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Structural Diversity and African Origin of the 17q21.31 Inversion Polymorphism
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 2700 individuals with an emphasis on African populations. We characterize eight structural haplotypes that...
Autores principales: | , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3408829/ https://www.ncbi.nlm.nih.gov/pubmed/22751100 http://dx.doi.org/10.1038/ng.2335 |
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author | Steinberg, Karyn Meltz Antonacci, Francesca Sudmant, Peter H. Kidd, Jeffrey M. Campbell, Catarina D. Vives, Laura Malig, Maika Scheinfeldt, Laura Beggs, William Ibrahim, Muntaser Lema, Godfrey Nyambo, Thomas B. Omar, Sabah A. Bodo, Jean-Marie Froment, Alain Donnelly, Michael P. Kidd, Kenneth K. Tishkoff, Sarah A. Eichler, Evan E. |
author_facet | Steinberg, Karyn Meltz Antonacci, Francesca Sudmant, Peter H. Kidd, Jeffrey M. Campbell, Catarina D. Vives, Laura Malig, Maika Scheinfeldt, Laura Beggs, William Ibrahim, Muntaser Lema, Godfrey Nyambo, Thomas B. Omar, Sabah A. Bodo, Jean-Marie Froment, Alain Donnelly, Michael P. Kidd, Kenneth K. Tishkoff, Sarah A. Eichler, Evan E. |
author_sort | Steinberg, Karyn Meltz |
collection | PubMed |
description | 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 2700 individuals with an emphasis on African populations. We characterize eight structural haplotypes that vary in size from 1.08 to 1.49 Mbp as a result of complex rearrangements and provide evidence for a 30 kbp H1/H2 double recombination event. We show that recurrent partial duplications of the KANSL1 (previously known as KIAA1267) gene have occurred on both H1 and H2 haplotypes and risen to high frequency in European populations. We identify a likely ancestral H2 haplotype (H2′) lacking these duplications, enriched among African hunter-gatherer groups yet essentially absent from West Africans populations. While H1 and H2 segmental duplications arose independently and prior to the human migration out of Africa, they have reached high frequencies recently among Europeans either due to extraordinary genetic drift or selective sweeps. |
format | Online Article Text |
id | pubmed-3408829 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
record_format | MEDLINE/PubMed |
spelling | pubmed-34088292013-02-01 Structural Diversity and African Origin of the 17q21.31 Inversion Polymorphism Steinberg, Karyn Meltz Antonacci, Francesca Sudmant, Peter H. Kidd, Jeffrey M. Campbell, Catarina D. Vives, Laura Malig, Maika Scheinfeldt, Laura Beggs, William Ibrahim, Muntaser Lema, Godfrey Nyambo, Thomas B. Omar, Sabah A. Bodo, Jean-Marie Froment, Alain Donnelly, Michael P. Kidd, Kenneth K. Tishkoff, Sarah A. Eichler, Evan E. Nat Genet Article 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 2700 individuals with an emphasis on African populations. We characterize eight structural haplotypes that vary in size from 1.08 to 1.49 Mbp as a result of complex rearrangements and provide evidence for a 30 kbp H1/H2 double recombination event. We show that recurrent partial duplications of the KANSL1 (previously known as KIAA1267) gene have occurred on both H1 and H2 haplotypes and risen to high frequency in European populations. We identify a likely ancestral H2 haplotype (H2′) lacking these duplications, enriched among African hunter-gatherer groups yet essentially absent from West Africans populations. While H1 and H2 segmental duplications arose independently and prior to the human migration out of Africa, they have reached high frequencies recently among Europeans either due to extraordinary genetic drift or selective sweeps. 2012-07-01 /pmc/articles/PMC3408829/ /pubmed/22751100 http://dx.doi.org/10.1038/ng.2335 Text en Users may view, print, copy, download and text and data- mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use: http://www.nature.com/authors/editorial_policies/license.html#terms |
spellingShingle | Article Steinberg, Karyn Meltz Antonacci, Francesca Sudmant, Peter H. Kidd, Jeffrey M. Campbell, Catarina D. Vives, Laura Malig, Maika Scheinfeldt, Laura Beggs, William Ibrahim, Muntaser Lema, Godfrey Nyambo, Thomas B. Omar, Sabah A. Bodo, Jean-Marie Froment, Alain Donnelly, Michael P. Kidd, Kenneth K. Tishkoff, Sarah A. Eichler, Evan E. Structural Diversity and African Origin of the 17q21.31 Inversion Polymorphism |
title | Structural Diversity and African Origin of the 17q21.31 Inversion Polymorphism |
title_full | Structural Diversity and African Origin of the 17q21.31 Inversion Polymorphism |
title_fullStr | Structural Diversity and African Origin of the 17q21.31 Inversion Polymorphism |
title_full_unstemmed | Structural Diversity and African Origin of the 17q21.31 Inversion Polymorphism |
title_short | Structural Diversity and African Origin of the 17q21.31 Inversion Polymorphism |
title_sort | structural diversity and african origin of the 17q21.31 inversion polymorphism |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3408829/ https://www.ncbi.nlm.nih.gov/pubmed/22751100 http://dx.doi.org/10.1038/ng.2335 |
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