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Population History and Gene Divergence in Native Mexicans Inferred from 76 Human Exomes.
Ávila-Arcos, María C; McManus, Kimberly F; Sandoval, Karla; Rodríguez-Rodríguez, Juan Esteban; Villa-Islas, Viridiana; Martin, Alicia R; Luisi, Pierre; Peñaloza-Espinosa, Rosenda I; Eng, Celeste; Huntsman, Scott; Burchard, Esteban G; Gignoux, Christopher R; Bustamante, Carlos D; Moreno-Estrada, Andrés.
Afiliação
  • Ávila-Arcos MC; International Laboratory for Human Genome Research (LIIGH), UNAM Juriquilla, Queretaro, Mexico.
  • McManus KF; Department of Genetics, Stanford University School of Medicine, Stanford, CA.
  • Sandoval K; Department of Biology, Stanford University, Stanford, CA.
  • Rodríguez-Rodríguez JE; Department of Biomedical Informatics, Stanford School of Medicine, Stanford, CA.
  • Villa-Islas V; National Laboratory of Genomics for Biodiversity (LANGEBIO), UGA, CINVESTAV, Irapuato, Guanajuato 36821, Mexico.
  • Martin AR; National Laboratory of Genomics for Biodiversity (LANGEBIO), UGA, CINVESTAV, Irapuato, Guanajuato 36821, Mexico.
  • Luisi P; International Laboratory for Human Genome Research (LIIGH), UNAM Juriquilla, Queretaro, Mexico.
  • Peñaloza-Espinosa RI; Department of Genetics, Stanford University School of Medicine, Stanford, CA.
  • Eng C; Centro de Investigación y Desarrollo en Inmunología y Enfermedades Infecciosas, Consejo Nacional de Investigaciones Científicas y Técnicas, Córdoba, Argentina.
  • Huntsman S; Facultad de Filosofía y Humanidades, Universidad Nacional de Córdoba, Córdoba, Argentina.
  • Burchard EG; Division of Biological and Health Sciences, Department of Biological Systems, Universidad Autónoma Metropolitana-Xochimilco, Mexico City, Mexico.
  • Gignoux CR; Department Bioengineering & Therapeutic Sciences and Medicine, University of California San Francisco, San Francisco, CA.
  • Bustamante CD; Department Bioengineering & Therapeutic Sciences and Medicine, University of California San Francisco, San Francisco, CA.
  • Moreno-Estrada A; Department Bioengineering & Therapeutic Sciences and Medicine, University of California San Francisco, San Francisco, CA.
Mol Biol Evol ; 37(4): 994-1006, 2020 04 01.
Article em En | MEDLINE | ID: mdl-31848607
Native 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.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Variação Genética / Adaptação Biológica / Evolução Molecular / Indígena Americano ou Nativo do Alasca País/Região como assunto: Mexico Idioma: En Ano de publicação: 2020 Tipo de documento: Article País de afiliação: México

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Variação Genética / Adaptação Biológica / Evolução Molecular / Indígena Americano ou Nativo do Alasca País/Região como assunto: Mexico Idioma: En Ano de publicação: 2020 Tipo de documento: Article País de afiliação: México