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Genetic ancestry, admixture and health determinants in Latin America

BACKGROUND: Modern Latin American populations were formed via genetic admixture among ancestral source populations from Africa, the Americas and Europe. We are interested in studying how combinations of genetic ancestry in admixed Latin American populations may impact genomic determinants of health...

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Autores principales: Norris, Emily T., Wang, Lu, Conley, Andrew B., Rishishwar, Lavanya, Mariño-Ramírez, Leonardo, Valderrama-Aguirre, Augusto, Jordan, I. King
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6288849/
https://www.ncbi.nlm.nih.gov/pubmed/30537949
http://dx.doi.org/10.1186/s12864-018-5195-7
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author Norris, Emily T.
Wang, Lu
Conley, Andrew B.
Rishishwar, Lavanya
Mariño-Ramírez, Leonardo
Valderrama-Aguirre, Augusto
Jordan, I. King
author_facet Norris, Emily T.
Wang, Lu
Conley, Andrew B.
Rishishwar, Lavanya
Mariño-Ramírez, Leonardo
Valderrama-Aguirre, Augusto
Jordan, I. King
author_sort Norris, Emily T.
collection PubMed
description BACKGROUND: Modern Latin American populations were formed via genetic admixture among ancestral source populations from Africa, the Americas and Europe. We are interested in studying how combinations of genetic ancestry in admixed Latin American populations may impact genomic determinants of health and disease. For this study, we characterized the impact of ancestry and admixture on genetic variants that underlie health- and disease-related phenotypes in population genomic samples from Colombia, Mexico, Peru, and Puerto Rico. RESULTS: We analyzed a total of 347 admixed Latin American genomes along with 1102 putative ancestral source genomes from Africans, Europeans, and Native Americans. We characterized the genetic ancestry, relatedness, and admixture patterns for each of the admixed Latin American genomes, finding a spectrum of ancestry proportions within and between populations. We then identified single nucleotide polymorphisms (SNPs) with anomalous ancestry-enrichment patterns, i.e. SNPs that exist in any given Latin American population at a higher frequency than expected based on the population’s genetic ancestry profile. For this set of ancestry-enriched SNPs, we inspected their phenotypic impact on disease, metabolism, and the immune system. All four of the Latin American populations show ancestry-enrichment for a number of shared pathways, yielding evidence of similar selection pressures on these populations during their evolution. For example, all four populations show ancestry-enriched SNPs in multiple genes from immune system pathways, such as the cytokine receptor interaction, T cell receptor signaling, and antigen presentation pathways. We also found SNPs with excess African or European ancestry that are associated with ancestry-specific gene expression patterns and play crucial roles in the immune system and infectious disease responses. Genes from both the innate and adaptive immune system were found to be regulated by ancestry-enriched SNPs with population-specific regulatory effects. CONCLUSIONS: Ancestry-enriched SNPs in Latin American populations have a substantial effect on health- and disease-related phenotypes. The concordant impact observed for same phenotypes across populations points to a process of adaptive introgression, whereby ancestry-enriched SNPs with specific functional utility appear to have been retained in modern populations by virtue of their effects on health and fitness. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12864-018-5195-7) contains supplementary material, which is available to authorized users.
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spelling pubmed-62888492018-12-14 Genetic ancestry, admixture and health determinants in Latin America Norris, Emily T. Wang, Lu Conley, Andrew B. Rishishwar, Lavanya Mariño-Ramírez, Leonardo Valderrama-Aguirre, Augusto Jordan, I. King BMC Genomics Research BACKGROUND: Modern Latin American populations were formed via genetic admixture among ancestral source populations from Africa, the Americas and Europe. We are interested in studying how combinations of genetic ancestry in admixed Latin American populations may impact genomic determinants of health and disease. For this study, we characterized the impact of ancestry and admixture on genetic variants that underlie health- and disease-related phenotypes in population genomic samples from Colombia, Mexico, Peru, and Puerto Rico. RESULTS: We analyzed a total of 347 admixed Latin American genomes along with 1102 putative ancestral source genomes from Africans, Europeans, and Native Americans. We characterized the genetic ancestry, relatedness, and admixture patterns for each of the admixed Latin American genomes, finding a spectrum of ancestry proportions within and between populations. We then identified single nucleotide polymorphisms (SNPs) with anomalous ancestry-enrichment patterns, i.e. SNPs that exist in any given Latin American population at a higher frequency than expected based on the population’s genetic ancestry profile. For this set of ancestry-enriched SNPs, we inspected their phenotypic impact on disease, metabolism, and the immune system. All four of the Latin American populations show ancestry-enrichment for a number of shared pathways, yielding evidence of similar selection pressures on these populations during their evolution. For example, all four populations show ancestry-enriched SNPs in multiple genes from immune system pathways, such as the cytokine receptor interaction, T cell receptor signaling, and antigen presentation pathways. We also found SNPs with excess African or European ancestry that are associated with ancestry-specific gene expression patterns and play crucial roles in the immune system and infectious disease responses. Genes from both the innate and adaptive immune system were found to be regulated by ancestry-enriched SNPs with population-specific regulatory effects. CONCLUSIONS: Ancestry-enriched SNPs in Latin American populations have a substantial effect on health- and disease-related phenotypes. The concordant impact observed for same phenotypes across populations points to a process of adaptive introgression, whereby ancestry-enriched SNPs with specific functional utility appear to have been retained in modern populations by virtue of their effects on health and fitness. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12864-018-5195-7) contains supplementary material, which is available to authorized users. BioMed Central 2018-12-11 /pmc/articles/PMC6288849/ /pubmed/30537949 http://dx.doi.org/10.1186/s12864-018-5195-7 Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Norris, Emily T.
Wang, Lu
Conley, Andrew B.
Rishishwar, Lavanya
Mariño-Ramírez, Leonardo
Valderrama-Aguirre, Augusto
Jordan, I. King
Genetic ancestry, admixture and health determinants in Latin America
title Genetic ancestry, admixture and health determinants in Latin America
title_full Genetic ancestry, admixture and health determinants in Latin America
title_fullStr Genetic ancestry, admixture and health determinants in Latin America
title_full_unstemmed Genetic ancestry, admixture and health determinants in Latin America
title_short Genetic ancestry, admixture and health determinants in Latin America
title_sort genetic ancestry, admixture and health determinants in latin america
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6288849/
https://www.ncbi.nlm.nih.gov/pubmed/30537949
http://dx.doi.org/10.1186/s12864-018-5195-7
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