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Genetic characterization of Greek population isolates reveals strong genetic drift at missense and trait-associated variants.
Panoutsopoulou, Kalliope; Hatzikotoulas, Konstantinos; Xifara, Dionysia Kiara; Colonna, Vincenza; Farmaki, Aliki-Eleni; Ritchie, Graham R S; Southam, Lorraine; Gilly, Arthur; Tachmazidou, Ioanna; Fatumo, Segun; Matchan, Angela; Rayner, Nigel W; Ntalla, Ioanna; Mezzavilla, Massimo; Chen, Yuan; Kiagiadaki, Chrysoula; Zengini, Eleni; Mamakou, Vasiliki; Athanasiadis, Antonis; Giannakopoulou, Margarita; Kariakli, Vassiliki-Eirini; Nsubuga, Rebecca N; Karabarinde, Alex; Sandhu, Manjinder; McVean, Gil; Tyler-Smith, Chris; Tsafantakis, Emmanouil; Karaleftheri, Maria; Xue, Yali; Dedoussis, George; Zeggini, Eleftheria.
Afiliação
  • Panoutsopoulou K; Department of Human Genetics, Wellcome Trust Sanger Institute, Hinxton CB10 1HH, UK.
  • Hatzikotoulas K; Department of Human Genetics, Wellcome Trust Sanger Institute, Hinxton CB10 1HH, UK.
  • Xifara DK; 1] Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford OX3 7BN, UK [2] Department of Statistics, University of Oxford, Oxford OX1 3TG, UK.
  • Colonna V; Institute of Genetics and Biophysics 'A. Buzzati-Traverso', National Research Council (CNR), Naples 80131, Italy.
  • Farmaki AE; Department of Nutrition and Dietetics, Harokopio University of Athens, Athens 17671, Greece.
  • Ritchie GR; 1] Department of Human Genetics, Wellcome Trust Sanger Institute, Hinxton CB10 1HH, UK [2] European Molecular Biology Laboratory, European Bioinformatics Institute, Hinxton, Cambridge CB10 1SD, UK.
  • Southam L; 1] Department of Human Genetics, Wellcome Trust Sanger Institute, Hinxton CB10 1HH, UK [2] Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford OX3 7BN, UK.
  • Gilly A; Department of Human Genetics, Wellcome Trust Sanger Institute, Hinxton CB10 1HH, UK.
  • Tachmazidou I; Department of Human Genetics, Wellcome Trust Sanger Institute, Hinxton CB10 1HH, UK.
  • Fatumo S; 1] Department of Human Genetics, Wellcome Trust Sanger Institute, Hinxton CB10 1HH, UK [2] H3Africa Bioinformatics Network (H3ABioNet) Node, National Biotechnology Development Agency (NABDA), Federal Ministry of Science and Technology (FMST), Abuja 900107, Nigeria [3] International Health Research G
  • Matchan A; Department of Human Genetics, Wellcome Trust Sanger Institute, Hinxton CB10 1HH, UK.
  • Rayner NW; 1] Department of Human Genetics, Wellcome Trust Sanger Institute, Hinxton CB10 1HH, UK [2] Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford OX3 7BN, UK [3] Oxford Centre for Diabetes, Endocrinology and Metabolism, University of Oxford, Churchill Hospital, Oxford OX3 7LJ, UK.
  • Ntalla I; 1] Department of Nutrition and Dietetics, Harokopio University of Athens, Athens 17671, Greece [2] Department of Health Sciences, University of Leicester, Leicester LE1 7RH, UK.
  • Mezzavilla M; 1] Department of Human Genetics, Wellcome Trust Sanger Institute, Hinxton CB10 1HH, UK [2] Division of Medical Genetics, Department of Reproductive Sciences and Development, IRCCS-Burlo Garofolo, University of Trieste, Trieste 34137, Italy.
  • Chen Y; Department of Human Genetics, Wellcome Trust Sanger Institute, Hinxton CB10 1HH, UK.
  • Kiagiadaki C; Anogia Medical Centre, Anogia 74051, Greece.
  • Zengini E; 1] Dromokaiteio Psychiatric Hospital of Athens, Chaidari, Athens 12461, Greece [2] Department of Human Metabolism, University of Sheffield, Sheffield S10 2TN, UK.
  • Mamakou V; 1] Dromokaiteio Psychiatric Hospital of Athens, Chaidari, Athens 12461, Greece [2] School of Medicine, National and Kapodistrian University of Athens, Goudi, Athens 11527, Greece.
  • Athanasiadis A; Echinos Medical Centre, Xanthi 67300, Greece.
  • Giannakopoulou M; School of Health Sciences, Faculty of Nursing, National and Kapodistrian University of Athens, Goudi, Athens 11527, Greece.
  • Kariakli VE; Department of Nutrition and Dietetics, Harokopio University of Athens, Athens 17671, Greece.
  • Nsubuga RN; Medical Research Council/Uganda Virus Research Institute, Uganda Research Unit on AIDS, PO Box 49, Entebbe, Uganda.
  • Karabarinde A; Medical Research Council/Uganda Virus Research Institute, Uganda Research Unit on AIDS, PO Box 49, Entebbe, Uganda.
  • Sandhu M; 1] Department of Human Genetics, Wellcome Trust Sanger Institute, Hinxton CB10 1HH, UK [2] International Health Research Group, Department of Public Health and Primary Care, University of Cambridge, Cambridge CB1 8NR, UK.
  • McVean G; Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford OX3 7BN, UK.
  • Tyler-Smith C; Department of Human Genetics, Wellcome Trust Sanger Institute, Hinxton CB10 1HH, UK.
  • Tsafantakis E; Anogia Medical Centre, Anogia 74051, Greece.
  • Karaleftheri M; Echinos Medical Centre, Xanthi 67300, Greece.
  • Xue Y; Department of Human Genetics, Wellcome Trust Sanger Institute, Hinxton CB10 1HH, UK.
  • Dedoussis G; Department of Nutrition and Dietetics, Harokopio University of Athens, Athens 17671, Greece.
  • Zeggini E; Department of Human Genetics, Wellcome Trust Sanger Institute, Hinxton CB10 1HH, UK.
Nat Commun ; 5: 5345, 2014 Nov 06.
Article em En | MEDLINE | ID: mdl-25373335
ABSTRACT
Isolated populations are emerging as a powerful study design in the search for low-frequency and rare variant associations with complex phenotypes. Here we genotype 2,296 samples from two isolated Greek populations, the Pomak villages (HELIC-Pomak) in the North of Greece and the Mylopotamos villages (HELIC-MANOLIS) in Crete. We compare their genomic characteristics to the general Greek population and establish them as genetic isolates. In the MANOLIS cohort, we observe an enrichment of missense variants among the variants that have drifted up in frequency by more than fivefold. In the Pomak cohort, we find novel associations at variants on chr11p15.4 showing large allele frequency increases (from 0.2% in the general Greek population to 4.6% in the isolate) with haematological traits, for example, with mean corpuscular volume (rs7116019, P=2.3 × 10(-26)). We replicate this association in a second set of Pomak samples (combined P=2.0 × 10(-36)). We demonstrate significant power gains in detecting medical trait associations.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: População / Variação Genética / Mutação de Sentido Incorreto / Deriva Genética / Genética Populacional / Genótipo Tipo de estudo: Etiology_studies / Incidence_studies / Observational_studies / Risk_factors_studies Limite: Adolescent / Humans País/Região como assunto: Europa Idioma: En Revista: Nat Commun Ano de publicação: 2014 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: População / Variação Genética / Mutação de Sentido Incorreto / Deriva Genética / Genética Populacional / Genótipo Tipo de estudo: Etiology_studies / Incidence_studies / Observational_studies / Risk_factors_studies Limite: Adolescent / Humans País/Região como assunto: Europa Idioma: En Revista: Nat Commun Ano de publicação: 2014 Tipo de documento: Article