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   Charting the Y-chromosome ancestry of present-day Argentinean Mennonites  
   
نویسنده Toscanini Ulises ,Brisighelli Francesca ,Llull Cintia ,Berardi Gabriela ,Gómez Andrea ,Andreatta Fernando ,Pardo-Seco Jacobo ,Gómez-Carballa Alberto ,Martinón-Torres Federico ,Álvarez-Iglesias Vanesa ,Salas Antonio
منبع journal of human genetics - 2016 - دوره : 61 - شماره : 6 - صفحه:507 -513
چکیده    Old order mennonite communities initially arose in northern europe (centered in the netherlands) and derived from the anabaptist movement of the 16th century. mennonites migrated to the new world in the early 18th century, first to north america, and more recently to mesoamerica and south america. we analyzed y-chromosome short tandem repeats (strs) and single nucleotide polymorphisms in males from a community of mennonites, ‘la nueva esperanza’, which arrived to argentina in 1985 from colonies in bolivia and mexico. molecular diversity indices coupled with demographic simulations show that mennonites have a reduced variability when compared with local argentinean populations and 69 european population samples. mennonite y-str haplotypes were mainly observed in central europe. in agreement, multidimensional scaling analyses based on rst genetic distances indicate that mennonite y-chromosomes are closely related to central/northern europeans (the netherlands, switzerland and denmark). in addition, statistical inferences made on the most likely geographic origin of y-chromosome haplotypes point more specifically to the netherlands as the populations that best represent the majority of the mennonite y-chromosomes. overall, y-chromosome variation of mennonites shows the signatures of moderate reduction of variability when compared with source populations, which is in good agreement with their lifestyle in small endogamous demes. these genetic singularities could also help to understand disease conditions that are more prevalent among mennonites.
آدرس PRICAI-Fundación Favaloro, Argentina. Universidade de Santiago de Compostela, Departamento de Anatomía Patolóxica e Ciencias Forenses, Unidade de Xenética, Grupo de Medicina Xenómica (GMX), Spain, Universidade de Santiago de Compostela, Departamento de Anatomía Patolóxica e Ciencias Forenses, Unidade de Xenética, Grupo de Medicina Xenómica (GMX), Spain, PRICAI-Fundación Favaloro, Argentina, PRICAI-Fundación Favaloro, Argentina, PRICAI-Fundación Favaloro, Argentina, Hospital Dr Manuel Freire, Argentina, Universidade de Santiago de Compostela, Departamento de Anatomía Patolóxica e Ciencias Forenses, Unidade de Xenética, Grupo de Medicina Xenómica (GMX), Spain. Hospital Clínico Universitario and Universidade de Santiago de Compostela (USC), Grupo de Investigación en Genética, Spain, Universidade de Santiago de Compostela, Departamento de Anatomía Patolóxica e Ciencias Forenses, Unidade de Xenética, Grupo de Medicina Xenómica (GMX), Spain. Hospital Clínico Universitario and Universidade de Santiago de Compostela (USC), Grupo de Investigación en Genética, Spain, Hospital Clínico Universitario and Universidade de Santiago de Compostela (USC), Grupo de Investigación en Genética, Spain. Hospital Clínico Universitario de Santiago de Compostela, Department of Pediatrics, Spain, Universidade de Santiago de Compostela, Departamento de Anatomía Patolóxica e Ciencias Forenses, Unidade de Xenética, Grupo de Medicina Xenómica (GMX), Spain, Universidade de Santiago de Compostela, Departamento de Anatomía Patolóxica e Ciencias Forenses, Unidade de Xenética, Grupo de Medicina Xenómica (GMX), Spain. Hospital Clínico Universitario and Universidade de Santiago de Compostela (USC), Grupo de Investigación en Genética, Spain
 
     
   
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