Haplogroup T (mtDNA)

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Haplogroup T
Possible time of origin25,149 ± 4,668 years before present
Possible place of origin Near East, and/or Caucasus
Ancestor JT
DescendantsT1 and T2
Defining mutationsG709A, G1888A, A4917G, G8697A, T10463C, G13368A, G14905A, A15607G, G15928A, C16294T

Haplogroup T is a human mitochondrial DNA (mtDNA) haplogroup. It is believed to have originated around 25,100 years ago in the Near East.[ citation needed ]

Contents

Origins

Mitochondrial clade T derives from the haplogroup JT, which also gave rise to the mtDNA haplogroup J. The T maternal clade is thought to have emanated from the Near East.[ citation needed ]

Distribution

Projected spatial frequency distribution for haplogroup T. Frequency maps based on HVS-I data for haplogroups T.png
Projected spatial frequency distribution for haplogroup T.

The basal haplogroup T* is found among Algerians in Oran (1.67%) and Reguibate Sahrawi (0.93%). [1] It is also distributed among the Soqotri (1.2%). [2]

Haplogroup T is present at low frequencies throughout Western and Central Asia and Europe, with varying degrees of prevalence and certainly might have been present in other groups from the surrounding areas. T is found in approximately 10% of native Europeans. [3] [4] It is also common among modern day Iranians. Based on a sample of over 400 modern day Iranians,[ citation needed ] the T haplogroup represents roughly 8.3% of the population (about 1 out of 12 individuals), with the more specific T1 subtype constituting roughly half of those. Furthermore, the specific subtype T1 tends to be found further east and is common in Central Asian and modern Turkic populations ( Lalueza-Fox 2004 ), who inhabit much of the same territory as the ancient Saka, Sarmatian, Andronovo, and other putative Iranian peoples of the 2nd and 1st millennia BC. Lalueza-Fox et al. (2004) also found several T and T1 sequences in ancient burials, including Kurgans, in the Kazakh steppe between the 14th-10th centuries BC, as well as later into the 1st millennia BC. These coincide with the latter part of the Andronovo period and the Saka period in the region. [5]

The geographic distribution within subclade T2 varies greatly with the ratio of subhaplogroup T2e to T2b reported to vary 40-fold across examined populations from a low in Britain and Ireland, to a high in Saudi Arabia ( Bedford 2012 ). Within subhaplogroup T2e, a very rare motif is identified among Sephardic Jews of Turkey and Bulgaria and suspected conversos from the New World ( Bedford 2012 ).

Found in Svan population from Caucasus (Georgia) T* 10,4% and T1 4,2%. T1a1a1 is particularly common in countries with high levels of Y-haplogroup R1a, such as Central and Northeast Europe. The clade is also found everywhere in Central Asia and deep into North Asia, as far east as Mongolia.

T2c and T2d appear to have a Near Eastern origin around the time of the Last Glacial Maximum (LGM) and more recent dispersals into Europe. Most of T2c comprises haplogroup T2c1. Apart from a peak in Cyprus, T2c1 is most common in the Persian Gulf region but is also found in the Levant and in Mediterranean Europe, with a more far-flung distribution at very low levels. [6]

T2 is also found among the Soqotri (7.7%). [2]

Archaeology

Wilde et al. (2014) tested mtDNA samples from the Yamna culture, the presumed homeland of Proto-Indo-European speakers. They found T2a1b in the Middle Volga region and Bulgaria, and T1a both in central Ukraine and the Middle Volga. The frequency of T1a and T2 in Yamna samples were each 14.5%, a percentage higher than in any country today and only found in similarly high frequencies among the Udmurts of the Volga-Ural region. [7]

Haplogroup T has also been found among Iberomaurusian specimens dating from the Epipaleolithic at the Afalou prehistoric site in Algeria. One ancient individual carried the T2b subclade (1/9; 11%). [8] Additionally, haplogroup T has been observed among ancient Egyptian mummies excavated at the Abusir el-Meleq archaeological site in Middle Egypt, which date from the Pre-Ptolemaic/late New Kingdom (T1, T2), Ptolemaic (T1, T2), and Roman (undifferentiated T, T1) periods. [9] Fossils excavated at the Late Neolithic site of Kelif el Boroud in Morocco, which have been dated to around 3,000 BCE, have also been observed to carry the T2 subclade. [10] Additionally, haplogroup T has been observed in ancient Guanche fossils excavated in Gran Canaria and Tenerife on the Canary Islands, which have been radiocarbon-dated to between the 7th and 11th centuries CE. The clade-bearing individuals were inhumed at the Tenerife site, with one specimen found to belong to the T2c1d2 subclade (1/7; 14%). [11]

Africa

In Africa, haplogroup T is primarily found among Afro-Asiatic-speaking populations, including the basal T* clade. [1] Some non-basal T clades are also commonly found among the Niger-Congo-speaking Serer due to diffusion from the Maghreb, likely with the spread of Islam. [12]

PopulationLocationLanguage FamilyNFrequencySource
AmharaEthiopiaAfro-Asiatic > Semitic5/1204.17% Kivisild 2004
BejaSudanAfro-Asiatic > Cushitic1/482.1% Hassan 2009
Beta IsraelEthiopiaAfro-Asiatic > Cushitic0/290.00% Behar 2008a
CoptEgyptAfro-Asiatic > Egyptian5/2917.2% Hassan 2009
Dawro K.EthiopiaAfro-Asiatic > Omotic2/1371.46% Castrì 2008 and Boattini 2013
Egyptians (El-Hayez)EgyptAfro-Asiatic > Semitic10/3528.6% Kujanova 2009
EthiopiaEthiopiaUndetermined2/772.60% Soares 2011
Ethiopian JewEthiopiaAfro-Asiatic > Cushitic0/410.00% Non 2011
GurageEthiopiaAfro-Asiatic > Semitic0/210.00% Kivisild 2004
HamerEthiopiaAfro-Asiatic > Omotic0/110.00% Castrì 2008 and Boattini 2013
OngotaEthiopiaAfro-Asiatic > Cushitic0/190.00% Castrì 2008 and Boattini 2013
OromoEthiopiaAfro-Asiatic > Cushitic0/330.00% Kivisild 2004
TigraiEthiopiaAfro-Asiatic > Semitic3/446.82% Kivisild 2004
DaasanachKenyaAfro-Asiatic > Cushitic0/490.00% Poloni 2009
ElmoloKenyaAfro-Asiatic > Cushitic0/520.00% Castrì 2008 and Boattini 2013
LuoKenyaNilo-Saharan0/490.00% Castrì 2008 and Boattini 2013
MaasaiKenyaNilo-Saharan0/810.00% Castrì 2008 and Boattini 2013
NairobiKenyaNiger-Congo0/1000.00% Brandstatter 2004
NyangatomKenyaNilo-Saharan0/1120.00% Poloni 2009
RendilleKenyaAfro-Asiatic > Cushitic0/170.00% Castrì 2008 and Boattini 2013
SamburuKenyaNilo-Saharan0/350.00% Castrì 2008 and Boattini 2013
TurkanaKenyaNilo-Saharan0/510.00% Castrì 2008 and Boattini 2013
HutuRwandaNiger-Congo0/420.00% Castrì 2009
DinkaSudanNilo-Saharan0/460.00% Krings 1999
SudanSudanUndetermined3/1022.94% Soares 2011
BurungeTanzaniaAfro-Asiatic > Cushitic0/380.00% Tishkoff 2007
DatogaTanzaniaNilo-Saharan1/571.75% Tishkoff 2007 and Knight 2003
IraqwTanzaniaAfro-Asiatic > Cushitic0/120.00% Knight 2003
SukumaTanzaniaNiger-Congo0/320.00% Tishkoff 2007 and Knight 2003
TuruTanzaniaNiger-Congo0/290.00% Tishkoff 2007
YemeniYemenAfro-Asiatic > Semitic1/1140.88% Kivisild 2004

Asia

Europe

Subclades

Schematic tree of mtDNA haplogroup T. Ages (in ka) indicated are maximum likelihood estimates obtained for the whole-mtDNA genome. Schematic tree of mtDNA haplogroup T.png
Schematic tree of mtDNA haplogroup T. Ages (in ka) indicated are maximum likelihood estimates obtained for the whole-mtDNA genome.

Tree

This phylogenetic tree of haplogroup I subclades is based on the paper ( van Oven 2008 ) and subsequent published research ( Behar 2012b ).

Health issues

One study has shown Haplogroup T to be associated with increased risk for coronary artery disease.[ citation needed ] However, some studies have also shown that people of Haplogroup T are less prone to diabetes (Chinnery 2007 and González 2012).

A few tentative medical studies have demonstrated that Haplogroup T may offer some resistance to both Parkinson's disease and Alzheimer's disease.[ citation needed ]

One study has found that among the Spanish population, hypertrophic cardiomyopathy (HCM) also referred to as hypertrophic obstructive cardiomyopathy (HOCM) is more likely to happen in those of T2 ancestry than those in other maternal haplogroups. [13] It is unknown whether or not this is specific to this subclaude of haplogroup T or is a risk factor shared by all of haplogroup T. With a statistically significant difference found in such a small sample, it may be advisable for those of known haplogroup T maternal ancestry to be aware of this and have their physician check for evidence of this condition when having a routine exam at an early age. It is usually symptom-less and increases the risk of sudden cardiac death, which often happens to those of as early in life as teenagers and may affect those who are active and have no other risk factors. [14]

Certain medical studies had shown mitochondrial Haplogroup T to be associated with reduced sperm motility in males, although these results have been challenged ( Mishmar 2002 ). According to the Departamento de Bioquimica y Biologica Molecular y Celular, Universidad de Zaragoza, Haplogroup T can predispose to asthenozoospermia ( Ruiz-Pesini 2000 ). However, these findings have been disputed due to a small sample size in the study ( Mishmar 2002 ).

Famous members

During the BBC One documentary Meet the Izzards, the actor and comedian Eddie Izzard learns that her mitochondrial DNA is of Haplogroup T, specifically the subclade T2f1a1. [15]

Henry Louis Gates Jr. belongs to haplogroup T2b2. [16]

Nicholas II of Russia

The last Russian Tsar, Nicholas II, has been shown to be of Haplogroup T, specifically subclade T2 ( Ivanov 1996 ). Assuming all relevant pedigrees are correct, this includes all female-line descendants of his female line ancestor Barbara of Celje (1390–1451), wife of Sigismund, Holy Roman Emperor. This includes a great number of European nobles, including George I of Great Britain and Frederick William I of Prussia (through the Electress Sophia of Hanover), Charles I of England, George III of the United Kingdom, George V of the United Kingdom, Charles X Gustav of Sweden, Gustavus Adolphus of Sweden, Maurice of Nassau, Prince of Orange, Olav V of Norway, and George I of Greece.

See also

Genetics

Backbone mtDNA Tree

Phylogenetic tree of human mitochondrial DNA (mtDNA) haplogroups

  Mitochondrial Eve (L)  
L0 L1–6 
L1 L2   L3    L4 L5 L6
M N  
CZ D E G Q   O A S R   I W X Y
C Z B F R0   pre-JT   P   U
HV JT K
H V J T

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References

Footnotes

    Citations

    1. 1 2 Asmahan Bekada; Lara R. Arauna; Tahria Deba; Francesc Calafell; Soraya Benhamamouch; David Comas (September 24, 2015). "Genetic Heterogeneity in Algerian Human Populations". PLOS ONE. 10 (9): e0138453. Bibcode:2015PLoSO..1038453B. doi: 10.1371/journal.pone.0138453 . PMC   4581715 . PMID   26402429.; S5 Table
    2. 1 2 Černý, Viktor; et al. (2009). "Out of Arabia—the settlement of island Soqotra as revealed by mitochondrial and Y chromosome genetic diversity" (PDF). American Journal of Physical Anthropology. 138 (4): 439–447. doi:10.1002/ajpa.20960. PMID   19012329. Archived from the original (PDF) on 6 October 2016. Retrieved 13 June 2016.
    3. ↑ Bryan Sykes (2001). The Seven Daughters of Eve. London; New York: Bantam Press. ISBN   978-0393020182.
    4. ↑ "Maternal Ancestry". Oxford Ancestors. Archived from the original on 15 July 2017. Retrieved 7 February 2013.
    5. ↑ Bennett, Casey; Kaestle, Frederika A. (2010). "Investigation of Ancient DNA from Western Siberia and the Sargat Culture". Human Biology. 82 (2): 143–156. arXiv: 1112.2014 . doi:10.3378/027.082.0202. PMID   20649397. S2CID   54566651.
    6. ↑ Pala, M; Olivieri, A; Achilli, A; Accetturo, M; Metspalu, E; Reidla, M; Tamm, E; Karmin, M; Reisberg, T; Hooshiar Kashani, B; Perego, UA; Carossa, V; Gandini, F; Pereira, JB; Soares, P; Angerhofer, N; Rychkov, S; Al-Zahery, N; Carelli, V; Sanati, MH; Houshmand, M; Hatina, J; Macaulay, V; Pereira, L; Woodward, SR; Davies, W; Gamble, C; Baird, D; Semino, O; Villems, R; Torroni, A; Richards, MB (4 May 2012). "Mitochondrial DNA Signals of Late Glacial Recolonization of Europe from Near Eastern Refugia". The American Journal of Human Genetics. 90 (5): 915–924. doi:10.1016/j.ajhg.2012.04.003. PMC   3376494 . PMID   22560092. http://haplogroup.org/sources/mitochondrial-dna-signals-of-late-glacial-recolonization-of-europe-from-near-eastern-refugia/ Archived 2023-02-07 at the Wayback Machine
    7. ↑ Wilde, Sandra (2014). "Direct evidence for positive selection of skin, hair, and eye pigmentation in Europeans during the last 5,000 y". Proceedings of the National Academy of Sciences. 111 (13): 4832–4837. Bibcode:2014PNAS..111.4832W. doi: 10.1073/pnas.1316513111 . PMC   3977302 . PMID   24616518.
    8. ↑ Kefi, Rym; et al. (2018). "On the origin of Iberomaurusians: new data based on ancient mitochondrial DNA and phylogenetic analysis of Afalou and Taforalt populations". Mitochondrial DNA Part A. 29 (1): 147–157. doi:10.1080/24701394.2016.1258406. PMID   28034339. S2CID   4490910.
    9. ↑ Schuenemann, Verena J.; et al. (2017). "Ancient Egyptian mummy genomes suggest an increase of Sub-Saharan African ancestry in post-Roman periods". Nature Communications. 8: 15694. Bibcode:2017NatCo...815694S. doi:10.1038/ncomms15694. PMC   5459999 . PMID   28556824.
    10. ↑ Fregel; et al. (2018). "Ancient genomes from North Africa evidence prehistoric migrations to the Maghreb from both the Levant and Europe". bioRxiv   10.1101/191569 .
    11. ↑ Rodrı́guez-Varela; et al. (2017). "Genomic Analyses of Pre-European Conquest Human Remains from the Canary Islands Reveal Close Affinity to Modern North Africans". Current Biology. 27 (1–7): 3396–3402.e5. doi: 10.1016/j.cub.2017.09.059 . hdl: 2164/13526 . PMID   29107554.
    12. ↑ Ball, Edward (2007). The Genetic Strand: Exploring a Family History Through DNA. Simon and Schuster. p. 233. ISBN   978-1416554257 . Retrieved 31 May 2016.
    13. ↑ Castro, M (2006). "Mitochondrial DNA haplogroups in Spanish patients with hypertrophic cardiomyopathy". Int J Cardiol. 112 (2): 202–6. doi:10.1016/j.ijcard.2005.09.008. PMID   16313983.
    14. ↑ Chen, Michael. "Hypertrophic cardiomyopathy - Medical Encyclopedia". Medline Plus. National Library of Medicine. Retrieved 2015-10-03.
    15. ↑ Meet the Izzards: The Mum's Line. BBC One. 2013-03-12. 48 minutes in.
    16. ↑ Gates Jr., Henry Louis (2010). Faces of America: How 12 Extraordinary People Discovered Their Pasts. New York University Press. p. 4.

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