Movatterモバイル変換


[0]ホーム

URL:


Jump to content
WikipediaThe Free Encyclopedia
Search

Haplogroup J-M267

From Wikipedia, the free encyclopedia
Human Y-chromosome DNA haplogroup
"Haplogroup J1" redirects here; not to be confused withHaplogroup J (mtDNA).

Haplogroup J-M267
Interpolated geographical frequency distribution.[1]
Possible time of origin17,000[2]–24,000 years before present (Di Giacomo 2004)
Possible place of originSomewhere betweennorthwestern Iran, theCaucasus and theArmenian Highland[3][4][5][6]
AncestorJ-P209
DescendantsJ-M62, J-M365.1, J-L136, J-Z1828
Defining mutationsM267, L255, L321, L765, L814, L827, L1030

Haplogroup J-M267, also commonly known asHaplogroup J1, is asubclade (branch) ofY-DNA haplogroup J-P209 (commonly known ashaplogroup J) along with its siblingcladehaplogroup J-M172 (commonly known ashaplogroup J2). (All these haplogroups have had other historical names listed below.[Phylogenetics 1][Phylogenetics 2])

The oldest J-M267 positive remains found so far are from aCaucasus Hunter-Gatherer fromSatsurblia cave,Georgia.[7]

Men from this lineage share a commonpaternal ancestor, which is demonstrated and defined by the presence of thesingle 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 theArabian Peninsula andWestern Asia. Out of its nativeAsian Continent, it is found at very high frequencies inSudan. It is also found at very high but lesser extent in parts of theCaucasus,Ethiopia and parts ofNorth Africa and amongst most Levant peoples, includingJewish groups, especially those withCohen surnames. It can also be found much less commonly, but still occasionally in significant amounts, in parts ofsouthern Europe and as far east asCentral Asia.[citation needed]

Origins

[edit]

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.[4][8][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 theNeolithic, 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-M62Y 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.

Haplogroup J-P58 is strongly associated with ancient populations from theCaucasus and ancientIran. Current DNA research indicates that this haplogroup was absent in allNatufian and Neolithic Levant male individuals examined thus far, but emerged during the Bronze Age inLebanon andJordan along with ancestry related to Chalcolithic Iranians. This ancestry penetrated the Levant between 3,300 and 5,900 YBP and Arabia between 2,000 and 3,500 YBP. These times overlap with the dates for the Bronze Age origin and spread ofSemitic languages in the Middle East estimated from lexical data.[6][5]

Distribution

[edit]

Africa

[edit]

North Africa and Horn of Africa

[edit]

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 andSemino 2004). However theCanary 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 amongBerber 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).

PopulationSample sizeJ*(xJ-M172)total J-M267J-M267(xP58)J-P58publicationprevious research on same samples
Algeria (Arabs fromOran)102NA22.5%NANARobino 2007
Algeria20NA35%NANASemino 2004
Egypt147NA21.1%1.4%19.7%Chiaroni 2009Luis 2004
Egypt124NA19.8%NANAEl-Sibai 2009
Egypt (Siwa,Western Desert)35NA31.4%NANAKujanová 2009
Libya (Tuareg)47NA0%NANAOttoni 2011
Libya (Benghazi)238NA39.5%NANAAlvarez 2014[9]Elmrghni 2012
Morocco (Arabs)87NA26.4%NANAFadhlaoui-Zid 2013[10]
Morocco (Arabs)49NA20.4%NANASemino 2004
Morocco (Arabs)28NA60.7%NANAUnderhill 2000[11]
Morocco (Arabs)19NA31.5%NANAFrancalacci 2008[12]
Morocco (Berbers)64NA6.3%NANASemino 2004
Morocco (Berbers)103NA10.7%NANASemino 2004
Morocco (Rabat)267NA21.3%NANAAlvarez 2014Aboukhalid 2010
Morocco (Casablanca)166NA15.7%NANAAlvarez 2014Laouina 2011
Morocco (Figuig)96NA29.2%NANAAlvarez 2014Palet 2010
Morocco (El Jadida)49NA8.2%NANAAlvarez 2014
Morocco (Fes)108NA16.7%0.0%16.7%Regueiro 2015
Tunisia73NA34.2%NANASemino 2004
Tunisia601Na16.64%NANAPestano J, et al. (2013)[13]
Tunisia (Sousse)220NA25.9%0.0%25.9%Fadhlaoui-Zid 2015[14]
Tunisia (Tunis)148NA32.4%1.3%31.1%Grugni 2012Arredi 2004
Tunisia52NA34.6%NANAOnofri 2008
Tunisia (Bou OmranBerbers)40NA0%NANAEnnafaa 2011
Tunisia (Bou SaadBerbers)40NA5%0%5%Ennafaa 2011
Tunisia (JerbianArabs)46NA8.7%NANAEnnafaa 2011
Tunisia (JerbianBerbers)47NA0%NANAEnnafaa 2011
Tunisia (SenedBerbers)35NA31.4%0%31.4%Fadhlaoui-Zid 2011
Tunisia (AndalusiZaghouan)32NA43.8%0%43.8%Fadhlaoui-Zid 2011
Tunisia (CosmopolitanTunis)33NA24.20%24.2%Fadhlaoui-Zid 2011
Tunisia (Sejenane)47NA34.0%NANAAlvarez 2014Frigi 2011
Tunisia (Sfax)56NA25%0.0%25%Regueiro 2015
Tunisia (Beja)72NA15.3%0.0%15.3%Regueiro 2015
Canary Islands (pre-Hispanic)30NA16.7%NANAFregel 2009
Canary Islands (17th-18th c)42NA11.9%NANAFregel 2009
Canary Islands652NA3.5%NANAFregel 2009
Sahrawis89NA20.2%NANAFregel 2009Bosch 2001 andFlores 2001
Sudan (Khartoum)35NA74.3%0.0%74.3%Chiaroni 2009Tofanelli 2009 andHassan 2008
Sudan (Sudanese Arabs)35NA17.1%0.0%17.1%Chiaroni 2009Hassan 2008
Sudan (Nilo-Saharans)61NA4.9%3.3%1.6%Chiaroni 2009Hassan 2008
Ethiopia (Oromo)78NA2.6%2.6%0.0%Chiaroni 2009Semino 2004
Ethiopia (Amhara)48NA29.2%8.3%20.8%Chiaroni 2009Semino 2004
Ethiopia (Arsi)8522%NANANAMoran 2004
Ethiopia9521%NANANAMoran 2004
Somalis[1]2010.5%2.5%NA2.5%Sanchez 2005J-P58 might be 5% in upcoming study
Comoros293NA5.0%NANAMsaidie 2011
South Africa (Lemba)76NA39.5%26.3%13.2%Soodyall 2011
Zimbabwe (Lemba)54NA9.3%9.3%NASoodyall 2011

Asia

[edit]

South Asia

[edit]

J*(xJ-M172) was found in India among Indian Muslims.[15]

PopulationSample sizeJ*(xJ-M172)total J-M267J-M267(xP58)J-P58Publication
India (Shia)16110.6%NANANAEaaswarkhanth 2009
India (Sunni)1292.3%NANANAEaaswarkhanth 2009
India (Mappla)4010%NANANAEaaswarkhanth 2009

West Asia

[edit]

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.

PopulationSample sizeTotal J-M267J-M267(xP58)J-P58PublicationPrevious research on same samples
Turkey5239.0%3.1%5.9%Chiaroni 2009Cinnioğlu 2004
Iran15011.3%2.7%8.7%Chiaroni 2009Regueiro 2006
Iran (Khuzestan)NA33.4%NANAKivisild 2012[16]
Iraq (Kurds)9311.8%4.3%7.5%Chiaroni 2009
Iraq (Assyrians)2828.6%17.9%10.7%Chiaroni 2009
Iraq (Arabs)5664.1%1.8%62.3%Chiaroni 2009Tofanelli 2009
Iran (Assyrians)3116.1%9.7%6.5%Chiaroni 2009
Iran923.2%NANAEl-Sibai 2009
Turkey (Assyrians)2520.0%16.0%4.0%Chiaroni 2009

Levant and Semitic populations

[edit]

J-M267 is very common throughout this region, dominated by J-P58, but some specific sub-populations have notably low frequencies.

PopulationSample sizeTotal J-M267J-M267(xP58)J-P58PublicationPrevious research on same samples
Syria55433.6%NANAEl-Sibai 2009Zalloua 2008a
Syria (Jabel Druze)3414.7%2.9%11.8%Chiaroni 2009
Syria (HamaSunnis)3647.2%2.8%44.4%Chiaroni 2009
Syria (Ma'loulaAramaeans)446.8%4.5%2.3%Chiaroni 2009
Syria (SednayaSyriac Catholic)1414.3%0.0%14.3%Chiaroni 2009
Syria (DamascusSyriac Catholic)429.5%0.0%9.5%Chiaroni 2009
Syria (Alawites)4526.7%0.0%26.7%Chiaroni 2009
Syria (North-eastAssyrians)303.3%0.0%3.3%Chiaroni 2009
Syria (DamascusIsmailis)5158.8%0.0%58.8%Chiaroni 2009
Lebanon95125%NANAZalloua 2008a
GalileeDruze17213.4%1.2%12.2%Chiaroni 2009Shlush 2008
Palestinians (Akka)10139.2%NANAZalloua 2008b
Palestinians4932.7%0.0%32.7%Chiaroni 2009
Jordan7648.7%0.0%48.7%Chiaroni 2009
Jordan27335.5%NANAEl-Sibai 2009
Jordan (Amman)10140.6%NANAFlores 2005
Jordan (Dead Sea)458.9%NANAFlores 2005
Jews (Trás-os-Montes,Portugal)5712.3%NANANogueiro 2009
Jews (Cohanim)21546.0%0.0%46.0%Hammer 2009
Jews (non-CohanimAshkenazi)1,36014.9%0.9%14.0%Hammer 2009
Bedouin (Negev)2867.9%3.6%64.3%Chiaroni 2009Cann 2002

Arabian peninsula

[edit]
This article needs to beupdated. Please help update this article to reflect recent events or newly available information.(January 2018)

J-P58 is the most common Y-Chromosome haplogroup among men from all of this region.

PopulationSample sizeTotal J-M267J-M267(xP58)J-P58PublicationPrevious research on same samples
Saudi Arabia15740.1%NANAAbu-Amero 2009
Qatar7258.3%1.4%56.9%Chiaroni 2009Cadenas 2008
United Arab Emirates16434.8%0.0%34.8%Chiaroni 2009Cadenas 2008
Yemen6272.6%4.8%67.7%Chiaroni 2009Cadenas 2008
Kuwait11745.2%NANA[17]
Oman12138.0%0.8%37.2%Chiaroni 2009Luis 2004

Europe

[edit]

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 2018 genetic study (Finocchio et al. 2018) with the extant variation strongly suggests the Caucasus and regions North of it as likely to be an origin of the Greek and Italian J-M267 haplogroup.[18]

PopulationSample sizeTotal J-M267J-M267(xP58)J-P58publication
Albania563.6%NANASemino 2004
North Macedonia (Albanian speakers)646.3%NANABattaglia 2008
Malta907.8%NANAEl-Sibai 2009[19]
Greece (Crete)1938.3%NANAKing 2008
Greece (mainland)1714.7%NANAKing 2008
Greece (Macedonia)561.8%NANASemino 2004
Greece2491.6%NANADi Giacomo 2004
Bulgaria8083.4%NANAKarachanak 2013
Romania1301.5%NANADi Giacomo 2004
Russia2230.4%NANADi Giacomo 2004
Croatia (OsijekCroats)290%NANABattaglia 2008
Slovenia751.3%NANABattaglia 2008
Italy (northeastItalians)670%NANABattaglia 2008
Italy (Italians)9150.7%NANACapelli 2009
Italy (Sicily)2363.8%NANADi Gaetano 2008
France (Provence)512%NANAKing 2011
Portugal (North)1011%NANAGonçalves 2005
Portugal (Centre)1024.9%NANAGonçalves 2005
Portugal (South)1007%NANAGonçalves 2005
Portugal (Açores)1212.5%NANAGonçalves 2005
Portugal (Madeira)1290%NANAGonçalves 2005

Caucasus

[edit]

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.

PopulationSample sizeTotal J-M267J-M267(xP58)J-P58Publication
Avars11559%58%1%Balanovsky 2011
Dargins10170%69%1%Balanovsky 2011
Kubachi6599%99%0%Balanovsky 2011
Kaitak3385%85%0%Balanovsky 2011
Lezghins8144.4%44.4%0%Balanovsky 2011
Shapsug1000%0%0%Balanovsky 2011
Abkhaz580%0%0%Balanovsky 2011
Circassians14211.9%4.9%7%Balanovsky 2011
Ingush1432.8%2.8%0%Balanovsky 2011
Ossetians3571.3%1.3%0.0%Balanovsky 2011
Chechens (Ingushetia)11221%21%0%Balanovsky 2011
Chechens (Chechnya)11825%25%0%Balanovsky 2011
Chechens (Dagestan)10016%16%0%Balanovsky 2011
Azerbaijan4615.2%NANADi Giacomo 2004

Subclade Distribution

[edit]

J-P58

[edit]

The P58 marker which defines subgroupJ1c3 was announced in (Karafet 2008), but had been announced earlier under the namePage08 in (Repping 2006 and called that again inChiaroni 2009). It is very prevalent in many areas where J-M267 is common, especially in parts ofNorth 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 thePre-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 theZarzianmaterial culture may be ancestral. They also propose that this movement of people may also be linked to the dispersal ofSemitic languages byhunter-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 andChiaroni 2008).

According to this scenario, after the initial neolithic expansion involvingSemitic languages, which possibly reached as far as Yemen, a more recent dispersal occurred during theChalcolithic or EarlyBronze Age (approximately 3000–5000 BCE), and this involved the branch of Semitic which leads to theArabic language. The authors propose that this involved a spread of some J-P58 from the direction of Syria towards Arab populations of theArabian Peninsula andNegev.

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:

  1. 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".
  2. The Armenian Highlands, 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.
  3. 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

[edit]

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 bySTR 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 andHammer 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 includesArabic speakers fromMaghreb,Sudan,Iraq andQatar, 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 includesEuropeans,Kurds,Iranians andEthiopians (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 theGulf of Oman in the dispersal ofAsian andEast Africangenes."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 "Galileemodal haplotype" (GMH) and "Palestinian & Israeli Arab modalhaplotype", both of which are associated withPalestinian/Israeli Arabs byNebel 2000 andHammer 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 theMaghreb 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 bySemino 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 theCohen 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 inCohanim. 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 ofTofanelli 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."[20]

J-M368

[edit]

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 andAnatolia, but also found in Ethiopia (Tofanelli 2009).

Phylogenetics and distribution

[edit]

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 the Armenian Highlands and parts of the Caucasus.
  • J1a (M62) Found at very low frequency in Europe.
  • J1b (M365.1) Found at low frequency in the Armenian Highlands, Iran, Qatar 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 (bothRabbinical andKaraitic).[21]
        • 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)

Ancient DNA

[edit]

Caucasian hunter-gatherer (12,000-11,000BC)

An ancient sample of J1 was found atSatsurblia Cave InGeorgia circa 11,000 BC, specifically belonging to the rare J1-FT34521 subclade. The ancient individual from Satsurblia was male with black hair, brown eyes, and light skin.[22]

Eastern European hunter-gatherer (8,000-5,000)

Haplogroup J1 was found amongEastern hunter-gatherers. J1 was found among several samples from Minino,Vologda Oblast, three samples from Yuzhnyy Oleni Ostrov,Republic of Karelia and two samples from Popovo,Arkhangelsk Oblast.[23][24][25][26]

Anatolian Neolithic Farmers(6,000-5,000BC)

Haplogroup J1 was found among samples from Anatolian farmers. Two samples fromÇatalhöyük belonged to haplogroup J1.[27]

Tell Kurdu (5,661-5,630BC)

One out of 4 male individuals from Tell Kurdu who lived circa 5661-5630 BC, belonged to J1-L620.[28]

Khvalynsk culture (5206-4935 BC)

An ancient sample of J1 was found among individuals fromKhvalynsk culture.[29]

Kura–Araxes culture(3,500-2200)

Haplogroup J1 was found among several samples from Kura-Araxes culture.[30][31][32][33]

Arslantepe archaeological complex (3491-3122 BC)

One out of 18 male individuals from Arslantepe who lived c. 3491-3122 BC, belonged to haplogroup J1-Z1824.[28]

Ancient city of Ebla (2565-1896 BC)

Three out of 6 individuals from Ebla who lived between 2565-1896 BC, belonged to J1-P58.[28]

Amorite city-state(1930-1325 BC)

Five out 12 male individuals from Alalakh who lived between 1930-1325 BC, belonged to haplogroup J1-P58.[28]

See also

[edit]

Genetics

[edit]

Y-DNA J Subclades

[edit]

Y-DNA Backbone Tree

[edit]
This article needs to beupdated. Please help update this article to reflect recent events or newly available information.(February 2021)
Footnotes
  1. ^Van Oven M, Van Geystelen A, Kayser M, Decorte R, Larmuseau HD (2014). "Seeing the wood for the trees: a minimal reference phylogeny for the human Y chromosome".Human Mutation.35 (2):187–91.doi:10.1002/humu.22468.PMID 24166809.S2CID 23291764.
  2. ^International Society of Genetic Genealogy (ISOGG; 2015),Y-DNA Haplogroup Tree 2015. (Access date: 1 February 2015.)
  3. ^Haplogroup A0-T is also known as A-L1085 (and previously as A0'1'2'3'4).
  4. ^Haplogroup A1 is also known as A1'2'3'4.
  5. ^ F-Y27277, sometimes known as F2'4, is both the parent clade of F2 and F4 and a child of F-M89.
  6. ^Haplogroup LT (L298/P326) is also known as Haplogroup K1.
  7. ^Between 2002 and 2008,Haplogroup T-M184 was known as "Haplogroup K2". That name has since been re-assigned toK-M526, the sibling of Haplogroup LT.
  8. ^ Haplogroup K2b (M1221/P331/PF5911) is also known as Haplogroup MPS.
  9. ^ Haplogroup K2b1 (P397/P399) is also known as Haplogroup MS, but has a broader and more complex internal structure.
  10. ^ Haplogroup P (P295) is also klnown as K2b2.
  11. ^K-M2313*, which as yet has no phylogenetic name, has been documented in two living individuals, who have ethnic ties to India and South East Asia. In addition, K-Y28299, which appears to be a primary branch of K-M2313, has been found in three living individuals from India. See: Poznikop. cit.;YFull YTree v5.08, 2017, "K-M2335", and;PhyloTree, 2017, "Details of the Y-SNP markers included in the minimal Y tree" (Access date of these pages: 9 December 2017)
  12. ^ Haplogroup M, as of 2017, is also known as K2b1b. (Previously the name Haplogroup M was assigned to K2b1d.)
  13. ^ Haplogroup S, as of 2017, is also known as K2b1a. (Previously the name Haplogroup S was assigned to K2b1a4.)

References

[edit]
  1. ^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.
  2. ^J1
  3. ^abSahakyan, 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 (23 March 2021)."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.
  4. ^abRebai, Ahmed."Synthetic review on the genetic relatedness between North Africa and Arabia deduced from paternal lineage distributions".
  5. ^abAlmarri, Mohamed A.; Haber, Marc; Lootah, Reem A.; Hallast, Pille; Al Turki, Saeed; Martin, Hilary C.; Xue, Yali; Tyler-Smith, Chris (2 September 2021)."The genomic history of the Middle East".Cell.184 (18): 4612–4625.e14.doi:10.1016/j.cell.2021.07.013.ISSN 1097-4172.PMC 8445022.PMID 34352227.
  6. ^abHaber, Marc; Doumet-Serhal, Claude; Scheib, Christiana; Xue, Yali; Danecek, Petr; Mezzavilla, Massimo; Youhanna, Sonia; Martiniano, Rui; Prado-Martinez, Javier; Szpak, Michał; Matisoo-Smith, Elizabeth; Schutkowski, Holger; Mikulski, Richard; Zalloua, Pierre; Kivisild, Toomas (3 August 2017)."Continuity and Admixture in the Last Five Millennia of Levantine History from Ancient Canaanite and Present-Day Lebanese Genome Sequences".The American Journal of Human Genetics.101 (2):274–282.doi:10.1016/j.ajhg.2017.06.013.ISSN 0002-9297.PMC 5544389.PMID 28757201.
  7. ^Jones, Eppie R; Gonzalez-Fortes, Gloria; Connell, Sarah; Siska, Veronika; Eriksson, Anders; Martiniano, Rui; McLaughlin, Russell L; Llorente, Marcos Gallego; Cassidy, Lara M; Gamba, Cristina; Meshveliani, Tengiz; Bar-Yosef, Ofer; Müller, Werner; Belfer-Cohen, Anna; Matskevich, Zinovi (16 November 2015)."Upper Palaeolithic genomes reveal deep roots of modern Eurasians".Nature Communications.6 8912.Bibcode:2015NatCo...6.8912J.doi:10.1038/ncomms9912.PMC 4660371.PMID 26567969.
  8. ^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.
  9. ^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.
  10. ^Fadhlaoui-Zid, Karima; Haber, Marc; Martínez-Cruz, Begoña; Zalloua, Pierre; Benammar Elgaaied, Amel; Comas, David (27 November 2013)."Genome-Wide and Paternal Diversity Reveal a Recent Origin of Human Populations in North Africa".PLOS ONE.8 (11) e80293.Bibcode:2013PLoSO...880293F.doi:10.1371/journal.pone.0080293.ISSN 1932-6203.PMC 3842387.PMID 24312208.
  11. ^Underhill, Peter A (December 2000)."Y chromosome sequence variation and the history of human populations".Nature Genetics.26 (3): 360.doi:10.1038/81685.PMID 11062480.S2CID 12893406.
  12. ^Francalacci, Paolo (2008)."History and geography of human Y-chromosome in Europe: a SNP perspective"(PDF).Journal of Anthropological Sciences.86:59–89.PMID 19934469. Archived fromthe original(PDF) on 28 March 2012. Retrieved9 October 2022.
  13. ^Bekada, Asmahan; Fregel, Rosa; Cabrera, Vicente M.; Larruga, José M.; Pestano, José; Benhamamouch, Soraya; González, Ana M. (19 February 2013)."Introducing the Algerian Mitochondrial DNA and Y-Chromosome Profiles into the North African Landscape".PLOS ONE.8 (2) e56775.Bibcode:2013PLoSO...856775B.doi:10.1371/journal.pone.0056775.ISSN 1932-6203.PMC 3576335.PMID 23431392.
  14. ^Fadhlaoui-Zid, Karima (2014)."Sousse: extreme genetic heterogeneity in North Africa".Journal of Human Genetics.60 (1):41–49.doi:10.1038/jhg.2014.99.PMID 25471516.S2CID 25186140.
  15. ^Eaaswarkhanth, M; Haque, I; Ravesh, Z; et al. (March 2010)."Traces of sub-Saharan and Middle Eastern lineages in Indian Muslim populations".European Journal of Human Genetics.18 (3):354–63.doi:10.1038/ejhg.2009.168.PMC 2859343.PMID 19809480.
  16. ^Grugni, Viola; Battaglia, Vincenza; Hooshiar Kashani, Baharak; Parolo, Silvia; Al-Zahery, Nadia; Achilli, Alessandro; Olivieri, Anna; Gandini, Francesca; Houshmand, Massoud; Sanati, Mohammad Hossein; Torroni, Antonio; Semino, Ornella (18 July 2012)."Ancient Migratory Events in the Middle East: New Clues from the Y-Chromosome Variation of Modern Iranians".PLOS ONE.7 (7) e41252.Bibcode:2012PLoSO...741252G.doi:10.1371/journal.pone.0041252.ISSN 1932-6203.PMC 3399854.PMID 22815981.
  17. ^Triki-Fendri, Soumaya; Sánchez-Diz, Paula; Rey-González, Danel; Alfadhli, Suad; Ayadi, Imen; Ben Marzoug, Riadh; Carracedo, Ángel; Rebai, Ahmed (4 March 2016). "Genetic structure of the Kuwaiti population revealed by paternal lineages: Genetic Structure of Kuwait".American Journal of Human Biology.28 (2):203–212.doi:10.1002/ajhb.22773.PMID 26293354.
  18. ^Finocchio, Andrea; Trombetta, Beniamino; Messina, Francesco; D'Atanasio, Eugenia; Akar, Nejat; Loutradis, Aphrodite; Michalodimitrakis, Emmanuel I.; Cruciani, Fulvio; Novelletto, Andrea (10 May 2018)."A finely resolved phylogeny of Y chromosome Hg J illuminates the processes of Phoenician and Greek colonizations in the Mediterranean".Scientific Reports.8 (1): 7465.Bibcode:2018NatSR...8.7465F.doi:10.1038/s41598-018-25912-9.ISSN 2045-2322.PMC 5945646.PMID 29748665.
  19. ^El-Sibai et al.,2009,Percentage of haplogroups
  20. ^Tofanelli, Sergio (10 November 2014)."Mitochondrial and Y chromosome haplotype motifs as diagnostic markers of Jewish ancestry: a reconsideration".Frontiers in Genetics.5: 384.doi:10.3389/fgene.2014.00384.PMC 4229899.PMID 25431579.
  21. ^Brook, Kevin A. (Summer 2014)."The Genetics of Crimean Karaites"(PDF).Karadeniz Araştırmaları (Journal of Black Sea Studies).11 (42): 69–84 on page 83.doi:10.12787/KARAM859.
  22. ^Jones, Eppie R.; Gonzalez-Fortes, Gloria; Connell, Sarah; Siska, Veronika; Eriksson, Anders; Martiniano, Rui; McLaughlin, Russell L.; Gallego Llorente, Marcos; Cassidy, Lara M.; Gamba, Cristina; Meshveliani, Tengiz; Bar-Yosef, Ofer; Müller, Werner; Belfer-Cohen, Anna; Matskevich, Zinovi (16 November 2015)."Upper Palaeolithic genomes reveal deep roots of modern Eurasians".Nature Communications.6 8912.Bibcode:2015NatCo...6.8912J.doi:10.1038/ncomms9912.ISSN 2041-1723.PMC 4660371.PMID 26567969.
  23. ^Posth, Cosimo; Yu, He; Ghalichi, Ayshin; Rougier, Hélène; Crevecoeur, Isabelle; Huang, Yilei; Ringbauer, Harald; Rohrlach, Adam B.; Nägele, Kathrin; Villalba-Mouco, Vanessa; Radzeviciute, Rita; Ferraz, Tiago; Stoessel, Alexander; Tukhbatova, Rezeda; Drucker, Dorothée G. (March 2023)."Palaeogenomics of Upper Palaeolithic to Neolithic European hunter-gatherers".Nature.615 (7950):117–126.Bibcode:2023Natur.615..117P.doi:10.1038/s41586-023-05726-0.ISSN 1476-4687.PMC 9977688.PMID 36859578.
  24. ^Mathieson, Iain; Lazaridis, Iosif; Rohland, Nadin; Mallick, Swapan; Patterson, Nick; Roodenberg, Songül Alpaslan; Harney, Eadaoin; Stewardson, Kristin; Fernandes, Daniel; Novak, Mario; Sirak, Kendra; Gamba, Cristina; Jones, Eppie R.; Llamas, Bastien; Dryomov, Stanislav (December 2015)."Genome-wide patterns of selection in 230 ancient Eurasians".Nature.528 (7583):499–503.Bibcode:2015Natur.528..499M.doi:10.1038/nature16152.hdl:1871.1/9f8d37bf-03b3-4304-9a8d-a3d4fb4bdbd4.ISSN 1476-4687.PMC 4918750.PMID 26595274.
  25. ^Hofmanová, Zuzana; Reyna-Blanco, Carlos S.; Becdelièvre, Camille de; Schulz, Ilektra; Blöcher, Jens; Jovanović, Jelena; Winkelbach, Laura; Figarska, Sylwia M.; Schulz, Anna (28 June 2022). "Between fishing and farming: palaeogenomic analyses reveal cross-cultural interactions triggered by the arrival of the Neolithic in the Danube Gorges".bioRxiv 10.1101/2022.06.24.497512.
  26. ^Mittnik, Alissa; Wang, Chuan-Chao; Pfrengle, Saskia; Daubaras, Mantas; Zariņa, Gunita; Hallgren, Fredrik; Allmäe, Raili; Khartanovich, Valery; Moiseyev, Vyacheslav; Tõrv, Mari; Furtwängler, Anja; Andrades Valtueña, Aida; Feldman, Michal; Economou, Christos; Oinonen, Markku (30 January 2018)."The genetic prehistory of the Baltic Sea region".Nature Communications.9 (1): 442.Bibcode:2018NatCo...9..442M.doi:10.1038/s41467-018-02825-9.ISSN 2041-1723.PMC 5789860.PMID 29382937.
  27. ^Yüncü, Eren; Doğu, Ayça Küçükakdağ; Kaptan, Damla; Kılıç, Muhammed Sıddık; Mazzucato, Camilla; Güler, Merve N.; Eker, Elifnaz; Katırcıoğlu, Büşra; Chyleński, Maciej; Vural, Kıvılcım Başak; Sağlıcan, Ekin; Atağ, Gözde; Bozkurt, Defne; Pearson, Jessica; Sevkar, Arda (26 June 2025)."Female lineages and changing kinship patterns in Neolithic Çatalhöyük".Science.388 (6754) eadr2915.doi:10.1126/science.adr2915.hdl:11511/115277.PMID 40570118.
  28. ^abcdSkourtanioti, Eirini; Erdal, Yilmaz S.; Frangipane, Marcella; Restelli, Francesca Balossi; Yener, K. Aslıhan; Pinnock, Frances; Matthiae, Paolo; Özbal, Rana; Schoop, Ulf-Dietrich; Guliyev, Farhad; Akhundov, Tufan; Lyonnet, Bertille; Hammer, Emily L.; Nugent, Selin E.; Burri, Marta (28 May 2020)."Genomic History of Neolithic to Bronze Age Anatolia, Northern Levant, and Southern Caucasus".Cell.181 (5): 1158–1175.e28.doi:10.1016/j.cell.2020.04.044.hdl:11586/476148.ISSN 0092-8674.PMID 32470401.
  29. ^Lazaridis, Iosif; et al. (2025)."The genetic origin of the Indo-Europeans".Nature.639 (8053):132–142.Bibcode:2025Natur.639..132L.bioRxiv 10.1101/2024.04.17.589597.doi:10.1038/s41586-024-08531-5.PMC 11922553.PMID 39910300.
  30. ^Ghalichi, Ayshin; Reinhold, Sabine; Rohrlach, Adam B.; Kalmykov, Alexey A.; Childebayeva, Ainash; Yu, He; Aron, Franziska; Semerau, Lena; Bastert-Lamprichs, Katrin; Belinskiy, Andrey B.; Berezina, Natalia Y.; Berezin, Yakov B.; Broomandkhoshbacht, Nasreen; Buzhilova, Alexandra P.; Erlikh, Vladimir R. (November 2024)."The rise and transformation of Bronze Age pastoralists in the Caucasus".Nature.635 (8040):917–925.Bibcode:2024Natur.635..917G.doi:10.1038/s41586-024-08113-5.ISSN 1476-4687.PMC 11602729.PMID 39478221.
  31. ^Wang, Chuan-Chao; Reinhold, Sabine; Kalmykov, Alexey; Wissgott, Antje; Brandt, Guido; Jeong, Choongwon; Cheronet, Olivia; Ferry, Matthew; Harney, Eadaoin; Keating, Denise; Mallick, Swapan; Rohland, Nadin; Stewardson, Kristin; Kantorovich, Anatoly R.; Maslov, Vladimir E. (4 February 2019)."Ancient human genome-wide data from a 3000-year interval in the Caucasus corresponds with eco-geographic regions".Nature Communications.10 (1): 590.Bibcode:2019NatCo..10..590W.doi:10.1038/s41467-018-08220-8.ISSN 2041-1723.PMC 6360191.PMID 30713341.
  32. ^Lazaridis, Iosif; Alpaslan-Roodenberg, Songül; Acar, Ayşe; Açıkkol, Ayşen; Agelarakis, Anagnostis; Aghikyan, Levon; Akyüz, Uğur; Andreeva, Desislava; Andrijašević, Gojko; Antonović, Dragana; Armit, Ian; Atmaca, Alper; Avetisyan, Pavel; Aytek, Ahmet İhsan; Bacvarov, Krum (26 August 2022)."The genetic history of the Southern Arc: A bridge between West Asia and Europe".Science.377 (6609) eabm4247.doi:10.1126/science.abm4247.ISSN 1095-9203.PMC 10064553.PMID 36007055.
  33. ^Skourtanioti, Eirini; Jia, Xiaowen; Tavartkiladze, Nino; Bitadze, Liana; Shengelia, Ramaz; Tushabramishvili, Nikoloz; Neumann, Gunnar U.; Bianco, Raffaela Angelina; Mötsch, Angela (13 June 2024). "The Genetic History of the South Caucasus from the Bronze to the Early Middle Ages: 5000 years of genetic continuity despite high mobility".bioRxiv 10.1101/2024.06.11.597880.

Footnotes

[edit]

Works cited

[edit]

Journals

[edit]
  • Onofri, Valerio; Alessandrini, Federica; Turchi, Chiara; Pesaresi, Mauro; Tagliabracci, Adriano (2008). "Y-chromosome markers distribution in Northern Africa: High-resolution SNP and STR analysis in Tunisia and Morocco populations".Forensic Science International: Genetics Supplement Series.1:235–236.doi:10.1016/j.fsigss.2007.10.173.
  • Regueiro, M.; Cadenas, A.M.; Gayden, T.; Underhill, P.A.; Herrera, R.J. (2006). "Iran: tricontinental nexus for Y-chromosome driven migration".Human Heredity.61 (3):132–143.doi:10.1159/000093774.PMID 16770078.S2CID 7017701.
  • Repping, S; van Daalen, SK; Brown, LG; Korver, Cindy M; Lange, Julian; Marszalek, Janet D; Pyntikova, Tatyana; van der Veen, Fulco; et al. (2006). "High mutation rates have driven extensive structural polymorphism among human Y chromosomes".Nat Genet.38 (4):463–467.CiteSeerX 10.1.1.537.1822.doi:10.1038/ng1754.PMID 16501575.S2CID 17083896.
  • Robino, C.; Crobu, F.; Di Gaetano, C.; Bekada, A.; Benhamamouch, S.; Cerutti, N.; Piazza, A.; Inturri, S.; Torre, C. (2008). "Analysis of Y-chromosomal SNP haplogroups and STR haplotypes in an Algerian population sample".International Journal of Legal Medicine.122 (3):251–255.doi:10.1007/s00414-007-0203-5.PMID 17909833.S2CID 11556974.
  • Shen, Peidong; Lavi, Tal; Kivisild, Toomas; Chou, Vivian; Sengun, Deniz; Gefel, Dov; Shpirer, Issac; Woolf, Eilon; et al. (2004). "Reconstruction of patrilineages and matrilineages of Samaritans and other Israeli populations from Y-chromosome and mitochondrial DNA sequence variation".Human Mutation.24 (3):248–260.doi:10.1002/humu.20077.PMID 15300852.S2CID 1571356.

Websites

[edit]

Haplogroups/Phylogeny

Haplotype/SNP research Projects. See alsoY-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

Further reading

[edit]

Phylogenetic Notes

[edit]
  1. ^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-M267J-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)J1J1a
    YCC 2008 (Longhand)J1J1a
    YCC 2010r (Longhand)J1J1a
  2. ^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 200124 is a subclade of23.
    YCC 2002/2008 (Shorthand)J-P209
    (AKA J-12f2.1 or J-M304)
    Jobling and Tyler-Smith 20009
    Underhill 2000VI
    Hammer 2001Med
    Karafet 200123
    Semino 2000Eu10
    Su 1999H4
    Capelli 2001B
    YCC 2002 (Longhand)J*
    YCC 2005 (Longhand)J
    YCC 2008 (Longhand)J
    YCC 2010r (Longhand)J

External links

[edit]
Retrieved from "https://en.wikipedia.org/w/index.php?title=Haplogroup_J-M267&oldid=1337373986"
Categories:
Hidden categories:

[8]ページ先頭

©2009-2026 Movatter.jp