Your browser doesn't support javascript.
loading
Selection scan in Native Americans of Mexico identifies FADS2 rs174616: Evidence of gene-diet interactions affecting lipid levels and Delta-6-desaturase activity.
Romero-Hidalgo, Sandra; Sagaceta-Mejía, Janine; Villalobos-Comparán, Marisela; Tejero, María Elizabeth; Domínguez-Pérez, Mayra; Jacobo-Albavera, Leonor; Posadas-Sánchez, Rosalinda; Vargas-Alarcón, Gilberto; Posadas-Romero, Carlos; Macías-Kauffer, Luis; Vadillo-Ortega, Felipe; Contreras-Sieck, Miguel Angel; Acuña-Alonzo, Víctor; Barquera, Rodrigo; Macín, Gastón; Binia, Aristea; Guevara-Chávez, Jose Guadalupe; Sebastián-Medina, Leticia; Menjívar, Martha; Canizales-Quinteros, Samuel; Carnevale, Alessandra; Villarreal-Molina, Teresa.
Affiliation
  • Romero-Hidalgo S; Departamento de Genómica Computacional, Instituto Nacional de Medicina Genómica, Mexico City, Mexico.
  • Sagaceta-Mejía J; Laboratorio de Nutrigenética y Nutrigenómica, Instituto Nacional de Medicina Genómica, Mexico City, Mexico.
  • Villalobos-Comparán M; Departamento de Genómica Computacional, Instituto Nacional de Medicina Genómica, Mexico City, Mexico.
  • Tejero ME; Laboratorio de Nutrigenética y Nutrigenómica, Instituto Nacional de Medicina Genómica, Mexico City, Mexico.
  • Domínguez-Pérez M; Laboratorio de Genómica de Enfermedades Cardiovasculares, Instituto Nacional de Medicina Genómica, Mexico City, Mexico.
  • Jacobo-Albavera L; Laboratorio de Genómica de Enfermedades Cardiovasculares, Instituto Nacional de Medicina Genómica, Mexico City, Mexico.
  • Posadas-Sánchez R; Departamento de Endocrinología, Instituto Nacional de Cardiología "Ignacio Chávez", Mexico City, Mexico.
  • Vargas-Alarcón G; Departmento de Biología Molecular y Dirección de Investigación, Instituto Nacional de Cardiología Ignacio Chávez, Mexico City, Mexico.
  • Posadas-Romero C; Departamento de Endocrinología, Instituto Nacional de Cardiología "Ignacio Chávez", Mexico City, Mexico.
  • Macías-Kauffer L; Unidad de Genómica de Poblaciones Aplicada a la Salud, Facultad de Química UNAM e Instituto Nacional de Medicina Genómica, Mexico City, Mexico.
  • Vadillo-Ortega F; Unidad de Vinculación de la Facultad de Medicina UNAM en el Instituto Nacional de Medicina Genómica, Mexico City, Mexico.
  • Contreras-Sieck MA; Laboratorio de Genética Molecular, Escuela Nacional de Antropología e Historia, Mexico City, Mexico.
  • Acuña-Alonzo V; Laboratorio de Genética Molecular, Escuela Nacional de Antropología e Historia, Mexico City, Mexico.
  • Barquera R; Department of Archaeogenetics, Max Planck Institute for Evolutionary Anthropology (MPI-EVA), Leipzig, Germany.
  • Macín G; Anthropology (MPI-EVA), Leipzig, Germany.
  • Binia A; Escuela Nacional de Antropología e Historia, Mexico City, Mexico.
  • Guevara-Chávez JG; Nestlé Institute of Health Sciences, Innovation Park, EPFL, Lausanne, Switzerland.
  • Sebastián-Medina L; Laboratorio de Genómica de Enfermedades Cardiovasculares, Instituto Nacional de Medicina Genómica, Mexico City, Mexico.
  • Menjívar M; Laboratorio de Nutrigenética y Nutrigenómica, Instituto Nacional de Medicina Genómica, Mexico City, Mexico.
  • Canizales-Quinteros S; Departamento de Biología, Facultad de Química UNAM, Mexico City and Unidad Académica de Ciencias y Tecnología, UNAM-Yucatán, Mérida, Mexico.
  • Carnevale A; Unidad de Genómica de Poblaciones Aplicada a la Salud, Facultad de Química UNAM e Instituto Nacional de Medicina Genómica, Mexico City, Mexico.
  • Villarreal-Molina T; Laboratorio de Enfermedades Mendelianas, Instituto Nacional de Medicina Genómica, Mexico City, Mexico.
Heliyon ; 10(15): e35477, 2024 Aug 15.
Article in En | MEDLINE | ID: mdl-39166092
ABSTRACT
Searching for positive selection signals across genomes has identified functional genetic variants responding to environmental change. In Native Americans of Mexico, we used the fixation index (Fst) and population branch statistic (PBS) to identify SNPs suggesting positive selection. The 103 most differentiated SNPs were tested for associations with metabolic traits, the most significant association was FADS2/rs174616 with body mass index (BMI). This variant lies within a linkage disequilibrium (LD) block independent of previously reported FADS selection signals and has not been clearly associated with metabolic phenotypes. We tested this variant in two independent cohorts with cardiometabolic data. In the Genetics of Atherosclerotic Disease (GEA) cohort, the derived allele (T) was associated with increased BMI, lower LDL-C levels and a decreased risk of subclinical atherosclerosis in women. Significant gene-diet interactions affected lipid, apolipoprotein and adiponectin levels with differences according to sex, involving mainly total and complex dietary carbohydrate%. In the Genotype-related Effects of PUFA trial, the derived allele was associated with lower Δ-6 desaturase activity and erythrocyte membrane dihomo-gamma-linolenic acid (DGLA) levels, and with increased Δ-5 desaturase activity and eicosapentaenoic acid levels. This variant interacted with dietary carbohydrate% affecting Δ-6 desaturase activity. Notably, the relationship of DGLA and other erythrocyte membrane LC-PUFA indices with HOMA-IR differed according to rs174616 genotype, which has implications regarding how these indices should be interpreted. In conclusion, this observational study identified rs174616 as a signal suggesting selection in an independent linkage disequilibrium block, was associated with cardiometabolic and erythrocyte measurements of LC-PUFA in two independent Mexican cohorts and showed significant gene-diet interactions.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Country/Region as subject: Mexico Language: En Journal: Heliyon Year: 2024 Document type: Article Affiliation country: Mexico Country of publication: United kingdom

Full text: 1 Collection: 01-internacional Database: MEDLINE Country/Region as subject: Mexico Language: En Journal: Heliyon Year: 2024 Document type: Article Affiliation country: Mexico Country of publication: United kingdom