Demographic history differences between Hispanics and Brazilians imprint haplotype features

Author:

da Cruz Pedro Rodrigues Sousa1ORCID,Ananina Galina1ORCID,Secolin Rodrigo23ORCID,Gil-da-Silva-Lopes Vera Lúcia2ORCID,Lima Carmen Silvia Passos4ORCID,de França Paulo Henrique Condeixa5ORCID,Donatti Amanda23ORCID,Lourenço Gustavo Jacob6ORCID,de Araujo Tânia Kawasaki2ORCID,Simioni Milena2ORCID,Lopes-Cendes Iscia23ORCID,Costa Fernando Ferreira7ORCID,de Melo Mônica Barbosa1ORCID

Affiliation:

1. Laboratory of Human Genetics, Center for Molecular Biology and Genetic Engineering (CBMEG), University of Campinas—UNICAMP , Campinas, SP 13083-875, Brazil

2. Department of Medical Genetics and Genomic Medicine, School of Medical Sciences, University of Campinas—UNICAMP , Campinas, SP 13083-887, Brazil

3. The Brazilian Institute of Neuroscience and Neurotechnology (BRAINN) , Campinas, SP 13083-887, Brazil

4. Clinical Oncology Service, Department of Internal Medicine, School of Medical Sciences, University of Campinas—UNICAMP , Campinas, SP 13083-887, Brazil

5. Joinville Stroke Biobank, University of Region of Joinville—UNIVILLE , Joinville, SC 89202-190, Brazil

6. Laboratory of Cancer Genetics, School of Medical Sciences, University of Campinas—UNICAMP , Campinas, SP 13083-887, Brazil

7. Hematology and Hemotherapy Center, University of Campinas—UNICAMP, Campinas, SP, 13083-878 , Brazil

Abstract

Abstract Admixture is known to greatly impact the genetic landscape of a population and, while genetic variation underlying human phenotypes has been shown to differ among populations, studies on admixed subjects are still scarce. Latin American populations are the result of complex demographic history, such as 2 or 3-way admixing events, bottlenecks and/or expansions, and adaptive events unique to the American continent. To explore the impact of these events on the genetic structure of Latino populations, we evaluated the following haplotype features: linkage disequilibrium, shared identity by descent segments, runs of homozygosity, and extended haplotype homozygosity (integrated haplotype score) in Latinos represented in the 1000 Genome Project along with array data from 171 Brazilians sampled in the South and Southeast regions of Brazil. We found that linkage disequilibrium decay relates to the amount of American and African ancestry. The extent of identity by descent sharing positively correlates with historical effective population sizes, which we found to be steady or growing, except for Puerto Ricans and Colombians. Long runs of homozygosity, a particular instance of autozygosity, was only enriched in Peruvians and Native Americans. We used simulations to account for random sampling and linkage disequilibrium to filter positive selection indexes and found 244 unique markers under selection, 26 of which are common to 2 or more populations. Some markers exhibiting positive selection signals had estimated time to the most recent common ancestor consistent with human adaptation to the American continent. In conclusion, Latino populations present highly divergent haplotype characteristics that impact genetic architecture and underlie complex phenotypes.

Funder

São Paulo Research Foundation

Publisher

Oxford University Press (OUP)

Subject

Genetics (clinical),Genetics,Molecular Biology

Reference89 articles.

1. A map of human genome variation from population-scale sequencing;1000 Genomes Project Consortium;Nature,2010

2. A global reference for human genetic variation;1000 Genomes Project Consortium;Nature,2015

3. The genetic diversity of the Americas;Adhikari;Annu Rev Genomics Hum Genet,2017

4. Population history and natural selection shape patterns of genetic variation in 132 genes;Akey;PLoS Biol,2004

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