 76 | NA | 39.5% | 26.3% | 13.2% | Soodyall 2011 | |
| Zimbabwe (Lemba) | 54 | NA | 9.3% | 9.3% | NA | Soodyall 2011 | |
Asia
South Asia
J*(xJ-M172) was found in India among Indian Muslims.[13]
| Population | Sample size | J*(xJ-M172) | total J-M267 | J-M267(xP58) | J-P58 | Publication |
| India (Shia) | 161 | 10.6% | NA | NA | NA | Eaaswarkhanth 2009 |
| India (Sunni) | 129 | 2.3% | NA | NA | NA | Eaaswarkhanth 2009 |
| India (Mappla) | 40 | 10% | NA | NA | NA | Eaaswarkhanth 2009 |
West Asia
The area including eastern Turkey and the Zagros and Taurus mountains, has been identified as a likely area of ancient J-M267 diversity. Both J-P58 and other types of J-M267 are present, sometimes with similar frequencies.
| Population | Sample size | Total J-M267 | J-M267(xP58) | J-P58 | Publication | Previous research on same samples |
| Turkey | 523 | 9.0% | 3.1% | 5.9% | Chiaroni 2009 | Cinnioğlu 2004 |
| Iran | 150 | 11.3% | 2.7% | 8.7% | Chiaroni 2009 | Regueiro 2006 |
| Iran (Khuzestan) | NA | 33.4% | NA | NA | Kivisild 2012[14] | |
| Iraq (Kurds) | 93 | 11.8% | 4.3% | 7.5% | Chiaroni 2009 | |
| Iraq (Assyrians) | 28 | 28.6% | 17.9% | 10.7% | Chiaroni 2009 | |
| Iraq (Arabs) | 56 | 64.1% | 1.8% | 62.3% | Chiaroni 2009 | Tofanelli 2009 |
| Iran (Assyrians) | 31 | 16.1% | 9.7% | 6.5% | Chiaroni 2009 | |
| Iran | 92 | 3.2% | NA | NA | El-Sibai 2009 | |
| Turkey (Assyrians) | 25 | 20.0% | 16.0% | 4.0% | Chiaroni 2009 | |
Levant and Semitic populations
J-M267 is very common throughout this region, dominated by J-P58, but some specific sub-populations have notably low frequencies.
Arabian peninsula
J-P58 is the most common Y-Chromosome haplogroup among men from all of this region.
| Population | Sample size | Total J-M267 | J-M267(xP58) | J-P58 | Publication | Previous research on same samples |
| Saudi Arabia | 157 | 40.1% | NA | NA | Abu-Amero 2009 | |
| Qatar | 72 | 58.3% | 1.4% | 56.9% | Chiaroni 2009 | Cadenas 2008 |
| United Arab Emirates | 164 | 34.8% | 0.0% | 34.8% | Chiaroni 2009 | Cadenas 2008 |
| Yemen | 62 | 72.6% | 4.8% | 67.7% | Chiaroni 2009 | Cadenas 2008 |
| Kuwait | 117 | 45.2% | NA | NA | [15] | |
| Oman | 121 | 38.0% | 0.8% | 37.2% | Chiaroni 2009 | Luis 2004 |
Europe
J-M267 is uncommon in most of Northern and Central Europe. It is, however, found in significant pockets at levels of 5–10% among many populations in southern Europe. A recent study with the extant variation concludes that the Caucasus is likely to be the source of the Greek and Italian haplogroup J1-M267 chromosomes.[16]
| Population | Sample size | Total J-M267 | J-M267(xP58) | J-P58 | publication |
| Albania | 56 | 3.6% | NA | NA | Semino 2004 |
| North Macedonia (Albanian speakers) | 64 | 6.3% | NA | NA | Battaglia 2008 |
| Malta | 90 | 7.8% | NA | NA | El-Sibai 2009[17] |
| Greece (Crete) | 193 | 8.3% | NA | NA | King 2008 |
| Greece (mainland) | 171 | 4.7% | NA | NA | King 2008 |
| Greece (Macedonia) | 56 | 1.8% | NA | NA | Semino 2004 |
| Greece | 249 | 1.6% | NA | NA | Di Giacomo 2004 |
| Bulgaria | 808 | 3.4% | NA | NA | Karachanak 2013 |
| Romania | 130 | 1.5% | NA | NA | Di Giacomo 2004 |
| Russia | 223 | 0.4% | NA | NA | Di Giacomo 2004 |
| Croatia (Osijek Croats) | 29 | 0% | NA | NA | Battaglia 2008 |
| Slovenia | 75 | 1.3% | NA | NA | Battaglia 2008 |
| Italy (northeast Italians) | 67 | 0% | NA | NA | Battaglia 2008 |
| Italy (Italians) | 915 | 0.7% | NA | NA | Capelli 2009 |
| Italy (Sicily) | 236 | 3.8% | NA | NA | Di Gaetano 2008 |
| France (Provence) | 51 | 2% | NA | NA | King 2011 |
| Portugal (North) | 101 | 1% | NA | NA | Gonçalves 2005 |
| Portugal (Centre) | 102 | 4.9% | NA | NA | Gonçalves 2005 |
| Portugal (South) | 100 | 7% | NA | NA | Gonçalves 2005 |
| Portugal (Açores) | 121 | 2.5% | NA | NA | Gonçalves 2005 |
| Portugal (Madeira) | 129 | 0% | NA | NA | Gonçalves 2005 |
Caucasus
The Caucasus has areas of both high and low J-M267 frequency. The J-M267 in the Caucasus is also notable because most of it is not within the J-P58 subclade.
| Population | Sample size | Total J-M267 | J-M267(xP58) | J-P58 | Publication |
| Avars | 115 | 59% | 58% | 1% | Balanovsky 2011 |
| Dargins | 101 | 70% | 69% | 1% | Balanovsky 2011 |
| Kubachi | 65 | 99% | 99% | 0% | Balanovsky 2011 |
| Kaitak | 33 | 85% | 85% | 0% | Balanovsky 2011 |
| Lezghins | 81 | 44.4% | 44.4% | 0% | Balanovsky 2011 |
| Shapsug | 100 | 0% | 0% | 0% | Balanovsky 2011 |
| Abkhaz | 58 | 0% | 0% | 0% | Balanovsky 2011 |
| Circassians | 142 | 11.9% | 4.9% | 7% | Balanovsky 2011 |
| Ingush | 143 | 2.8% | 2.8% | 0% | Balanovsky 2011 |
| Ossetians | 357 | 1.3% | 1.3% | 0.0% | Balanovsky 2011 |
| Chechens (Ingushetia) | 112 | 21% | 21% | 0% | Balanovsky 2011 |
| Chechens (Chechnya) | 118 | 25% | 25% | 0% | Balanovsky 2011 |
| Chechens (Dagestan) | 100 | 16% | 16% | 0% | Balanovsky 2011 |
| Azerbaijan | 46 | 15.2% | NA | NA | Di Giacomo 2004 |
Subclade Distribution
J-P58
The P58 marker which defines subgroup J1c3 was announced in (Karafet 2008), but had been announced earlier under the name Page08 in (Repping 2006 and called that again in Chiaroni 2009). It is very prevalent in many areas where J-M267 is common, especially in parts of North Africa and throughout the Arabian peninsula. It also makes up approximately 70% of the J-M267 among the Amhara of Ethiopia. Notably, it is not common among the J-M267 of the Caucasus.
Chiaroni 2009 proposed that J-P58 (that they refer to as J1e) might have first dispersed during the Pre-Pottery Neolithic B period, "from a geographical zone, including northeast Syria, northern Iraq and eastern Turkey toward Mediterranean Anatolia, Ismaili from southern Syria, Jordan, Palestine and northern Egypt." They further propose that the Zarzian material culture may be ancestral. They also propose that this movement of people may also be linked to the dispersal of Semitic languages by hunter-herders, who moved into arid areas during periods known to have had low rainfall. Thus, while other haplogroups including J-M267 moved out of the area with agriculturalists who followed the rainfall, populations carrying J-M267 remained with their flocks (King 2002 and Chiaroni 2008).
According to this scenario, after the initial neolithic expansion involving Semitic languages, which possibly reached as far as Yemen, a more recent dispersal occurred during the Chalcolithic or Early Bronze Age (approximately 3000–5000 BCE), and this involved the branch of Semitic which leads to the Arabic language. The authors propose that this involved a spread of some J-P58 from the direction of Syria towards Arab populations of the Arabian Peninsula and Negev.
On the other hand, the authors agree that later waves of dispersion in and around this area have also had complex effects upon the distributions of some types of J-P58 in some regions. They list three regions which are particularly important to their proposal:
- The Levant (Syria, Jordan, Israel and Palestine). In this area, Chiaroni 2009 note a "patchy distribution of J1c3 or J-P58 frequency" which is difficult to interpret, and which "may reflect the complex demographic dynamics of religion and ethnicity in the region".
- The Eastern Anatolia, northern Iraq and western Iran. In this area, Chiaroni 2009 recognize signs that J-M267 might have an older presence, and on balance they accept the evidence but note that it could be in error.
- The southern area of Oman, Yemen and Ethiopia. In this area, Chiaroni 2009 recognize similar signs, but reject it as possibly a result of "either sampling variability and/or demographic complexity associated with multiple founders and multiple migrations."
The "YCAII=22-22 and DYS388≥15" cluster
Studies show that J-P58 group is not only in itself very dominant in many areas where J-M267 or J1 are common, but it also contains a large cluster which had been recognized before the discovery of P58. It is still a subject of research though.
This relatively young cluster, compared to J-M267 overall, was identified by STR markers haplotypes - specifically YCAII as 22-22, and DYS388 having unusual repeat values of 15 or higher, instead of more typical 13 (Chiaroni 2009) This cluster was found to be relevant in some well-publicized studies of Jewish and Palestinian populations (Nebel 2000 and Hammer 2009). More generally, since then this cluster has been found to be frequent among men in the Middle East and North Africa, but less frequent in areas of Ethiopia and Europe where J-M267 is nevertheless common. The genetical pattern is therefore similar to the pattern of J-P58 generally, described above, and may be caused by the same movements/migration of people (Chiaroni 2009).
Tofanelli 2009 refers to this overall cluster with YCAII=22-22 and high DYS388 values as an "Arabic" as opposed to a "Eurasian" type of J-M267. This Arabic type includes Arabic speakers from Maghreb, Sudan, Iraq and Qatar, and it is a relatively homogeneous group, implying that it might have dispersed relatively recently compared to J-M267 generally. The more diverse "Eurasian" group includes Europeans, Kurds, Iranians and Ethiopians (despite Ethiopia being outside of Eurasia), and is much more diverse. The authors also say that "Omanis show a mix of Eurasian pool-like and typical Arabic haplotypes as expected, considering the role of corridor played at different times by the Gulf of Oman in the dispersal of Asian and East African genes." Chiaroni 2009 also noted the anomalously high apparent age of Omani J-M267 when looking more generally at J-P58 and J-M267 more generally.
This cluster in turn contains three well-known related sub-clusters. First, it contains the majority of the Jewish "Cohen modal haplotype", found among Jewish populations, but especially in men with surnames related to Cohen. It also contains the "Galilee modal haplotype" (GMH) and "Palestinian & Israeli Arab modal haplotype", both of which are associated with Palestinian/Israeli Arabs by Nebel 2000 and Hammer 2009. Nebel 2002 then pointed out that the GMH is also the most frequent type of J-P209 haplotype found in north-west Africans and Yemenis, so it is not restricted to Israel and Palestine. However, this particular variant "is absent" from two particular "non-Arab Middle Eastern populations", namely "Jews and Muslim Kurds" (even though both of these populations do have high levels of J-P209). Nebel 2002 noted not only the presence of the GMH in the Maghreb but also that J-M267 in this region had very little diversity. They concluded that J-M267 in this region is a result of two distinct migration events: "early Neolithic dispersion" and "expansions from the Arabian peninsula" during the 7th century.Semino 2004 later agreed that this seemed consistent with the evidence and generalized from this that distribution of the entire YCAII=22-22 cluster of J-M267 in the Arabic-speaking areas of the Middle East and North Africa might in fact mainly have an origin in historical times.
More recent studies have emphasized doubt that the Islamic expansions are old enough to completely explain the major patterns of J-M267 frequencies. Chiaroni 2009 rejected this for J-P58 as a whole, but accepted that "some of the populations with low diversity, such as Bedouins from Israel, Qatar, Sudan and UAE, are tightly clustered near high-frequency haplotypes suggesting founder effects with star burst expansion in the Arabian Desert". They did not comment on the Maghreb.
Tofanelli 2009 take a stronger position of rejecting any strong correlation between the Arab expansion and either the YCAII=22-22 STR-defined sub-cluster as discussed by Semino 2004 or the smaller "Galilee modal haplotype" as discussed by (Nebel 2002). They also estimate that the Cohen modal haplotype must be older than 4500 years old, and maybe as much as 8600 years old - well before the supposed origin of the Cohanim. Only the "Palestinian & Israeli Arab" modal had a strong correlation to an ethnic group, but it was also rare. In conclusion, the authors were negative about the usefulness of STR defined modals for any "forensic or genealogical purposes" because "they were found across ethnic groups with different cultural or geographic affiliation".
Hammer 2009 disagreed, at least concerning the Cohen modal haplotype. They said that it was necessary to look at a more detailed STR haplotype in order to define a new "Extended Cohen Modal Haplotype" which is extremely rare outside Jewish populations, and even within Jewish populations is mainly only found in Cohanim. They also said that by using more markers and a more restrictive definition, the estimated age of the Cohanim lineage is lower than the estimates of Tofanelli 2009, and it is consistent with a common ancestor at the approximate time of founding of the priesthood which is the source of Cohen surnames.
Tofanelli et al. 2014 responded by saying: "In conclusion, while the observed distribution of sub-clades of haplotypes at mitochondrial and Y chromosome non-recombinant genomes might be compatible with founder events in recent times at the origin of Jewish groups as Cohenite, Levite, Ashkenazite, the overall substantial polyphyletism as well as their systematic occurrence in non-Jewish groups highlights the lack of support for using them either as markers of Jewish ancestry or Biblical tales."[18]
J-M368
The correspondence between P58 and high DYS388 values, and YCAII=22-22 is not perfect. For example the J-M267 subclade of J-P58 defined by SNP M368 has DYS388=13 and YCAII=19-22, like other types of J-M267 outside the "Arabic" type of J-M267, and it is therefore believed to be a relatively old offshoot of J-P58, that did not take part in the most recent waves of J-M267 expansion in the Middle East (Chiaroni 2009). These DYS388=13 haplotypes are most common in the Caucasus and Anatolia, but also found in Ethiopia (Tofanelli 2009).
Phylogenetics and distribution
There are several confirmed and proposed phylogenetic trees available for haplogroup J-M267. The following phylogeny or family tree of J-M267 haplogroup subclades is based on the ISOGG (2012) tree, which is in turn based upon the YCC 2008 tree and subsequent published research.
J1 (L255, L321, M267)
- J1* J1* clusters are found in Eastern Anatolia and parts of the Caucasus.
- J1a (M62) Found at very low frequency in Britain.
- J1b (M365.1) Found at low frequency in Eastern Anatolia, Iran and parts of Europe.
- J1c (L136)
- J1c* Found at low frequency in Europe.
- J1c1 (M390)
- J1c2 (P56) Found sporadically in Anatolia, East Africa, the Arabian Peninsula and Europe.
- J1c3
- J1c3* Found at low frequency in the Levant and the Arabian Peninsula.
- J1c3a (M367.1, M368.1) Previously known as J1e1.
- J1c3b (M369) Previously known as J1e2.
- J1c3c (L92, L93) Found at low frequency in South Arabia.
- J1c3d (L147.1) Accounts for the majority of J1, the predominant haplogroup in the Arabian peninsula.
- J1c3d* Accounts for the majority of J1 in Yemen, Cohen Jews (both Rabbinical and Karaitic),[19] but missing from Quraysh including Sharif of Makkah of Banu Hashem clan.
- J1c3d1 (L174.1)
- J1c3d2 (L222.2) Accounts for the majority of J1c3d in Saudi Arabia. An important element of J1c3d in North Africa.
- J1c3d2*
- J1c3d2a (L65.2/S159.2)
- J1c3d2*
Ancient DNA
Alalakh Amorite city-state
Five out 12 male individuals from Alalakh who lived between 1930-1325 BC, belonged to haplogroup J1-P58.[20][21]
Arslantepe archaeological complex
One out of 18 male individuals from Arslantepe who lived c. 3491-3122 BC, belonged to haplogroup J1-Z1824.[22][23]
Ancient city of Ebla
Three out of 6 individuals from Ebla who lived between 2565-1896 BC, belonged to J1-P58.[24][25] Ebla was an ancient East Semitic-speaking city and kingdom in Syria in the early Bronze age that was destroyed by the Akkadians.
Karelia
A member of haplogroup J1-M267 is found among eastern hunter-gatherers from Karelia, Northeast Europe living ~ 8.3 kya. This branch is absent in other ancient European hunter-gatherers. Unfortunately, it is not possible to put this sample in the context of the current haplogroup J1-M267 variation because of the poor quality of the DNA sequence.[3]
Sardinia
Olivieri et al. found a J1c3 haplotype in one of their ancient samples from Sardinia, dated to 6190–6000 calBP.[26]
Satsurblia
An ancient sample of J1 was found at Satsurblia Cave circa 11,000 BC, specifically belonging to the rare J1-FT34521 subclade.[27] The ancient individual from Satsurblia was male with black hair, brown eyes, and light skin.
Tell Kurdu
One out of 4 male individuals from Tell Kurdu who lived circa 5706-5622 BC, belonged to J1-L620.[28][29]
See also
Genetics
- Genetic history of the Middle East
- Genetic history of Europe
- Conversion table for Y chromosome haplogroups
- Genetic Genealogy
- Haplogroup
- Haplotype
- Human Y-chromosome DNA haplogroup
- Molecular phylogenetics
- Paragroup
- Subclade
- Y-chromosomal Aaron
- Y-chromosome haplogroups in populations of the world
- Y-DNA haplogroups in populations of Europe
- Y-DNA haplogroups in populations of East and Southeast Asia
- Y-DNA haplogroups in populations of the Near East
- Y-DNA haplogroups in populations of North Africa
- Y-DNA haplogroups in populations of the Caucasus
- Y-DNA haplogroups by ethnic group
Y-DNA J Subclades
Y-DNA Backbone Tree
References
- ↑ Singh S; Singh A; Rajkumar R; Sampath Kumar K; Kadarkarai Samy S; Nizamuddin S; et al. (2016). "Dissecting the influence of Neolithic demic diffusion on Indian Y-chromosome pool through J2-M172 haplogroup". Scientific Reports. 6: 19157. Bibcode:2016NatSR...619157S. doi:10.1038/srep19157. PMC 4709632. PMID 26754573.
- ↑ J1
- 1 2 3 Sahakyan, Hovhannes; Margaryan, Ashot; Saag, Lauri; Karmin, Monika; Flores, Rodrigo; Haber, Marc; Kushniarevich, Alena; Khachatryan, Zaruhi; Bahmanimehr, Ardeshir; Parik, Jüri; Karafet, Tatiana; Yunusbayev, Bayazit; Reisberg, Tuuli; Solnik, Anu; Metspalu, Ene (2021-03-23). "Origin and diffusion of human Y chromosome haplogroup J1-M267". Scientific Reports. 11 (1): 6659. Bibcode:2021NatSR..11.6659S. doi:10.1038/s41598-021-85883-2. ISSN 2045-2322. PMC 7987999. PMID 33758277.
- ↑ Rebai, Ahmed. "Synthetic review on the genetic relatedness between North Africa and Arabia deduced from paternal lineage distributions".
- ↑ Rebai, Ahmed. "Synthetic review on the genetic relatedness between North Africa and Arabia deduced from paternal lineage distributions".
- ↑ Chiaroni, Jacques; King, Roy J.; Myres, Natalie M.; Henn, Brenna M.; Ducourneau, Axel; Mitchell, Michael J.; Boetsch, Gilles; Sheikha, Issa; Lin, Alice A.; Nik-Ahd, Mahnoosh; Ahmad, Jabeen; Lattanzi, Francesca; Herrera, Rene J.; Ibrahim, Muntaser E.; Brody, Aaron; Semino, Ornella; Kivisild, Toomas; Underhill, Peter A. (2010). "The emergence of Y-chromosome haplogroup J1e among Arabic-speaking populations". European Journal of Human Genetics. 18 (3): 348–353. doi:10.1038/ejhg.2009.166. PMC 2987219. PMID 19826455.
- ↑ Alvarez, Luis; Ciria, Estela; Marques, Sofia L.; Santos, Cristina; Aluja, Maria Pilar (2014). "Y-chromosome analysis in a Northwest Iberian population: Unraveling the impact of Northern African lineages". American Journal of Human Biology. 26 (6): 740–746. doi:10.1002/ajhb.22602. PMID 25123837. S2CID 205303372.
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Footnotes
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- Shlush, Liran I.; Behar, Doron M.; Yudkovsky, Guennady; Templeton, Alan; Hadid, Yarin; Basis, Fuad; Hammer, Michael; Itzkovitz, Shalev; Skorecki, Karl (2008). "The Druze: a population genetic refugium of the Near East". PLOS ONE. 3 (5): e2105. Bibcode:2008PLoSO...3.2105S. doi:10.1371/journal.pone.0002105. PMC 2324201. PMID 18461126.
- Tofanelli, Sergio; Ferri, Gianmarco; Bulayeva, Kazima; Caciagli, Laura; Onofri, Valerio; Taglioli, Luca; Bulayev, Oleg; Boschi, Ilaria; et al. (2009). "J1-M267 Y lineage marks climate-driven pre-historical human displacements". European Journal of Human Genetics. 17 (11): 1520–1524. doi:10.1038/ejhg.2009.58. PMC 2986692. PMID 19367321.
- Y Chromosome Consortium "YCC" (2002). "A Nomenclature System for the Tree of Human Y-Chromosomal Binary Haplogroups". Genome Research. 12 (2): 339–48. doi:10.1101/gr.217602. PMC 155271. PMID 11827954.
- Zalloua, Pierre A.; Xue, Yali; Khalife, Jade; Makhoul, Nadine; Debiane, Labib; Platt, Daniel E.; Royyuru, Ajay K.; Herrera, Rene J.; et al. (2008). "Y-chromosomal diversity in Lebanon is structured by recent historical events". American Journal of Human Genetics. 82 (4): 873–882. doi:10.1016/j.ajhg.2008.01.020. PMC 2427286. PMID 18374297.
- Zalloua, Pierre A.; Platt, Daniel E.; El Sibai, Mirvat; Khalife, Jade; Makhoul, Nadine; Haber, Marc; Xue, Yali; Izaabel, Hassan; et al. (2008). "Identifying Genetic Traces of Historical Expansions: Phoenician Footprints in the Mediterranean". American Journal of Human Genetics. 83 (5): 633–642. doi:10.1016/j.ajhg.2008.10.012. PMC 2668035. PMID 18976729.
Websites
Haplogroups/Phylogeny
- ISOGG; Schrack, Janzen (2013). "Y-DNA Haplogroup J and its Subclades". International Society of Genetic Genealogists "ISOGG". Ongoing Corrections/Additions by citizen scientists.
Haplotype/SNP research Projects. See also Y-DNA haplogroup projects (ISOGG Wiki)
- Schrack; Janzen; Rottensteiner; Ricci; Mas (2013). "Y-DNA J Haplogroup Project". Family Tree DNA. This is an ongoing research project by citizen scientists. Over 2300 members.
- Givargidze; Hrechdakian (2013). "J1* Y-DNA Project". Family Tree DNA. This is an ongoing research project by citizen scientists. Over 150 members.
- Al Haddad (2013). "J1c3 (J-L147)". Family Tree DNA. This is an ongoing research project by citizen scientists. Over 550 members.
- Cone; Al Gazzah; Sanders (2013). "J-M172 Y-DNA Project (J2)". Family Tree DNA. This is an ongoing research project by citizen scientists. Over 1050 members.
- Aburto; Katz; Al Gazzah; Janzen (2013). "J-L24-Y-DNA Haplogroup Project (J2a1h)". Family Tree DNA. This is an ongoing research project by citizen scientists. Over 450 members.
Haplogroup-Specific Ethnic/Geographical Group Projects
- Eddali (2013). "Arab Tribes". Family Tree DNA. This is an ongoing research project by citizen scientists. Over 950 J members.
- Al Gazzah (2013). "J2-Middle East Project مشروع سلالة ج2 في العالم العربي والشرق الأوسط". Family Tree DNA. This is an ongoing research project by citizen scientists. Over 400 members.
Further reading
- Behar, Doron M.; Thomas, Mark G.; Skorecki, Karl; Hammer, Michael F.; Bulygina, Ekaterina; Rosengarten, Dror; Jones, Abigail L.; Held, Karen; et al. (2003). "Multiple Origins of Ashkenazi Levites: Y Chromosome Evidence for Both Near Eastern and European Ancestries". The American Journal of Human Genetics. 73 (4): 768–79. doi:10.1086/378506. PMC 1180600. PMID 13680527.
- Behar, Doron M.; Garrigan, Daniel; Kaplan, Matthew E.; Mobasher, Zahra; Rosengarten, Dror; Karafet, Tatiana M.; Quintana-Murci, Lluis; Ostrer, Harry; et al. (2004). "Contrasting patterns of Y chromosome variation in Ashkenazi Jewish and host non-Jewish European populations". Human Genetics. 114 (4): 354–65. doi:10.1007/s00439-003-1073-7. PMID 14740294. S2CID 10310338.
- Firasat, Sadaf; Khaliq, Shagufta; Mohyuddin, Aisha; Papaioannou, Myrto; Tyler-Smith, Chris; Underhill, Peter A; Ayub, Qasim (2006). "Y-chromosomal evidence for a limited Greek contribution to the Pathan population of Pakistan". European Journal of Human Genetics. 15 (1): 121–6. doi:10.1038/sj.ejhg.5201726. PMC 2588664. PMID 17047675.
- Flores, Carlos; Maca-Meyer, Nicole; González, Ana M; Oefner, Peter J; Shen, Peidong; Pérez, Jose A; Rojas, Antonio; Larruga, Jose M; Underhill, Peter A (2004). "Reduced genetic structure of the Iberian peninsula revealed by Y-chromosome analysis: Implications for population demography". European Journal of Human Genetics. 12 (10): 855–63. doi:10.1038/sj.ejhg.5201225. PMID 15280900.
- Semino, O.; Passarino, G; Oefner, PJ; Lin, AA; Arbuzova, S; Beckman, LE; De Benedictis, G; Francalacci, P; et al. (2000). "The Genetic Legacy of Paleolithic Homo sapiens sapiens in Extant Europeans: A Y Chromosome Perspective". Science. 290 (5494): 1155–9. Bibcode:2000Sci...290.1155S. doi:10.1126/science.290.5494.1155. PMID 11073453.
Phylogenetic Notes
- ↑ This table shows the historic names for J-M267 and its earlier discovered and named subclade J-M62 in published peer reviewed literature.
YCC 2002/2008 (Shorthand) J-M267 J-M62 Jobling and Tyler-Smith 2000 - 9 Underhill 2000 - VI Hammer 2001 - Med Karafet 2001 - 23 Semino 2000 - Eu10 Su 1999 - H4 Capelli 2001 - B YCC 2002 (Longhand) - J1 YCC 2005 (Longhand) J1 J1a YCC 2008 (Longhand) J1 J1a YCC 2010r (Longhand) J1 J1a - ↑ This table shows the historic names for J-P209 (AKA J-12f2.1 or J-M304) in published peer reviewed literature. Note that in Semino 2000 Eu09 is a subclade of Eu10 and in Karafet 2001 24 is a subclade of 23.
YCC 2002/2008 (Shorthand) J-P209
(AKA J-12f2.1 or J-M304)Jobling and Tyler-Smith 2000 9 Underhill 2000 VI Hammer 2001 Med Karafet 2001 23 Semino 2000 Eu10 Su 1999 H4 Capelli 2001 B YCC 2002 (Longhand) J* YCC 2005 (Longhand) J YCC 2008 (Longhand) J YCC 2010r (Longhand) J