4.3 Article

Demographic history differences between Hispanics and Brazilians imprint haplotype features

Journal

G3-GENES GENOMES GENETICS
Volume 12, Issue 7, Pages -

Publisher

OXFORD UNIV PRESS INC
DOI: 10.1093/g3journal/jkac111

Keywords

Latinos; haplotypes; population; selection; ROH; IBD sharing; linkage disequilibrium; diversity

Funding

  1. Sao Paulo Research Foundation (FAPESP) [2006/07054-5, 2006/06231-0, 2008/57441-0, 2014/00984-3, 2019/18886-1, 2008/10596-0, 2012/06438-5, 2015/13152-9]
  2. National Council for Scientific and Technological Development (CNPq) [8367/2011-1, 150398/2013-1, 304455/2012-1, 310938/2014-7, 306765/2020-9, 309494/2014-1]
  3. Brazilian Synchrotron Light Laboratory
  4. Brazilian Institute of Neuroscience and Neurotechnology (BRAINN-FAPESP) [2013/07559-3]
  5. Regional University of Joinville

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The genetic structure of Latino populations is affected by their complex demographic history, including multiple admixing events, bottlenecks and/or expansions, and unique adaptive events. The study found that the amount of American and African ancestry is related to the decay of linkage disequilibrium, and the extent of identity by descent sharing is correlated with historical effective population sizes. Long runs of homozygosity were only enriched in Peruvians and Native Americans. Positive selection signals were observed in certain markers, indicating human adaptation to the American continent.
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.

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