Vicente M. Cabrera1*, Patricia Marrero, , Khaled K.
Abu-Amero,Jose M. Larruga. (2017). Carriers of mitochondrial DNA
macrohaplogroup L3 basic lineages migrated back to Africa from Asia around
70,000 years ago. https://www.biorxiv.org/content/biorxiv/early/2017/12/13/233502.full.pdf
Cabrera et al, argue that the basic lineages for L3 migrated
back to Africa 70,000 years ago. The proposition is not supported by any
archaeological evidence. Absent any archaeological evidence this proposal lacks
any credibility. It is more likely that L3 had already spread across Africa
prior to 100,000 BC. This is obvious by the fact that the Aurignacians carried
L3 (N).
The
TMRCA mtDNA ancestor of hgs L3, M and N lived around 94.3kya(3).
There appears to have been a serial expansion of haplogroup N from the Great Lakes region of Africa
to other parts of Africa 93kya (3a). From Tanzania Khoisan speaking people
probably spread the haplogroup into Ethiopia by 80kya. this agrees with Cabrera et al's contention that L3, had early spread into East Africa.
The mtDNA haplogroup N has the common
transitions 73,7028,11719, 12705,14766 and 16223. The defining mutations include
8701,9540,10398, 10873 and 15301. Haplogroup N is a branch of L3 (M,N).
There
are also N hgs found in Africa . Haplogroups
N,N* and N1 is found in low frequencies
within Sub-Saharan groups including
Senegambians (9), Tanzanians (3) and modern
Ethiopians (1) .In Egypt 8.8 percent of the Gurma carry hg N1b (25).
Much of
the ancient mtDNA found in Iberia
has no relationship to the people presently living in Iberia (1a).
Dominguez found that the lineages recovered from ancient skeletons are the
African lineages L1b,L2 and L3. Almost 50% of the lineages from the Abauntz
Chalcolithic deposits and Tres Montes, in Navarre are the Sub-Saharan
lineages L1b,L2 and L3.
Discussion
Until
recently it was assumed that the earliest dates for hg N were in Eastern Eurasia . This view has changed recently as a
result of the extraction and examination of ancient mtDNA from Cro Magnon
skeletons dating to the Aurignacian period (26).
The archaeological evidence indicates that AMH
replaced Neanderthal during the Aurignacian period in Europe
between 32-35kya (27).
The Aurignacian civilization appears to have expanded from West to East (28-30).The
founders of this culture came from Africa (28,29,31).
Some researchers have argued that the Aurignacian culture was introduced to Europe from Africa (1a,32).
They based this conclusion on the fact that its tool kit was foreign to the
Mousterian type, and the culture appears in a mature form throughout Europe from France to Central Europe (1a,3a, 32-33).
Around 40,000 BC Europe
was occupied mainly by Neanderthals. They begin to be replaced in Europe around 32,000 by the CroMagnon
people at Les Eyzies inFrance
(29). It is also evident that archaic humans were replaced in much
of the Levant by the Levantine Aurignacian
culture bearers by a local variant of this technology at Ksar Akil Xlll-Vll
32kya , not 60-50kya.
people at Les Eyzies in
The Cro Magnon
DNA found in the ancient skeletons dates back to the Aurignacian period.
The Cro magnon skeletons belong to the N
haplogroup (26).
The Cro
Magnon skeletons carried N1a,N1b,N1c and N* (26). It is
characterized by motifs 00073G,10873C, 10238T and A4CC between nucleotide
positions 10397 and 10400. Most of the skeletons carried hg N*.
It
appears that the hg N was the most frequent mtDNA carried by Western European
populations for over 20,000 years. This gene as discussed earlier is found
primarily today outside Western Europe . The
Cro Magnon people were mainly hunter-gathers.
Haak et
al. found that the twenty-four samples included haplogroups H or V, T, K, J ,
N1a and U3 (36). The frequency of N1a among ancient samples ranged
from 8% to 42%. The archaeological evidence make it clear that the
Cro Magnon people probably originated in Africa
where we find hg N among African populations throughout the continent (3-3a,9).
The spread of Cro Magnon populations from Iberia eastward into Eastern Europe and the Levant
support the view that haplogroup N was
carried into Eurasia by Cro Magnon population
from Africa across the Straits of Gibraltar into
Iberia
(28).
The dates for the hg N in East Asia are
far later than the dates for hg N among Cro Magnon populations in western Eurasia . This
suggest that the hg N was carried into Iberia by Cro Magnon people.
The
Aurignacian culture did not enter Europe from
the Levant . The Aurignacian civilization
appears to have expanded from West to East (29-30) . The spread of
the Aurignacian culture from Western to Eastern Eurasian suggest that while hg
N*,N1 was already present among Western Eurasians , by around 12-14 kya hgs N2- N3 probably
originated in Siberia , not East
Asia . It would appear that the presence of these haplogroups in Eastern Europe are the result of a back migration from Siberia .
The high
frequency of hg N among the ancient Western Eurasians
make it clear that eventhough hg M and hg N may have exited Africa
along the southern coastal route out of Africa
65kya most carriers of hg N probably left Africa
during the migratory trajectory across the Straits of Gibraltar. Low
frequencies of hg N in East Asia and Oceania today, are probably the result of the southern
coastal route out of Africa from the Red Sea on into Asia.This view is supported by the
ancient M and N lineages found in Asia .
Conclusion
In
conclusion, the ‘Classic Aurignacian’
culture probably began in Africa , crossed the
Straits of Gibraltar into Iberia ,
and expanded eastward across Europe (3a,40-41,44)
. The archaeological record informs us that CroMagnon people carried hg N and
replaced the Neanderthal population of the Levant, at Ksar Akil around 32, 000 years ago (42-43),
not the Natufians who entered the Levant almost 20,000 years later. Moreover,
by 7000 BC the dominant haplogroup of Western Eurasians
remained hg N1(36) .
The
appearance of phylogenetically related sequences of hg L3 present
in many ancient Iberian skeletons
suggest that this haplogroup may have a
long history in Iberia .
The fact that hg N came to Iberia
with the Cro-Magnon people in Aurignacian times suggest that carries of L3 may
have also been part of this population movement.
The
mtDNA, skeletal and archaeological record generally, support a third migration event out of Africa before the expansion of the Natufians into the Levant 10,000-20,000 ybp (35). This third out
of Africa event took place between 40-35kya,
when modern man crossed from Africa into Iberia carrying
haplogroups N and L3, and began to
replace Neanderthal as the dominant population in western Eurasia .
Reference:
1.
Quibtanana-Murci L, Semino O,Bandelt H J, Passaro
G, McElreadey K, Santachiara-Benerecetti A S. Genetic Evidence of an early exit
of Homo sapiens from Africa through eastern Africa, Nat. Genet (1999); 23:437-441.
1a. Domínguez E.F. Polimorfismos de DNA mitocondrial
en poblaciones antiguas de la cuenca
mediterránea.
Universitat de Barcelona.
Departament de Biologia Animal, 2005 (PhD thesis).
2.
Rootsi S, Zhehvotsky LA, Baldovi M, Kayer M, Kutnev
IA, Khusainova R, Bermisheva MA, Gubina M. A counter-clockwise northern route
of the Y-chromosome haplogroup N from Southeast Asia
towards Europe . Eur J Hum Genet (2007)15, 204-211.
3.
Gonder
MK, Mortensen HM, Reed FA, de Sousa A, Tishkoff SA. (2006). Whole mtDNA Genome
Sequence Analysis of Ancient African Lineages. Mol Biol Evol. 2006 Dec
28.
3a. Winters,C. Origin and spread of
the Haplogroup N. Bioresearch Bull (2010) 3:116-122.
4.
Karafet TM, Osipova LP, Gubina MA, Posukh OL,
Zegura SL, Hammer MF: High levels of Y-chromosome differentiation among native
Siberian populations and the genetic signature of a boreal hunter-gatherer way
of life. Hum Biol 2002; 74: 761–789. | PubMed | ISI |
5.
Zerjal T, Dashnyam B, Pandya A et al:
Genetic relationships of Asians and Northern Europeans, revealed by Y-chromosomal
DNA analysis. Am J Hum Genet 1997; 60: 1174–1183. | PubMed | ISI | ChemPort |
6.
Tambets K, Rootsi S, Kivisild T et al:
The western and eastern roots of the Saami – the story of genetic 'outliers'
told by mtDNA and Y-chromosome. Am J Hum Genet 2004; 74: 661:682. | Article |
7.
Palanichamy MG, Sun C, Agrawal B, Kong Q-P,
Khan F, Wang C-Y, Palla V, Zhang Y-P. Phylogeny of Mitochondrial DNA
Macrohaplogroup N Based on complete sequencing: Implications for South Asia ,
Am J Hum Genet 2004; 75(6), 966-978.
8. Rosa A, Ornelas C, Jobling MA, Brehm A,
Villems R. Y-chromosome diversit6y in the population of Guinea-Bissau: a
multiethnic perspective, BMC Evolutionary Biology 2007; 7, 124-.
9. González, A. M., V. M.
Cabrera, J. M. Larruga, A. Tounkara, G. Noumsi, B. N. Thomas and J. M. Moulds. Mitochondrial DNA Variation in Mauritania and Mali and their
Genetic Relationship to Other Western Africa Populations. Annals of Human Genetics 2006;70,5.
http://www.blackwell-synergy.com/doi/abs/10.1111/j.1469-1809.2006.00259.x?cookieSet=1&journalCode=ahg
10.
Su B, Jin L: Natives or immigrants: modern
human origin in East Asia. Nat Rev 2000; 1: 126–133. | Article | ChemPort |
11.
Wendorf, F. The History of Nubia,
1968. Dallas.
12.
Hammer MF, Karafet TM, Park H et al:
Dual origins of the Japanese: common ground for hunter-gatherer and farmer Y
chromosomes. J Hum Genet 2006; 51: 47–58. | Article | PubMed |
13.
Tajima A, Pan IH, Fucharoen G et al:
Three major lineages of Asian Y chromosomes: implications for the peopling of
east and southeast Asia. Hum Genet 2002; 110: 80–88. | Article | PubMed | ISI | ChemPort |
14.
Dupuy BM, Stenersen M, Egeland T, Olaisen B:
Y-chromosomal microsatellite mutation rates: differences in mutation rate
between and within loci. Hum Mutat 2004; 23: 117–124. | Article | PubMed | ChemPort |
15.
Cinnioglu C, King R, Kivisild T et al:
Excavating Y-chromosome haplotype strata in Anatolia. Hum Genet 2004; 114: 127–148. | Article | PubMed |
16.
Kayser M, Brauer S, Weiss G et al:
Reduced Y-chromosome, but not mitochondrial DNA, diversity in human populations
from West New Guinea. Am J Hum Genet 2003; 72: 281–302. | Article | PubMed | ISI | ChemPort |
17.
Su B, Xiao J, Underhill P et al:
Y-Chromosome evidence for a northward migration of modern humans into Eastern
Asia during the last ice age. Am J Hum Genet 1999; 65: 1718–1724. | Article | PubMed | ISI | ChemPort |
18.
Bergen AW, Wang CY, Tsai J et al: An
Asian-Native American paternal lineage identified by RPS4Y resequencing and by
microsatellite haplotyping. Ann Hum Genet 1999; 63: 63–80. | Article | PubMed | ISI | ChemPort |
19.
Karafet TM, Zegura SL, Posukh O et al:
Ancestral Asian source(s) of new world Y-chromosome founder haplotypes. Am J Hum Genet
1999; 64: 817–831. | Article | PubMed | ISI | ChemPort |
20.
Lell JT, Sukernik RI, Starikovskaya YB et
al: The dual origin and Siberian affinities of Native American Y
chromosomes. Am J Hum Genet 2002; 70: 192–206. | Article | PubMed | ISI | ChemPort |
21.
Seielstad M, Yuldasheva N, Singh N et al:
A novel Y-chromosome variant puts an upper limit on the timing of first entry
into the Americas. Am J Hum Genet 2003; 73: 700–705. | Article | PubMed | ChemPort |
24.
Darenko M, Malyarchuk B, Denisova G., Wozniak
M, Grzybouski T, Dambueva I, Zakharov I. Y-chromosome haplogroup N dispersals
from South Siberia to Europe, J Hum Genet 2007, 52 (9), 763-770.
25.
Stevanovitch A, Gilles A, Bouzaid E, Kefi R,
Paris,F. Mitochondrial DNA sequence diversity in a Sedentary population from
Egypt, Ann Hum Gent 2003; 68, 23-30.
26.
Caramelli,D.,Lalueza-Fox,C., Vernesi,C.,
Lari,M.,Casoli,A., Mallegni,B.C., Dupanloup, I., Bertranpetit,J., Barbujani,G.,
Bertorelle,G. Evidence for a genetic discontinuity between Neandertals and
24,000 year-old anatomically modern Europeans. Proc Natl Acad Sci U S A. 2003,;100
(11):6593-6597.
27.
Lindly LM, G. A.
Clark; O. Bar-Yosef; D. Lieberman; J. Shea; Harold L. Dibble; Phillip G. Chase; Clive Gamble; Robert H.
Gargett; Ken Jacobs; Paul Mellars; Anne Pike-Tay; Yuri Smirnov; Lawrence Guy
Straus; C. B. Stringer; Erik Trinkaus; Randall White .(1990). Symbolism and
Modern Human Origins [and Comments and Reply] Current Anthropology,
31( 3): 233-261.
28.
Winters
C.(2008). Aurignacian Culture: Evidence of a Western Exit for Anatomically
Modern Humans. South Asian Anthropologist , Forthcoming March.
29.
Diop, A.( 1991 ) . Civilization
or Barbarism. Lawrence Hill Books.
30.
Diop,A.(1974).
The African Origin of Civilization. Lawrence Hill Books .
31.
Boule,
M., HV Vallois . (1957). Fossil Man .
Dryden Press New York Bordes,
Francois.(1972 ). L’Origine de l’homme moderne.Paris, UNESCO. Bordes,
Francois.(1972 ). L’Origine de l’homme moderne.Paris, UNESCO.
32.
Mellars, P.A.
(1992).Archaeology and the Population-Dispersal Hypothesis of Modern Human
Origins in Europe. The Origin of Modern Humans and the Impact of
Chronometric Dating. .Philosophical Transactions: Biological Sciences, 337( 1280) : 225-234.
33.
Verneaux,R.(1926). Les Origines de l’humanite. Paris : F. Riedder & Cie.
34.
Holiday, T. (2000). Evolution at the
Crossroads:Modern Human Emergence in Western Asia ,
American Anthropologist,102(1) .
35.
Haak
W et al. 2005. Ancient DNA from the first European farmers 7500-year-old
Neolithic sites. Science 310:1016-1018.
36.
Barral,L. & Charles,R.P. (1963)
Nouvelles donnees anthropometriques et precision sue les affinities
systematiques des negroides de Grimaldi, Bulletin du Musee d’anthropologie prehistorique de Monaco ,
No.10:123-139.
37.
Brace,
C.L. , Noriko Seguchi, Conrad B. Quintyn, Sherry C. Fox, A. Russell Nelson, Sotiris K. Manolis,**
and Pan Qifeng. (2006). The questionable contribution of the Neolithic and
the Bronze Age to European craniofacial form. Proc Natl Acad Sci U S A.
2006 January 3; 103(1): 242–247.
38.
Balter M. 2005. Ancient DNA yields clues to
the puzzle of European origins. Science 310:964-965. Full text
(subscription)
39.
Haak
W et al. 2005. Ancient DNA from the first European farmers 7500-year-old
Neolithic sites. Science 310:1016-1018.
40. Mellars,P.A.
(2006).Going East:New Genetic and Archaeological Perspectives on the Modern Human
Colonization of Eurasia. Science 333 (11 August):796-800.
41. Brown, S.J. (2006). Neanderthals and modern
humans in western Asia . Retrieved 2/7/2007 at: http://karmak.org/archive/2003/01/westasia.html
42.
Steven,L.K. Stiner,M.C., Reese,D.S. & Gulec,E. (2001). Ornaments of the
earliest Upper Paleolithic:New insights from the Levant .
PNAS, 98(13):7641-7646.
43. Gilead ,I. (2005). The
Upper Paleolithic period in the Levant . Journal
of World History, 5(2): 105-154.
44. Winters
C.(2008). Aurignacian Culture: Evidence of Western Exit for Anatomically Modern
Humans, South Asian Anthropologist, 81(1):79-81.
No comments:
Post a Comment