Haplogroup T (mtDNA): Difference between revisions
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{{Short description|Human mitochondrial DNA haplogroup}} |
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{{About|the human mtDNA Haplogroup T|the unrelated human Y-Chromosome Haplogroup T-M184|Haplogroup T-M184}} |
{{About|the human mtDNA Haplogroup T|the unrelated human Y-Chromosome Haplogroup T-M184|Haplogroup T-M184}} |
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{{Infobox haplogroup |
{{Infobox haplogroup |
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|name=T |
|name=T |
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|origin-date=25,149 ± 4,668 years before present |
|origin-date=25,149 ± 4,668 years before present |
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|origin-place=[[Near East]] |
|origin-place=[[Near East]], and/or [[Caucasus]] |
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|ancestor=[[Haplogroup JT (mtDNA)|JT]] |
|ancestor=[[Haplogroup JT (mtDNA)|JT]] |
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|descendants=T1 and T2 |
|descendants=T1 and T2 |
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}} |
}} |
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'''Haplogroup T''' is a [[Human mitochondrial DNA (mtDNA) haplogroup|human mitochondrial DNA]] (mtDNA) haplogroup. It is believed to have originated around 25,100 years ago in the [[Near East]]. |
'''Haplogroup T''' is a [[Human mitochondrial DNA (mtDNA) haplogroup|human mitochondrial DNA]] (mtDNA) haplogroup. It is believed to have originated around 25,100 years ago in the [[Near East]].{{CN|date=November 2023}} |
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{{TOC limit|3}} |
{{TOC limit|3}} |
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==Origins== |
==Origins== |
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Mitochondrial clade T derives from the haplogroup [[Haplogroup JT (mtDNA)|JT]], which also gave rise to the mtDNA [[Haplogroup J (mtDNA)|haplogroup J]]. The T maternal clade is thought to have emanated from the [[Near East]] |
Mitochondrial clade T derives from the haplogroup [[Haplogroup JT (mtDNA)|JT]], which also gave rise to the mtDNA [[Haplogroup J (mtDNA)|haplogroup J]]. The T maternal clade is thought to have emanated from the [[Near East]].{{CN|date=May 2023}} |
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==Distribution== |
==Distribution== |
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[[File:Frequency maps based on HVS-I data for haplogroups T.png|thumb|Projected spatial frequency distribution for haplogroup T.]] |
[[File:Frequency maps based on HVS-I data for haplogroups T.png|thumb|Projected spatial frequency distribution for haplogroup T.]] |
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The basal haplogroup T* is found among [[Algeria]]ns in [[Oran]] (1.67%) and [[Reguibat tribe|Reguibate]] [[Sahrawi people|Sahrawi]] (0.93%).<ref name="Bekada2015">{{cite journal|author1=Asmahan Bekada |author2=Lara R. Arauna |author3=Tahria Deba |author4=Francesc Calafell |author5=Soraya Benhamamouch |author6=David Comas |title=Genetic Heterogeneity in Algerian Human Populations|journal=PLOS ONE|date=September 24, 2015|volume=10|issue=9|doi=10.1371/journal.pone.0138453|pages=e0138453 |pmid=26402429 |pmc=4581715|bibcode=2015PLoSO..1038453B}}; [http://journals.plos.org/plosone/article/asset?unique&id=info:doi/10.1371/journal.pone.0138453.s007 S5 Table]</ref> It is also distributed among the [[Soqotri people|Soqotri]] (1.2%).<ref name="Cerny2009">{{cite journal|last1=Černý, Viktor|title=Out of Arabia—the settlement of island Soqotra as revealed by mitochondrial and Y chromosome genetic diversity|journal=American Journal of Physical Anthropology|date=2009|volume=138|issue=4|pages=439–447|url=http://ychrom.invint.net/upload/iblock/f30/Cerny%202009%20Out%20of%20ArabiarusThe%20Settlement%20of%20Island%20Soqotra%20as%20Revealed%20by%20Mitochondrial%20and%20Y.pdf|access-date=13 June 2016|display-authors=etal|doi=10.1002/ajpa.20960|pmid=19012329|url-status=dead|archive-url=https://web.archive.org/web/20161006125303/http://ychrom.invint.net/upload/iblock/f30/Cerny%202009%20Out%20of%20ArabiarusThe%20Settlement%20of%20Island%20Soqotra%20as%20Revealed%20by%20Mitochondrial%20and%20Y.pdf|archive-date=6 October 2016}}</ref> |
The basal haplogroup T* is found among [[Algeria]]ns in [[Oran]] (1.67%) and [[Reguibat tribe|Reguibate]] [[Sahrawi people|Sahrawi]] (0.93%).<ref name="Bekada2015">{{cite journal|author1=Asmahan Bekada |author2=Lara R. Arauna |author3=Tahria Deba |author4=Francesc Calafell |author5=Soraya Benhamamouch |author6=David Comas |title=Genetic Heterogeneity in Algerian Human Populations|journal=PLOS ONE|date=September 24, 2015|volume=10|issue=9|doi=10.1371/journal.pone.0138453|pages=e0138453 |pmid=26402429 |pmc=4581715|bibcode=2015PLoSO..1038453B|doi-access=free }}; [http://journals.plos.org/plosone/article/asset?unique&id=info:doi/10.1371/journal.pone.0138453.s007 S5 Table]</ref> It is also distributed among the [[Soqotri people|Soqotri]] (1.2%).<ref name="Cerny2009">{{cite journal|last1=Černý, Viktor|title=Out of Arabia—the settlement of island Soqotra as revealed by mitochondrial and Y chromosome genetic diversity|journal=American Journal of Physical Anthropology|date=2009|volume=138|issue=4|pages=439–447|url=http://ychrom.invint.net/upload/iblock/f30/Cerny%202009%20Out%20of%20ArabiarusThe%20Settlement%20of%20Island%20Soqotra%20as%20Revealed%20by%20Mitochondrial%20and%20Y.pdf|access-date=13 June 2016|display-authors=etal|doi=10.1002/ajpa.20960|pmid=19012329|url-status=dead|archive-url=https://web.archive.org/web/20161006125303/http://ychrom.invint.net/upload/iblock/f30/Cerny%202009%20Out%20of%20ArabiarusThe%20Settlement%20of%20Island%20Soqotra%20as%20Revealed%20by%20Mitochondrial%20and%20Y.pdf|archive-date=6 October 2016}}</ref> |
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Haplogroup T is present at low frequencies |
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.<ref>{{cite book|author=Bryan Sykes|title=The Seven Daughters of Eve|year=2001|publisher=Bantam Press|location=London; New York|isbn=978-0393020182|title-link=The Seven Daughters of Eve|author-link=Bryan Sykes}}</ref><ref>{{cite web|title=Maternal Ancestry|url=http://www.oxfordancestors.com/content/view/35/55/|publisher=Oxford Ancestors|access-date=7 February 2013|archive-url=https://web.archive.org/web/20170715205636/http://www.oxfordancestors.com/content/view/35/55/|archive-date=15 July 2017|url-status=dead}}</ref> It is also common among modern day [[Demographics of Iran|Iranians]]. Based on a sample of over 400 modern day Iranians,{{CN|date=May 2023}} 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 Asia]]n and modern [[Turkic peoples|Turkic]] populations {{harv|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 [[Kurgan]]s, 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.<ref>{{cite journal | last1 = Bennett | first1 = Casey | last2 = Kaestle | first2 = Frederika A. | year = 2010 | title = Investigation of Ancient DNA from Western Siberia and the Sargat Culture | journal = Human Biology | volume = 82 | issue = 2| pages = 143–156 | doi=10.3378/027.082.0202| pmid = 20649397 | arxiv = 1112.2014 | s2cid = 54566651 }}</ref> |
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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 {{harv|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 {{harv|Bedford|2012}}. |
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 {{harv|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 {{harv|Bedford|2012}}. |
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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. |
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. |
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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.<ref>{{cite journal|title=Mitochondrial DNA Signals of Late Glacial Recolonization of Europe from Near Eastern Refugia|date=4 May 2012|pages=915–924|doi=10.1016/j.ajhg.2012.04.003|volume=90|issue=5|journal=The American Journal of Human Genetics|pmid=22560092|pmc=3376494 | last1 = Pala | first1 = M | last2 = Olivieri | first2 = A | last3 = Achilli | first3 = A | last4 = Accetturo | first4 = M | last5 = Metspalu | first5 = E | last6 = Reidla | first6 = M | last7 = Tamm | first7 = E | last8 = Karmin | first8 = M | last9 = Reisberg | first9 = T | last10 = Hooshiar Kashani | first10 = B | last11 = Perego | first11 = UA | last12 = Carossa | first12 = V | last13 = Gandini | first13 = F | last14 = Pereira | first14 = JB | last15 = Soares | first15 = P | last16 = Angerhofer | first16 = N | last17 = Rychkov | first17 = S | last18 = Al-Zahery | first18 = N | last19 = Carelli | first19 = V | last20 = Sanati | first20 = MH | last21 = Houshmand | first21 = M | last22 = Hatina | first22 = J | last23 = Macaulay | first23 = V | last24 = Pereira | first24 = L | last25 = Woodward | first25 = SR | last26 = Davies | first26 = W | last27 = Gamble | first27 = C | last28 = Baird | first28 = D | last29 = Semino | first29 = O | last30 = Villems | first30 = R | last31 = Torroni | first31 = A | last32 = Richards | first32 = MB}}http://haplogroup.org/sources/mitochondrial-dna-signals-of-late-glacial-recolonization-of-europe-from-near-eastern-refugia/</ref> |
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.<ref>{{cite journal|title=Mitochondrial DNA Signals of Late Glacial Recolonization of Europe from Near Eastern Refugia|date=4 May 2012|pages=915–924|doi=10.1016/j.ajhg.2012.04.003|volume=90|issue=5|journal=The American Journal of Human Genetics|pmid=22560092|pmc=3376494 | last1 = Pala | first1 = M | last2 = Olivieri | first2 = A | last3 = Achilli | first3 = A | last4 = Accetturo | first4 = M | last5 = Metspalu | first5 = E | last6 = Reidla | first6 = M | last7 = Tamm | first7 = E | last8 = Karmin | first8 = M | last9 = Reisberg | first9 = T | last10 = Hooshiar Kashani | first10 = B | last11 = Perego | first11 = UA | last12 = Carossa | first12 = V | last13 = Gandini | first13 = F | last14 = Pereira | first14 = JB | last15 = Soares | first15 = P | last16 = Angerhofer | first16 = N | last17 = Rychkov | first17 = S | last18 = Al-Zahery | first18 = N | last19 = Carelli | first19 = V | last20 = Sanati | first20 = MH | last21 = Houshmand | first21 = M | last22 = Hatina | first22 = J | last23 = Macaulay | first23 = V | last24 = Pereira | first24 = L | last25 = Woodward | first25 = SR | last26 = Davies | first26 = W | last27 = Gamble | first27 = C | last28 = Baird | first28 = D | last29 = Semino | first29 = O | last30 = Villems | first30 = R | last31 = Torroni | first31 = A | last32 = Richards | first32 = MB}}http://haplogroup.org/sources/mitochondrial-dna-signals-of-late-glacial-recolonization-of-europe-from-near-eastern-refugia/ {{Webarchive|url=https://web.archive.org/web/20230207084159/https://haplogroup.org/sources/mitochondrial-dna-signals-of-late-glacial-recolonization-of-europe-from-near-eastern-refugia/ |date=2023-02-07 }}</ref> |
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T2 is also found among the Soqotri (7.7%).<ref name="Cerny2009"/> |
T2 is also found among the Soqotri (7.7%).<ref name="Cerny2009"/> |
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===Archaeology=== |
===Archaeology=== |
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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.<ref>{{cite journal | doi = 10.1073/pnas.1316513111 | pmid=24616518 | volume=111 | issue=13 | title=Direct evidence for positive selection of skin, hair, and eye pigmentation in Europeans during the last 5,000 y | journal=Proceedings of the National Academy of Sciences | pages=4832–4837 | year=2014 | last1 = Wilde | first1 = Sandra| pmc=3977302 | bibcode=2014PNAS..111.4832W }}</ref> |
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.<ref>{{cite journal | doi = 10.1073/pnas.1316513111 | pmid=24616518 | volume=111 | issue=13 | title=Direct evidence for positive selection of skin, hair, and eye pigmentation in Europeans during the last 5,000 y | journal=Proceedings of the National Academy of Sciences | pages=4832–4837 | year=2014 | last1 = Wilde | first1 = Sandra| pmc=3977302 | bibcode=2014PNAS..111.4832W | doi-access=free }}</ref> |
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Haplogroup T has also been found among [[Iberomaurusian]] specimens dating from the [[Epipaleolithic]] at the [[Mechta-Afalou|Afalou]] prehistoric site in [[Algeria]]. One ancient individual carried the T2b subclade (1/9; 11%).<ref name="Kefi2016">{{cite journal|last1=Kefi, Rym|display-authors=etal|title=On the origin of Iberomaurusians: new data based on ancient mitochondrial DNA and phylogenetic analysis of Afalou and Taforalt populations|journal=Mitochondrial DNA Part A|year=2018|volume=29|issue=1|pages=147–157|doi=10.1080/24701394.2016.1258406|pmid=28034339|s2cid=4490910}}</ref> Additionally, haplogroup T has been observed among [[ancient Egypt]]ian mummies excavated at the [[Abusir|Abusir el-Meleq]] archaeological site in Middle Egypt, which date from the Pre-[[Ptolemaic Kingdom|Ptolemaic]]/late [[New Kingdom of Egypt|New Kingdom]] (T1, T2), Ptolemaic (T1, T2), and [[Egypt (Roman province)|Roman]] (undifferentiated T, T1) periods.<ref>{{cite journal|last1=Schuenemann, Verena J.|display-authors=etal|title=Ancient Egyptian mummy genomes suggest an increase of Sub-Saharan African ancestry in post-Roman periods|journal=Nature Communications|date=2017|volume=8|page=15694|pmid=28556824|doi=10.1038/ncomms15694|pmc=5459999|bibcode=2017NatCo...815694S}}</ref> 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.<ref>{{cite |
Haplogroup T has also been found among [[Iberomaurusian]] specimens dating from the [[Epipaleolithic]] at the [[Mechta-Afalou|Afalou]] prehistoric site in [[Algeria]]. One ancient individual carried the T2b subclade (1/9; 11%).<ref name="Kefi2016">{{cite journal|last1=Kefi, Rym|display-authors=etal|title=On the origin of Iberomaurusians: new data based on ancient mitochondrial DNA and phylogenetic analysis of Afalou and Taforalt populations|journal=Mitochondrial DNA Part A|year=2018|volume=29|issue=1|pages=147–157|doi=10.1080/24701394.2016.1258406|pmid=28034339|s2cid=4490910}}</ref> Additionally, haplogroup T has been observed among [[ancient Egypt]]ian mummies excavated at the [[Abusir|Abusir el-Meleq]] archaeological site in Middle Egypt, which date from the Pre-[[Ptolemaic Kingdom|Ptolemaic]]/late [[New Kingdom of Egypt|New Kingdom]] (T1, T2), Ptolemaic (T1, T2), and [[Egypt (Roman province)|Roman]] (undifferentiated T, T1) periods.<ref>{{cite journal|last1=Schuenemann, Verena J.|display-authors=etal|title=Ancient Egyptian mummy genomes suggest an increase of Sub-Saharan African ancestry in post-Roman periods|journal=Nature Communications|date=2017|volume=8|page=15694|pmid=28556824|doi=10.1038/ncomms15694|pmc=5459999|bibcode=2017NatCo...815694S}}</ref> 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.<ref>{{cite bioRxiv |last1=Fregel |display-authors=etal |year=2018 |title=Ancient genomes from North Africa evidence prehistoric migrations to the Maghreb from both the Levant and Europe <!-- unsupported parameter |url=https://www.biorxiv.org/content/early/2018/02/20/191569.full.pdf --> |biorxiv=10.1101/191569}}</ref> Additionally, haplogroup T has been observed in ancient [[Guanches|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%).<ref>{{cite journal|last1=Rodrı́guez-Varela|display-authors=etal|title=Genomic Analyses of Pre-European Conquest Human Remains from the Canary Islands Reveal Close Affinity to Modern North Africans|journal=Current Biology|date=2017|volume=27|issue=1–7|doi=10.1016/j.cub.2017.09.059|pmid=29107554|pages=3396–3402.e5|doi-access=free|hdl=2164/13526|hdl-access=free}}</ref> |
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===Africa=== |
===Africa=== |
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In Africa, haplogroup T is primarily found among [[Afroasiatic languages|Afro-Asiatic]]-speaking populations, including the basal T* clade.<ref name="Bekada2015"/> Some non-basal T clades are also commonly found among the [[Niger-Congo languages|Niger-Congo]]-speaking [[Serer people|Serer]] due to diffusion from the [[Maghreb]], likely with the spread of Islam |
In Africa, haplogroup T is primarily found among [[Afroasiatic languages|Afro-Asiatic]]-speaking populations, including the basal T* clade.<ref name="Bekada2015"/> Some non-basal T clades are also commonly found among the [[Niger-Congo languages|Niger-Congo]]-speaking [[Serer people|Serer]] due to diffusion from the [[Maghreb]], likely with the spread of Islam.<ref>{{cite book|last1=Ball|first1=Edward|title=The Genetic Strand: Exploring a Family History Through DNA|date=2007|publisher=Simon and Schuster|page=233|isbn=978-1416554257|url=https://books.google.com/books?id=cj8_GbJhY6sC|access-date=31 May 2016}}</ref> |
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{|class="wikitable sortable collapsible" |
{|class="wikitable sortable collapsible" |
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!scope="col" |'''Population''' |
!scope="col" |'''Population''' |
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***T1a |
***T1a |
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****T1a1 |
****T1a1 |
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****T1a2 |
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***T1b |
***T1b |
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**T2 |
**T2 |
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==Health issues== |
==Health issues== |
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One study has shown Haplogroup T to be associated with increased risk for [[coronary artery disease]] |
One study has shown Haplogroup T to be associated with increased risk for [[coronary artery disease]].{{CN|date=May 2023}} However, some studies have also shown that people of Haplogroup T are less prone to [[diabetes]] ({{harvnb|Chinnery|2007}} and {{harvnb|González|2012}}). |
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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|date=August 2019}} |
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|date=August 2019}} |
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One study has found that among the Spanish population, |
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.<ref name="Castro et al">{{cite journal|last1=Castro|first1=M|title=Mitochondrial DNA haplogroups in Spanish patients with hypertrophic cardiomyopathy. |pmid=16313983|doi=10.1016/j.ijcard.2005.09.008|volume=112|issue=2|pages=202–6|journal=Int J Cardiol|year=2006}}</ref> 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.<ref name="Chen 2014">{{cite web|last1=Chen|first1=Michael|title=Hypertrophic cardiomyopathy - Medical Encyclopedia|url=https://www.nlm.nih.gov/medlineplus/ency/article/000192.htm|website=Medline Plus|publisher=National Library of Medicine|access-date=2015-10-03}}</ref> |
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Certain medical studies had shown mitochondrial Haplogroup T to be associated with reduced [[sperm motility]] in males, although these results have been challenged {{harv|Mishmar|2002}}. According to the Departamento de Bioquimica y Biologica Molecular y Celular, Universidad de Zaragoza, Haplogroup T can predispose to [[asthenozoospermia]] {{harv|Ruiz-Pesini|2000}}. However, these findings have been disputed due to a small sample size in the study {{harv|Mishmar|2002}}. |
Certain medical studies had shown mitochondrial Haplogroup T to be associated with reduced [[sperm motility]] in males, although these results have been challenged {{harv|Mishmar|2002}}. According to the Departamento de Bioquimica y Biologica Molecular y Celular, Universidad de Zaragoza, Haplogroup T can predispose to [[asthenozoospermia]] {{harv|Ruiz-Pesini|2000}}. However, these findings have been disputed due to a small sample size in the study {{harv|Mishmar|2002}}. |
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==Famous members== |
==Famous members== |
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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.<ref>{{cite AV media|title= Meet the Izzards: The Mum's Line |publisher= [[BBC One]] |minutes= 48 |date= 2013-03-12}}</ref> |
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.<ref>{{cite AV media|title= Meet the Izzards: The Mum's Line |publisher= [[BBC One]] |minutes= 48 |date= 2013-03-12}}</ref> |
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[[Henry Louis Gates Jr.]] belongs to haplogroup T2b2.<ref>{{cite book |last=Gates Jr.|first=Henry Louis|page=4|date=2010|title=Faces of America: How 12 Extraordinary People Discovered Their Pasts|publisher=New York University Press}}</ref> |
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===Nicholas II of Russia=== |
===Nicholas II of Russia=== |
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*[[Human mitochondrial molecular clock]] |
*[[Human mitochondrial molecular clock]] |
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*[[Mitochondrial Eve]] |
*[[Mitochondrial Eve]] |
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*[[mtDna haplogroups by populations|mtDNA Haplogroups by Populations]] |
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*[[Population genetics]] |
*[[Population genetics]] |
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<references /> |
<references /> |
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===Sources=== |
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*{{cite journal|last1=Hartmann|year=2009|ref={{harvid|Hartmann|2009}}|doi=10.1002/humu.20816|pmid=18623076|first1=A|last2=Thieme|first2=M|last3=Nanduri|first3=LK|last4=Stempfl|first4=T|last5=Moehle|first5=C|last6=Kivisild|first6=T|last7=Oefner|first7=PJ|title=Validation of microarray-based resequencing of 93 worldwide mitochondrial genomes|volume=30|issue=1|pages=115–22|journal=Human Mutation|s2cid=205918494}} |
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*{{cite web|last1=Hassan|first1=Hisham Yousif|year=2009|title=Genetic Patterns of Y-chromosome and Mitochondrial DNA Variation, with Implications to the Peopling of the Sudan|url=http://khartoumspace.uofk.edu/bitstream/handle/123456789/6376/Genetic%20Patterns%20of%20Y-chromosome%20and%20Mitochondrial.pdf?sequence=1|publisher=University of Khartoum|access-date=2016-04-18|archive-date=2020-11-10|archive-url=https://web.archive.org/web/20201110063820/http://khartoumspace.uofk.edu/handle/123456789/6376/restricted-resource?bitstreamId=11199|url-status=dead}} |
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*{{cite journal|last1=Helgason|year=2001|ref={{harvid|Helgason|2001}}|doi=10.1086/318785|title=mtDNA and the Islands of the North Atlantic: Estimating the Proportions of Norse and Gaelic Ancestry|first1=Agnar|last2=Hickey|first2=Eileen|last3=Goodacre|first3=Sara|last4=Bosnes|first4=Vidar|last5=Stefánsson|first5=Kári|last6=Ward|first6=Ryk|last7=Sykes|first7=Bryan|journal=The American Journal of Human Genetics|volume=68|issue=3|pages=206–15|pmc=1274484|pmid=11179019}} |
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*{{cite journal|last1=Hofreiter|year=2010|ref={{harvid|Hofreiter|2010}}|doi=10.1371/journal.pone.0011898|quote=The overall occurrence of haplogroups did not deviate from extant Scandinavians, however, haplogroup I was significantly more frequent among the ancient Danes (average 13%) than among extant Danes and Scandinavians (~2.5%) as well as among other ancient population samples reported. Haplogroup I could therefore have been an ancient Southern Scandinavian type “diluted” by later immigration events.|title=Genetic Diversity among Ancient Nordic Populations|editor1-last=Hofreiter|editor1-first=Michael|first1=Linea|last2=Lynnerup|first2=Niels|last3=Siegismund|first3=Hans R.|last4=Kivisild|first4=Toomas|last5=Dissing|first5=Jørgen|journal=PLOS ONE|volume=5|issue=7|pages=e11898|pmid=20689597|pmc=2912848|bibcode=2010PLoSO...511898M}} |
*{{cite journal|last1=Hofreiter|year=2010|ref={{harvid|Hofreiter|2010}}|doi=10.1371/journal.pone.0011898|quote=The overall occurrence of haplogroups did not deviate from extant Scandinavians, however, haplogroup I was significantly more frequent among the ancient Danes (average 13%) than among extant Danes and Scandinavians (~2.5%) as well as among other ancient population samples reported. Haplogroup I could therefore have been an ancient Southern Scandinavian type “diluted” by later immigration events.|title=Genetic Diversity among Ancient Nordic Populations|editor1-last=Hofreiter|editor1-first=Michael|first1=Linea|last2=Lynnerup|first2=Niels|last3=Siegismund|first3=Hans R.|last4=Kivisild|first4=Toomas|last5=Dissing|first5=Jørgen|journal=PLOS ONE|volume=5|issue=7|pages=e11898|pmid=20689597|pmc=2912848|bibcode=2010PLoSO...511898M|doi-access=free}} |
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*{{cite journal|last1=Mikkelsen|year=2010|ref={{harvid|Mikkelsen|2010}}|doi=10.1016/j.fsigen.2009.07.007|pmid=20457038|title=Mitochondrial DNA HV1 and HV2 variation in Danes|first1=Martin|last2=Sørensen|first2=Erik|last3=Rasmussen|first3=Erik Michael|last4=Morling|first4=Niels|journal=Forensic Science International: Genetics|volume=4|issue=4|pages=e87–8}} |
||
*{{cite journal|last1=Mishmar|year=2003|ref={{harvid|Mishmar| |
*{{cite journal|last1=Mishmar|year=2003|ref={{harvid|Mishmar|2002}}|doi=10.1073/pnas.0136972100|pmid=12509511|first1=D|last2=Ruiz-Pesini|first2=E|last3=Golik|first3=P|last4=MacAulay|first4=V|last5=Clark|first5=AG|last6=Hosseini|first6=S|last7=Brandon|first7=M|last8=Easley|first8=K|last9=Chen|first9=E|last10=Brown|first10=M. D.|last11=Sukernik|first11=R. I.|last12=Olckers|first12=A.|last13=Wallace|first13=D. C.|title=Natural selection shaped regional mtDNA variation in humans|volume=100|issue=1|pages=171–6|pmc=140917|journal=Proceedings of the National Academy of Sciences of the United States of America|display-authors=8|bibcode=2003PNAS..100..171M|doi-access=free}} |
||
*{{cite journal|last1=Musilová|year=2011|ref={{harvid|Musilová|2011}}|doi=10.1002/ajpa.21522|title=Population history of the Red Sea-genetic exchanges between the Arabian Peninsula and East Africa signaled in the mitochondrial DNA HV1 haplogroup|first1=Eliška|last2=Fernandes|first2=Verónica|last3=Silva|first3=Nuno M.|last4=Soares|first4=Pedro|last5=Alshamali|first5=Farida|last6=Harich|first6=Nourdin|last7=Cherni|first7=Lotfi|last8=Gaaied|first8=Amel Ben Ammar El|last9=Al-Meeri|first9=Ali|last10=Pereira|first10=Luísa|last11=Černý|first11=Viktor|journal=American Journal of Physical Anthropology|volume=145|issue=4|pages=592–8|pmid=21660931|display-authors=8}} |
*{{cite journal|last1=Musilová|year=2011|ref={{harvid|Musilová|2011}}|doi=10.1002/ajpa.21522|title=Population history of the Red Sea-genetic exchanges between the Arabian Peninsula and East Africa signaled in the mitochondrial DNA HV1 haplogroup|first1=Eliška|last2=Fernandes|first2=Verónica|last3=Silva|first3=Nuno M.|last4=Soares|first4=Pedro|last5=Alshamali|first5=Farida|last6=Harich|first6=Nourdin|last7=Cherni|first7=Lotfi|last8=Gaaied|first8=Amel Ben Ammar El|last9=Al-Meeri|first9=Ali|last10=Pereira|first10=Luísa|last11=Černý|first11=Viktor|journal=American Journal of Physical Anthropology|volume=145|issue=4|pages=592–8|pmid=21660931|display-authors=8}} |
||
*{{cite journal|last1=Nikitin|year=2009|ref={{harvid|Nikitin|2009}}|doi=10.3378/027.081.0104|title=Mitochondrial DNA Sequence Variation in the Boyko, Hutsul, and Lemko Populations of the Carpathian Highlands|journal=Human Biology|first1=Alexey G.|last2=Kochkin|first2=Igor T.|last3=June|first3=Cynthia M.|last4=Willis|first4=Catherine M.|last5=McBain|first5=Ian|last6=Videiko|first6=Mykhailo Y.|volume=81|pages=43–58|pmid=19589018|issue=1|s2cid=45791162}} |
*{{cite journal|last1=Nikitin|year=2009|ref={{harvid|Nikitin|2009}}|doi=10.3378/027.081.0104|title=Mitochondrial DNA Sequence Variation in the Boyko, Hutsul, and Lemko Populations of the Carpathian Highlands|journal=Human Biology|first1=Alexey G.|last2=Kochkin|first2=Igor T.|last3=June|first3=Cynthia M.|last4=Willis|first4=Catherine M.|last5=McBain|first5=Ian|last6=Videiko|first6=Mykhailo Y.|volume=81|pages=43–58|pmid=19589018|issue=1|s2cid=45791162}} |
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*{{cite journal|last1=Richards|year=2000|ref={{harvid|Richards|2000}}|doi=10.1016/S0002-9297(07)62954-1|title=Tracing European Founder Lineages in the Near Eastern mtDNA Pool|first1=Martin|last2=MacAulay|first2=Vincent|last3=Hickey|first3=Eileen|last4=Vega|first4=Emilce|last5=Sykes|first5=Bryan|last6=Guida|first6=Valentina|last7=Rengo|first7=Chiara|last8=Sellitto|first8=Daniele|last9=Cruciani|first9=Fulvio|last10=Kivisild|first10=Toomas|last11=Villems|first11=Richard|last12=Thomas|first12=Mark|last13=Rychkov|first13=Serge|last14=Rychkov|first14=Oksana|last15=Rychkov|first15=Yuri|last16=Gölge|first16=Mukaddes|last17=Dimitrov|first17=Dimitar|last18=Hill|first18=Emmeline|last19=Bradley|first19=Dan|last20=Romano|first20=Valentino|last21=Calì|first21=Francesco|last22=Vona|first22=Giuseppe|last23=Demaine|first23=Andrew|last24=Papiha|first24=Surinder|last25=Triantaphyllidis|first25=Costas|last26=Stefanescu|first26=Gheorghe|last27=Hatina|first27=Jiři|last28=Belledi|first28=Michele|last29=Di Rienzo|first29=Anna|last30=Novelletto|first30=Andrea|journal=The American Journal of Human Genetics|volume=67|issue=5|pages=1251–76|pmid=11032788|pmc=1288566|display-authors=8}} |
*{{cite journal|last1=Richards|year=2000|ref={{harvid|Richards|2000}}|doi=10.1016/S0002-9297(07)62954-1|title=Tracing European Founder Lineages in the Near Eastern mtDNA Pool|first1=Martin|last2=MacAulay|first2=Vincent|last3=Hickey|first3=Eileen|last4=Vega|first4=Emilce|last5=Sykes|first5=Bryan|last6=Guida|first6=Valentina|last7=Rengo|first7=Chiara|last8=Sellitto|first8=Daniele|last9=Cruciani|first9=Fulvio|last10=Kivisild|first10=Toomas|last11=Villems|first11=Richard|last12=Thomas|first12=Mark|last13=Rychkov|first13=Serge|last14=Rychkov|first14=Oksana|last15=Rychkov|first15=Yuri|last16=Gölge|first16=Mukaddes|last17=Dimitrov|first17=Dimitar|last18=Hill|first18=Emmeline|last19=Bradley|first19=Dan|last20=Romano|first20=Valentino|last21=Calì|first21=Francesco|last22=Vona|first22=Giuseppe|last23=Demaine|first23=Andrew|last24=Papiha|first24=Surinder|last25=Triantaphyllidis|first25=Costas|last26=Stefanescu|first26=Gheorghe|last27=Hatina|first27=Jiři|last28=Belledi|first28=Michele|last29=Di Rienzo|first29=Anna|last30=Novelletto|first30=Andrea|journal=The American Journal of Human Genetics|volume=67|issue=5|pages=1251–76|pmid=11032788|pmc=1288566|display-authors=8}} |
||
*{{cite journal|last1=Richards|year=2003|ref={{harvid|Richards|2003}}|doi=10.1086/374384|title=Extensive Female-Mediated Gene Flow from Sub-Saharan Africa into Near Eastern Arab Populations|first1=Martin|last2=Rengo|first2=Chiara|last3=Cruciani|first3=Fulvio|last4=Gratrix|first4=Fiona|last5=Wilson|first5=James F.|last6=Scozzari|first6=Rosaria|last7=MacAulay|first7=Vincent|last8=Torroni|first8=Antonio|journal=The American Journal of Human Genetics|volume=72|issue=4|pages=1058–64|pmid=12629598|pmc=1180338}} |
*{{cite journal|last1=Richards|year=2003|ref={{harvid|Richards|2003}}|doi=10.1086/374384|title=Extensive Female-Mediated Gene Flow from Sub-Saharan Africa into Near Eastern Arab Populations|first1=Martin|last2=Rengo|first2=Chiara|last3=Cruciani|first3=Fulvio|last4=Gratrix|first4=Fiona|last5=Wilson|first5=James F.|last6=Scozzari|first6=Rosaria|last7=MacAulay|first7=Vincent|last8=Torroni|first8=Antonio|journal=The American Journal of Human Genetics|volume=72|issue=4|pages=1058–64|pmid=12629598|pmc=1180338}} |
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*{{cite journal|last1=Rogaev|year=2009|doi=10.1073/pnas.0811190106|pmid=19251637|pmc=2664067|title=Genomic identification in the historical case of the Nicholas II royal family|first1=E. I.|last2=Grigorenko|first2=A. P.|last3=Moliaka|first3=Y. K.|last4=Faskhutdinova|first4=G.|last5=Goltsov|first5=A.|last6=Lahti|first6=A.|last7=Hildebrandt|first7=C.|last8=Kittler|first8=E. L. W.|last9=Morozova|first9=I.|journal=Proceedings of the National Academy of Sciences|volume=106|issue=13|pages=5258–63|bibcode=2009PNAS..106.5258R}} |
*{{cite journal|last1=Rogaev|year=2009|doi=10.1073/pnas.0811190106|pmid=19251637|pmc=2664067|title=Genomic identification in the historical case of the Nicholas II royal family|first1=E. I.|last2=Grigorenko|first2=A. P.|last3=Moliaka|first3=Y. K.|last4=Faskhutdinova|first4=G.|last5=Goltsov|first5=A.|last6=Lahti|first6=A.|last7=Hildebrandt|first7=C.|last8=Kittler|first8=E. L. W.|last9=Morozova|first9=I.|journal=Proceedings of the National Academy of Sciences|volume=106|issue=13|pages=5258–63|bibcode=2009PNAS..106.5258R|doi-access=free}} |
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*{{cite journal|last1=Ruiz-Pesini|year=2000|doi=10.1086/303040|pmid=10936107|pmc=1287528|title=Human mtDNA Haplogroups Associated with High or Reduced Spermatozoa Motility|first1=Eduardo|last2=Lapeña|first2=Ana-Cristina|last3=Díez-Sánchez|first3=Carmen|last4=Pérez-Martos|first4=Acisclo|last5=Montoya|first5=Julio|last6=Alvarez|first6=Enrique|last7=Díaz|first7=Miguel|last8=Urriés|first8=Antonio|last9=Montoro|first9=Luis|last10=López-Pérez|first10=Manuel J.|last11=Enríquez|first11=José A.|journal=The American Journal of Human Genetics|volume=67|issue=3|pages=682–96|display-authors=8}} |
*{{cite journal |ref={{harvid|Ruiz-Pesini|2000}} |last1=Ruiz-Pesini|year=2000|doi=10.1086/303040|pmid=10936107|pmc=1287528|title=Human mtDNA Haplogroups Associated with High or Reduced Spermatozoa Motility|first1=Eduardo|last2=Lapeña|first2=Ana-Cristina|last3=Díez-Sánchez|first3=Carmen|last4=Pérez-Martos|first4=Acisclo|last5=Montoya|first5=Julio|last6=Alvarez|first6=Enrique|last7=Díaz|first7=Miguel|last8=Urriés|first8=Antonio|last9=Montoro|first9=Luis|last10=López-Pérez|first10=Manuel J.|last11=Enríquez|first11=José A.|journal=The American Journal of Human Genetics|volume=67|issue=3|pages=682–96|display-authors=8}} |
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*{{cite journal|last1=Shlush|year=2008|ref={{harvid|Shlush|2008}}|doi=10.1371/journal.pone.0002105|title=The Druze: A Population Genetic Refugium of the Near East|editor1-last=Gemmell|editor1-first=Neil John|first1=Liran I.|last2=Behar|first2=Doron M.|last3=Yudkovsky|first3=Guennady|last4=Templeton|first4=Alan|last5=Hadid|first5=Yarin|last6=Basis|first6=Fuad|last7=Hammer|first7=Michael|last8=Itzkovitz|first8=Shalev|last9=Skorecki|first9=Karl|journal=PLOS ONE|volume=3|issue=5|pages=e2105|pmid=18461126|pmc=2324201|bibcode=2008PLoSO...3.2105S}} |
*{{cite journal|last1=Shlush|year=2008|ref={{harvid|Shlush|2008}}|doi=10.1371/journal.pone.0002105|title=The Druze: A Population Genetic Refugium of the Near East|editor1-last=Gemmell|editor1-first=Neil John|first1=Liran I.|last2=Behar|first2=Doron M.|last3=Yudkovsky|first3=Guennady|last4=Templeton|first4=Alan|last5=Hadid|first5=Yarin|last6=Basis|first6=Fuad|last7=Hammer|first7=Michael|last8=Itzkovitz|first8=Shalev|last9=Skorecki|first9=Karl|journal=PLOS ONE|volume=3|issue=5|pages=e2105|pmid=18461126|pmc=2324201|bibcode=2008PLoSO...3.2105S|doi-access=free}} |
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*{{cite journal|last1=Soares|year=2011|ref={{harvid|Soares|2011}}|doi=10.1093/molbev/msr245|title=The Expansion of mtDNA Haplogroup L3 within and out of Africa|first1=P.|last2=Alshamali|first2=F.|last3=Pereira|first3=J. B.|last4=Fernandes|first4=V.|last5=Silva|first5=N. M.|last6=Afonso|first6=C.|last7=Costa|first7=M. D.|last8=Musilova|first8=E.|last9=MacAulay|first9=V.|last10=Richards|first10=M. B.|last11=Cerny|first11=V.|last12=Pereira|first12=L.|journal=Molecular Biology and Evolution|volume=29|issue=3|pages=915–27|pmid=22096215|display-authors=8|doi-access=free}} |
*{{cite journal|last1=Soares|year=2011|ref={{harvid|Soares|2011}}|doi=10.1093/molbev/msr245|title=The Expansion of mtDNA Haplogroup L3 within and out of Africa|first1=P.|last2=Alshamali|first2=F.|last3=Pereira|first3=J. B.|last4=Fernandes|first4=V.|last5=Silva|first5=N. M.|last6=Afonso|first6=C.|last7=Costa|first7=M. D.|last8=Musilova|first8=E.|last9=MacAulay|first9=V.|last10=Richards|first10=M. B.|last11=Cerny|first11=V.|last12=Pereira|first12=L.|journal=Molecular Biology and Evolution|volume=29|issue=3|pages=915–27|pmid=22096215|display-authors=8|doi-access=free}} |
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*{{cite journal|last1=Stanger|year=2007|doi=10.1016/j.mito.2007.08.034|title=30 Mitochondrial haplogroup T is associated with coronary artery disease|first1=Olaf|last2=Müller|first2=Edith|last3=Zimmermann|first3=Franz|last4=Wiesbauer|first4=Martina|last5=Mayr|first5=Johannes A.|last6=Paulweber|first6=Bernhard|last7=Iglseder|first7=Bernhard|last8=Renner|first8=Wilfried|last9=Eder|first9=Waltraud|last10=Kofler|first10=Barbara|journal=Mitochondrion|volume=7|issue=6|pages=412|display-authors=8}} |
*{{cite journal|last1=Stanger|year=2007|doi=10.1016/j.mito.2007.08.034|title=30 Mitochondrial haplogroup T is associated with coronary artery disease|first1=Olaf|last2=Müller|first2=Edith|last3=Zimmermann|first3=Franz|last4=Wiesbauer|first4=Martina|last5=Mayr|first5=Johannes A.|last6=Paulweber|first6=Bernhard|last7=Iglseder|first7=Bernhard|last8=Renner|first8=Wilfried|last9=Eder|first9=Waltraud|last10=Kofler|first10=Barbara|journal=Mitochondrion|volume=7|issue=6|pages=412|display-authors=8}} |
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*{{cite journal|last1=Tishkoff|year=2007|ref={{harvid|Tishkoff|2007}}|doi=10.1093/molbev/msm155|pmid=17656633|title=History of Click-Speaking Populations of Africa Inferred from mtDNA and Y Chromosome Genetic Variation|first1=S. A.|last2=Gonder|first2=M. K.|last3=Henn|first3=B. M.|last4=Mortensen|first4=H.|last5=Knight|first5=A.|last6=Gignoux|first6=C.|last7=Fernandopulle|first7=N.|last8=Lema|first8=G.|last9=Nyambo|first9=T. B.|last10=Ramakrishnan|first10=U.|last11=Reed|first11=F. A.|last12=Mountain|first12=J. L.|journal=Molecular Biology and Evolution|volume=24|issue=10|pages=2180–95|display-authors=8|doi-access=free}} |
*{{cite journal|last1=Tishkoff|year=2007|ref={{harvid|Tishkoff|2007}}|doi=10.1093/molbev/msm155|pmid=17656633|title=History of Click-Speaking Populations of Africa Inferred from mtDNA and Y Chromosome Genetic Variation|first1=S. A.|last2=Gonder|first2=M. K.|last3=Henn|first3=B. M.|last4=Mortensen|first4=H.|last5=Knight|first5=A.|last6=Gignoux|first6=C.|last7=Fernandopulle|first7=N.|last8=Lema|first8=G.|last9=Nyambo|first9=T. B.|last10=Ramakrishnan|first10=U.|last11=Reed|first11=F. A.|last12=Mountain|first12=J. L.|journal=Molecular Biology and Evolution|volume=24|issue=10|pages=2180–95|display-authors=8|doi-access=free}} |
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*{{cite journal|last1=Topf|year=2005|ref={{harvid|Topf|2005}}|doi=10.1093/molbev/msj013|title=Tracing the Phylogeography of Human Populations in Britain Based on 4th-11th Century mtDNA Genotypes|first1=A. L.|journal=Molecular Biology and Evolution|volume=23|pages=152–61|pmid=16151183|last2=Gilbert|first2=MT|last3=Dumbacher|first3=JP|last4=Hoelzel|first4=AR|issue=1|doi-access=free}} |
*{{cite journal|last1=Topf|year=2005|ref={{harvid|Topf|2005}}|doi=10.1093/molbev/msj013|title=Tracing the Phylogeography of Human Populations in Britain Based on 4th-11th Century mtDNA Genotypes|first1=A. L.|journal=Molecular Biology and Evolution|volume=23|pages=152–61|pmid=16151183|last2=Gilbert|first2=MT|last3=Dumbacher|first3=JP|last4=Hoelzel|first4=AR|issue=1|doi-access=free}} |
||
*{{cite journal|last1=Torroni|year=1996|ref={{harvid|Torroni|1996}}|title=Classification of European mtDNAs From an Analysis of Three European Populations|journal=Genetics|pmid=8978068|first1=A|last2=Huoponen|first2=K|last3=Francalacci|first3=P|last4=Petrozzi|first4=M|last5=Morelli|first5=L|last6=Scozzari|first6=R|last7=Obinu|first7=D|last8=Savontaus|first8=ML|last9=Wallace|first9=DC|volume=144|issue=4|pages=1835–50|pmc=1207732}} |
*{{cite journal|last1=Torroni|year=1996|ref={{harvid|Torroni|1996}}|title=Classification of European mtDNAs From an Analysis of Three European Populations|journal=Genetics|pmid=8978068|first1=A|last2=Huoponen|first2=K|last3=Francalacci|first3=P|last4=Petrozzi|first4=M|last5=Morelli|first5=L|last6=Scozzari|first6=R|last7=Obinu|first7=D|last8=Savontaus|first8=ML|last9=Wallace|first9=DC|volume=144|issue=4|pages=1835–50|doi=10.1093/genetics/144.4.1835|pmc=1207732}} |
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*{{cite journal|last1=van Oven|year=2009|ref={{harvid|van Oven| |
*{{cite journal|last1=van Oven|year=2009|ref={{harvid|van Oven|2008}}|doi=10.1002/humu.20921|title=Updated comprehensive phylogenetic tree of global human mitochondrial DNA variation|first1=Mannis|last2=Kayser|first2=Manfred|journal=Human Mutation|volume=30|issue=2|pages=E386–94|pmid=18853457|s2cid=27566749|doi-access=free}} |
||
<!-- Per Richards et al. (2006), Watson et al. (1997) made a statistical error, as it "was based largely on control-region sequence data, which fails to resolve many mtDNA haplogroups" -- see Non (2010) for the actual relative frequencies: http://etd.fcla.edu/UF/UFE0041981/non_a.pdf --> |
<!-- Per Richards et al. (2006), Watson et al. (1997) made a statistical error, as it "was based largely on control-region sequence data, which fails to resolve many mtDNA haplogroups" -- see Non (2010) for the actual relative frequencies: http://etd.fcla.edu/UF/UFE0041981/non_a.pdf --> |
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====Websites==== |
====Websites==== |
||
*{{cite web|last1=Behar|last2=Family Tree DNA|year=2012|ref={{harvid|Behar and Family Tree DNA|2012}}|title=mtDNA Community|url=http://www.mtdnacommunity.org/human-mtdna-phylogeny.aspx}} |
*{{cite web|last1=Behar|last2=Family Tree DNA|year=2012|ref={{harvid|Behar and Family Tree DNA|2012}}|title=mtDNA Community|url=http://www.mtdnacommunity.org/human-mtdna-phylogeny.aspx|access-date=2013-01-12|archive-date=2018-01-02|archive-url=https://web.archive.org/web/20180102091357/http://www.mtdnacommunity.org/human-mtdna-phylogeny.aspx|url-status=dead}} |
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===Further reading=== |
===Further reading=== |
||
*{{cite journal|last1=Černý|year=2009|ref={{harv|Černý|2009}}|doi=10.1002/ajpa.20960|title=Out of Arabia-The settlement of Island Soqotra as revealed by mitochondrial and Y chromosome genetic diversity|first1=Viktor|last2=Pereira|first2=Luísa|last3=Kujanová|first3=Martina|last4=VašÍková|first4=Alžběta|last5=Hájek|first5=Martin|last6=Morris|first6=Miranda|last7=Mulligan|first7=Connie J.|journal=American Journal of Physical Anthropology|volume=138|issue=4|pages=439–47|pmid=19012329}} |
*{{cite journal|last1=Černý|year=2009|ref={{harv|Černý|2009}}|doi=10.1002/ajpa.20960|title=Out of Arabia-The settlement of Island Soqotra as revealed by mitochondrial and Y chromosome genetic diversity|first1=Viktor|last2=Pereira|first2=Luísa|last3=Kujanová|first3=Martina|last4=VašÍková|first4=Alžběta|last5=Hájek|first5=Martin|last6=Morris|first6=Miranda|last7=Mulligan|first7=Connie J.|journal=American Journal of Physical Anthropology|volume=138|issue=4|pages=439–47|pmid=19012329}} |
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*{{cite journal|last1=Kitchen|year=2009|doi=10.1098/rspb.2009.0408|title=Bayesian phylogenetic analysis of Semitic languages identifies an Early Bronze Age origin of Semitic in the Near East|first1=A.|last2=Ehret|first2=C.|last3=Assefa|first3=S.|last4=Mulligan|first4=C. J.|journal=Proceedings of the Royal Society B: Biological Sciences|volume=276|issue=1668|pages=2703–10|pmid=19403539|pmc=2839953}} |
*{{cite journal|last1=Kitchen|year=2009|doi=10.1098/rspb.2009.0408|title=Bayesian phylogenetic analysis of Semitic languages identifies an Early Bronze Age origin of Semitic in the Near East|first1=A.|last2=Ehret|first2=C.|last3=Assefa|first3=S.|last4=Mulligan|first4=C. J.|journal=Proceedings of the Royal Society B: Biological Sciences|volume=276|issue=1668|pages=2703–10|pmid=19403539|pmc=2839953}} |
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*{{cite journal|last1=Petit-Maire|year=2000|doi=10.18814/epiiugs/2000/v23i4/001|title=Geological records of the recent past, a key to the near future world environments|first1=Nicole|journal=Episodes|volume=23|issue=4|pages=230–246|last2=Bouysse|first2=Philippe|url=http://www.episodes.co.in/www/backissues/234/230-246%20Petit.pdf}} |
*{{cite journal|last1=Petit-Maire|year=2000|doi=10.18814/epiiugs/2000/v23i4/001|title=Geological records of the recent past, a key to the near future world environments|first1=Nicole|journal=Episodes|volume=23|issue=4|pages=230–246|last2=Bouysse|first2=Philippe|url=http://www.episodes.co.in/www/backissues/234/230-246%20Petit.pdf|doi-access=free}} |
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==External links== |
==External links== |
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**[https://web.archive.org/web/20080405220810/https://www3.nationalgeographic.com/genographic/pdf/PLOS_paper.pdf The Genographic Project Public Participation Mitochondrial DNA Database] |
**[https://web.archive.org/web/20080405220810/https://www3.nationalgeographic.com/genographic/pdf/PLOS_paper.pdf The Genographic Project Public Participation Mitochondrial DNA Database] |
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*'''Haplogroup T''' |
*'''Haplogroup T''' |
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**YFull MTree's [https://www.yfull.com/mtree/T/ Haplogroup T] |
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**[http://lists.rootsweb.ancestry.com/index/other/DNA/MTDNA-HAPLOGROUP-T.html Discussion List at RootsWeb] |
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**MITOMAP's [https://mitomap.org/cgi-bin/haplo_distribution?hg=T Haplogroup T] |
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**[[Family TreeDNA]]'s mtDNA Haplotree: [https://www.familytreedna.com/public/mt-dna-haplotree/T Haplogroup T] |
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**[https://web.archive.org/web/20061117000120/https://www3.nationalgeographic.com/genographic/atlas.html?card=mm019 Spread of Haplogroup T], from [[National Geographic (magazine)|National Geographic]] |
**[https://web.archive.org/web/20061117000120/https://www3.nationalgeographic.com/genographic/atlas.html?card=mm019 Spread of Haplogroup T], from [[National Geographic (magazine)|National Geographic]] |
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**[ |
**[https://web.archive.org/web/20090211131223/https://www.jengod.com/genealogy/family/genetic.html Genetic Genealogy: A Personal Perspective on Tara, Karelians and Kent, England] |
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**[http://www.u.arizona.edu/~bedford/mitochondrialdna%20for%20posting.htm Analysis of a Haplogroup T sequence (T5/T2)] |
**[http://www.u.arizona.edu/~bedford/mitochondrialdna%20for%20posting.htm Analysis of a Haplogroup T sequence (T5/T2)] |
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**[http://www.jogg.info/21/Pike.html Phylogenetic Networks for the Human mtDNA Haplogroup T] |
**[http://www.jogg.info/21/Pike.html Phylogenetic Networks for the Human mtDNA Haplogroup T] {{Webarchive|url=https://web.archive.org/web/20080531032822/http://www.jogg.info/21/Pike.html |date=2008-05-31 }} |
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**[http://www.familytreedna.com/public/T_FGS/default.aspx mtDNA Haplogroup T - Full Genomic Sequence Research Project] |
**[http://www.familytreedna.com/public/T_FGS/default.aspx mtDNA Haplogroup T - Full Genomic Sequence Research Project] |
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[[Category:Human mtDNA haplogroups|T]] |
[[Category:Human mtDNA haplogroups|T]] |
Revision as of 05:27, 23 August 2024
Haplogroup T | |
---|---|
Possible time of origin | 25,149 ± 4,668 years before present |
Possible place of origin | Near East, and/or Caucasus |
Ancestor | JT |
Descendants | T1 and T2 |
Defining mutations | G709A, 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
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]
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
Tree
This phylogenetic tree of haplogroup I subclades is based on the paper (van Oven 2008) and subsequent published research (Behar 2012b). For brevity, only the first three levels of subclades (branches) are shown.
- T
- T1
- T1a
- T1a1
- T1a2
- T1b
- T1a
- T2
- T2a
- T2a1
- T2b
- T2b1
- T2b2
- T2b3
- T2b4
- T2b5
- T2b6
- T2c
- T2c1
- T2d
- T2e
- T2e2
- T2f
- T2f1
- T2g
- T2a
- T1
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 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 |
References
Footnotes
Citations
- ^ a b 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
- ^ a b 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.
- ^ Bryan Sykes (2001). The Seven Daughters of Eve. London; New York: Bantam Press. ISBN 978-0393020182.
- ^ "Maternal Ancestry". Oxford Ancestors. Archived from the original on 15 July 2017. Retrieved 7 February 2013.
- ^ 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.
- ^ 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
- ^ 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.
- ^ 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.
- ^ 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.
- ^ 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.
- ^ 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.
- ^ Ball, Edward (2007). The Genetic Strand: Exploring a Family History Through DNA. Simon and Schuster. p. 233. ISBN 978-1416554257. Retrieved 31 May 2016.
- ^ 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.
- ^ Chen, Michael. "Hypertrophic cardiomyopathy - Medical Encyclopedia". Medline Plus. National Library of Medicine. Retrieved 2015-10-03.
- ^ Meet the Izzards: The Mum's Line. BBC One. 2013-03-12. 48 minutes in.
- ^ Gates Jr., Henry Louis (2010). Faces of America: How 12 Extraordinary People Discovered Their Pasts. New York University Press. p. 4.
Sources
- Pike DA, Barton TJ, Bauer SL, Kipp E (2010). "mtDNA Haplogroup T Phylogeny Based on Full Mitochondrial Sequences". Journal of Genetic Genealogy. 6 (1). Archived from the original on 2016-04-22. Retrieved 2011-10-19.
- Malyarchuk, B. A.; Derenko, M. V. (November 1999). "Molecular instability of the mitochondrial haplogroup T sequences at nucleotide positions 16292 and 16296". Annals of Human Genetics. 63 (6): 489–497. doi:10.1017/S0003480099007794. PMID 11246451.
- Abu-Amero, Khaled K; Larruga, José M; Cabrera, Vicente M; González, Ana M (2008). "Mitochondrial DNA structure in the Arabian Peninsula". BMC Evolutionary Biology. 8 (1): 45. Bibcode:2008BMCEE...8...45A. doi:10.1186/1471-2148-8-45. PMC 2268671. PMID 18269758.
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- Bedford, Felice L (2012). "Sephardic signature in haplogroup T mitochondrial DNA". European Journal of Human Genetics. 20 (4): 441–8. doi:10.1038/ejhg.2011.200. PMC 3306851. PMID 22108605.
- Behar, DM; Metspalu, E; Kivisild, T; Rosset, S; Tzur, S; Hadid, Y; Yudkovsky, G; Rosengarten, D; et al. (2008). MacAulay, Vincent (ed.). "Counting the founders: The matrilineal genetic ancestry of the Jewish Diaspora". PLOS ONE. 3 (4): e2062. Bibcode:2008PLoSO...3.2062B. doi:10.1371/journal.pone.0002062. PMC 2323359. PMID 18446216.
- Behar, Doron M.; Van Oven, Mannis; Rosset, Saharon; Metspalu, Mait; Loogväli, Eva-Liis; Silva, Nuno M.; Kivisild, Toomas; Torroni, Antonio; Villems, Richard (2012). "A "Copernican" Reassessment of the Human Mitochondrial DNA Tree from its Root". The American Journal of Human Genetics. 90 (4): 675–84. doi:10.1016/j.ajhg.2012.03.002. PMC 3322232. PMID 22482806.
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- Bosch, E.; Calafell, F.; Gonzalez-Neira, A.; Flaiz, C.; Mateu, E.; Scheil, H.-G.; Huckenbeck, W.; Efremovska, L.; et al. (2006). "Paternal and maternal lineages in the Balkans show a homogeneous landscape over linguistic barriers, except for the isolated Aromuns". Annals of Human Genetics. 70 (4): 459–87. doi:10.1111/j.1469-1809.2005.00251.x. PMID 16759179. S2CID 23156886.
- Brandstatter, Anita; Peterson, Christine T.; Irwin, Jodi A.; Mpoke, Solomon; Koech, Davy K.; Parson, Walther; Parsons, Thomas J. (2004). "Mitochondrial DNA control region sequences from Nairobi (Kenya): Inferring phylogenetic parameters for the establishment of a forensic database". International Journal of Legal Medicine. 118 (5): 294–306. doi:10.1007/s00414-004-0466-z. PMID 15248073. S2CID 19703169.
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- Castrì, Loredana; Tofanelli, Sergio; Garagnani, Paolo; Bini, Carla; Fosella, Xenia; Pelotti, Susi; Paoli, Giorgio; Pettener, Davide; Luiselli, Donata (2009). "MtDNA variability in two Bantu-speaking populations (Shona and Hutu) from Eastern Africa: Implications for peopling and migration patterns in sub-Saharan Africa". American Journal of Physical Anthropology. 140 (2): 302–11. doi:10.1002/ajpa.21070. PMID 19425093.
- Chinnery, P F; Mowbray, C; Patel, S K; Elson, J L; Sampson, M; Hitman, G A; McCarthy, M I; Hattersley, A T; Walker, M (2007). "Mitochondrial DNA haplogroups and type 2 diabetes: A study of 897 cases and 1010 controls". Journal of Medical Genetics. 44 (6): e80. doi:10.1136/jmg.2007.048876. PMC 2740896. PMID 17551080.
- Coble, Michael D.; Loreille, Odile M.; Wadhams, Mark J.; Edson, Suni M.; Maynard, Kerry; Meyer, Carna E.; Niederstätter, Harald; Berger, Cordula; et al. (2009). Hofreiter, Michael (ed.). "Mystery Solved: The Identification of the Two Missing Romanov Children Using DNA Analysis". PLOS ONE. 4 (3): e4838. Bibcode:2009PLoSO...4.4838C. doi:10.1371/journal.pone.0004838. PMC 2652717. PMID 19277206.
- Costa, MD; Cherni, L; Fernandes, V; Freitas, F; Ammar El Gaaied, AB; Pereira, L (2009). "Data from complete mtDNA sequencing of Tunisian centenarians: Testing haplogroup association and the "golden mean" to longevity". Mechanisms of Ageing and Development. 130 (4): 222–6. doi:10.1016/j.mad.2008.12.001. PMID 19133286. S2CID 6102820.
- Cvjetan, S; Tolk, HV; Lauc, LB; Colak, I; Dordević, D; Efremovska, L; Janićijević, B; Kvesić, A; et al. (2004). "Frequencies of mtDNA haplogroups in southeastern Europe--Croatians, Bosnians and Herzegovinians, Serbians, Macedonians and Macedonian Romani". Collegium Antropologicum. 28 (1): 193–8. PMID 15636075.
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Websites
- Behar; Family Tree DNA (2012). "mtDNA Community". Archived from the original on 2018-01-02. Retrieved 2013-01-12.
Further reading
- Černý, Viktor; Pereira, Luísa; Kujanová, Martina; VašÍková, Alžběta; Hájek, Martin; Morris, Miranda; Mulligan, Connie J. (2009). "Out of Arabia-The settlement of Island Soqotra as revealed by mitochondrial and Y chromosome genetic diversity". American Journal of Physical Anthropology. 138 (4): 439–47. doi:10.1002/ajpa.20960. PMID 19012329.
- Kitchen, A.; Ehret, C.; Assefa, S.; Mulligan, C. J. (2009). "Bayesian phylogenetic analysis of Semitic languages identifies an Early Bronze Age origin of Semitic in the Near East". Proceedings of the Royal Society B: Biological Sciences. 276 (1668): 2703–10. doi:10.1098/rspb.2009.0408. PMC 2839953. PMID 19403539.
- Petit-Maire, Nicole; Bouysse, Philippe (2000). "Geological records of the recent past, a key to the near future world environments" (PDF). Episodes. 23 (4): 230–246. doi:10.18814/epiiugs/2000/v23i4/001.
External links
- General
- Ian Logan's Mitochondrial DNA Site
- Mannis van Oven's Phylotree
- The Genographic Project Public Participation Mitochondrial DNA Database
- Haplogroup T
- YFull MTree's Haplogroup T
- MITOMAP's Haplogroup T
- Family TreeDNA's mtDNA Haplotree: Haplogroup T
- Spread of Haplogroup T, from National Geographic
- Genetic Genealogy: A Personal Perspective on Tara, Karelians and Kent, England
- Analysis of a Haplogroup T sequence (T5/T2)
- Phylogenetic Networks for the Human mtDNA Haplogroup T Archived 2008-05-31 at the Wayback Machine
- Phylogenetic Networks for the Human mtDNA Haplogroup T Archived 2008-05-09 at the Wayback Machine
- mtDNA Haplogroup T - Full Genomic Sequence Research Project