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Haplogroup T-L206

From Wikipedia, the free encyclopedia
Human Y-chromosome DNA haplogroup
This article is about the Y-chromosome haplogroup T1. For the unrelated mtDNA haplogroup, seeHaplogroup T (mtDNA).
Haplogroup T-L206
Possible time of origin26,800 BP[1]
Possible place of originWestern Asia[2][3][4]
AncestorT (T-M184)
DescendantsT1a (T-M70)

Haplogroup T-L206, also known ashaplogroup T1, is ahuman Y-chromosome DNA haplogroup. TheSNP that defines the T1 clade is L206. The haplogroup is one of two primary branches ofT (T-M184), the other subclade being T2 (T-PH110).

T1 is the most common descendant of the T-M184 haplogroup, being the lineage of more than 95% of all T-M184 members inAfrica andEurasia (as well as countries to which those populations have migrated in the modern era, in the Americas and Australasia). T1 lineages are now found at high frequencies among northernSomali clans. It is hypothesized that T1* (if not some of its subclades) originated inWestern Asia, and spread intoEurope andNorth Africa with thePre-Pottery Neolithic B culture (PPNB).

Thebasal clade T1* is rare, but has been found in at least three males from widely separated regions: aBerber fromTunisia, aSyrian, and aMacedonian.[5][6][7]

T-L206's sole primary branch, T1a (M70), is believed to have originated about 15,900 – 23,900 BP,[8] in the Levant. It appears that a number of individuals bearing T-M70 later migrated south to Africa.[9]

Structure

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Phylogenetic T-M184 tree
  • T1 (L206, L490) Found in Syria.
    • T1a (M70/Page46/PF5662, PAGES78) Found in Early Neolithic skeleton found in Karsdorf, Germany, 7200 years old. Also in Iran, Iraq, Saudi Arabia, Ossetia, England, Italy and Portugal.
      • T1a1 (L162/Page21, L299, L453/PF5617, L454) Found on Eivissa, northern Anatolia and Germany.
        • T1a1a (L208/Page2, L905) Mostly found in Upper Egypt, Horn of Africa, western Europe, eastern Anatolia, Iran and the Arabian Peninsula. Some spots in western Morocco, Sahrawis and Canarias.
          • T1a1a1 (P77,CTS8512) Mostly found in Middle East, Western Europe and Ashkenazi Jews.
          • T1a1a2 (P321) Found in Syria and Ashkenazi Jews.
            • T1a1a2a (P317) Found in Syria, Italian Jews and Ashkenazi Jews.
      • T1a2 (L131) Mostly found in northern Europe, eastern Europe, southeastern Europe and Anatolia. Also found in Xinjiang, Lemba, Tunisia, south and east Iberian Peninsula.
        • T1a2a (P322, P328) Found in Scandinavia, Denmark, Germany and Netherlands. Some spots in Yemenite Jews and Palestine(P327).
        • T1a2b (L446) Found in Northwest Europe and eastern Alps.
      • T1a3 (L1255) Found in Kuwait.

Subclade distribution

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T1* (T-L206*)

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This lineage could have arrived in theLevant through thePPNB expansion from northeasternAnatolia.

PopulationLanguageLocationMembers/Sample sizePercentageSourceNotes
BerbersSiwi (Berber)Sejenane1/472.1%[5]
SyriansUnspecifiedSyria1/951.1%[6]
MacedoniansMacedonian
(Balto-Slavic)
Macedonia1/2010.5%[7]Orthodox Christians of Macedonian ethnicity
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This sectionneeds expansion. You can help byadding to it.(September 2016)

T1a (M70)

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Initial research on T1a-M70 (previously K2)

M70 is believed to have originated in Asia after the emergence of the K-M9 polymorphism (45–30 ky) (Underhill et al. 2001a). As deduced from the collective data (Underhill et al. 2000; Cruciani et al. 2002; Semino et al. 2002; present study), K2-M70 individuals, at some later point, proceeded south to Africa. While these chromosomes are seen in relatively high frequencies in Egypt, Oman, Tanzania, Ethiopia, they are especially prominent in theFulbe 18%( [Scozzari et al. 1997, 1999])

J. R. Luis et al. 2004, [10]
Three genetically different populations in the Balearic Islands, Catalonia, Spain

The population of the Pityusic Islands does present a clear genetic divergence in relation to the Mallorcan and Menorcan populations. Neither [does it show] a confluence with the Catalan and Valencian populations ...[T]he data provided by the Pityusic population [compared] with other circumediterranean populations surprises [in] that practically there is no convergence with any of these populations, not even with ... North African populations. The Pityusic case is paradigmatic: ... some markers shows affinities with [Middle Eastern] ... mtDNA variables ... but [the Pityusic population] diverges from these populations when considering other markers. [It] is a separate case, a island, not [just] in the geographical sense but [also a] genetical [island].

Misericòrdia Ramon Juanpere et al., 1998-2004
PopulationLanguageLocationMembers/Sample sizePercentageSourceNotes
Pityusic IslandsEivissenc (Ibizan) (Romance)Ibiza,Balearic Islands,Catalonia,Spain9/5416.7%[11][12]L454+. All individuals carry typical Ibizan surnames and had paternal grandfathers born in Ibiza.
Pityusic IslandsEivissencIbiza7/967.3%[13]L454+
Pityusic IslandsEivissencIbiza3/456.7%[14]L454+

T1a1 (L162; xL208)

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T1a1 formed 17,400-14,600 BP, is the largest lineage downstream from T1a-M70 and became widespread across Eurasia and Africa before the modern era.

This extremely rare subclade has been found inIbizan (Eivissan) islanders andPontic Greeks fromGiresun. The first Y-STR haplotype belonging to this lineage appeared in the paper of Tomas et al in 2006 among a sample of Eivissan individuals but is not until August 2009 when the first T1a1-L162(xL208) individual was reported in a 23andMe customer of Pontic Greek background and Metaxopoulos surname, thanks to the public Adriano Squecco's Y-Chromosome Genome Comparison Project.

Pontic Greeks from Giresun descend fromSinope colonists and Sinope was colonised byIonians fromMiletus. It is interesting to note that there existed an Ionian colony known asPityussa, just like the known Greek name for EivissaPityuses. In Eivissa, archaeological findings include the famous bust ofDemeter which has been confused with thePunicgoddessTanit for decades. The bust belonging to Demeter has been analysed and was found to contain black particles of volcanic sand, originating fromMount Etna. It is thought that the bust was made inSicily, with red clays typical of the easternTrinacria, which was colonized by the Ionians. The Ionians could be arrived to Eivissa c.2700 YBP. This lineage could be an Ionian marker.T1a1 formed 17,400-14,600 BP, is the largest lineage downstream from T1a-M70 and became widespread across Eurasia and Africa before the modern era.

T1a1a (L208)

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This lineage, formed 14,200-11,000 BP, is the largest branch downstream T1a1-L162. First discovered and reported in August 2009 in a 23andMe customer of Iberian ancestry that participated in the public Squecco's Y-Chromosome Genome Comparison Project and appearing there as "Avilés" and as "AlpAstur" in 23andMe. Named as "L208" at November 2009.

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T1a1a1a1b1a1 (Y3782; xY3836)

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This sectionneeds expansion. You can help byadding to it.(September 2016)
PopulationLanguageLocationMembers/Sample sizePercentageSourceNotes
SardiniansCampidanese (Romance languages)Casteddu1/1870.5%[15]

T1a1a1a1b1a1a (Y3836)

[edit]

This lineage is mostly found among individuals from the Iberian Peninsula, where is found their highest diversity. The first Y-STR haplotype of this lineage, characterized by DYS437=13, was found in the public FTDNA Y-DNA Haplogroup T project, appearing there at April 2009 as kit E8011. However, is not until June 2014 when the Y-SNP Y3836 was discovered in the public YFULL project among two of their participants of Iberian ancestry, appearing there as YF01637 and YF01665.

PopulationLanguageLocationMembers/Sample sizePercentageSourceNotes
PanamaniansPanamian Castilian (Romance languages)Los Santos Province1/303.3%[16]
ColombiansColombian Castilian (Romance languages)Caldas2/752.7%YHRDMestizo individuals
PanamaniansPanamian Castilian (Romance languages)Panama Province1/432.3%[16]
NorthwestArgentiniansArgentinian Castilian (Romance languages)Mountainous region ofJujuy1/502%[17] YHRDAdmixed population
Puerto RicansPuerto Rican Castilian (Romance languages)SoutheastPuerto Rico2/1101.8%[18]
Northeastern Portuguese JewsJudaeo-Portuguese (Romance)Bragança,Argozelo,Carção,Mogadouro, andVilarinho dos Galegos1/571.8%[19][20][21]
Native Mirandese speakersMirandese Astur-leonese (Romance)Miranda de l Douro1/581.7%[22][23]
DominicansDominican Castilian (Romance languages)Dominican Republic4/2611.5%[24]
PanamaniansPanamian Castilian (Romance languages)Chiriquí Province1/921.1%[16]
MecklenburgersEast Low Saxon (West Germanic)Rostock2/2001%[25]
ColombiansColombian Castilian (Romance languages)Bogotá2/1951%YHRDMestizo individuals
ColombiansColombian Castilian (Romance languages)Valle del Cauca1/1031%YHRDMestizo individuals
VenezuelansVenezuelan Castilian (Romance languages)Maracaibo1/1110.9%[26]
VenezuelansVenezuelan Castilian (Romance languages)Central Region1/1150.9%[27]
EuropeansBrazilian Portuguese (Romance languages)São Paulo1/1200.8YHRDEuropean descents
EcuadoriansEcuadorian Castilian (Romance languages)Quito1/1200.8%[28]
ColombiansColombian Castilian (Romance languages)Antioquia6/7770.7%[29]
MexicansMexican Castilian (Romance languages)Tuxtla Gutiérrez1/1540.7YHRDMestizo individuals
MexicansMexican Castilian (Romance languages)Mérida1/1590.6%YHRDMestizo individuals
EasternAndalusiansAndalusian (Romance)Granada1/1800.6%[30]
ColombiansColombian Castilian (Romance languages)Santander1/1930.5%YHRDMestizo individuals
ChileansChilean Castilian (Romance languages)Concepción1/1980.5%YHRD
MexicansMexican Spanish (Romance languages)Guadalajara1/2460.4%YHRDMestizo individuals
EuropeansBrazilian Portuguese (Romance languages)Rio Grande do Sul1/2550.4%[31]

Geographical distribution

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Europe

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Cretan Greeks fromLasithi possess Haplogroup T, almost certainly T1a (M70), at a level of 18% (9/50).[32]

Unconfirmed but probable T-M70+ : 14% (3/23) ofRussians inYaroslavl,[33] 12.5% (3/24) ofItalians inMatera,[34] 10.3% (3/29) ofItalians inAvezzano,[34] 10% (3/30) ofTyroleans inNonstal,[34] 10% (2/20) ofItalians inPescara,[34] 8.7% (4/46) ofItalians inBenevento,[34] 7.8% (4/51) ofItalians in SouthLatium,[35] 7.4% (2/27) ofItalians inPaola,[34] 7.3% (11/150) ofItalians in Central-SouthItaly,[36] 7.1% (8/113) ofSerbs inSerbia,[37] 4.7% (2/42) ofAromanians inRomania,[38] 3.7% (3/82) of Italians inBiella,[39] 3.7% (1/27) ofAndalusians inCórdoba,[40] 3.3% (2/60) ofLeoneses inLeón,[40] 3.2% (1/31) of Italians inPostua,[39] 3.2% (1/31) of Italians inCavaglià,[39] 3.1% (3/97) of Calabrians inReggio Calabria,[41] 2.8% (1/36) ofRussians inRyazan Oblast,[42] 2.8% (2/72) ofItalians in SouthApulia,[43] 2.7% (1/37) of Calabrians inCosenza,[41] 2.6% (3/114) ofSerbs inBelgrade,[44] 2.5% (1/40) ofRussians inPskov,[33] 2.4% (1/42) ofRussians inKaluga,[33] 2.2% (2/89) ofTransylvanians inMiercurea Ciuc,[45] 2.2% (2/92) of Italians inTrino Vercellese,[39] 1.9% (2/104) of Italians inBrescia,[46] 1.9% (2/104) ofRomanians inRomania,[47] 1.7% (4/237) ofSerbs andMontenegrins inSerbia andMontenegro,[48] 1.7% (1/59) ofItalians inMarche,[43] 1.7% (1/59) of Calabrians inCatanzaro,[41] 1.6% (3/183) ofGreeks in NorthernGreece,[49] 1.3% (2/150) ofSwiss Germans inZürich Area,[50] 1.3% (1/79) ofItalians in SouthTuscany and NorthLatium,[43] 1.1% (1/92) of Dutch inLeiden,[51] 0.5% (1/185) ofSerbs inNovi Sad (Vojvodina),[52] 0.5% (1/186) ofPolish inPodlasie[53]

Middle East & Caucasus

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PopulationLanguageLocationMembers/Sample sizePercentageSourceNotes
Iraqi JewsJudeo-Iraqi Arabic (Central Semitic)Iraq7/3221.9%[6]12.5% T1a1a1a1a1a1-P77 and 9.4% T1a3-Y11151
Armenian SasuntzisWestern Armenian dialect,Kurmanji andDimli (Northwestern Iranian) languagesSasun21/10420.2%[2]T1a1 and T1a2 subclades
Kurdish JewsJudeo-Aramaic (Central Semitic)Kurdistan9/5018%[6]10% T1a1a1a1a1a1-P77 and 8% T1a1-L162
Iranian JewsJudeo-Iranian (Southwestern Iranian)Iran3/2213.6%[6]4.5% T1a1a1a1a1a1-P77 and 9.1% T1a3-Y11151
Mountain JewsJudeo-Tat (Southwestern Iranian)Derbentsky District2/1711.8%[54]All belong to T1a1a1a1a1a1-P77
Not specifiedNot specifiedBirjand1/273.7%[55]All T1a3-Y12871
Not specifiedNot specifiedMashhad2/1291.6%[55]0.8% T1a3-Y11151 (xY8614)

Unconfirmed but probable T-M70+ : 28% (7/25) ofLezginians inDagestan,[56] 21.7% (5/23) ofOssetians inZamankul,[57] 14% (7/50) ofIranians inIsfahan,[56] 13% (3/23) ofOssetians inZil'ga,[57] 12.6% (11/87) ofKurmanjiKurds inEastern Turkey,[58] 11.8% (2/17) ofPalestinian Arabs inPalestine,[59] 8.3% (1/12) ofIranians inShiraz,[60] 8.3% (2/24) ofOssetians inAlagir,[57] 8% (2/25) ofKurmanjiKurds inGeorgia,[58] 7.5% (6/80) ofIranians inTehran,[56][61] 7.4% (10/135) ofPalestinian Arabs inIsraeli Village,[59] 7% (10/143) ofPalestinian Arabs inIsrael andPalestine,[59] 5% (1/19) ofChechens inChechenia,[56][61] 4.2% (3/72) ofAzerbaijanians inAzerbaijan,[56][61] 4.1% (2/48) ofIranians inIsfahan,[61] 4% (4/100) ofArmenians inArmenia,[56][61] 4% (1/24) ofBedouins inIsrael[59] and 2.6% (1/39) ofTurks inAnkara.[61]

North & East Asia

[edit]

Barghut Mongolians from |different localities ofHulun Buir Aimak have T1a (M70) at a level of 1.3% (1/76).[62] In the 12–13th centuries, the Barga (Barghuts) Mongols appeared as tribes near Lake Baikal, named Bargujin.

Unconfirmed but probable T-M70+: 2% (4/204) ofHui inLiaoning province,[63] and 0.9% (1/113) ofBidayuh inSarawak.[64]

South Asia

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Haplogroup T1a-M70 in South Asia is considered to be of West Eurasian origin.[65]

TheGaro people ofTangail District appear to possess T-P77 (T1a1a1b2b2b1a) at a rate of 0.8% (1/120).[66]||Likely +

Unconfirmed but probable T-M70+ : 56.6% (30/53) ofKunabhis inUttar Kannada,[67] 32.5% (13/40) ofKammas inAndhra Pradesh,[68] 26.8% (11/41) ofBrahmins inVisakhapatnam,[68] 25% (1/4) ofKattunaiken inSouth India,[69] 22.4% (11/49) ofTelugus inAndhra Pradesh,[70] 20% (1/5) ofAnsari inSouth Asia, (2/20) ofPoroja inAndhra Pradesh,[68] 9.8% (5/51) ofKashmiri Pandits inKashmir,[71] 8.2% (4/49) ofGujars inKashmir,[71] 7.7% (1/13) ofSiddis (migrants fromEthiopia) inAndhra Pradesh,[68] 5.5% (3/55) ofAdi inNortheast India,[72] 5.5% (7/128) ofPardhans inAdilabad,[70] 5.3% (2/38) ofBrahmins inBihar,[71] 4.3% (1/23) ofBagata inAndhra Pradesh,[68] 4.2% (1/24) ofValmiki inAndhra Pradesh,[68] (1/32) ofBrahmins inMaharashtra,[71] 3.1% (2/64) ofBrahmins inGujarat,[71] 2.9% (1/35) ofRajput inUttar Pradesh,[73] 2.3% (1/44) ofBrahmins inPeruru,[68] and 1.7% (1/59) ofManghi inMaharashtra.[70]

Also inDesasth-Brahmins inMaharashtra (1/19 or 5.3%) andChitpavan-Brahmins inKonkan (1/21 or 4.8%),Chitpavan-Brahmins inKonkan (2/66 or 3%).

Africa

[edit]
PopulationLanguageLocationMembers/Sample sizePercentageSourceNotes
Somalis (Dir clan)Somali (EastCushitic)Djibouti24/24100%[74]The main sub-clans of the Dir clan in Djibouti are the Issa and Gadabuursi.
Somalis (Dire Dawa)Somali (EastCushitic)Dire Dawa14/1782.4%[75]Dir sub-clans of Dire Dawa are Issa, Gurgura and Gadabuursi.
AnteonyAntemoro (Plateau Malagasy)old Antemoro Kingdom22/3759.5%[76]The Anteony are the descendants of aristocrats, from whom the Antemoro king is chosen. Can be grouped into the Silamo, because they have the right to undertake the ritual slaughter of animals (Sombily)
Somalis (Dir clan) andAfarsSomali andAfar (EastCushitic)Djibouti30/5456.6%[77]Mixed sample of Somali and Afar individuals.[failed verification]
Somalis (Ethiopia)Somali (EastCushitic)Shilavo (woreda) (Ogaden)5/1050%[74]The geographic location of this Ethiopia sample as seen in Fig.1.
Somalis (Isaaq)Somali (EastCushitic)Somaliland4/4100%[78]All belonging to the T1a-Y16897 subclade
ToubouToubouChad31%[79]All belonging to the T1a-PF5662 subclade
LembaVenda andShona (Bantu)Zimbabwe/South Africa6/3417.6%[6]Exclusively belong to T1a2* (old T1b*). Possible recent founder effect. Low frequency of T1a2 has been observed in Bulgarian Jews and Turks but is not found in other Jewish communities. Y-str Haplotypes close to some T1a2 Armenians.
BaribasBaatonum (Niger–Congo)Benin1/571.8%[80]T1a-M70(xT1a2-L131)

Ancient DNA

[edit]

Peki'in Cave Israel

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During the Chalcolithic Period, (the "Copper Age") in the NorthernGalilee town ofPeki'in here's a burial cave that dates to over 6,500 years ago. The cave is the largest one known inIsrael and contains a wealth of ancient artifacts: decorated ossuaries which some claim is the protoIsraeliteBurial, burial offerings, jars, stone tools. We find that the individuals buried in Peqi'in Cave represent a relatively genetically homogeneous population. This homogeneity is evident not only in the genome-wide analyses but also in the fact that most of the male individuals (nine out of ten) belong to theY-DNAHaplogroup T a lineage thought to have diversified in theNear East. 2x T-L208 Peqi'in 1155,1160, 1x T-FT13419 Peqi'in 1165, 4x T-Y4119 Peqi'in ,1166,1170,1172,1178, 2x T-L454 Peqi'in 1180,1187 expressing the upstream and downstream diversity of Haplogroup T-M184 in West Asia its most likely point of divergence.

Kulubnarti Nubian Christian

[edit]

Kulubnarti 6340 was a 18 month old baby boy who lived between 770 - 960 CE Kulubnarti 6328 was a 7 year old boy who lived between 700 - 990 CE during theNorth AfricaChristian Age and was found in the region now known as the elite R cemetery inKulubnarti,Sudan.They were associated with the KulubnartiNubians cultural group theY-DNA was T-Y31479 and T-FT338883 they along with aHaplogroup LT were the three outliers amongst the Nubian elite R cemetery.

Notable members

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Elite endurance runners

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Possible patterns between Y-chromosome and elite endurance runners were studied in an attempt to find a genetic explanation to the Ethiopian endurance running success. Given the superiority of East African athletes in international distance running over the past four decades, it has been speculated that they are genetically advantaged. Elite marathon runners from Ethiopia were analysed for K*(xP) which according to the previously published Ethiopian studies is attributable to the haplogroup T[81]

According to further studies,[6] T1a1a* (L208) was found to be proportionately more frequent in the elite marathon runners sample than in the control samples than any other haplogroup, therefore this y-chromosome could play a significant role in determining Ethiopian endurance running success. Haplogroup T1a1a* was found in 14% of the elite marathon runners sample of whom 43% of this sample are from Arsi province. In addition, haplogroup T1a1a* was found in only 4% of the Ethiopian control sample and only 1% of the Arsi province control sample. T1a1a* is positively associated with aspects of endurance running, whereas E1b1b1 (old E3b1) is negatively associated.[82]

Royal House of Khalifa

[edit]

The House of Khalifa (Arabic: آل خليفة,romanized: Āl Khalīfah) is the ruling family of theKingdom of Bahrain. The Al Khalifas professSunniIslam and belong to theAnizah tribe, some members of this tribe joined theUtub alliance which migrated from CentralArabia toKuwait, then ruled all ofQatar, more specificallyAl Zubarah, which they built and ruled over before settling in Bahrain in the early 17th century. The current head of the family isHamad bin Isa Al Khalifa, who became the Emir ofBahrain in 1999 and proclaimed himself King of Bahrain in 2002, in fact becoming a constitutional monarch.[citation needed]

Thomas Jefferson

[edit]
Thomas Jefferson

Phylogenetic network analysis of its Y-STR (short tandem repeat) haplotype shows that it is most closely related to an Egyptian K2 [now T/K1a] haplotype, but the presence of scattered and diverse European haplotypes within the network is nonetheless consistent with Jefferson's patrilineage belonging to an ancient and rare indigenous European type. This is supported by the observation that two of 85 unrelated British men sharing the surname Jefferson also share the President's Y-STR haplotype within haplogroup K2.

Turi E. Kinget al., [83]
See also:Jefferson–Hemings controversy

A notable member of the T-M184 haplogroup is the third US President,Thomas Jefferson. He reportedly belongs to a subclade of T-M184 which is most commonly found in theIberian Peninsula (e.g. Spain). His most distant known ancestor is Samuel Jeffreason [sic], born 11 October 1607 atPettistree, Suffolk, England, although there is also a widespread belief that the President hadWelsh ancestry.

There was controversy for almost two centuries regarding allegations that Thomas Jefferson had fathered the children of hisslaveSally Hemings. The controversy effectively began on September 1,1802 with an article by James Callender, printed in a Richmond newspaper.[84] Anoral tradition in theHemings family and other historical evidence was countered in the early 19th century by some Jefferson's grandchildren, who asserted that a son of Thomas Jefferson's sister, by the name of Carr, had been the father of Hemings' children. However, a 1998 study of Jefferson male-line DNA found that it matched that of a descendant of Sally Hemings' youngest son,Eston Hemings. Most historians[who?] now believe that Jefferson had a relationship with Hemings for 38 years, and probably fathered her seven known children, five of whom lived to adulthood. In addition, the testing conclusively disproved any connection between the Hemings descendant and the Carr male line.[citation needed]

Subclades

[edit]

Tree

[edit]
Phylogenetic Tree of the Eurasian Haplogroup T-M184 and their closest macro-lineages
Latest 2015 tree (ISOGG 2015)
Branching of T-M184
LT<br /> L298 (43900ybp)
LT*(xM184, M20)

All cases without M184 or M20

TM184 (39,300‑45,100ybp)
T*(xL206)

All cases without L206 or PH110

<br />T1L206 (26600ybp)
T1*(xM70)

Syria

<br />T1aM70 (19,000-30,000ybp)[6]
T1a*(xL162,L131,Y11151)

All cases without L162, L131 or Y11151

<br />T1a1L162 (15400ybp)
T1a1*(xL208)

Pityusic Islanders,Pontic Greeks from Giresun, Germany andBalkars.

<br />T1a1aL208 (14800ybp)
T1a1a*(xCTS11451, Y16897)

All cases without CTS11451 or Y16897

<br />T1a1a1CTS11451 (9500ybp)
T1a1a1*(xY4119, Y6671)

All cases without Y4119 or Y6671

<br />T1a1a1aY4119 (9200ybp)
T1a1a1a*(xCTS2214)

All cases without CTS2214

<br />T1a1a1a1CTS2214 (8900ybp)
T2<br />PH110 (26600ybp)

Ossetian Irons, Leoneses, Germans and Bhutaneses

L<br />M20
L1<br />M22

West Asia, Europe, Central and South Asia.

<br />L2<br />L595

Widely widespread in Europe, where is found the highest diversity of this lineage.

Macro-Haplogroup LT

Phylogenetic history

[edit]
Main article:Conversion table for Y chromosome haplogroups

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.

YCC 2002/2008 (Shorthand)(α)(β)(γ)(δ)(ε)(ζ)(η)YCC 2002 (Longhand)YCC 2005 (Longhand)YCC 2008 (Longhand)YCC 2010r (Longhand)ISOGG 2006ISOGG 2007ISOGG 2008ISOGG 2009ISOGG 2010ISOGG 2011ISOGG 2012ISOGG 2013
T-M18426VIII1U25Eu16H5FK*KTTK2K2TTTTTT
K-M70/T-M7026VIII1U25Eu15H5FK2K2TT1K2K2TTTT1T1aT1a
T-P7726VIII1U25Eu15H5FK2K2T2T1a2K2K2T2T2T2a1T1a1bT1a1a1T1a1a1

Original research publications

[edit]

The following research teams per their publications were represented in the creation of the YCC Tree.

αJobling and Tyler-Smith 2000 andKaladjieva 2001

βUnderhill 2000

γHammer 2001

δKarafet 2001

εSemino 2000

ζSu 1999

ηCapelli 2001

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

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Original research

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Other works cited

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