The American Journal of Human GeneticsGenomicsPeer-reviewed journal article
Understanding the Hidden Complexity of Latin American Population Isolates
Jazlyn A. MooneyiD, Christian D. HuberiD, Susan K. ServiceiD, Jae Hoon SuliD, Clare Diana Marsden, Zhongyang ZhangiD, Chiara SabattiiD, Andrés Ruiz‐LinaresiD, Gabriel BedoyaiD, Nelson B. FreimeriD, Kirk E. LohmuelleriD, Scott C. FearsiD, Bárbara KremeyeriD, Carmen Araya Lic, Xinia Araya Lic, Julio BejaranoiD, Margarita Ramirez Lic, Gabriel CastrillóniD, Maria C. Lopez, Gabriel Montoya, Patricia Montoya, Terri M. Teshiba, Lori Altshuler, George Bartzokis, Javier I. EscobariD, , Giovanni CoppolaiD
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Abstract
Most population isolates examined to date were founded from a single ancestral population. Consequently, there is limited knowledge about the demographic history of admixed population isolates. Here we investigate genomic diversity of recently admixed population isolates from Costa Rica and Colombia and compare their diversity to a benchmark population isolate, the Finnish. These Latin American isolates originated during the 16th century from admixture between a few hundred European males and Amerindian females, with a limited contribution from African founders. We examine whole genome sequence data from 449 individuals, ascertained as families to build mutigenerational pedigrees, with a mean sequencing depth of coverage of approximately 24X. We find that Latin American isolates have increased genetic diversity relative to the Finnish. However, there is an increase in the amount of identity by descent (IBD) segments in the Latin American isolates relative to the Finnish. The increase in IBD segments is likely a consequence of a very recent and severe population bottleneck during the founding of the admixed population isolates. Furthermore, the proportion of the genome that falls within a long run of homozygosity (ROH) in Costa Rican and Colombian individuals was significantly greater than that in the Finnish, suggesting more recent consanguinity in the Latin American isolates relative to that seen in the Finnish. Lastly, we found that recent consanguinity increased the number of deleterious variants found in the homozygous state, which is relevant if deleterious variants are recessive. Our study suggests there is no single genetic signature of a population isolate.
- organism: human
- assay: whole-genome sequencing
- research focus: variant calling
- research focus: genome assembly
- approach: statistical model
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