Haplogroup T (mtDNA)

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Haplogroup T
Possible time of origin25,149 ± 4,668 years before present
Possible place of origin
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
]

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.

The basal haplogroup T* is found among

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.

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

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

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

Niger-Congo-speaking Serer due to diffusion from the Maghreb, likely with the spread of Islam.[12]

Population Location Language Family N Frequency Source
Amhara Ethiopia Afro-Asiatic > Semitic 5/120 4.17% Kivisild 2004
Beja Sudan Afro-Asiatic > Cushitic 1/48 2.1% Hassan 2009
Beta Israel Ethiopia Afro-Asiatic > Cushitic 0/29 0.00% Behar 2008a
Copt Egypt Afro-Asiatic > Egyptian 5/29 17.2% Hassan 2009
Dawro K. Ethiopia Afro-Asiatic > Omotic 2/137 1.46% Castrì 2008 and Boattini 2013
Egyptians (El-Hayez) Egypt Afro-Asiatic > Semitic 10/35 28.6% Kujanova 2009
Ethiopia Ethiopia Undetermined 2/77 2.60% Soares 2011
Ethiopian Jew Ethiopia Afro-Asiatic > Cushitic 0/41 0.00% Non 2011
Gurage Ethiopia Afro-Asiatic > Semitic 0/21 0.00% Kivisild 2004
Hamer Ethiopia Afro-Asiatic > Omotic 0/11 0.00% Castrì 2008 and Boattini 2013
Ongota Ethiopia Afro-Asiatic > Cushitic 0/19 0.00% Castrì 2008 and Boattini 2013
Oromo Ethiopia Afro-Asiatic > Cushitic 0/33 0.00% Kivisild 2004
Tigrai Ethiopia Afro-Asiatic > Semitic 3/44 6.82% Kivisild 2004
Daasanach Kenya Afro-Asiatic > Cushitic 0/49 0.00% Poloni 2009
Elmolo Kenya Afro-Asiatic > Cushitic 0/52 0.00% Castrì 2008 and Boattini 2013
Luo Kenya Nilo-Saharan 0/49 0.00% Castrì 2008 and Boattini 2013
Maasai Kenya Nilo-Saharan 0/81 0.00% Castrì 2008 and Boattini 2013
Nairobi Kenya Niger-Congo 0/100 0.00% Brandstatter 2004
Nyangatom Kenya Nilo-Saharan 0/112 0.00% Poloni 2009
Rendille Kenya Afro-Asiatic > Cushitic 0/17 0.00% Castrì 2008 and Boattini 2013
Samburu Kenya Nilo-Saharan 0/35 0.00% Castrì 2008 and Boattini 2013
Turkana Kenya Nilo-Saharan 0/51 0.00% Castrì 2008 and Boattini 2013
Hutu Rwanda Niger-Congo 0/42 0.00% Castrì 2009
Dinka Sudan Nilo-Saharan 0/46 0.00% Krings 1999
Sudan Sudan Undetermined 3/102 2.94% Soares 2011
Burunge Tanzania Afro-Asiatic > Cushitic 0/38 0.00% Tishkoff 2007
Datoga Tanzania Nilo-Saharan 1/57 1.75% Tishkoff 2007 and Knight 2003
Iraqw Tanzania Afro-Asiatic > Cushitic 0/12 0.00% Knight 2003
Sukuma Tanzania Niger-Congo 0/32 0.00% Tishkoff 2007 and Knight 2003
Turu Tanzania Niger-Congo 0/29 0.00% Tishkoff 2007
Yemeni Yemen Afro-Asiatic > Semitic 1/114 0.88% Kivisild 2004

Asia

Europe

Subclades

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 (

subclades
(branches) are shown.

  • T
    • T1
      • T1a
        • T1a1
        • T1a2
      • T1b
    • T2
      • T2a
        • T2a1
      • T2b
        • T2b1
        • T2b2
        • T2b3
        • T2b4
        • T2b5
        • T2b6
      • T2c
        • T2c1
      • T2d
      • T2e
        • T2e2
      • T2f
        • T2f1
      • T2g

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 his 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

Olav V of Norway, and George I of Greece
.

See also

Genetics

Backbone mtDNA Tree

Phylogenetic tree of human mitochondrial DNA (mtDNA) haplogroups

 
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

References

Footnotes

Citations

  1. ^
  2. ^
    PMID 19012329. Archived from the original
    (PDF) on 6 October 2016. Retrieved 13 June 2016.
  3. .
  4. ^ "Maternal Ancestry". Oxford Ancestors. Archived from the original on 15 July 2017. Retrieved 7 February 2013.
  5. S2CID 54566651
    .
  6. .
  7. .
  8. .
  9. .
  10. .
  11. . Retrieved 31 May 2016.
  12. .
  13. ^ Chen, Michael. "Hypertrophic cardiomyopathy - Medical Encyclopedia". Medline Plus. National Library of Medicine. Retrieved 2015-10-03.
  14. ^ Meet the Izzards: The Mum's Line. BBC One. 2013-03-12. 48 minutes in.
  15. ^ Gates Jr., Henry Louis (2010). Faces of America: How 12 Extraordinary People Discovered Their Pasts. New York University Press. p. 4.

Sources

Websites

Further reading

External links