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
Latin American Collaborative Study of Congenital Malformations (ECLAMC) and National Institute of Population Medical Genetics (INAGEMP), Departmento de Genética, Instituto de Biologia, Universidade Federal do Rio de Janeiro (UFRJ), Rio de Janeiro, RJ, Brazil.
Neonatal Service, Department of Obstetrics and Gynecology, Hospital Clínico de La Universidad del Chile, Santiago, Chile.
Genet Mol Biol. 2016 Oct-Dec;39(4):573-579. doi: 10.1590/1678-4685-GMB-2015-0273. Epub 2016 Aug 4.
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.
美洲原住民、欧洲人和非洲人的存在促使智利形成了一个多民族的混合人口。本研究旨在为智利三个地区单亲遗传结构的特征描述做出贡献。对来自圣地亚哥、马乌莱和洛斯里奥斯智利地区的独立、普罗维登西亚、圣地亚哥、库里科、考克内斯、瓦尔迪维亚和蒙特港公社七家医院的新生儿进行了研究。确定了美洲原住民线粒体DNA(mtDNA)单倍群以及Y染色体非重组区域中存在的两个标记DYS199和DYS287的存在情况,这两个标记分别指示美洲原住民和非洲血统。在所有三个研究地区都发现美洲原住民母系贡献高,而美洲原住民和非洲父系贡献低。正如之前在智利混合人群中所发现的那样,圣地亚哥的美洲原住民母系贡献低于其他研究地区。然而,圣地亚哥一个研究公社中美洲原住民血统的贡献出人意料地更高,这可能是由于来自该国其他地区的高移民率所致。由于常染色体和X染色体标记可能存在分层现象,我们使用少数单亲标记在圣地亚哥检测到的群体遗传亚结构需要进一步证实。