scholarly journals The Polynesian gene pool: an early contribution by Amerindians to Easter Island

2012 ◽  
Vol 367 (1590) ◽  
pp. 812-819 ◽  
Author(s):  
Erik Thorsby

It is now generally accepted that Polynesia was first settled by peoples from southeast Asia. An alternative that eastern parts of Polynesia were first inhabited by Amerindians has found little support. There are, however, many indications of a ‘prehistoric’ (i.e. before Polynesia was discovered by Europeans) contact between Polynesia and the Americas, but genetic evidence of a prehistoric Amerindian contribution to the Polynesian gene pool has been lacking. We recently carried out genomic HLA (human leucocyte antigen) typing as well as typing for mitochondrial DNA (mtDNA) and Y chromosome markers of blood samples collected in 1971 and 2008 from reputedly non-admixed Easter Islanders. All individuals carried HLA alleles and mtDNA types previously found in Polynesia, and most of the males carried Y chromosome markers of Polynesian origin (a few had European Y chromosome markers), further supporting an initial Polynesian population on Easter Island. The HLA investigations revealed, however, that some individuals also carried HLA alleles which have previously almost only been found in Amerindians. We could trace the introduction of these Amerindian alleles to before the Peruvian slave trades, i.e. before the 1860s, and provide suggestive evidence that they were introduced already in prehistoric time. Our results demonstrate an early Amerindian contribution to the Polynesian gene pool on Easter Island, and illustrate the usefulness of typing for immunogenetic markers such as HLA to complement mtDNA and Y chromosome analyses in anthropological investigations.

2020 ◽  
Vol 56 (7) ◽  
pp. 849-855
Author(s):  
V. N. Kharkov ◽  
L. M. Novikova ◽  
O. V. Shtygasheva ◽  
F. A. Luzina ◽  
I. Yu. Khitrinskaya ◽  
...  

Author(s):  
Y. V. Bogunov ◽  
◽  
O. V. Maltseva ◽  
A. A. Bogunova ◽  
E. V. Balanovskaya ◽  
...  

2014 ◽  
Vol 50 (2) ◽  
pp. 180-190 ◽  
Author(s):  
V. N. Kharkov ◽  
K. V. Khamina ◽  
O. F. Medvedeva ◽  
K. V. Simonova ◽  
E. R. Eremina ◽  
...  

2015 ◽  
Vol 57 (1) ◽  
pp. 95-98
Author(s):  
Ruslan G. Krivda ◽  
◽  
Aymen A. Jassim ◽  
Tatiana B. Fernandez Trokhimtchouk ◽  
◽  
...  

2003 ◽  
Vol 30 ◽  
pp. 159-167 ◽  
Author(s):  
Martin Richards

The major pattern in the European gene pool is a southeast-northwest frequency gradient of classic genetic markers such as blood groups, which population geneticists initially attributed to the demographic impact of Neolithic farmers dispersing from the Near East. Molecular genetics has enriched this picture, with analyses of mitochondrial DNA and the Y chromosome allowing a more detailed exploration of alternative models for the spread of the Neolithic into Europe. This paper considers a range of possible models in the light of the detailed information now emerging from genetic studies.


Author(s):  
Aleksandr Pilipenko ◽  
Stepan Cherdantsev ◽  
Rostislav Trapezov ◽  
Matvey Tomilin ◽  
Mariya Balabanova ◽  
...  

Introduction. The article presents the results of the analysis of mitochondrial DNA and Y-chromosome samples obtained from the representatives of Sarmatian populations from the Lower Volga region belonging to all stages of the culture. Methods and materials. The authors have screened samples from 202 individuals representing three cultural and chronological Sarmatian groups (Early Sarmatian, Middle Sarmatian and Late Sarmatian cultures). As a result, the researchers have determined the structure and phylogenetic position of 62 mitochondrial DNA samples and 12 Y-chromosome samples, carried out a comprehensive analysis of the results. The authors have interpreted the obtained results in terms of the formation of the Sarmatian genetic composition and their genetic relationships. Results and discussion. The paper shows that the Sarmatian mitochondrial DNA pool is characterized by a high level of diversity, which is also typical for other Early Iron Age nomadic groups. The mitochondrial DNA lineages of Western Eurasian origin dominate in the Sarmatian gene pool, while lineages of Eastern Eurasian haplogroups cover less than 13% of the total sample. Data on both genetic markers suggests that the formation of the main features of the Sarmatian gene pool could be alternatively influenced by populations from more eastern regions, genetically more related to the Andronovo historical and cultural community, which is consistent with the data of physical paleoanthropology, or autochthonous populations of the Lower Volga and adjacent regions. The mitochondrial DNA data indicates a significant genetic influence of the populations from more southern regions of the Eurasian steppe belt on the Sarmatian gene pool. In addition, the authors show the presence of Eastern Eurasian components in the gene pools of all chronological Sarmatian groups, which may indicate the genetic influence of early nomads from eastern regions of the Eurasian steppe belt. The exact time of the appearance of these eastern genetic components in the Lower Volga region remains unclear. At the same time, the authors did not find the signs of an increase in the role of eastern components during the transition from the Early to Middle and to Late stages of the Sarmatian culture, which could be expected based on the data of archaeology and physical anthropology. Prospects. Prospects for a more detailed reconstruction of the Sarmatian genetic history in the Lower Volga region are associated with the further development of the diachronic model, including the accumulation of more mitochondrial DNA and Y-chromosome data for the population of each stage of the Sarmatian culture, the involvement of groups preceding the Sarmatians in the region in the study and the analysis of additional markers of nuclear DNA.


2012 ◽  
Vol 48 (6) ◽  
pp. 640-650 ◽  
Author(s):  
E. K. Khusnutdinova ◽  
S. S. Litvinov ◽  
I. A. Kutuev ◽  
B. B. Yunusbayev ◽  
R. I. Khusainova ◽  
...  

2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Rossana Santiago de Sousa Azulay ◽  
Luís Cristóvão Porto ◽  
Dayse Aparecida Silva ◽  
Maria da Glória Tavares ◽  
Roberta Maria Duailibe Ferreira Reis ◽  
...  

AbstractThis study aimed to investigate the relationship between genetic ancestry inferred from autosomal and Y chromosome markers and HLA genotypes in patients with Type 1 Diabetes from an admixed Brazilian population. Inference of autosomal ancestry; HLA-DRB1, -DQA1 and -DQB1 typifications; and Y chromosome analysis were performed. European autosomal ancestry was about 50%, followed by approximately 25% of African and Native American. The European Y chromosome was predominant. The HLA-DRB1*03 and DRB1*04 alleles presented risk association with T1D. When the Y chromosome was European, DRB1*03 and DRB1*04 homozygote and DRB1*03/DRB1*04 heterozygote genotypes were the most frequent. The results suggest that individuals from Maranhão have a European origin as their major component; and are patrilineal with greater frequency from the R1b haplogroup. The predominance of the HLA-DRB1*03 and DRB1*04 alleles conferring greater risk in our population and being more frequently related to the ancestry of the European Y chromosome suggests that in our population, the risk of T1D can be transmitted by European ancestors of our process miscegenation. However, the Y sample sizes of Africans and Native Americans were small, and further research should be conducted with large mixed sample sizes to clarify this possible association.


2017 ◽  
Vol 29 (5) ◽  
pp. 703-713
Author(s):  
Rhiannon E. McGeehan ◽  
Lewis A. Cockram ◽  
D. Timothy J. Littlewood ◽  
Kathleen Keatley ◽  
Diana M. Eccles ◽  
...  

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