Haplogroup_I_(mtDNA)

Haplogroup I (mtDNA)

Haplogroup I (mtDNA)

Human mitochondrial DNA haplogroup


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.

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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]

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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.

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Europe

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]

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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).

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Historic and prehistoric 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 8850–8750 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 Paternanbidea, 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
UneticeGermanyEsperstedt2050–1800 BCI1Adler 2012; Brandt 2013
Bell BeakerGermany2600–2500 BCI1a1Lee 2012; Oliveiri 2013
UneticeGermanyPlotzkau 32200–1550 BCI1a1Brandt 2013
UneticeGermanyEulau1979–1921 BCI1a1Brandt 2013
SrubnayaRussiaRozhdestveno I, Samara Steppes, Samara1850–1600 BCI1a1Mathieson 2015
Seh GabiIran3972–3800 BCI1cLazaridis 2016
Cami de Can GrauSpain3500–3000 BCI1c1Sampietro 2007; Olivieri 2013
Late Dynastic-PtolemaicEgypt806 BC – 124 ADI2Khairat 2013
Su CarroppuItaly9124–7851 BCI3Modi 2017
ScythianRussiaRostov-on-Don500–200 BCI3Der Sarkissian 2011
UneticeGermanyBenzingerode-Heimburg1653–1627 BCI3aBrandt 2013
UneticeGermanyEsperstedt2131–1979 BCI3aAdler 2012; Brandt 2013; Haak 2015; Mathieson 2015
UneticeGermanyEsperstedt2199–2064 BCI3aAdler 2012; Brandt 2013; Haak 2015
PoltavkaRussiaLopatino II, Sok River, Samara2885–2665 BCI3aMathieson 2015
KarasukRussiaSabinka 21416–1268 BCI4a1Allentoft 2015
MinoanGreeceAyios Charalambos2400–1700 BCI5Hughey 2013
MinoanGreeceAyios Charalambos2400–1700 BCI5Hughey 2013
MinoanGreeceAyios Charalambos2400–1700 BCI5Hughey 2013
Christian NubiaSudanKulubnarti550–800 ADI5Sirak 2016
Late Bronze AgeArmeniaNorabak1209–1009 BCI5cAllentoft 2015
MezhovskavaRussiaKapova cave1598–1398 BCI5cAllentoft 2015

Samples with unknown subclades

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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)
N1a1b28.623.5–33.9
I20.118.4–21.9
I116.314.6–18.0
I1a11.69.9–13.3
I1a14.94.2–5.6
I1a1a3.83.3–4.4
I1a1b1.40.5–2.2
I1a1c2.51.3–3.7
I1a1d1.81.0–2.6
I1b13.411.3–15.5
I1c10.38.4–12.2
I1c17.25.4–9.0
I1c1a4.02.5–5.4
I2'312.610.4–14.7
I26.86.0–7.6
I2a4.73.8–5.7
I2a13.22.1–4.4
I2b1.70.5–2.9
I2c4.73.6–5.8
I2d3.01.1–4.8
I2e3.11.4–4.8
I310.68.8–12.4
I3a7.46.1–8.7
I3a16.14.7–7.5
I3b2.61.1–4.2
I3c9.47.6–11.2
I415.112.3–18.0
I4a6.45.4–7.4
I4a15.74.5–6.7
I4b8.45.8–10.9
I518.416.4–20.3
I5a16.014.0–17.9
I5a19.27.1–11.3
I5a212.310.2–14.4
I5a2a1.61.0–2.1
I5a34.82.8–6.8
I5a45.63.5–7.8
I5b8.86.3–11.2
I618.416.2–20.6
I6a5.33.5–7.0
I6b13.110.4–15.8
I79.16.3–11.9

Distribution

I1

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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).

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I1a
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The subclade frequency peaks (circa 2.8%) are mostly located in North-Eastern Europe (Olivieri 2013).

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I1a1
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I1a1a
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I1a1a1
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I1a1a2
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I1a1b
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I1a1c
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I1a1d
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I1a1e
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I1b
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I1c
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I1c1
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I1c1a1
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I1c1a2
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I1d
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I1e
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I1f
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I2'3

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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
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I2a
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I2a1
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I2a1a
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I2a2
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I2a3
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I2b
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I2c
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I2d
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I2e
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I3
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I3a
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I3a1
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I3b
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I3c
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I3d
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I4

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

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I4a
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I4a1
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I4a2
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I4b
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I5

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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).

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I5a
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I5a1
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I5a1a
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I5a1b
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I5a1c
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I5a2
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I5a2a
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I5a3
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I5a4
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I5b
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I5c
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I5c1
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I6

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

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I6a
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I7

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

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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. 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: 115–116.

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."

Works cited

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