Revision as of 18:19, 3 July 2014 editJeezuuz1934 (talk | contribs)73 edits →Main genetic compositions← Previous edit | Revision as of 18:23, 3 July 2014 edit undoJeezuuz1934 (talk | contribs)73 edits →Links with African populations: Can get rid of this for now. Can work on it in talk pageTag: section blankingNext edit → | ||
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Haplogroup composition of the ancient Iberians was very similar to that found in the modern Iberian Peninsula populations, suggesting a long-term genetic continuity since pre-Roman times.<ref>{{cite journal |doi=10.1111/j.1529-8817.2005.00194.x |title=The Genetics of the Pre-Roman Iberian Peninsula: A mtDNA Study of Ancient Iberians |year=2005 |last1=Sampietro |first1=M. L. |first2=D. |first3=O. |first4=F. |first5=D. |first6=M. |first7=B. |first8=J. |first9=C. |journal=Annals of Human Genetics |volume=69 |pmid=16138912 |issue=Pt 5 |last2=Caramelli |last3=Lao |last4=Calafell |last5=Comas |last6=Lari |last7=Agustí |last8=Bertranpetit |last9=Lalueza-Fox |pages=535–48|display-authors=9 }}</ref><ref>{{cite journal |doi=10.1007/s004390000370 |title=Alu insertion polymorphisms in NW Africa and the Iberian Peninsula: evidence for a strong genetic boundary through the Gibraltar Straits |year=2000 |last1=Comas |first1=David |first2=Francesc |first3=Noufissa |first4=Ahmed |first5=Gerard |first6=Mark |first7=Mark A. |first8=Jaume |first9=Antti |journal=Human Genetics |volume=107 |pmid=11129330 |issue=4 |last2=Calafell |last3=Benchemsi |last4=Helal |last5=Lefranc |last6=Stoneking |last7=Batzer |last8=Bertranpetit |last9=Sajantila |pages=312–9|display-authors=9 }}</ref> | Haplogroup composition of the ancient Iberians was very similar to that found in the modern Iberian Peninsula populations, suggesting a long-term genetic continuity since pre-Roman times.<ref>{{cite journal |doi=10.1111/j.1529-8817.2005.00194.x |title=The Genetics of the Pre-Roman Iberian Peninsula: A mtDNA Study of Ancient Iberians |year=2005 |last1=Sampietro |first1=M. L. |first2=D. |first3=O. |first4=F. |first5=D. |first6=M. |first7=B. |first8=J. |first9=C. |journal=Annals of Human Genetics |volume=69 |pmid=16138912 |issue=Pt 5 |last2=Caramelli |last3=Lao |last4=Calafell |last5=Comas |last6=Lari |last7=Agustí |last8=Bertranpetit |last9=Lalueza-Fox |pages=535–48|display-authors=9 }}</ref><ref>{{cite journal |doi=10.1007/s004390000370 |title=Alu insertion polymorphisms in NW Africa and the Iberian Peninsula: evidence for a strong genetic boundary through the Gibraltar Straits |year=2000 |last1=Comas |first1=David |first2=Francesc |first3=Noufissa |first4=Ahmed |first5=Gerard |first6=Mark |first7=Mark A. |first8=Jaume |first9=Antti |journal=Human Genetics |volume=107 |pmid=11129330 |issue=4 |last2=Calafell |last3=Benchemsi |last4=Helal |last5=Lefranc |last6=Stoneking |last7=Batzer |last8=Bertranpetit |last9=Sajantila |pages=312–9|display-authors=9 }}</ref> | ||
== Links with African populations == | |||
===North-African admixture=== | |||
A number of studies have tried to find out the genetic impact of North African and Middle Eastern population movements on the modern Spanish and Portuguese ancestry, through comparison of genetic markers in Spain and Portugal with North Africa and the Near East. The most recent and thorough study about Moorish influence in the Iberian Peninsula was conducted April 2013 by Pompeu Fabra University using genome-wide SNP data for over 2000 individuals. This study concluded that the Iberian Peninsula holds significantly higher levels of both North African and Sub-Saharan ancestry than the rest of the European continent with a sharp difference between Iberia and France. Estimates of shared ancestry with North African populations were found to be much higher than previously reported, averaging 4% to 20% of individual genomes, whereas these do not exceed 2% in Southern European populations outside Spain and Portugal and are practically inexistent north of the Pyrenees.<ref></ref> | |||
Iberia has the greatest presence of the typically ]n Y-chromosome haplotype marker E-M81 in Europe.<ref name=capelli2009>{{cite journal |doi=10.1038/ejhg.2008.258 |title=Moors and Saracens in Europe: estimating the medieval North African male legacy in southern Europe |year=2009 |last1=Capelli |first1=Cristian |first2=Valerio |first3=Francesca |first4=Ilaria |first5=Francesca |pmc=2947089 |first6=Mara |first7=Gianmarco |first8=Sergio |first9=Adriano |journal=European Journal of Human Genetics |volume=17 |pmid=19156170 |issue=6 |last2=Onofri |last3=Brisighelli |last4=Boschi |last5=Scarnicci |last6=Masullo |last7=Ferri |last8=Tofanelli |last9=Tagliabracci |last10=Gusmao |first10=Leonor |last11=Amorim |first11=Antonio |last12=Gatto |first12=Francesco |last13=Kirin |first13=Mirna |last14=Merlitti |first14=Davide |last15=Brion |first15=Maria |last16=Verea |first16=Alejandro Blanco |last17=Romano |first17=Valentino |last18=Cali |first18=Francesco |last19=Pascali |first19=Vincenzo |pages=848–52}}</ref><ref>{{cite journal |doi=10.1086/386295 |title=Origin, Diffusion, and Differentiation of Y-Chromosome Haplogroups E and J: Inferences on the Neolithization of Europe and Later Migratory Events in the Mediterranean Area |year=2004 |last1=Semino |first1=Ornella |last2=Magri |first2=Chiara |last3=Benuzzi |first3=Giorgia |last4=Lin |first4=Alice A. |last5=Al-Zahery |first5=Nadia |last6=Battaglia |first6=Vincenza |last7=MacCioni |first7=Liliana |last8=Triantaphyllidis |first8=Costas |last9=Shen |first9=Peidong |last10=Oefner |first10=Peter J. |last11=Zhivotovsky |first11=Lev A. |last12=King |first12=Roy |last13=Torroni |first13=Antonio |last14=Cavalli-Sforza |first14=L. Luca |last15=Underhill |first15=Peter A. |last16=Santachiara-Benerecetti |first16=A. Silvana |journal=The American Journal of Human Genetics |volume=74 |issue=5 |pages=1023–34 |pmid=15069642 |pmc=1181965}}</ref> and Haplotype Va.<ref>{{cite journal |doi=10.1353/hub.2006.0045 |title=North African Berber and Arab Influences in the Western Mediterranean Revealed by Y-Chromosome DNA Haplotypes |year=2006 |last1=Gérard |first1=Nathalie |last2=Berriche |first2=Sala |last3=Aouizérate |first3=Annie |last4=Diéterlen |first4=Florent |last5=Lucotte |first5=Gérard |journal=Human Biology |volume=78 |issue=3 |pages=307–16 |pmid=17216803}}</ref> | |||
According to a widely publicized recent study (December 2008) published in the ], 19.8 percent of modern Iberians (Spain + Portugal) have DNA reflecting Near Eastern and 10.6 percent having DNA reflecting North African ancestors.<ref name=adams2008/> The study's speculation on Sephardic origin of the Levantine markers has been widely contested since it is likely that such markers also reflect other migrations, including Levantine Arabs, earlier Phoenician colonization or even population movements during the Neolithic.<ref name=adams2008/><ref name=adams2008/><ref name=gonzalez2003/><ref>{{cite journal |doi=10.1007/s00439-004-1168-9 |title=Y chromosomal haplogroup J as a signature of the post-neolithic colonization of Europe |year=2004 |last1=Giacomo |first1=F. |first2=F. |first3=L. O. |first4=N. |first5=N. |first6=J. |first7=R. |first8=G. |first9=F. |last10=Ciavarella |first10=G. |last11=Cucci |first11=F. |last12=Stasi |first12=L. |last13=Gavrila |first13=L. |last14=Kerimova |first14=M. G. |last15=Kovatchev |first15=D. |last16=Kozlov |first16=A. I. |last17=Loutradis |first17=A. |last18=Mandarino |first18=V. |last19=Mammi′ |first19=C. |last20=Michalodimitrakis |first20=E. N. |last21=Paoli |first21=G. |last22=Pappa |first22=K. I. |last23=Pedicini |first23=G. |last24=Terrenato |first24=L. |last25=Tofanelli |first25=S. |last26=Malaspina |first26=P. |last27=Novelletto |first27=A. |journal=Human Genetics |volume=115 |pmid=15322918 |issue=5 |last2=Luca |last3=Popa |last4=Akar |last5=Anagnou |last6=Banyko |last7=Brdicka |last8=Barbujani |last9=Papola |pages=357–71|display-authors=8 }}</ref><ref>{{cite journal |doi=10.1080/03014460500475870 |title=Toward resolution of the debate regarding purported crypto-Jews in a Spanish-American population: Evidence from the Y chromosome |year=2006 |last1=Sutton |first1=Wesley K. |first2=Alec |first3=Peter A. |first4=Judith S. |first5=Todd R. |first6=Joanna L. |journal=Annals of Human Biology |volume=33 |pmid=16500815 |issue=1 |last2=Knight |last3=Underhill |last4=Neulander |last5=Disotell |last6=Mountain |pages=100–11}}</ref><ref name=zalloua2008>{{cite journal |doi=10.1016/j.ajhg.2008.10.012 |title=Identifying Genetic Traces of Historical Expansions: Phoenician Footprints in the Mediterranean |year=2008 |last1=Zalloua |first1=P |first2=D |first3=M |first4=J |first5=N |first6=M |first7=Y |first8=H |first9=E |last10=Adams |first10=Susan M. |last11=Arroyo |first11=Eduardo |last12=López-Parra |first12=Ana María |last13=Aler |first13=Mercedes |last14=Picornell |first14=Antònia |last15=Ramon |first15=Misericordia |last16=Jobling |first16=Mark A. |last17=Comas |first17=David |last18=Bertranpetit |first18=Jaume |last19=Wells |first19=R. Spencer |last20=Tyler-Smith |first20=Chris |last21=Genographic |first21=Consortium |journal=The American Journal of Human Genetics |volume=83 |pmid=18976729 |last2=Platt |last3=El Sibai |last4=Khalife |last5=Makhoul |last6=Haber |last7=Xue |last8=Izaabel |last9=Bosch |issue=5 |pmc=2668035 |pages=633–42|display-authors=8 }}</ref><ref name="publico">"La cifra de los sefardíes puede estar sobreestimada, ya que en estos genes hay mucha diversidad y quizá absorbieron otros genes de Oriente Medio" ''('''"The Sephardic result may be overestimated''', since there is much diversity in those genes and maybe absorbed other genes from the Middle East")''. ¿Pone en duda Calafell la validez de los tests de ancestros? "Están bien para los americanos, nosotros ya sabemos de dónde venimos" ''(Puts Calafell in doubt the validity of ancestry tests? "They can be good for the Americans, we already know from where we come from)''.''''' ''" </ref><ref>"El doctor Calafell matiza que (...) los marcadores genéticos usados para distinguir a la población con ancestros sefardíes pueden producir distorsiones". "ese 20% de españoles que el estudio señala como descendientes de sefardíes podrían haber heredado ese rasgo de movimiento más antiguos, como el de los fenicios o, incluso, primeros pobladores neolíticos hace miles de años." "Dr. Calafell clarifies that (...) '''the genetic markers used to distinguish the population with Sephardim ancestry may produce distortions. The 20% of Spaniards that are identified as having Sephardim ancestry in the study could have inherited that same marker from other population movements such as Arabs, Phoenicians, or even the first Neolithic settlers thousands of years ago'''" http://www.elmundo.es/elmundo/2008/12/04/ciencia/1228409780.html</ref> Chris Tyler-Smith, a collaborator with the team that carried the study,<ref>{{dead link|date=July 2010}}</ref> argues that the individual differences in Y-chromosome markers suggests a common ancestry more recent than several millennia.<ref>, ], December 4, 2008</ref> | |||
Priorly, Capelli et al. 2009 reported that North African ], especially E1b1b1b (E-M81), E1b1b1a-b (M78 derived chromosomes showing the rare DYS439 allele 10, or E-V65) and a subset of J1 (M267 derived), represented, on average, 7-8% of the current Iberian male lineages.<ref>{{cite journal|doi=10.1038/ejhg.2008.258|pmc=2947089|pmid=19156170|title=Moors and Saracens in Europe: Estimating the medieval North African male legacy in southern Europe|year=2009|last1=Capelli|first1=Cristian|last2=Onofri|first2=Valerio|last3=Brisighelli|first3=Francesca|last4=Boschi|first4=Ilaria|last5=Scarnicci|first5=Francesca|last6=Masullo|first6=Mara|last7=Ferri|first7=Gianmarco|last8=Tofanelli|first8=Sergio|last9=Tagliabracci|first9=Adriano|last10=Gusmao|first10=Leonor|last11=Amorim|first11=Antonio|last12=Gatto|first12=Francesco|last13=Kirin|first13=Mirna|last14=Merlitti|first14=Davide|last15=Brion|first15=Maria|last16=Verea|first16=Alejandro Blanco|last17=Romano|first17=Valentino|last18=Cali|first18=Francesco|last19=Pascali|first19=Vincenzo|journal=European Journal of Human Genetics|volume=17|issue=6|pages=848–52|display-authors=8}} </ref> | |||
{| class="wikitable sortable" border=1 | |||
|+Historically introduced NW African types in Iberia (Capelli et al. (2009)) | |||
! scope="col" |Sample | |||
! scope="col" |N | |||
! scope="col" |] | |||
! scope="col" |] | |||
! scope="col" |] (subset) | |||
! scope="col" |Total % | |||
|- | |||
| Spain||717||5.2||1||1.5||7.7 | |||
|- | |||
| Portugal||659||5||0.3||1.8||7.1 | |||
|- | |||
| Iberia||1376||5.1||0.7||1.7||7.4 | |||
|} | |||
An earlier European-wide study had pointed to a small North African and Arab element in modern day Iberian ancestry when compared to the pre-Islamic ancestral basis, and the Gibraltar Strait seems to have functioned much more as a genetic barrier than a bridge.<ref name=pmid15044595>{{cite journal |doi=10.1093/molbev/msh135 |title=Estimating the Impact of Prehistoric Admixture on the Genome of Europeans |year=2004 |last1=Dupanloup |first1=I. |journal=Molecular Biology and Evolution |volume=21 |issue=7 |pages=1361–72 |pmid=15044595 |last2=Bertorelle |first2=G |last3=Chikhi |first3=L |last4=Barbujani |first4=G}}</ref><ref>{{cite journal |doi=10.1086/319521 |title=High-Resolution Analysis of Human Y-Chromosome Variation Shows a Sharp Discontinuity and Limited Gene Flow between Northwestern Africa and the Iberian Peninsula |year=2001 |last1=Bosch |first1=Elena |last2=Calafell |first2=Francesc |last3=Comas |first3=David |last4=Oefner |first4=Peter J. |last5=Underhill |first5=Peter A. |last6=Bertranpetit |first6=Jaume |journal=The American Journal of Human Genetics |volume=68 |issue=4 |pages=1019–29 |pmid=11254456 |pmc=1275654}}</ref><ref>{{cite journal |doi=10.1007/s004390000370 |title=Alu insertion polymorphisms in NW Africa and the Iberian Peninsula: Evidence for a strong genetic boundary through the Gibraltar Straits |year=2000 |last1=Comas |first1=David |last2=Calafell |first2=Francesc |last3=Benchemsi |first3=Noufissa |last4=Helal |first4=Ahmed |last5=Lefranc |first5=Gerard |last6=Stoneking |first6=Mark |last7=Batzer |first7=Mark A. |last8=Bertranpetit |first8=Jaume |last9=Sajantila |first9=Antti |journal=Human Genetics |volume=107 |issue=4 |pages=312–9 |pmid=11129330|display-authors=9 }}</ref> | |||
As for Mtdna analysis (Mitochondrial DNA), although present at only low levels, Iberia has much higher frequencies of typically North African Haplogroup U6 than those generally observed in Europe.<ref name=adams2008>{{cite journal |doi=10.1016/j.ajhg.2008.11.007 |laysummary=http://www.sciencenews.org/view/generic/id/39056/title/Spanish_Inquisition_couldn%E2%80%99t_quash_Moorish,_Jewish_genes |laysource=] |laydate=3 January 2009 |title=The Genetic Legacy of Religious Diversity and Intolerance: Paternal Lineages of Christians, Jews, and Muslims in the Iberian Peninsula |year=2008 |last1=Adams |first1=Susan M. |first2=Elena |first3=Patricia L. |first4=Stéphane J. |first5=Andrew C. |first6=Eduardo |first7=Ana M. |first8=Mercedes |first9=Marina S. Gisbert |journal=The American Journal of Human Genetics |volume=83 |pmid=19061982 |last2=Bosch |last3=Balaresque |last4=Ballereau |last5=Lee |last6=Arroyo |last7=López-Parra |last8=Aler |last9=Grifo |issue=6 |pmc=2668061 |last10=Brion |first10=Maria |last11=Carracedo |first11=Angel |last12=Lavinha |first12=João |last13=Martínez-Jarreta |first13=Begoña |last14=Quintana-Murci |first14=Lluis |last15=Picornell |first15=Antònia |last16=Ramon |first16=Misericordia |last17=Skorecki |first17=Karl |last18=Behar |first18=Doron M. |last19=Calafell |first19=Francesc |last20=Jobling |first20=Mark A. |pages=725–36}}</ref><ref name=gonzalez2003>{{cite journal |doi=10.1002/ajpa.10168 |title=Mitochondrial DNA affinities at the Atlantic fringe of Europe |year=2003 |last1=González |first1=Ana M. |first2=Antonio |first3=José A. |first4=Nicole |first5=Carlos |first6=Vicente M. |journal=American Journal of Physical Anthropology |volume=120 |pmid=12627534 |issue=4 |last2=Brehm |last3=Pérez |last4=Maca-Meyer |last5=Flores |last6=Cabrera |pages=391–404}}</ref><ref name=plaza2003>{{cite journal |doi=10.1046/j.1469-1809.2003.00039.x |title=Joining the Pillars of Hercules: mtDNA Sequences Show Multidirectional Gene Flow in the Western Mediterranean |year=2003 |last1=Plaza |first1=S. |first2=F. |first3=A. |first4=N. |first5=G. |first6=J. |first7=D. |journal=Annals of Human Genetics |volume=67 |pmid=12914566 |issue=Pt 4 |last2=Calafell |last3=Helal |last4=Bouzerna |last5=Lefranc |last6=Bertranpetit |last7=Comas |pages=312–28}}</ref><ref name=pereira2005>{{cite journal |doi=10.1353/hub.2005.0041 |title=African Female Heritage in Iberia: A Reassessment of mtDNA Lineage Distribution in Present Times |year=2005 |last1=Pereira |first1=Luisa |first2=Carla |first3=Cintia |first4=Antonio |journal=Human Biology |volume=77 |last2=Cunha |last3=Alves |last4=Amorim |pmid=16201138 |issue=2 |pages=213–29}}</ref> It is difficult to ascertain whether U6's presence is the consequence of Islam's expansion into Europe during the Middle Ages, or it is rather the result of ancient demic processes that predate the Islamic presence.<ref name=gonzalez2003/><ref>{{cite journal |doi=10.1111/j.1529-8817.2005.00161.x |title=Y-chromosome Lineages from Portugal, Madeira and Acores Record Elements of Sephardim and Berber Ancestry |year=2005 |last1=Goncalves |first1=Rita |last2=Freitas |first2=Ana |last3=Branco |first3=Marta |last4=Rosa |first4=Alexandra |last5=Fernandes |first5=Ana T. |last6=Zhivotovsky |first6=Lev A. |last7=Underhill |first7=Peter A. |last8=Kivisild |first8=Toomas |last9=Brehm |first9=Antonio |journal=Annals of Human Genetics |volume=69 |issue=4 |pages=443–54 |pmid=15996172|display-authors=9 }}</ref> | |||
{| class="wikitable sortable" border=1 | |||
| align="center" style="background:#f0f0f0;"|'''Country''' | |||
| align="center" style="background:#f0f0f0;"|'''Region''' | |||
| align="center" style="background:#f0f0f0;"|'''Number tested''' | |||
| align="center" style="background:#f0f0f0;"|'''Study''' | |||
| align="center" style="background:#f0f0f0;"|'''%''' | |||
|- | |||
| Italy || Countrywide ||583||Brisighelli et al. (2012)||0.8% | |||
|- | |||
| Italy || Countrywide ||411||Plaza et al. (2003)||0.1% | |||
|- | |||
| Italy || ] ||169||Plaza et al. (2003)||0.6% | |||
|- | |||
| Italy || ] ||106||Maca-Meyer et al. (2003)||0.94% | |||
|- | |||
| Spain|| Central Spain ||50||Plaza et al. (2003)||2.0% | |||
|- | |||
| Spain || ] ||103||Plaza et al. (2003)||1.9% | |||
|- | |||
| Spain || ] ||135||Maca-Meyer et al. (2003)||2.2% | |||
|- | |||
| Spain || ] ||118||Maca-Meyer et al. (2003)||1.6% | |||
|- | |||
| Spain ||] ||135||Hernandez et al. (2014)||8.8% | |||
|- | |||
| Spain || Maragatos ||49||Maca-Meyer et al. (2003)||8.1% | |||
|- | |||
| Spain || ] ||300||Brehm et al. (2003)||14.0% | |||
|- | |||
| Portugal|| Countrywide ||54||Plaza et al. (2003)||5.6% | |||
|- | |||
| Portugal|| North Portugal ||184||Maca-Meyer et al. (2003)||4.3% | |||
|- | |||
| Portugal|| Central Portugal ||161||Brehm et al. (2003)||1.9% | |||
|- | |||
| Portugal|| ] ||155||Brehm et al. (2003)||3.9% | |||
|- | |||
| Iberia|| ] & ]||887||Plaza et al. (2003)||1.8% | |||
|} | |||
A 2007 study (published 2007) had estimated the contribution of northern African lineages to the entire male gene pool of Iberia as 5.6%."<ref>{{cite journal |doi=10.1093/molbev/msm049 |title=Tracing Past Human Male Movements in Northern/Eastern Africa and Western Eurasia: New Clues from Y-Chromosomal Haplogroups E-M78 and J-M12 |year=2007 |last1=Cruciani |first1=F. |last2=La Fratta |first2=R. |last3=Trombetta |first3=B. |last4=Santolamazza |first4=P. |last5=Sellitto |first5=D. |last6=Colomb |first6=E. B. |last7=Dugoujon |first7=J.-M. |last8=Crivellaro |first8=F. |last9=Benincasa |first9=T. |last10=Pascone |first10=R. |last11=Moral |first11=P. |last12=Watson |first12=E. |last13=Melegh |first13=B. |last14=Barbujani |first14=G. |last15=Fuselli |first15=S. |last16=Vona |first16=G. |last17=Zagradisnik |first17=B. |last18=Assum |first18=G. |last19=Brdicka |first19=R. |last20=Kozlov |first20=A. I. |last21=Efremov |first21=G. D. |last22=Coppa |first22=A. |last23=Novelletto |first23=A. |last24=Scozzari |first24=R. |journal=Molecular Biology and Evolution |volume=24 |issue=6 |pages=1300–11 |pmid=17351267}}</ref> | |||
===Haplogroup L lineages frequencies=== | |||
Haplogroup L is the dominant haplogroup of Sub-Saharan Africa (96-100%) with lower levels occurring also in adjacent areas of North Africa, the Arabian Peninsula and parts of the Middle East. | |||
{| class="toccolours" style="float: right; margin-left: 1em; margin-right: 2em; font-size: 85%; background:#c6dbf7; color:black; width:30em; max-width: 40%;" cellspacing="5" | |||
| style="text-align: left;" | Map (in the link) <ref name="genome.cshlp.org">http://genome.cshlp.org/content/22/5/821/F1.large.jpg</ref> showing the distribution of ] mtDNA (shown in '''red''') in Europe<BR> Map is From '''Cerezo et al. 2012''' <ref>http://genome.cshlp.org/content/22/5/821.full#ref-12</ref><BR>''Universidad de Santiago de Compostela''<BR>] (Spain & Portugal) having the highest amount and strongest concentration of ] mtDNA in Europe.<ref name="genome.cshlp.org"/> | |||
|- | |||
|} | |||
In ] the mean frequency of Haplogroup L lineages reaches 3.83% and the frequency is higher in ] (5.83%) than in ] (2.9% average) and without parallel in the rest of Europe. In both countries frequencies vary widely between regions with increase frequencies observed for Madeira (Portugal), Southern Portugal, Cordoba (Southern Spain) and North Western Castile (Spain).<ref>{{cite journal |author=Pereira L, Cunha C, Alves C, Amorim A |title=African female heritage in Iberia: a reassessment of mtDNA lineage distribution in present times |journal=Human Biology |volume=77 |issue=2 |pages=213–29 |date=April 2005 |pmid=16201138 |doi=10.1353/hub.2005.0041 |ref=harv}}</ref> In the ], L haplogroups constituted about 13% of the lineages in ], significantly more than in the ].<ref name="Brehm A, Pereira L, Kivisild T, Amorim A 2003 77–86">{{cite journal |author=Brehm A, Pereira L, Kivisild T, Amorim A |title=Mitochondrial portraits of the Madeira and Açores archipelagos witness different genetic pools of its settlers |journal=Human Genetics |volume=114 |issue=1 |pages=77–86 |date=December 2003 |pmid=14513360 |doi=10.1007/s00439-003-1024-3 |ref=harv}}</ref> In the Spanish archipelago of ], frequencies have been reported at 6.6%.<ref name="Brehm A, Pereira L, Kivisild T, Amorim A 2003 77–86"/> Regarding Iberia, current debates are concerned with whether these lineages are associated with prehistoric migrations, the Islamic occupation of Iberia or the slave trade. {{Harvcoltxt|Pereira et al.|2000}} suggested that African lineages in Iberia were predominantly the result of Atlantic Slave Trade. {{Harvcoltxt|Gonzalez et al.|2003}} revealed that most of the L lineages in Iberia matched Northwest African L lineages rather than contemporary Sub-Saharan L lineages. The authors suggest this pattern indicates that most of the Sub-Saharan L lineages entered Iberia in Islamic or even prehistoric time rather than during the slave trade. However, according to {{Harvcoltxt|Pereira et al.|2005}}, the sub-Saharan lineages found in Iberia matched lineages from diverse regions in Africa. They suggest this pattern is more compatible with recent arrival of these lineages after slave trading began in the 15th century. According to the study, alternative scenarios that invoke much older and demographically more significant introductions ({{Harvcoltxt|Gonzalez et al.|2003}}) or that claim a substantial role of the Roman and/or Islamic periods on the introduction of sub-Saharan lineages seem unlikely. {{Harvcoltxt|Casas et al.|2006}} extracted DNA from human remains that were exhumed from old burial sites in ], Spain. The remains date to between 12th-13th century. The frequency of Sub-Saharan lineages detected in the medieval samples was 14.6% and 8.3% in the present population of ]. The authors suggest the ] and prehistoric migrations before the Muslim occupation would have been the source of these lineages. The highest frequencies of Sub-Saharan lineages found so far in Europe were observed by Alvarez et al. 2010 in the ] of ] (18.2%) which is according to the authors "comparable to that described for the South of Portugal"<ref>{{cite paper | author = Alvarez et al. | year = 2010 | pmid = 20127843 | title = Mitochondrial DNA Patterns in the Iberian Northern Plateau: Population Dynamics and Substructure of the Zamora Province}}</ref><ref>''As regards sub-Saharan Hgs (L1b, L2b, and L3b), the high frequency found in the southern regions of Zamora, 18.2% in Sayago and 8.1% in Bajo Duero, is comparable to that described for the South of Portugal'', Alvarez et al. (2010)</ref> and by Pereira et al. 2010 in ] (22%).<ref>{{cite doi|10.1002/ajhb.21049}}</ref> | |||
A study by Auton et al. 2009, which also contains an admixture analysis chart but no cluster membership | |||
coefficients, shows little to no sub-Saharan African influence in a wide array of non-Iberian European samples.<ref name="auton">{{cite journal |author=Auton A |title=Global distribution of genomic diversity underscores rich complex history of continental human populations |journal=Genome Research |volume=19 |issue=5 |pages=795–803 |date=May 2009 |pmid=19218534 |pmc=2675968 |doi=10.1101/gr.088898.108 |ref=harv |author-separator=, |author2=Bryc K |author3=Boyko AR |display-authors=3 |last4=Lohmueller |first4=K. E. |last5=Novembre |first5=J. |last6=Reynolds |first6=A. |last7=Indap |first7=A. |last8=Wright |first8=M. H. |last9=Degenhardt |first9=J. D.}}</ref> | |||
{| class="wikitable sortable" border=1 | |||
| align="center" style="background:#f0f0f0;"|'''Country''' | |||
| align="center" style="background:#f0f0f0;"|'''Region''' | |||
| align="center" style="background:#f0f0f0;"|'''Number tested''' | |||
| align="center" style="background:#f0f0f0;"|'''Study''' | |||
| align="center" style="background:#f0f0f0;"|'''%''' | |||
|- | |||
| Greece||]||202||Achilli et al. (2007)||0.99% | |||
|- | |||
| Cyprus||]||91||Irwin et al. (2008)||3.30% | |||
|- | |||
| Italy ||Countrywide||583||Brisighelli et al. (2012)||1.20%<ref></ref> | |||
|- | |||
| Italy ||] ||322||Achilli et al. (2007)||1.90% | |||
|- | |||
| Italy ||] ||138||Achilli et al. (2007)||2.90% | |||
|- | |||
| Italy ||] ||813||Achilli et al. (2007)||0.98% | |||
|- | |||
| Italy ||] ||114||Achilli et al. (2007)||2.60% | |||
|- | |||
| Italy ||] ||177||Achilli et al. (2007)||0.00% | |||
|- | |||
| Italy ||] ||169||Achilli et al. (2007)||0.00% | |||
|- | |||
| Italy ||] ||84||Pereira et al. (2005)||2.90% | |||
|- | |||
| Italy ||] (South Italy) ||313||Achilli et al. (2007)||0.32% | |||
|- | |||
| Italy ||] (South Italy) ||92||Ottoni et al. (2009)||2.20% | |||
|- | |||
| Italy ||] & ] (South Italy) ||226||Achilli et al. (2007)||0.00% | |||
|- | |||
| Italy ||] ||115||Sarno et al. (2014)||0.00% | |||
|- | |||
| Italy ||] ||105||Achilli et al. (2007)||1.90% | |||
|- | |||
| Italy ||] ||198||Sarno et al. (2014)||1.01% | |||
|- | |||
| Iberia||] & ] (South) ||310||Casas et al. (2006)||7.40% | |||
|- | |||
| Spain||Countrywide||312||Alvarez et al. (2007)||2.90% | |||
|- | |||
| Spain ||Central Spain||50||Plaza et al. (2003)||4.00% | |||
|- | |||
| Spain ||North-West Spain||216||Achilli et al. (2007)||3.70% | |||
|- | |||
| Spain || ] ||92||Pereira et al. (2005)||3.30% | |||
|- | |||
| Spain ||] ||214||Alvarez et al. (2010)||4.70% | |||
|- | |||
| Spain ||] ||33||Alvarez et al. (2010)||18.18% | |||
|- | |||
| Spain ||] ||108||Casas et al. (2006)||8.30% | |||
|- | |||
| Spain ||] ||135||Hernandez et al. (2014)||5.70% | |||
|- | |||
| Spain ||] ||30||Plaza et al. (2003)||3.40% | |||
|- | |||
| Spain ||]||101||Alvarez-Iglesias et al. (2009)||2.97% | |||
|- | |||
| Spain ||]||231||Picornell et al. (2005)||2.20% | |||
|- | |||
| Spain ||]||300||Brehm et al. (2003)||6.60% | |||
|- | |||
| Portugal||Countrywide||549||Pereira et al. (2005)||5.83% | |||
|- | |||
| Portugal||North||100||Pereira et al. (2010)||5.00% | |||
|- | |||
| Portugal||Center||82||Pereira et al. (2010)||9.70% | |||
|- | |||
| Portugal||South||195||Brehm et al. (2003)||11.30% | |||
|- | |||
| Portugal||South||303||Achilli et al. (2007)||10.80% | |||
|- | |||
| Portugal||]||160||Pereira et al. (2010)||8.70% | |||
|- | |||
| Portugal||]||75||Pereira et al. (2010)||3.90% | |||
|- | |||
| Portugal||Alcacer do Sal||50||Pereira et al. (2010)||22.00% | |||
|} | |||
==See also== | ==See also== |
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The ancestry of modern Iberians (Spanish and Portuguese) is consistent with the geographical situation of the Iberian Peninsula in the south-west of Europe:There is a strong connexion particularly with Atlantic Europe but also Mediterranean Europe and the Near East, albeit the latter is lesser than other Mediterranean countries (notably Greece) due to Spain being the furthest away from the Bosphorous region considered the main bridge of Neolithic expansions into Europe. Nevertheless, Iberia has the strongest link in Europe to both North African and Sub Saharan Africa, purportedly as a result of northward population movements during the seven centuries of Muslim rule over the peninsula. Iberia's Mediterranean and Near Eastern connexion is also likely to be largely of historical rather prehistorical origin, with the region's prehistorical ancestral basis being fundamentally western European.
Population Genetics: Methods and Limitations
One of the first scholars to perform genetic studies was Luigi Luca Cavalli-Sforza. He used classical genetic markers to analyse DNA by proxy. This method studies differences in the frequencies of particular allelic traits, namely polymorphisms from proteins found within human blood (such as the ABO blood groups, Rhesus blood antigens, HLA loci, immunoglobulins, G-6-P-D isoenzymes, among others). Subsequently his team calculated genetic distance between populations, based on the principle that two populations that share similar frequencies of a trait are more closely related than populations that have more divergent frequencies of the trait.
Since then, population genetics has progressed significantly and studies using direct DNA analysis are now abundant and may use mitochondrial DNA (mtDNA), the non-recombining portion of the Y chromosome (NRY) or autosomal DNA. MtDNA and NRY DNA share some similar features which have made them particularly useful in genetic anthropology. These properties include the direct, unaltered inheritance of mtDNA and NRY DNA from mother to offspring and father to son, respectively, without the 'scrambling' effects of genetic recombination. We also presume that these genetic loci are not affected by natural selection and that the major process responsible for changes in base pairs has been mutation (which can be calculated).
The smaller effective population size of the NRY and mtDNA enhances the consequences of drift and founder effect, relative to the autosomes, making NRY and mtDNA variation a potentially sensitive index of population composition. These biologically plausible assumptions are not concrete, Rosser suggests that climatic conditions may affect the fertility of certain lineages.
The underlying mutation rate used by the geneticists is more questionable. They often use different mutation rates and studies frequently arrive at vastly different conclusions. NRY and mtDNA may be so susceptible to drift, that some ancient patterns may have become obscured. Another assumption is that population genealogies are approximated by allele genealogies. Barbujani points out that this only holds if population groups develop from a genetically monomorphic set of founders. Barbujani argues that there is no reason to believe that Europe was colonized by monomorphic populations. This would result in an overestimation of haplogroup age, thus falsely extending the demographic history of Europe into the Late Paleolithic rather than the Neolithic era. (See also Genetic drift, Founder effect, Population bottleneck.) Greater certainty about chronology may be obtained from studies of ancient DNA (see below) but so far these have been comparatively few.
Whereas Y-DNA and mtDNA haplogroups represent but a small component of a person’s DNA pool, autosomal DNA has the advantage of containing hundreds and thousands of examinable genetic loci, thus giving a more complete picture of genetic composition. Descent relationships can only to be determined on a statistical basis, because autosomal DNA undergoes recombination. A single chromosome can record a history for each gene. Autosomal studies are much more reliable for showing the relationships between existing populations but do not offer the possibilities for unraveling their histories in the same way as mtDNA and NRY DNA studies promise, despite their many complications.
Genetic studies operate on numerous assumptions and suffer from methodological limitations such as selection bias and confounding. Phenomenon like genetic drift, foundation and bottleneck effects cause large errors, particularly in haplogroup studies. No matter how accurate the methodology, conclusions derived from such studies are compiled on the basis of how the author envisages their data fits with established archaeological or linguistic theories.
Analysis of prehistoric populations
2014 Study
A 2014 genetic study revealed that a Stone age man from the Mesolithic period, who lived in the Iberian Peninsula about 7,000 years ago, had blue eyes, black or brown hair, and dark skin. His DNA proved to be different from the genetic make up of most today's european populations.
Main genetic compositions
Overall Genetic make-up
DNA analysis shows that Spanish and Portuguese populations are most closely related to other populations of western Europe.
According to Dupanloup et al. (2004) the main components in the European genomes appear to derive from ancestors whose features were similar to those of modern Basques (Paleolithic) and Near Easterners (Neolithic), with average values greater than 35% for both these parental populations, regardless of whether or not molecular information is taken into account. The lowest degree of both Basque and Near Eastern admixture is found in Finland, whereas the highest values are, respectively, 70% ("Basque") in Spain and roughly 60% ("Near Eastern") in the Balkans.
However, a controversial study, published in January 2010, claimed that despite this apparent East-West cline, Western Europeans (including Iberians) are of a nearly equal combination of the European hunter gatherers of the earlier Paleolithic period and more recent Neolithic period ancestry from the Near East, that likely came from Anatolia.
Autosomal DNA
A 2007 European-wide study including Spanish Basques and Valencian Spaniards, found Iberian populations to cluster the furthest from other continental groups, implying that Iberia holds the most ancient European ancestry. In this study, the most prominent genetic stratification in Europe was found to run from the north to the south-east, while another important axis of differentiation runs east-west across the continent. It also found, despite the differences, that all Europeans are closely related.
Y-Chromosome DNA
Y-chromosome analysis had suggested Paleolithic ancestry among populations in the Iberian Peninsula and that Iberia may have played a role in the re-population of western Europe after the last glaciation. This shows an ancestral bond between Iberia and the rest of western Europe, and in particular with Atlantic Europe, which share high frequencies of these haplogroups. R1b1a2, the most common western European haplogroup, arose 4,000 to 8,000 years ago in southwest Asia and later spread to Europe.
Mitochondrial DNA
According to Dupanloup et al. (2004) the main components in the European genomes appear to derive from ancestors whose features were similar to those of modern Basques and Near Easterners, with average values greater than 35% for both these parental populations, regardless of whether or not molecular information is taken into account. The lowest degree of both Basque and Near Eastern admixture is found in Finland, whereas the highest values are, respectively, 70% ("Basque") in Spain and roughly 60% ("Near Eastern") in the Balkans.
DNA analysis shows that the Spanish and Portuguese are most closely related to other populations of western Europe: the French, the Andorrans, the Italians, the Irish, the British, the Germans, and the Swiss.
The results suggested that the lineage R1b1a2 (R-M269) (from 2003 to 2005 what is now R1b1a2 was designated R1b3; from 2005 to 2008 it was R1b1c and from 2008 to 2011 it was R1b1b2), like E1b1b or J lineages, spread together with farming from the Near East. Dr Patricia Balaresque added: "In total, this means that more than 80% of European Y chromosomes descend from incoming farmers. In contrast, most maternal genetic lineages seem to descend from hunter-gatherers. To us, this suggests a reproductive advantage for farming males over indigenous hunter-gatherer males during the switch from hunting and gathering, to farming".
Haplogroup composition of the ancient Iberians was very similar to that found in the modern Iberian Peninsula populations, suggesting a long-term genetic continuity since pre-Roman times.
See also
References
- Cavalli-Sforza (1993, p. 51) harvtxt error: no target: CITEREFCavalli-Sforza1993 (help)
- Milisauskas (2002, p. 58) harvtxt error: no target: CITEREFMilisauskas2002 (help)
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- Semino (2000) harvcoltxt error: no target: CITEREFSemino2000 (help)
- Barbujani & Bertorelle (2001:22–25) harvcoltxt error: no target: CITEREFBarbujaniBertorelle2001 (help)
- Swarthy, blue-eyed caveman revealed using DNA from ancient tooth
- Blue-Eyed Hunter-Gatherers Roamed Prehistoric Europe, Gene Map Reveals
- Stone Age Spaniard had blue eyes, dark skin
- Stone Age Europeans had dark skin and blue eyes, Spanish researchers say
- Nelis, Mari; Esko, Tõnu; Mägi, Reedik; Zimprich, Fritz; Zimprich, Alexander; Toncheva, Draga; Karachanak, Sena; Piskácková, Tereza; Balascák, Ivan; Peltonen, L; Jakkula, E; Rehnström, K; Lathrop, M; Heath, S; Galan, P; Schreiber, S; Meitinger, T; Pfeufer, A; Wichmann, HE; Melegh, B; Polgár, N; Toniolo, D; Gasparini, P; d'Adamo, P; Klovins, J; Nikitina-Zake, L; Kucinskas, V; Kasnauskiene, J; Lubinski, J; Debniak, T (2009). Fleischer, Robert C. (ed.). "Genetic Structure of Europeans: A View from the North–East". PLoS ONE. 4 (5): e5472. Bibcode:2009PLoSO...4.5472N. doi:10.1371/journal.pone.0005472. PMC 2675054. PMID 19424496.
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- Novembre, John; Johnson, Toby; Bryc, Katarzyna; Kutalik, Zoltán; Boyko, Adam R.; Auton, Adam; Indap, Amit; King, Karen S.; Bergmann, Sven; Nelson, Matthew R.; Stephens, Matthew; Bustamante, Carlos D. (2008). "Genes mirror geography within Europe". Nature. 456 (7218): 98–101. Bibcode:2008Natur.456...98N. doi:10.1038/nature07331. PMC 2735096. PMID 18758442.
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was invoked but never defined (see the help page). - ^ Balaresque, Patricia; Bowden, Georgina R.; Adams, Susan M.; Leung, Ho-Yee; King, Turi E.; Rosser, Zoë H.; Goodwin, Jane; Moisan, Jean-Paul; Richard, Christelle; Millward, Ann; Demaine, Andrew G.; Barbujani, Guido; Previderè, Carlo; Wilson, Ian J.; Tyler-Smith, Chris; Jobling, Mark A. (2010). Penny, David (ed.). "A Predominantly Neolithic Origin for European Paternal Lineages". PLoS Biology. 8 (1): e1000285. doi:10.1371/journal.pbio.1000285. PMC 2799514. PMID 20087410.
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- ^ Most European males 'descended from farmers', BBC News, 20 January 2010
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{{cite journal}}
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{{cite journal}}
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{{cite journal}}
: Invalid|display-authors=9
(help) - Nelis, Mari; Esko, Tõnu; Mägi, Reedik; Zimprich, Fritz; Zimprich, Alexander; Toncheva, Draga; Karachanak, Sena; Piskácková, Tereza; Balascák, Ivan; Peltonen, L; Jakkula, E; Rehnström, K; Lathrop, M; Heath, S; Galan, P; Schreiber, S; Meitinger, T; Pfeufer, A; Wichmann, HE; Melegh, B; Polgár, N; Toniolo, D; Gasparini, P; d'Adamo, P; Klovins, J; Nikitina-Zake, L; Kucinskas, V; Kasnauskiene, J; Lubinski, J; Debniak, T (2009). Fleischer, Robert C. (ed.). "Genetic Structure of Europeans: A View from the North–East". PLoS ONE. 4 (5): e5472. Bibcode:2009PLoSO...4.5472N. doi:10.1371/journal.pone.0005472. PMC 2675054. PMID 19424496.
{{cite journal}}
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suggested) (help)CS1 maint: unflagged free DOI (link) - Novembre, John; Johnson, Toby; Bryc, Katarzyna; Kutalik, Zoltán; Boyko, Adam R.; Auton, Adam; Indap, Amit; King, Karen S.; Bergmann, Sven; Nelson, Matthew R.; Stephens, Matthew; Bustamante, Carlos D. (2008). "Genes mirror geography within Europe". Nature. 456 (7218): 98–101. Bibcode:2008Natur.456...98N. doi:10.1038/nature07331. PMC 2735096. PMID 18758442.
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(help) - Comas, David; Calafell, Francesc; Benchemsi, Noufissa; Helal, Ahmed; Lefranc, Gerard; Stoneking, Mark; Batzer, Mark A.; Bertranpetit, Jaume; Sajantila, Antti (2000). "Alu insertion polymorphisms in NW Africa and the Iberian Peninsula: evidence for a strong genetic boundary through the Gibraltar Straits". Human Genetics. 107 (4): 312–9. doi:10.1007/s004390000370. PMID 11129330.
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(help)
Human genetics | |
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Sub-topics | |
Genetic history by region | |
Population genetics by group |
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