Population History and Gene Divergence in Native Mexicans Inferred from 76 Human Exomes

Author:

Ávila-Arcos María C12,McManus Kimberly F34,Sandoval Karla5,Rodríguez-Rodríguez Juan Esteban5,Villa-Islas Viridiana1,Martin Alicia R2,Luisi Pierre67,Peñaloza-Espinosa Rosenda I8,Eng Celeste9,Huntsman Scott9,Burchard Esteban G9,Gignoux Christopher R10,Bustamante Carlos D2,Moreno-Estrada Andrés5

Affiliation:

1. International Laboratory for Human Genome Research (LIIGH), UNAM Juriquilla, Queretaro, Mexico

2. Department of Genetics, Stanford University School of Medicine, Stanford, CA

3. Department of Biology, Stanford University, Stanford, CA

4. Department of Biomedical Informatics, Stanford School of Medicine, Stanford, CA

5. National Laboratory of Genomics for Biodiversity (LANGEBIO), UGA, CINVESTAV, Irapuato, Guanajuato 36821, Mexico

6. Centro de Investigación y Desarrollo en Inmunología y Enfermedades Infecciosas, Consejo Nacional de Investigaciones Científicas y Técnicas, Córdoba, Argentina

7. Facultad de Filosofía y Humanidades, Universidad Nacional de Córdoba, Córdoba, Argentina

8. Division of Biological and Health Sciences, Department of Biological Systems, Universidad Autónoma Metropolitana-Xochimilco, Mexico City, Mexico

9. Department Bioengineering & Therapeutic Sciences and Medicine, University of California San Francisco, San Francisco, CA

10. Division of Biomedical Informatics and Personalized Medicine, University of Colorado, Denver, CO

Abstract

AbstractNative American genetic variation remains underrepresented in most catalogs of human genome sequencing data. Previous genotyping efforts have revealed that Mexico’s Indigenous population is highly differentiated and substructured, thus potentially harboring higher proportions of private genetic variants of functional and biomedical relevance. Here we have targeted the coding fraction of the genome and characterized its full site frequency spectrum by sequencing 76 exomes from five Indigenous populations across Mexico. Using diffusion approximations, we modeled the demographic history of Indigenous populations from Mexico with northern and southern ethnic groups splitting 7.2 KYA and subsequently diverging locally 6.5 and 5.7 KYA, respectively. Selection scans for positive selection revealed BCL2L13 and KBTBD8 genes as potential candidates for adaptive evolution in Rarámuris and Triquis, respectively. BCL2L13 is highly expressed in skeletal muscle and could be related to physical endurance, a well-known phenotype of the northern Mexico Rarámuri. The KBTBD8 gene has been associated with idiopathic short stature and we found it to be highly differentiated in Triqui, a southern Indigenous group from Oaxaca whose height is extremely low compared to other Native populations.

Funder

Beijing Genomics Institute

BGI

Stanford Center for Computational, Evolutionary and Human Genomics

CEHG

Laboratorio Nacional de Visualización Científica Avanzada

Mexico’s CONACYT Basic Research Program

International Center for Genetic Engineering and Biotechnology

Health Care Research in Developing Countries

Programa de Apoyo a Proyectos de Investigación e Innovación Tecnológica

Universidad Nacional Autónoma de México

CONACYT Infrastructure

Publisher

Oxford University Press (OUP)

Subject

Genetics,Molecular Biology,Ecology, Evolution, Behavior and Systematics

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