Rare intronic variants of TCF7L2 arising by selective sweeps in an indigenous population from Mexico

التفاصيل البيبلوغرافية
العنوان: Rare intronic variants of TCF7L2 arising by selective sweeps in an indigenous population from Mexico
المؤلفون: Laura Carolina Correa-Acosta, Alma Cristal Hernández-Mondragón, Carlos A. Aguilar-Salinas, Berenice Chávez-Florencio, José L. Acosta, Elvia Yamilet Ramírez-Vega, Laura del Bosque-Plata, Teresa Tusié-Luna, Sandra Nathaly Cazañas-Padilla, Tulia Monge-Cázares
المصدر: BMC Genetics
بيانات النشر: Springer Nature
مصطلحات موضوعية: 0301 basic medicine, Linkage disequilibrium, endocrine system diseases, Population, Population genetics, 030105 genetics & heredity, Biology, 03 medical and health sciences, Genetic variation, Ethnicity, Genetics, Humans, Genetics(clinical), 1000 Genomes Project, education, Mexico, Genetics (clinical), Recombination hotspots, Genetic association, Recombination, Genetic, education.field_of_study, Genetic diversity, Polymorphism, Genetic, Haplotype, nutritional and metabolic diseases, TCF7L2 gene, Type 2 diabetes, Exons, Introns, Sweeps selection, 030104 developmental biology, Diabetes Mellitus, Type 2, Evolutionary biology, Mutation, Transcription Factor 7-Like 2 Protein, Research Article
الوصف: Background Genetic variations of the TCF7L2 gene are associated with the development of Type 2 diabetes (T2D). The associated mutations have demonstrated an adaptive role in some human populations, but no studies have determined the impact of evolutionary forces on genetic diversity in indigenous populations from Mexico. Here, we sequenced and analyzed the variation of the TCF7L2 gene in three Amerindian populations and compared the results with whole-exon-sequencing of Mestizo populations from Sigma and the 1000 Genomes Project to assess the roles of selection and recombination in diversity. Results The diversity in the indigenous populations was biased to intronic regions. Most of the variation was low frequency. Only mutations rs77961654 and rs61724286 were located on exon 15. We did not observe variation in intronic region 4–6 in any of the three indigenous populations. In addition, we identified peaks of selective sweeps in the mestizo samples from the Sigma Project within this region. By replicating the analysis of association with T2D between case-controls from the Sigma Project, we determined that T2D was most highly associated with the rs7903146 risk allele and to a lesser extent with the other six variants. All associated markers were located in intronic region 4–6, and their r2 values of linkage disequilibrium were significantly higher in the Mexican population than in Africans from the 1000 Genomes Project. We observed reticulations in both the haplotypes network analysis from seven marker associates and the neighborNet tree based on 6061 markers in the TCF7L2 gene identified from all samples of the 1000 Genomes Project. Finally, we identified two recombination hotspots in the upstream region and 3’ end of the TCF7L2 gene. Conclusions The lack of diversity in intronic region 4–6 in Indigenous populations could be an effect of selective sweeps generated by the selection of neighboring rare variants at T2D-associated mutations. The survivors’ variants make the intronic region 4–6 the area of the greatest population differentiation within the TCF7L2 gene. The abundance of selective peak sweeps in the downstream region of the TCF7L2 gene suggests that the TCF7L2 gene is part of a region that is in constant recombination between populations. Electronic supplementary material The online version of this article (doi:10.1186/s12863-016-0372-7) contains supplementary material, which is available to authorized users.
اللغة: English
تدمد: 1471-2156
DOI: 10.1186/s12863-016-0372-7
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bb8ace00ecb71a2a8553343da0edd6cfTest
حقوق: OPEN
رقم الانضمام: edsair.doi.dedup.....bb8ace00ecb71a2a8553343da0edd6cf
قاعدة البيانات: OpenAIRE
الوصف
تدمد:14712156
DOI:10.1186/s12863-016-0372-7