Haplogroup I (mtDNA)

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Haplogroup I
Possible time of origin20.1 kya (Olivieri 2013)
Possible place of originWest Asia (Terreros 2011 and Fernandes 2012)
AncestorN1a1b (former N1e'I), (Olivieri 2013)
DescendantsI1, I2'3, I4, I5, I6, I7 (Olivieri 2013)
Defining mutationsT10034C, G16129A!, G16391A (Behar & Family Tree DNA 2012)

Haplogroup I is a human mitochondrial DNA (mtDNA) haplogroup. It is believed to have originated about 21,000 years ago, during the Last Glacial Maximum (LGM) period in West Asia ((Olivieri 2013); Terreros 2011; Fernandes 2012). The haplogroup is unusual in that it is now widely distributed geographically, but is common in only a few small areas of East Africa, West Asia and Europe. It is especially common among the El Molo and Rendille peoples of Kenya, various regions of Iran, the Lemko people of Slovakia, Poland and Ukraine, the island of Krk in Croatia, the department of Finistère in France and some parts of Scotland and Ireland.

Origin[]

Haplogroup I is a descendant (subclade) of haplogroup N1a1b and sibling of haplogroup N1a1b1 (Olivieri 2013). It is believed to have arisen somewhere in West Asia between 17,263 and 24,451 years before present (BP) (Behar 2012b), with coalescence age of 20.1 thousand years ago (Olivieri 2013). It has been suggested that its origin may be in Iran or more generally the Near East (Terreros 2011). It has diverged to at least seven distinct clades i.e. branches I1-I7, dated between 16-6.8 thousand years (Olivieri 2013). The hypothesis about its Near Eastern origin is based on the fact that all haplogroup I clades, especially those from Late Glacial period (I1, I4, I5, and I6), include mitogenomes from the Near East (Olivieri 2013). The age estimates and dispersal of some subclades (I1, I2’3, I5) are similar to those of major subclades of the mtDNA haplogroups J and T, indicating possible dispersal of the I haplogroup into Europe during the Late Glacial period (c. 18–12 kya) and postglacial period (c. 10–11 kya), several millennia before the European Neolithic period. Some subclades (I1a1, I2, I1c1, I3) show signs of the Neolithic diffusion of agriculture and pastoralism within Europe (Olivieri 2013).

It is noteworthy that, with the exception of its northern neighbor Azerbaijan, Iran is the only population in which haplogroup I exhibits polymorphic levels. Also, a contour plot based on the regional phylogeographic distribution of the I haplogroup exhibits frequency clines consistent with an Iranian cradle ... Moreover, when compared with other populations in the region, those from the Levant (Iraq, Syria and Palestine) and the Arabian Peninsula (Oman and UAE) exhibit significantly lower proportions of I individuals ... this haplogroup has been detected in European groups (Krk, a tiny island off the coast of Croatia (11.3%), and Lemko, an isolate from the Carpathian Highlands (11.3%)) at comparable frequencies to those observed in the North Iranian population. However, the higher frequencies of the haplogroup within Europe are found in geographical isolates and are likely the result of founder effects and/or drift ... it is plausible that the high levels of haplogroup I present in Iran may be the result of a localized enrichment through the action of genetic drift or may signal geographical proximity to the location of origin.

— Terreros 2011

A similar view puts more emphasis on the Persian Gulf region of the Near East (Fernandes 2012).

Haplogroup I ... dates to ∼25 ka ago and is overall most frequent in Europe ..., but the facts that it has a frequency peak in the Gulf region and that its highest diversity values are in the Gulf, Anatolia, and southeast Europe suggest that its origin is most likely in the Near East and/or Arabia ...

Distribution[]

Projected frequencies of mtDNA haplogroup I.

Haplogroup I is found at moderate to low frequencies in East Africa, Europe, West Asia and South Asia (Fernandes 2012). In addition to the confirmed seven clades, the rare basal/paraphyletic clade I* has been observed in three individuals; two from Somalia and one from Iran (Olivieri 2013).

Africa[]

The highest frequencies of mitochondrial haplogroup I observed so far appear in the Cushitic-speaking El Molo (23%) and Rendille (>17%) in northern Kenya (Castrì 2008). The clade is also found at comparable frequencies among the Soqotri (~22%).[1]

Population Location Language Family N Frequency Source
Amhara Ethiopia Afro-Asiatic > Semitic 1/120 0.83% Kivisild 2004
Egyptians Egypt Afro-Asiatic > Semitic 2/34 5.9% Stevanovitch 2004
Beta Israel Ethiopia Afro-Asiatic > Cushitic 0/29 0.00% Behar 2008a
Dawro Konta Ethiopia Afro-Asiatic > Omotic 0/137 0.00% Castrì 2008 and Boattini 2013
Ethiopia Ethiopia Undetermined 0/77 0.00% Soares 2011
Ethiopian Jews Ethiopia Afro-Asiatic > Cushitic 0/41 0.00% Non 2011
Gurage Ethiopia Afro-Asiatic > Semitic 1/21 4.76% 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 0/44 0.00% Kivisild 2004
Daasanach Kenya Afro-Asiatic > Cushitic 0/49 0.00% Poloni 2009
Elmolo Kenya Afro-Asiatic > Cushitic 12/52 23.08% 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 1/112 0.89% Poloni 2009
Rendille Kenya Afro-Asiatic > Cushitic 3/17 17.65% Castrì 2008 and Boattini 2013
Samburu Kenya Nilo-Saharan 3/35 8.57% 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 0/102 0.00% Soares 2011
Burunge Tanzania Afro-Asiatic > Cushitic 1/38 2.63% Tishkoff 2007
Datoga Tanzania Nilo-Saharan 0/57 0.00% 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 0/114 0.00% Kivisild 2004

Asia[]

Haplogroup I is present across West Asia and Central Asia, and is also found at trace frequencies in South Asia. Its highest frequency area is perhaps in northern Iran (9.7%). Terreros 2011 notes that it also has high diversity there and reiterates past studies that have suggested that this may be its place of origin. Found in Svan population from Georgia(Caucasus) I* 4.2%."Sequence polymorphisms of the mtDNA control region in a human isolate: the Georgians from Swanetia."Alfonso-Sánchez MA1, Martínez-Bouzas C, Castro A, Peña JA, Fernández-Fernández I, Herrera RJ, de Pancorbo MM.[citation needed] The table below shows some of the populations where it has been detected.

Population Language Family N Frequency Source
Baluch Indo-European 0/39 0.00% Quintana-Murci 2004
Brahui Dravidian 0/38 0.00% Quintana-Murci 2004
Caucasus (Georgia)* Kartvelian 1/58 1.80% Quintana-Murci 2004
Druze - 11/311 3.54% Shlush 2008
Gilaki Indo-European 0/37 0.00% Quintana-Murci 2004
Gujarati Indo-European 0/34 0.00% Quintana-Murci 2004
Hazara Indo-European 0/23 0.00% Quintana-Murci 2004
Hunza Burusho Isolate 2/44 4.50% Quintana-Murci 2004
India - 8/2544 0.30% Metspalu 2004
Iran (North) - 3/31 9.70% Terreros 2011
Iran (South) - 2/117 1.70% Terreros 2011
Kalash Indo-European 0/44 0.00% Quintana-Murci 2004
Kurdish (Western Iran) Indo-European 1/20 5.00% Quintana-Murci 2004
Kurdish (Turkmenistan) Indo-European 1/32 3.10% Quintana-Murci 2004
Kurdish

(Turkey)

Indo-European 66/200 33.0% [citation needed]
Lur Indo-European 0/17 0.00% Quintana-Murci 2004
Makrani Indo-European 0/33 0.00% Quintana-Murci 2004
Mazandarian Indo-European 1/21 4.80% Quintana-Murci 2004
Pakistani Indo-European 0/100 0.00% Quintana-Murci 2004
Pakistan - 1/145 0.69% Metspalu 2004
Parsi Indo-European 0/44 0.00% Quintana-Murci 2004
Pathan Indo-European 1/44 2.30% Quintana-Murci 2004
Persian Indo-European 1/42 2.40% Quintana-Murci 2004
Shugnan Indo-European 1/44 2.30% Quintana-Murci 2004
Sindhi Indo-European 1/23 8.70% Quintana-Murci 2004
Turkish (Azerbaijan) Turkic 2/40 5.00% Quintana-Murci 2004
Turkish (Anatolia)* Turkic 1/50 2.00% Quintana-Murci 2004
Turkmen Turkic 0/41 0.00% Quintana-Murci 2004
Uzbek Turkic 0/42 0.00% Quintana-Murci 2004

Europe[]

Western Europe[]

In Western Europe, haplogroup I is most common in Northwestern Europe (Norway,[citation needed] the Isle of Skye, and the British Isles). The frequency in these areas is between 2 and 5 percent. Its highest frequency in Brittany, France where it is over 9 percent of the population in Finistère. It is uncommon and sometimes absent in other parts of Western Europe (Iberia, South-West France, and parts of Italy).

Population Language N Frequency Source
Austria/Switzerland - 4/187 2.14% Helgason 2001
Basque (Admix Zone) Basque/Labourdin côtier-haut navarrais 0/56 0.00% Martınez-Cruz 2012
Basque (Araba) Basque/Occidental 0/55 0.00% Martınez-Cruz 2012
Basque (Bizkaia) Basque/Biscayen 1/59 1.69% Martınez-Cruz 2012
Basque (Central/Western Navarre ) Basque/Haut-navarrais méridional 2/63 3.17% Martınez-Cruz 2012
Basque (Gipuskoa) Basque/Gipuzkoan 0/57 0.00% Martınez-Cruz 2012
Basque (Navarre Labourdin) Basque/Bas-navarrais 0/68 0.00% Martınez-Cruz 2012
Basque (North/Western Navarre) Basque/Haut-navarrais septentrional 0/51 0.00% Martınez-Cruz 2012
Basque (Roncal) Basque/Roncalais-salazarais 0/55 0.00% Martınez-Cruz 2012
Basque (Soule) Basque/Souletin 0/62 0.00% Martınez-Cruz 2012
Basque (South/Western Gipuskoa) Basque/Biscayen 0/64 0.00% Martınez-Cruz 2012
Béarn French 0/51 0.00% Martınez-Cruz 2012
Bigorre French 0/44 0.00% Martınez-Cruz 2012
Burgos Spanish 0/25 0.00% Martınez-Cruz 2012
Cantabria Spanish 0/18 0.00% Martınez-Cruz 2012
Chalosse French 0/58 0.00% Martınez-Cruz 2012
Denmark - 6/105 5.71% Mikkelsen 2010
England/Wales - 12/429 3.03% Helgason 2001
Finland - 1/49 2.04% Torroni 1996
Finland/Estonia - 5/202 2.48% Helgason 2001
France (Finistère) - 2/22 9.10% Dubut 2003
France (Morbihan) - 0/40 0.00% Dubut 2003
France (Normandy) - 0/39 0.00% Dubut 2003
France (Périgord-Limousin) - 2/72 2.80% Dubut 2003
France (Var) - 2/37 5.40% Dubut 2003
France/Italy - 2/248 0.81% Helgason 2001
Germany - 12/527 2.28% Helgason 2001
Iceland - 21/467 4.71% Helgason 2001
Ireland - 3/128 2.34% Helgason 2001
Italy (Tuscany) - 2/48 4.20% Torroni 1996
La Rioja Spanish 1/51 1.96% Martınez-Cruz 2012
North Aragon Spanish 0/26 0.00% Martınez-Cruz 2012
Orkney - 5/152 3.29% Helgason 2001
Saami - 0/176 0.00% Helgason 2001
Scandinavia - 12/645 1.86% Helgason 2001
Scotland - 39/891 4.38% Helgason 2001
Spain/Portugal - 2/352 0.57% Helgason 2001
Sweden - 0/37 0.00% Torroni 1996
Western Bizkaia Spanish 0/18 0.00% Martınez-Cruz 2012
Western Isles/Isle of Skye - 15/246 6.50% Helgason 2001

Eastern Europe[]

In Eastern Europe, the frequency of haplogroup I is generally lower than in Western Europe (1 to 3 percent), but its frequency is more consistent between populations with fewer places of extreme highs or lows. There are two notable exceptions. Nikitin 2009 found that Lemkos (a sub- or co-ethnic group of Rusyns) in the Carpathian mountains have the "highest frequency of haplogroup I (11.3%) in Europe, identical to that of the population of Krk Island (Croatia) in the Adriatic Sea".[Footnote 1][Footnote 2]

Population N Frequency Source
Boyko 0/20 0.00% Nikitin 2009
Hutsul 0/38 0.00% Nikitin 2009
Lemko 6/53 11.32% Nikitin 2009
Belorussians 2/92 2.17% Belyaeva 2003
Russia (European) 3/215 1.40% Helgason 2001
Romanians (Constanta) 59 0.00% Bosch 2006
Romanians (Ploiesti) 46 2.17% Bosch 2006
Russia 1/50 2.0% Malyarchuk 2001
Ukraine 0/18 0.00% Malyarchuk 2001
Croatia (Mainland) 4/277 1.44% Pericić 2005
Croatia (Krk) 15/133 11.28% Cvjetan 2004
Croatia (Brac) 1/105 0.95% Cvjetan 2004
Croatia (Hvar) 2/108 1.9% Cvjetan 2004
Croatia (Korcula) 1/98 1% Cvjetan 2004
Herzegovinians 1/130 0.8% Cvjetan 2004
Bosnians 6/247 2.4% Cvjetan 2004
Serbians 4/117 3.4% Cvjetan 2004
Macedonians 2/146 1.4% Cvjetan 2004
Macedonian Romani 7/153 4.6% Cvjetan 2004
Slovenians 2/104 1.92% Malyarchuk 2003
Bosnians 4/144 2.78% Malyarchuk 2003
Poles 8/436 1.83% Malyarchuk 2003
Caucasus (Georgia)* 1/58 1.80% Quintana-Murci 2004
Russians 5/201 2.49% Malyarchuk 2003
Bulgaria/Turkey 2/102 1.96% Helgason 2001

Historic and Pre-Historic Samples[]

Haplogroup I has until recently been absent from ancient European samples found in Paleolithic and Mesolithic grave sites. In 2017, in a site on Italian island of Sardinia was found a sample with the subclade I3 dated to 9124-7851 BC (Modi 2017), while in the Near East, in Levant was found a sample with yet-not-defined subclade dated 8,850-8,750 BC, while in Iran was found a younger sample with subclade I1c dated to 3972-3800 BC (Lazaridis 2016). In Neolithic Spain (c. 6090-5960 BC in , Navarre) was found a sample with yet-not-defined subclade (Olivieri 2013). Haplogroup I displays a strong connection with the Indo-European migrations; especially its I1, I1a1 and I3a subclades, which have been found in Poltavka and Srubnaya cultures in Russia (Mathieson 2015), among ancient Scythians (Der Sarkissian 2011), and in Corded Ware and Unetice Culture burials in Saxony (Brandt 2013).I3A has also been found in the Unetice Culture in Lubingine, Germany 2,200 B.C. to 1,800 B.C. courtesy article on Unetice Culture Wikipedia of 2 Skeletons that were DNA tested. Haplogroup I (with undetermined subclades) has also been noted at significant frequencies in more recent historic grave sites (Melchior 2008 and Hofreiter 2010).

In 2013, Nature announced the publication of the first genetic study utilizing next-generation sequencing to ascertain the ancestral lineage of an Ancient Egyptian individual. The research was led by Carsten Pusch of the University of Tübingen in Germany and Rabab Khairat, who released their findings in the Journal of Applied Genetics. DNA was extracted from the heads of five Egyptian mummies that were housed at the institution. All the specimens were dated to between 806 BC and 124 AD, a time frame corresponding with the Late Dynastic and Ptolemaic periods. The researchers observed that one of the mummified individuals likely belonged to the I2 subclade.[2] Haplogroup I has also been found among ancient Egyptian mummies excavated at the Abusir el-Meleq archaeological site in Middle Egypt, which date from the Pre-Ptolemaic/late New Kingdom, Ptolemaic, and Roman periods.[3]

Haplogroup I5 has also been observed among specimens at the mainland cemetery in Kulubnarti, Sudan, which date from the Early Christian period (AD 550-800).[4]

Samples with determined subclades[]

Culture Country Site Date Haplogroup Source
Unetice Germany Esperstedt 2050-1800 BC I1 Adler 2012; Brandt 2013
Bell Beaker Germany 2600-2500 BC I1a1 Lee 2012; Oliveiri 2013
Unetice Germany Plotzkau 3 2200-1550 BC I1a1 Brandt 2013
Unetice Germany Eulau 1979-1921 BC I1a1 Brandt 2013
Srubnaya Russia Rozhdestveno I, Samara Steppes, Samara 1850-1600 BC I1a1 Mathieson 2015
Seh Gabi Iran 3972-3800 BC I1c Lazaridis 2016
Cami de Can Grau Spain 3500-3000 BC I1c1 Sampietro 2007; Olivieri 2013
Late Dynastic-Ptolemaic Egypt 806 BC-124 AD I2 Khairat 2013
Su Carroppu Italy 9124–7851 BC I3 Modi 2017
Scythian Russia Rostov-on-Don 500-200 BC I3 Der Sarkissian 2011
Unetice Germany Benzingerode-Heimburg 1653-1627 BC I3a Brandt 2013
Unetice Germany Esperstedt 2131-1979 BC I3a Adler 2012; Brandt 2013; Haak 2015; Mathieson 2015
Unetice Germany Esperstedt 2199-2064 BC I3a Adler 2012; Brandt 2013; Haak 2015
Poltavka Russia Lopatino II, Sok River, Samara 2885-2665 BC I3a Mathieson 2015
Karasuk Russia Sabinka 2 1416-1268 BC I4a1 Allentoft 2015
Minoan Greece Ayios Charalambos 2400-1700 BC I5 Hughey 2013
Minoan Greece Ayios Charalambos 2400-1700 BC I5 Hughey 2013
Minoan Greece Ayios Charalambos 2400-1700 BC I5 Hughey 2013
Christian Nubia Sudan Kulubnarti 550-800 AD I5 Sirak 2016
Late Bronze Age Armenia Norabak 1209-1009 BC I5c Allentoft 2015
Mezhovskava Russia Kapova cave 1598-1398 BC I5c Allentoft 2015

Samples with unknown subclades[]

Populations N Frequency Source
Roman Iron Age sites
Bøgebjerggård (AD 1–400)
Simonsborg (AD 1–200)
Skovgaarde (AD 200–400)
3/24 12.5% Melchior 2008a, Hofreiter 2010
Viking Age burial sites
Galgedil (AD 1000)
Christian cemetery Kongemarken (AD 1000–1250)
medieval cemetery Riisby (AD 1250–1450)
4/29 13.79% Melchior 2008, Hofreiter 2010
Anglo-Saxon burial sites
Leicester:6
Lavington:6
Buckland:7
Norton:12
Norwich:17
1/48 2.08% Töpf 2006

We have previously observed a high frequency of Hg I's among Iron Age villagers (Bøgebjerggård) and individuals from the early Christian cemetery, Kongemarken [16], [17]. This trend was also found for the additional sites reported here, Simonsborg, Galgedil and Riisby. The overall frequency of Hg I among the individuals from the Iron Age to the Medieval Age is 13% (7/53) compared to 2.5% for modern Danes [35]. The higher frequencies of Hg I can not be ascribed to maternal kinship since only two individuals share the same common motif (K2 and K7 at Kongemarken). Except for Skovgaarde (no Hg I's observed) frequencies range between 9% and 29% and there seems to be no trend in relation to time. No Hg I's were observed at the Neolithic Damsbo and the Bronze Age site Bredtoftegård, where all three individuals harbored Hg U4 or Hg U5a (Table 1).

Hofreiter 2010

The frequency of haplogroup I may have undergone a reduction in Europe following the Middle Ages. An overall frequency of 13% was found in ancient Danish samples from the Iron Age to the Medieval Age (including Vikings) from Denmark and Scandinavia compared to only 2.5% in modern samples. As haplogroup I is not observed in any ancient Italian, Spanish [contradicted by the recent research as have been found in pre-Neolithic Italy as well Neolithic Spain], British, central European populations, early central European farmers and Neolithic samples, according to the authors "Haplogroup I could, therefore, have been an ancient Southern Scandinavian type "diluted" by later immigration events" (Hofreiter 2010).

Subclades[]

Phylogenetic tree of haplogroups I (left) and W (right). Kya in the left scale bar stands for thousand years ago (Olivieri 2013).

Tree[]

This phylogenetic tree of haplogroup I subclades with time estimates is based on the paper and published research (Olivieri 2013).

Hg (July 2013) Age estimate (thousand years) 95% confidence interval (thousand years)
N1a1b 28.6 23.5 - 33.9
I 20.1 18.4 - 21.9
I1 16.3 14.6 - 18.0
I1a 11.6 9.9 - 13.3
I1a1 4.9 4.2 - 5.6
I1a1a 3.8 3.3 - 4.4
I1a1b 1.4 0.5 - 2.2
I1a1c 2.5 1.3 - 3.7
I1a1d 1.8 1.0 - 2.6
I1b 13.4 11.3 - 15.5
I1c 10.3 8.4 - 12.2
I1c1 7.2 5.4 - 9.0
I1c1a 4.0 2.5 - 5.4
I2'3 12.6 10.4 - 14.7
I2 6.8 6.0 - 7.6
I2a 4.7 3.8 - 5.7
I2a1 3.2 2.1 - 4.4
I2b 1.7 0.5 - 2.9
I2c 4.7 3.6 - 5.8
I2d 3.0 1.1 - 4.8
I2e 3.1 1.4 - 4.8
I3 10.6 8.8 - 12.4
I3a 7.4 6.1 - 8.7
I3a1 6.1 4.7 - 7.5
I3b 2.6 1.1 - 4.2
I3c 9.4 7.6 - 11.2
I4 15.1 12.3 - 18.0
I4a 6.4 5.4 - 7.4
I4a1 5.7 4.5 - 6.7
I4b 8.4 5.8 - 10.9
I5 18.4 16.4 - 20.3
I5a 16.0 14.0 - 17.9
I5a1 9.2 7.1 - 11.3
I5a2 12.3 10.2 - 14.4
I5a2a 1.6 1.0 - 2.1
I5a3 4.8 2.8 - 6.8
I5a4 5.6 3.5 - 7.8
I5b 8.8 6.3 - 11.2
I6 18.4 16.2 - 20.6
I6a 5.3 3.5 - 7.0
I6b 13.1 10.4 - 15.8
I7 9.1 6.3 - 11.9

Distribution[]

I1[]

Haplogroup I1
Possible time of origin15,231 ± 3,402 BP (Behar 2012b)
Possible place of originInsufficient Data
AncestorI
Defining mutations455.1T, G6734A, G9966A, T16311C! (Behar & Family Tree DNA 2012)

It formed during the Last Glacial pre-warming period. It is found mainly in Europe, Near East, occasionally in North Africa and the Caucasus. It is the most frequent clade of the haplogroup (Olivieri 2013).

Genbank ID Population Source
JQ702472 Behar 2012b
JQ702567 Germany Behar 2012b
JQ704077 Germany Behar 2012b
JQ705190 Behar 2012b
JQ705840 Behar 2012b
I1a[]
Haplogroup I1a
Possible time of origin11,726 ± 3,306 BP (Behar 2012b)
Possible place of originInsufficient Data
AncestorI1
Defining mutationsT152C!, G207A (Behar & Family Tree DNA 2012)

The subclade frequency peaks (circa 2.8%) are mostly located in North-Eastern Europe (Olivieri 2013).

Genbank ID Population Source
EU694173 - FamilyTreeDNA
HM454265 Turkey (Armenian) FamilyTreeDNA
JQ245746 Chuvash Fernandes 2012
I1a1[]
Haplogroup I1a1
Possible time of origin5,294 ± 2,134 BP (Behar 2012b)
Possible place of originInsufficient Data
AncestorI1a
Defining mutationsG203A, C3990T, G9947A, A9966G!, T10915C! (Behar & Family Tree DNA 2012)
Genbank ID Population Source
EF177414 Portugal Pereira 2007
JQ701900 - Behar 2012b
JQ702519 - Behar 2012b
JQ702820 - Behar 2012b
JQ702882 - Behar 2012b
JQ703835 - Behar 2012b
JQ705025 - Behar 2012b
JQ705645 - Behar 2012b
FJ460562 Tunisia Costa 2009
JQ705889 - Behar 2012b
JQ245748 Czech Fernandes 2012
JQ245749 Czech Fernandes 2012
JQ245767 Turkey Fernandes 2012
JQ245802 Morocco Fernandes 2012
I1a1a[]
Haplogroup I1a1a
Possible time of origin3,327 ± 2,720 BP (Behar 2012b)
Possible place of originInsufficient Data
AncestorI1a1
Defining mutationsG9053A (Behar & Family Tree DNA 2012)
Genbank ID Population Source
AY339502 Finland Finnila 2001
AY339503 Finland Finnila 2001
AY339504 Finland Finnila 2001
AY339505 Finland Finnila 2001
AY339506 Finland Finnila 2001
AY339507 Finland Finnila 2001
AY339508 Finland Finnila 2001
AY339509 Finland Finnila 2001
JQ702939 - Behar 2012b
JQ703652 - Behar 2012b
JQ704013 - Behar 2012b
JQ705140 - Behar 2012b
JQ705378 - Behar 2012b
I1a1b[]
Haplogroup I1a1b
Possible time of origin2,608 ± 2,973 BP (Behar 2012b)
Possible place of originInsufficient Data
AncestorI1a1
Defining mutationsT14182C (Behar & Family Tree DNA 2012)
Genbank ID Population Source
JQ702470 - Behar 2012b
JQ705595 - Behar 2012b
JQ704690 - Behar 2012b
I1a1c[]
Haplogroup I1a1c
Possible time of originAbout 1,523 BP (Behar 2012b)
Possible place of originInsufficient Data
AncestorI1a1
Defining mutationsT6620C (Behar & Family Tree DNA 2012)
Genbank ID Population Source
JQ702023 - Behar 2012b
JQ702457 - Behar 2012b
GU123027 Mishar Tatars
(Buinsk)
Malyarchuk 2010b
I1a1d[]
Haplogroup I1a1d
Possible time of originAbout 1,892 BP (Behar 2012b)
Possible place of originInsufficient Data
AncestorI1a1
Defining mutationsA1836G, T4023C, T13488C, T16189C! (Behar & Family Tree DNA 2012)
Genbank ID Population Source
JQ702342 - Behar 2012b
JQ705189 - Behar 2012b
I1b[]
Haplogroup I1b
Possible time of origin11,135 ± 4,818 BP (Behar 2012b)
Possible place of originInsufficient Data
AncestorI1
Defining mutationsT6227C (Behar & Family Tree DNA 2012)
Genbank ID Population Source
AY195769 Caucasian Mishmar 2003
AY714041 India Palanichamy 2004
EF556153 Jewish Diaspora Behar 2008a
FJ234984 Armenian FamilyTreeDNA
FJ968796 - FamilyTreeDNA
JQ704018 - Behar 2012b
JQ705376 - Behar 2012b
KJ890387.1 Swedish FamilyTreeDNA
I1c[]
Haplogroup I1c
Possible time of origin8,216 ± 3,787 BP (Behar 2012b)
Possible place of originInsufficient Data
AncestorI1
Defining mutationsG8573A, C16264T, G16319A, T16362C (Behar & Family Tree DNA 2012)
GenBank ID Population Source
EU564849 - FamilyTreeDNA
JQ702655 - Behar 2012b
JQ705364 - Behar 2012b
JQ705932 - Behar 2012b

I2'3[]

Haplogroup I2'3
Possible time of origin11,308 ± 4,154 BP (Behar 2012b)
Possible place of originInsufficient Data
AncestorI
Defining mutationsT152C!, G207A (Behar & Family Tree DNA 2012)

It is the common root clade for subclades I2 and I3. There's a sample from Tanzania with which I2'3 shares a variant at position 152 from the root node of haplogroup I, and this "node 152" could be upstream I2'3s clade (Olivieri 2013). Both I2 and I3 might have formed during the Holocene period, and most of their subclades are from Europe, only few from the Near East (Olivieri 2013). Examples of this ancestral branch have not been documented.

I2[]
Haplogroup I2
Possible time of origin6,387 ± 2,449 BP (Behar 2012b)
Possible place of originInsufficient Data
AncestorI2'3
Defining mutationsA15758G (Behar & Family Tree DNA 2012)
GenBank ID Population Source
FJ911909 - FamilyTreeDNA
GU122984 Volga Tatars Malyarchuk 2010b
GU294854 - FamilyTreeDNA
HQ287882 - Pope 2011
JQ701942 - Behar 2012b
JQ702191 - Behar 2012b
JQ702284 - Behar 2012b
JQ703850 - Behar 2012b
JQ704705 - Behar 2012b
JQ704765 - Behar 2012b
JQ704936 - Behar 2012b
JQ705000 - Behar 2012b
JQ705304 - Behar 2012b
JQ705379 - Behar 2012b
EU570217 - FamilyTreeDNA
JQ245744 Chechnya Fernandes 2012
JQ245747 Czech Fernandes 2012
JQ245771 Turkey Fernandes 2012
I2a[]
Haplogroup I2a
Possible time of origin3,771 ± 2,143 BP (Behar 2012b)
Possible place of originInsufficient Data
AncestorI2
Defining mutationsA11065G, G16145A (Behar & Family Tree DNA 2012)
GenBank ID Population Source
HQ326985 - FamilyTreeDNA
HQ714959 Scotland FamilyTreeDNA
JQ703910 - Behar 2012b
JQ705175 - Behar 2012b
JQ705921 - Behar 2012b
HQ695930 - FamilyTreeDNA
I2a1[]
Haplogroup I2a1
Possible time of origin2,986 ± 1,968 BP (Behar 2012b)
Possible place of originInsufficient Data
AncestorI2a
Defining mutationsT3398C (Behar & Family Tree DNA 2012)
GenBank ID Population Source
AY339497 Finland Finnila 2001
HQ724528 Ireland FamilyTreeDNA
JN411083 Ireland FamilyTreeDNA
I2b[]
Haplogroup I2b
Possible time of originAbout 1,267 BP (Behar 2012b)
Possible place of originInsufficient Data
AncestorI2
Defining mutationsT6515C, 8281-8289d, A16166c (Behar & Family Tree DNA 2012)
GenBank ID Population Source
AY339498 Finland Finnila 2001
AY339499 Finland Finnila 2001
AY339500 Finland Finnila 2001
AY339501 Finland Finnila 2001
I2c[]
Haplogroup I2c
Possible time of originAbout 2,268 BP (Behar 2012b)
Possible place of originInsufficient Data
AncestorI2
Defining mutationsT460C, G9438A (Behar & Family Tree DNA 2012)
GenBank ID Population Source
JQ702163 - Behar 2012b
JQ702253 - Behar 2012b
JQ703024 - Behar 2012b
JQ705187 - Behar 2012b
JQ705666 - Behar 2012b
I2d[]
Haplogroup I2d
Possible time of originAbout 3,828 BP (Behar 2012b)
Possible place of originInsufficient Data
AncestorI2
Defining mutationsG6480A (Behar & Family Tree DNA 2012)
GenBank ID Population Source
JQ705244 - Behar 2012b
JQ703829 - Behar 2012b
I2e[]
Haplogroup I2e
Possible time of originAbout 2,936 BP (Behar 2012b)
Possible place of originInsufficient Data
AncestorI2
Defining mutationsG3591A (Behar & Family Tree DNA 2012)
GenBank ID Population Source
JQ702578 - Behar 2012b
JQ703106 - Behar 2012b
I3[]
Haplogroup I3
Possible time of origin8,679 ± 3,410 BP (Behar 2012b)
Possible place of originInsufficient Data
AncestorI2'3
Defining mutationsT239C (Behar & Family Tree DNA 2012)
GenBank ID Population Source
JQ702493 - Behar 2012b
JQ702647 - Behar 2012b
JQ703862 - Behar 2012b
JQ703883 - Behar 2012b
JQ245751 Greece Fernandes 2012
I3a[]
Haplogroup I3a
Possible time of origin6,091 ± 3,262 BP (Behar 2012b)
Possible place of originOldest sample from Poltavka culture (Russia-Lopatino II, Sok River, Samara, 2885-2665 BC) (Mathieson 2015)
AncestorI3
Defining mutationsT16086C (Behar & Family Tree DNA 2012)
GenBank ID Population Source
EU746658 France FamilyTreeDNA
EU869314 - FamilyTreeDNA
JQ702062 - Behar 2012b
JQ702109 - Behar 2012b
JQ702413 - Behar 2012b
JQ702041 - Behar 2012b
I3a1[]
Haplogroup I3a1
Possible time of origin5,070 ± 3,017 BP (Behar 2012b)
Possible place of originInsufficient Data
AncestorI3a
Defining mutationsG2849A (Behar & Family Tree DNA 2012)
GenBank ID Population Source
AY963586 Italy Bandelt
HQ420832 France FamilyTreeDNA
JQ704837 - Behar 2012b
I3b[]
Haplogroup I3b
Possible time of origin5,596 ± 3,629 BP (Behar 2012b)
Possible place of originInsufficient Data
AncestorI3
Defining mutationsC16494T (Behar & Family Tree DNA 2012)
GenBank ID Population Source
GU590993 Ireland FamilyTreeDNA
JQ705377 - Behar 2012b

I4[]

Haplogroup I4
Possible time of origin14,913 ± 5,955 BP (Behar 2012b)
Possible place of originInsufficient Data
AncestorI
Defining mutationsG8519A (Behar & Family Tree DNA 2012)

The clade splits into subclades I4a and newly defined I4b, with samples found in Europe, the Near East and the Caucasus (Olivieri 2013).

GenBank ID Population Source
JQ704976 - Behar 2012b
EF660987 Italy Gasparre 2007
I4a[]
Haplogroup I4a
Possible time of originAbout 2,124 BP (Behar 2012b)
Possible place of originInsufficient Data
AncestorI4
Defining mutationsA10819G (Behar & Family Tree DNA 2012)
GenBank ID Population Source
EF153786 Siberia Derenko 2007
EU091245 - FamilyTreeDNA
HM804481 - FamilyTreeDNA
JN660158 Armenian FamilyTreeDNA
JQ701909 - Behar 2012b
JQ701957 - Behar 2012b
JQ705060 - Behar 2012b
JQ705191 - Behar 2012b
JQ705303 - Behar 2012b
JQ705514 - Behar 2012b
JQ705906 - Behar 2012b
JQ706017 - Behar 2012b
JQ702369 - Behar 2012b

I5[]

Haplogroup I5
Possible time of origin18,806 ± 4,005 BP (Behar 2012b)
Possible place of originInsufficient Data
AncestorI
Defining mutationsA14233G (Behar & Family Tree DNA 2012)

Is the second most frequent clade of the haplogroup. Its subclades are found in Europe, e.g. I5a1, and the Near East, e.g. I5a2a and I5b (Olivieri 2013).

GenBank ID Population Source
HQ658465 German (north) FamilyTreeDNA
JQ245724 North Ossetia Fernandes 2012
I5a[]
Haplogroup I5a
Possible time of origin15,116 ± 4,128 BP (Behar 2012b)
Possible place of originInsufficient Data
AncestorI5
Defining mutationsT5074C, C16148T (Behar & Family Tree DNA 2012)
GenBank ID Population Source
FJ348190 Hutterite Pichler 2010
JQ701894 - Behar 2012b
JQ704768 - Behar 2012b
JQ245733 Dubai Fernandes 2012
JQ245772 Turkey Fernandes 2012
JQ245780 Yemen Fernandes 2012
JQ245781 Yemen Fernandes 2012
JQ245782 Yemen Fernandes 2012
JQ245783 Yemen Fernandes 2012
JQ245784 Yemen Fernandes 2012
JQ245785 Yemen Fernandes 2012
JQ245786 Yemen Fernandes 2012
I5a1[]
Haplogroup I5a1
Possible time of origin11,062 ± 4,661 BP (Behar 2012b)
Possible place of originInsufficient Data
AncestorI5a
Defining mutations8281-8289d, A12961G (Behar & Family Tree DNA 2012)
GenBank ID Population Source
AF382007 Leon Maca-Meyer 2001
EU597573 Bedouin (Israel) Hartmann 2009
JQ704713 - Behar 2012b
JQ705096 - Behar 2012b
EF660917 Italy Gasparre 2007
JQ245807 Bulgaria Fernandes 2012

I6[]

Haplogroup I6
Possible time of originAbout 18,400 BP (Olivieri 2013)
Possible place of originInsufficient Data
AncestorI
Defining mutationsT3645C (Behar & Family Tree DNA 2012)

The subclade is very rare, found until July 2013 only in four samples from the Near East (Olivieri 2013).

GenBank ID Population Source
JQ245773 Turkey Fernandes 2012
I6a[]
Haplogroup I6a
Possible time of originAbout 5,300 BP (Olivieri 2013)
Possible place of originInsufficient Data
AncestorI6
Defining mutations(G203A), G3915A, A6116G, A7804G, T15287C, (A16293c) (Behar & Family Tree DNA 2012)
GenBank ID Population Source
AY245555 - Janssen 2006
JQ705382 - Behar 2012b

I7[]

Haplogroup I7
Possible time of originAbout 9,100 BP (Olivieri 2013)
Possible place of originInsufficient Data
AncestorI
Defining mutationsC3534T, A4829G, T16324C

It is the rarest defined subclade, until July 2013 found only in two samples from the Near East and the Caucasus (Olivieri 2013).

GenBank ID Population Source
JF298212 Armenian FamilyTreeDNA
KF146253 Kuwait Olivieri 2013

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[]

  1. ^ Non, Amy. "ANALYSES OF GENETIC DATA WITHIN AN INTERDISCIPLINARY FRAMEWORK TO INVESTIGATE RECENT HUMAN EVOLUTIONARY HISTORY AND COMPLEX DISEASE" (PDF). University of Florida. Retrieved 12 April 2016.
  2. ^ Rabab Khairat; Markus Ball; Chun-Chi Hsieh Chang; Raffaella Bianucci; Andreas G. Nerlich; Martin Trautmann; Somaia Ismail; et al. (4 April 2013). "First insights into the metagenome of Egyptian mummies using next-generation sequencing". Journal of Applied Genetics. 54 (3): 309–325. doi:10.1007/s13353-013-0145-1. PMID 23553074. S2CID 5459033. Retrieved 8 June 2016.
  3. ^ 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.
  4. ^ Sirak, Kendra; Frenandes, Daniel; Novak, Mario; Van Gerven, Dennis; Pinhasi, Ron (2016). "Abstract Book of the IUAES Inter-Congress 2016 - A community divided? Revealing the community genome(s) of Medieval Kulubnarti using next- generation sequencing". Abstract Book of the Iuaes Inter-Congress 2016. IUAES: 115.

Footnotes[]

  1. ^ Nikitin 2009: 6/53 in Lemkos
    "Lemkos shared the highest frequency of haplogroup I ever reported and the highest frequency of haplogroup M* in the region."
  2. ^ Cvjetan 2004: 15/133

Works Cited[]

Journals[]

Websites[]

Further reading[]

External links[]

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