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]
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]
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]
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.
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]
^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. PMID28034339. S2CID4490910.
^Fregel; et al. (2018). "Ancient genomes from North Africa evidence prehistoric migrations to the Maghreb from both the Levant and Europe". bioRxiv10.1101/191569.
^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. PMID16313983.
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. PMID11246451.
Belyaeva, Olga; Bermisheva, Marina; Khrunin, Andrey; Slominsky, Petr; Bebyakova, Natalia; Khusnutdinova, E. K. (Elza Kamilevna); Mikulich, Aleksei Ignatevich; Limborskaia, S. A. (Svetlana Andreevna) (2003). "Mitochondrial DNA variations in Russian and Belorussian populations". Human Biology. 75 (5): 647–60. doi:10.1353/hub.2003.0069. PMID14763602. S2CID23876546.
Boattini, Alessio; Castrì, Loredana; Sarno, Stefania; Useli, Antonella; Cioffi, Manuela; Sazzini, Marco; Garagnani, Paolo; De Fanti, Sara; Pettener, Davide; Luiselli, Donata (2013). "MtDNA variation in East Africa unravels the history of afro-asiatic groups". American Journal of Physical Anthropology. 150 (3): 375–385. doi:10.1002/ajpa.22212. PMID23283748.
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. PMID16759179. S2CID23156886.
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. PMID15248073. S2CID19703169.
Castrì, Loredana; Garagnani, P; Useli, A; Pettener, D; Luiselli, D (2008). "Kenyan crossroads: migration and gene flow in six ethnic groups from Eastern Africa". Journal of Anthropological Sciences. 86: 189–192. PMID19934476.
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. PMID19425093.
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. PMID19133286. S2CID6102820.
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. PMID15636075.
Hofreiter, Linea; Lynnerup, Niels; Siegismund, Hans R.; Kivisild, Toomas; Dissing, Jørgen (2010). Hofreiter, Michael (ed.). "Genetic Diversity among Ancient Nordic Populations". PLOS ONE. 5 (7): e11898. Bibcode:2010PLoSO...511898M. doi:10.1371/journal.pone.0011898. PMC2912848. PMID20689597. 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.
Janssen, GM; Neu, A; 't Hart, LM; Van De Sande, CM; Antonie Maassen, J (2006). "Novel mitochondrial DNA length variants and genetic instability in a family with diabetes and deafness". Experimental and Clinical Endocrinology & Diabetes. 114 (4): 168–74. doi:10.1055/s-2006-924066. PMID16705548.
Keyser, Christine; Bouakaze, Caroline; Crubézy, Eric; Nikolaev, Valery G.; Montagnon, Daniel; Reis, Tatiana; Ludes, Bertrand (2009). "Ancient DNA provides new insights into the history of south Siberian Kurgan people". Human Genetics. 126 (3): 395–410. doi:10.1007/s00439-009-0683-0. PMID19449030. S2CID21347353.
Martina Kujanova; Luisa Pereira; Veronica Fernandes; Joana B. Pereira; Viktor Cerny (2009). "Near Eastern Neolithic Genetic Input in a Small Oasis of the Egyptian Western Desert". American Journal of Physical Anthropology. 140 (2): 336–346. doi:10.1002/ajpa.21078. PMID19425100.
Musilová, Eliška; Fernandes, Verónica; Silva, Nuno M.; Soares, Pedro; Alshamali, Farida; Harich, Nourdin; Cherni, Lotfi; Gaaied, Amel Ben Ammar El; et al. (2011). "Population history of the Red Sea-genetic exchanges between the Arabian Peninsula and East Africa signaled in the mitochondrial DNA HV1 haplogroup". American Journal of Physical Anthropology. 145 (4): 592–8. doi:10.1002/ajpa.21522. PMID21660931.
Nikitin, Alexey G.; Kochkin, Igor T.; June, Cynthia M.; Willis, Catherine M.; McBain, Ian; Videiko, Mykhailo Y. (2009). "Mitochondrial DNA Sequence Variation in the Boyko, Hutsul, and Lemko Populations of the Carpathian Highlands". Human Biology. 81 (1): 43–58. doi:10.3378/027.081.0104. PMID19589018. S2CID45791162.
Non, Amy L.; Al-Meeri, Ali; Raaum, Ryan L.; Sanchez, Luisa F.; Mulligan, Connie J. (2011). "Mitochondrial DNA reveals distinct evolutionary histories for Jewish populations in Yemen and Ethiopia". American Journal of Physical Anthropology. 144 (1): 1–10. doi:10.1002/ajpa.21360. PMID20623605.
Pericić, M; Barać Lauc, L; Martinović Klarić, I; Janićijević, B; Rudan, P (2005). "Review of Croatian genetic heritage as revealed by mitochondrial DNA and Y chromosomal lineages". Croatian Medical Journal. 46 (4): 502–13. PMID16100752.
Pope, AM; Carr, SM; Smith, KN; Marshall, HD; Marshall, H. D. (2011). "Mitogenomic and microsatellite variation in descendants of the founder population of Newfoundland: High genetic diversity in an historically isolated population". Genome. 54 (2): 110–9. doi:10.1139/G10-102. PMID21326367.
Stanger, Olaf; Müller, Edith; Zimmermann, Franz; Wiesbauer, Martina; Mayr, Johannes A.; Paulweber, Bernhard; Iglseder, Bernhard; Renner, Wilfried; et al. (2007). "30 Mitochondrial haplogroup T is associated with coronary artery disease". Mitochondrion. 7 (6): 412. doi:10.1016/j.mito.2007.08.034.
Stone, AC; Starrs, JE; Stoneking, M (2001). "Mitochondrial DNA analysis of the presumptive remains of Jesse James". Journal of Forensic Sciences. 46 (1): 173–6. doi:10.1520/JFS14932J. PMID11210907.
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. PMID19012329.