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Uniparental ancestry markers in Chilean populations
The presence of Native Americans, Europeans, and Africans has led to the development of a multi-ethnic, admixed population in Chile. This study aimed to contribute to the characterization of the uniparental genetic structure of three Chilean regions. Newborns from seven hospitals in Independencia, P...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Sociedade Brasileira de Genética
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5127147/ https://www.ncbi.nlm.nih.gov/pubmed/27561109 http://dx.doi.org/10.1590/1678-4685-GMB-2015-0273 |
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author | Vieira-Machado, Camilla Dutra Tostes, Maluah Alves, Gabrielle Nazer, Julio Martinez, Liliana Wettig, Elisabeth Pizarro Rivadeneira, Oscar Diaz Caamaño, Marcela Larenas Ascui, Jessica Pavez, Pedro Dutra, Maria da Graça Castilla, Eduardo Enrique Orioli, Ieda Maria |
author_facet | Vieira-Machado, Camilla Dutra Tostes, Maluah Alves, Gabrielle Nazer, Julio Martinez, Liliana Wettig, Elisabeth Pizarro Rivadeneira, Oscar Diaz Caamaño, Marcela Larenas Ascui, Jessica Pavez, Pedro Dutra, Maria da Graça Castilla, Eduardo Enrique Orioli, Ieda Maria |
author_sort | Vieira-Machado, Camilla Dutra |
collection | PubMed |
description | The presence of Native Americans, Europeans, and Africans has led to the development of a multi-ethnic, admixed population in Chile. This study aimed to contribute to the characterization of the uniparental genetic structure of three Chilean regions. Newborns from seven hospitals in Independencia, Providencia, Santiago, Curicó, Cauquenes, Valdívia, and Puerto Montt communes, belonging to the Chilean regions of Santiago, Maule, and Los Lagos, were studied. The presence of Native American mitochondrial DNA (mtDNA) haplogroups and two markers present in the non-recombinant region of the Y chromosome, DYS199 and DYS287, indicative of Native American and African ancestry, respectively, was determined. A high Native American matrilineal contribution and a low Native American and African patrilineal contributions were found in all three studied regions. As previously found in Chilean admixed populations, the Native American matrilineal contribution was lower in Santiago than in the other studied regions. However, there was an unexpectedly higher contribution of Native American ancestry in one of the studied communes in Santiago, probably due to the high rate of immigration from other regions of the country. The population genetic sub-structure we detected in Santiago using few uniparental markers requires further confirmation, owing to possible stratification for autosomal and X-chromosome markers. |
format | Online Article Text |
id | pubmed-5127147 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Sociedade Brasileira de Genética |
record_format | MEDLINE/PubMed |
spelling | pubmed-51271472016-12-08 Uniparental ancestry markers in Chilean populations Vieira-Machado, Camilla Dutra Tostes, Maluah Alves, Gabrielle Nazer, Julio Martinez, Liliana Wettig, Elisabeth Pizarro Rivadeneira, Oscar Diaz Caamaño, Marcela Larenas Ascui, Jessica Pavez, Pedro Dutra, Maria da Graça Castilla, Eduardo Enrique Orioli, Ieda Maria Genet Mol Biol Human and Medical Genetics The presence of Native Americans, Europeans, and Africans has led to the development of a multi-ethnic, admixed population in Chile. This study aimed to contribute to the characterization of the uniparental genetic structure of three Chilean regions. Newborns from seven hospitals in Independencia, Providencia, Santiago, Curicó, Cauquenes, Valdívia, and Puerto Montt communes, belonging to the Chilean regions of Santiago, Maule, and Los Lagos, were studied. The presence of Native American mitochondrial DNA (mtDNA) haplogroups and two markers present in the non-recombinant region of the Y chromosome, DYS199 and DYS287, indicative of Native American and African ancestry, respectively, was determined. A high Native American matrilineal contribution and a low Native American and African patrilineal contributions were found in all three studied regions. As previously found in Chilean admixed populations, the Native American matrilineal contribution was lower in Santiago than in the other studied regions. However, there was an unexpectedly higher contribution of Native American ancestry in one of the studied communes in Santiago, probably due to the high rate of immigration from other regions of the country. The population genetic sub-structure we detected in Santiago using few uniparental markers requires further confirmation, owing to possible stratification for autosomal and X-chromosome markers. Sociedade Brasileira de Genética 2016-08-04 2016 /pmc/articles/PMC5127147/ /pubmed/27561109 http://dx.doi.org/10.1590/1678-4685-GMB-2015-0273 Text en Copyright © 2016, Sociedade Brasileira de Genética. http://creativecommons.org/licenses/by/4.0/ License information: This is an open-access article distributed under the terms of the Creative Commons Attribution License (type CC-BY), which permits unrestricted use, distribution and reproduction in any medium, provided the original article is properly cited. |
spellingShingle | Human and Medical Genetics Vieira-Machado, Camilla Dutra Tostes, Maluah Alves, Gabrielle Nazer, Julio Martinez, Liliana Wettig, Elisabeth Pizarro Rivadeneira, Oscar Diaz Caamaño, Marcela Larenas Ascui, Jessica Pavez, Pedro Dutra, Maria da Graça Castilla, Eduardo Enrique Orioli, Ieda Maria Uniparental ancestry markers in Chilean populations |
title | Uniparental ancestry markers in Chilean populations |
title_full | Uniparental ancestry markers in Chilean populations |
title_fullStr | Uniparental ancestry markers in Chilean populations |
title_full_unstemmed | Uniparental ancestry markers in Chilean populations |
title_short | Uniparental ancestry markers in Chilean populations |
title_sort | uniparental ancestry markers in chilean populations |
topic | Human and Medical Genetics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5127147/ https://www.ncbi.nlm.nih.gov/pubmed/27561109 http://dx.doi.org/10.1590/1678-4685-GMB-2015-0273 |
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