Structural diversity and African origin of the 17q21.31 inversion polymorphism

被引:102
|
作者
Steinberg, Karyn Meltz [1 ]
Antonacci, Francesca [1 ]
Sudmant, Peter H. [1 ]
Kidd, Jeffrey M. [1 ]
Campbell, Catarina D. [1 ]
Vives, Laura [1 ]
Malig, Maika [1 ]
Scheinfeldt, Laura [2 ]
Beggs, William [2 ]
Ibrahim, Muntaser [3 ]
Lema, Godfrey [4 ]
Nyambo, Thomas B. [4 ]
Omar, Sabah A. [5 ]
Bodo, Jean-Marie [6 ]
Froment, Alain [7 ]
Donnelly, Michael P. [8 ]
Kidd, Kenneth K. [8 ]
Tishkoff, Sarah A. [2 ]
Eichler, Evan E. [1 ,9 ]
机构
[1] Univ Washington, Dept Genome Sci, Seattle, WA 98195 USA
[2] Univ Penn, Dept Genet & Biol, Philadelphia, PA 19104 USA
[3] Univ Khartoum, Inst Endem Dis, Dept Mol Biol, Khartoum, Sudan
[4] Muhimbili Univ Hlth & Allied Sci, Dept Biochem, Dar Es Salaam, Tanzania
[5] Ctr Biotechnol Res & Dev, Kenya Med Res Inst, Nairobi, Kenya
[6] Musee Homme Paris, MNHN, IRD, Unite Mixte Rech UMR 208, Paris, France
[7] Minist Rech Sci & Innovat, Yaounde, Cameroon
[8] Yale Univ, Dept Genet, New Haven, CT USA
[9] Univ Washington, Howard Hughes Med Inst, Seattle, WA 98195 USA
基金
加拿大自然科学与工程研究理事会; 美国国家卫生研究院; 美国国家科学基金会;
关键词
COPY NUMBER VARIATION; ADULT DEPRESSION; SEGMENTAL DUPLICATIONS; PARKINSON-DISEASE; COMMON INVERSION; KANSL1; CAUSE; HAPLOTYPE; MAPT; GENE; ASSOCIATION;
D O I
10.1038/ng.2335
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The 17q21.31 inversion polymorphism exists either as direct (H1) or inverted (H2) haplotypes with differential predispositions to disease and selection. We investigated its genetic diversity in 2,700 individuals, with an emphasis on African populations. We characterize eight structural haplotypes due to complex rearrangements that vary in size from 1.08-1.49 Mb and provide evidence for a 30-kb H1-H2 double recombination event. We show that recurrent partial duplications of the KANSL1 gene have occurred on both the H1 and H2 haplotypes and have risen to high frequency in European populations. We identify a likely ancestral H2 haplotype (H2') lacking these duplications that is enriched among African hunter-gatherer groups yet essentially absent from West African populations. Whereas H1 and H2 segmental duplications arose independently and before human migration out of Africa, they have reached high frequencies recently among Europeans, either because of extraordinary genetic drift or selective sweeps.
引用
收藏
页码:872 / +
页数:11
相关论文
共 50 条
  • [21] 17q21.31 Microdeletion Syndrome: Further Expanding the Clinical Phenotype
    Sharkey, F. H.
    Morrison, N.
    Murray, R.
    Iremonger, J.
    Stephen, J.
    Maher, E.
    Tolmie, J.
    Jackson, A. P.
    CYTOGENETIC AND GENOME RESEARCH, 2009, 127 (01) : 61 - 66
  • [22] SOCIAL COGNITION AND THE BEHAVIOURAL PHENOTYPE OF 17Q21.31 MICRODELETION SYNDROME
    Egger, J. I. M.
    Wingbermuhle, E.
    Verhoeven, W. M. A.
    Dijkman, M.
    Kessels, R. P. C.
    Koolen, D.
    EUROPEAN PSYCHIATRY, 2012, 27
  • [23] AORTIC ROOT DILITATION IN A CHILD WITH MICRODELETION 17Q21.31 SYNDROME
    Klein, R. L.
    Jones, M. C.
    JOURNAL OF INVESTIGATIVE MEDICINE, 2009, 57 (01) : 236 - 237
  • [24] Recurrent Inversion Events at 17q21.31 Microdeletion Locus Are Linked to the MAPT H2 Haplotype
    Rao, P. N.
    Li, W.
    Vissers, L. E. L. M.
    Veltman, J. A.
    Ophoff, R. A.
    CYTOGENETIC AND GENOME RESEARCH, 2010, 129 (04) : 275 - 279
  • [25] 17q21.31 microdeletion in a patient with pituitary stalk interruption syndrome
    El Chehadeh-Djebbar, Salima
    Callier, Patrick
    Masurel-Paulet, Alice
    Bensignor, Candace
    Mejean, Nathalie
    Payet, Muriel
    Ragon, Clemence
    Durand, Christine
    Marle, Nathalie
    Mosca-Boidron, Anne-Laure
    Huet, Frederic
    Mugneret, Francine
    Faivre, Laurence
    Thauvin-Robinet, Christel
    EUROPEAN JOURNAL OF MEDICAL GENETICS, 2011, 54 (03) : 369 - 373
  • [26] Phenotypic expansion and further characterisation of the 17q21.31 microdeletion syndrome
    Tan, T. Y.
    Aftimos, S.
    Worgan, L.
    Susman, R.
    Wilson, M.
    Ghedia, S.
    Kirk, E. P.
    Love, D.
    Ronan, A.
    Darmanian, A.
    Slavotinek, A.
    Hogue, J.
    Moeschler, J. B.
    Ozmore, J.
    Widmer, R.
    Savarirayan, R.
    Peters, G.
    JOURNAL OF MEDICAL GENETICS, 2009, 46 (07) : 480 - 489
  • [27] A 17q21.31 microdeletion encompassing the MAPT gene in a mentally impaired patient
    Varela, M. C.
    Krepischi-Santos, A. C. V.
    Paz, J. A.
    Knijnenburg, J.
    Szuhai, K.
    Rosenberg, C.
    Koiffmann, C. P.
    CYTOGENETIC AND GENOME RESEARCH, 2006, 114 (01) : 89 - 92
  • [28] Vitiligo in the Koolen-de Vries or 17q21.31 microdeletion syndrome
    Maley, Alexander M.
    Spraker, Mary K.
    de Vries, Bert B. A.
    Koolen, David A.
    CLINICAL DYSMORPHOLOGY, 2015, 24 (02) : 86 - 87
  • [29] The influence of 17q21.31 and APOE genetic ancestry on neurodegenerative disease risk
    Harerimana, Nadia V.
    Goate, Alison M.
    Bowles, Kathryn R.
    FRONTIERS IN AGING NEUROSCIENCE, 2022, 14
  • [30] TWO CASES WITH EPILEPSY AND DYSMORPHIC FEATURES ASSOCIATED WITH 17Q21.31 MICRODELETION SYNDROME
    Uctepe, E.
    Aktas, D.
    Kasifoglu, M. A.
    Gunduz, E.
    Sonmez, F. M.
    EPILEPSIA, 2015, 56 : 151 - 152