Demographic history differences between Hispanics and Brazilians imprint haplotype features.


Journal

G3 (Bethesda, Md.)
ISSN: 2160-1836
Titre abrégé: G3 (Bethesda)
Pays: England
ID NLM: 101566598

Informations de publication

Date de publication:
06 07 2022
Historique:
received: 31 01 2022
accepted: 27 04 2022
pubmed: 6 5 2022
medline: 9 7 2022
entrez: 5 5 2022
Statut: ppublish

Résumé

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.

Identifiants

pubmed: 35511163
pii: 6576632
doi: 10.1093/g3journal/jkac111
pmc: PMC9258545
pii:
doi:

Banques de données

figshare
['10.6084/m9.figshare.19640322']

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

© The Author(s) 2022. Published by Oxford University Press on behalf of Genetics Society of America.

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Auteurs

Pedro Rodrigues Sousa da Cruz (PRS)

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

Galina Ananina (G)

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

Rodrigo Secolin (R)

Department of Medical Genetics and Genomic Medicine, School of Medical Sciences, University of Campinas-UNICAMP, Campinas, SP 13083-887, Brazil.
The Brazilian Institute of Neuroscience and Neurotechnology (BRAINN), Campinas, SP 13083-887, Brazil.

Vera Lúcia Gil-da-Silva-Lopes (VL)

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

Carmen Silvia Passos Lima (CSP)

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

Paulo Henrique Condeixa de França (PHC)

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

Amanda Donatti (A)

Department of Medical Genetics and Genomic Medicine, School of Medical Sciences, University of Campinas-UNICAMP, Campinas, SP 13083-887, Brazil.
The Brazilian Institute of Neuroscience and Neurotechnology (BRAINN), Campinas, SP 13083-887, Brazil.

Gustavo Jacob Lourenço (GJ)

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

Tânia Kawasaki de Araujo (TK)

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

Milena Simioni (M)

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

Iscia Lopes-Cendes (I)

Department of Medical Genetics and Genomic Medicine, School of Medical Sciences, University of Campinas-UNICAMP, Campinas, SP 13083-887, Brazil.
The Brazilian Institute of Neuroscience and Neurotechnology (BRAINN), Campinas, SP 13083-887, Brazil.

Fernando Ferreira Costa (FF)

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

Mônica Barbosa de Melo (MB)

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

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