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A Worldwide Analysis of Beta-Defensin Copy Number Variation Suggests Recent Selection of a High-Expressing DEFB103 Gene Copy in East Asia

Beta-defensins are a family of multifunctional genes with roles in defense against pathogens, reproduction, and pigmentation. In humans, six beta-defensin genes are clustered in a repeated region which is copy-number variable (CNV) as a block, with a diploid copy number between 1 and 12. The role in...

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Autores principales: Hardwick, Robert J, Machado, Lee R, Zuccherato, Luciana W, Antolinos, Suzanne, Xue, Yali, Shawa, Nyambura, Gilman, Robert H, Cabrera, Lilia, Berg, Douglas E, Tyler-Smith, Chris, Kelly, Paul, Tarazona-Santos, Eduardo, Hollox, Edward J
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wiley Subscription Services, Inc., A Wiley Company 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3263423/
https://www.ncbi.nlm.nih.gov/pubmed/21387465
http://dx.doi.org/10.1002/humu.21491
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author Hardwick, Robert J
Machado, Lee R
Zuccherato, Luciana W
Antolinos, Suzanne
Xue, Yali
Shawa, Nyambura
Gilman, Robert H
Cabrera, Lilia
Berg, Douglas E
Tyler-Smith, Chris
Kelly, Paul
Tarazona-Santos, Eduardo
Hollox, Edward J
author_facet Hardwick, Robert J
Machado, Lee R
Zuccherato, Luciana W
Antolinos, Suzanne
Xue, Yali
Shawa, Nyambura
Gilman, Robert H
Cabrera, Lilia
Berg, Douglas E
Tyler-Smith, Chris
Kelly, Paul
Tarazona-Santos, Eduardo
Hollox, Edward J
author_sort Hardwick, Robert J
collection PubMed
description Beta-defensins are a family of multifunctional genes with roles in defense against pathogens, reproduction, and pigmentation. In humans, six beta-defensin genes are clustered in a repeated region which is copy-number variable (CNV) as a block, with a diploid copy number between 1 and 12. The role in host defense makes the evolutionary history of this CNV particularly interesting, because morbidity due to infectious disease is likely to have been an important selective force in human evolution, and to have varied between geographical locations. Here, we show CNV of the beta-defensin region in chimpanzees, and identify a beta-defensin block in the human lineage that contains rapidly evolving noncoding regulatory sequences. We also show that variation at one of these rapidly evolving sequences affects expression levels and cytokine responsiveness of DEFB103, a key inhibitor of influenza virus fusion at the cell surface. A worldwide analysis of beta-defensin CNV in 67 populations shows an unusually high frequency of high-DEFB103-expressing copies in East Asia, the geographical origin of historical and modern influenza epidemics, possibly as a result of selection for increased resistance to influenza in this region. Hum Mutat 32:743–750, 2011. © 2011 Wiley-Liss, Inc.
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spelling pubmed-32634232012-01-23 A Worldwide Analysis of Beta-Defensin Copy Number Variation Suggests Recent Selection of a High-Expressing DEFB103 Gene Copy in East Asia Hardwick, Robert J Machado, Lee R Zuccherato, Luciana W Antolinos, Suzanne Xue, Yali Shawa, Nyambura Gilman, Robert H Cabrera, Lilia Berg, Douglas E Tyler-Smith, Chris Kelly, Paul Tarazona-Santos, Eduardo Hollox, Edward J Hum Mutat Research Articles Beta-defensins are a family of multifunctional genes with roles in defense against pathogens, reproduction, and pigmentation. In humans, six beta-defensin genes are clustered in a repeated region which is copy-number variable (CNV) as a block, with a diploid copy number between 1 and 12. The role in host defense makes the evolutionary history of this CNV particularly interesting, because morbidity due to infectious disease is likely to have been an important selective force in human evolution, and to have varied between geographical locations. Here, we show CNV of the beta-defensin region in chimpanzees, and identify a beta-defensin block in the human lineage that contains rapidly evolving noncoding regulatory sequences. We also show that variation at one of these rapidly evolving sequences affects expression levels and cytokine responsiveness of DEFB103, a key inhibitor of influenza virus fusion at the cell surface. A worldwide analysis of beta-defensin CNV in 67 populations shows an unusually high frequency of high-DEFB103-expressing copies in East Asia, the geographical origin of historical and modern influenza epidemics, possibly as a result of selection for increased resistance to influenza in this region. Hum Mutat 32:743–750, 2011. © 2011 Wiley-Liss, Inc. Wiley Subscription Services, Inc., A Wiley Company 2011-07 2011-03-08 /pmc/articles/PMC3263423/ /pubmed/21387465 http://dx.doi.org/10.1002/humu.21491 Text en © 2011 Wiley-Liss, Inc. http://creativecommons.org/licenses/by/2.5/ Re-use of this article is permitted in accordance with the Creative Commons Deed, Attribution 2.5, which does not permit commercial exploitation.
spellingShingle Research Articles
Hardwick, Robert J
Machado, Lee R
Zuccherato, Luciana W
Antolinos, Suzanne
Xue, Yali
Shawa, Nyambura
Gilman, Robert H
Cabrera, Lilia
Berg, Douglas E
Tyler-Smith, Chris
Kelly, Paul
Tarazona-Santos, Eduardo
Hollox, Edward J
A Worldwide Analysis of Beta-Defensin Copy Number Variation Suggests Recent Selection of a High-Expressing DEFB103 Gene Copy in East Asia
title A Worldwide Analysis of Beta-Defensin Copy Number Variation Suggests Recent Selection of a High-Expressing DEFB103 Gene Copy in East Asia
title_full A Worldwide Analysis of Beta-Defensin Copy Number Variation Suggests Recent Selection of a High-Expressing DEFB103 Gene Copy in East Asia
title_fullStr A Worldwide Analysis of Beta-Defensin Copy Number Variation Suggests Recent Selection of a High-Expressing DEFB103 Gene Copy in East Asia
title_full_unstemmed A Worldwide Analysis of Beta-Defensin Copy Number Variation Suggests Recent Selection of a High-Expressing DEFB103 Gene Copy in East Asia
title_short A Worldwide Analysis of Beta-Defensin Copy Number Variation Suggests Recent Selection of a High-Expressing DEFB103 Gene Copy in East Asia
title_sort worldwide analysis of beta-defensin copy number variation suggests recent selection of a high-expressing defb103 gene copy in east asia
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3263423/
https://www.ncbi.nlm.nih.gov/pubmed/21387465
http://dx.doi.org/10.1002/humu.21491
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