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Mapping and genotypic analysis of the NK-lysin gene in chicken

BACKGROUND: Antimicrobial peptides (AMP) are important elements of the first line of defence against pathogens in animals. NK-lysin is a cationic AMP that plays a critical role in innate immunity. The chicken NK-lysin gene has been cloned and its antimicrobial and anticancer activity has been descri...

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Autores principales: Lee, Mi Ok, Yang, Ence, Morisson, Mireille, Vignal, Alain, Huang, Yong-Zhen, Cheng, Hans H, Muir, William M, Lamont, Susan J, Lillehoj, Hyun Soon, Lee, Sung Hyen, Womack, James E
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4120735/
https://www.ncbi.nlm.nih.gov/pubmed/25001618
http://dx.doi.org/10.1186/1297-9686-46-43
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author Lee, Mi Ok
Yang, Ence
Morisson, Mireille
Vignal, Alain
Huang, Yong-Zhen
Cheng, Hans H
Muir, William M
Lamont, Susan J
Lillehoj, Hyun Soon
Lee, Sung Hyen
Womack, James E
author_facet Lee, Mi Ok
Yang, Ence
Morisson, Mireille
Vignal, Alain
Huang, Yong-Zhen
Cheng, Hans H
Muir, William M
Lamont, Susan J
Lillehoj, Hyun Soon
Lee, Sung Hyen
Womack, James E
author_sort Lee, Mi Ok
collection PubMed
description BACKGROUND: Antimicrobial peptides (AMP) are important elements of the first line of defence against pathogens in animals. NK-lysin is a cationic AMP that plays a critical role in innate immunity. The chicken NK-lysin gene has been cloned and its antimicrobial and anticancer activity has been described but its location in the chicken genome remains unknown. Here, we mapped the NK-lysin gene and examined the distribution of a functionally significant single nucleotide polymorphism (SNP) among different chicken inbred lines and heritage breeds. RESULTS: A 6000 rad radiation hybrid panel (ChickRH6) was used to map the NK-lysin gene to the distal end of chromosome 22. Two additional genes, the adipocyte enhancer-binding protein 1-like gene (AEBP1) and the DNA polymerase delta subunit 2-like (POLD2) gene, are located in the same NW_003779909 contig as NK-lysin, and were thus indirectly mapped to chromosome 22 as well. Previously, we reported a functionally significant SNP at position 271 of the NK-lysin coding sequence in two different chicken breeds. Here, we examined this SNP and found that the A allele appears to be more common than the G allele in these heritage breeds and inbred lines. CONCLUSIONS: The chicken NK-lysin gene mapped to the distal end of chromosome 22. Two additional genes, AEBP1 and POLD2, were indirectly mapped to chromosome 22 also. SNP analyses revealed that the A allele, which encodes a peptide with a higher antimicrobial activity, is more common than the G allele in our tested inbred lines and heritage breeds.
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spelling pubmed-41207352014-08-05 Mapping and genotypic analysis of the NK-lysin gene in chicken Lee, Mi Ok Yang, Ence Morisson, Mireille Vignal, Alain Huang, Yong-Zhen Cheng, Hans H Muir, William M Lamont, Susan J Lillehoj, Hyun Soon Lee, Sung Hyen Womack, James E Genet Sel Evol Research BACKGROUND: Antimicrobial peptides (AMP) are important elements of the first line of defence against pathogens in animals. NK-lysin is a cationic AMP that plays a critical role in innate immunity. The chicken NK-lysin gene has been cloned and its antimicrobial and anticancer activity has been described but its location in the chicken genome remains unknown. Here, we mapped the NK-lysin gene and examined the distribution of a functionally significant single nucleotide polymorphism (SNP) among different chicken inbred lines and heritage breeds. RESULTS: A 6000 rad radiation hybrid panel (ChickRH6) was used to map the NK-lysin gene to the distal end of chromosome 22. Two additional genes, the adipocyte enhancer-binding protein 1-like gene (AEBP1) and the DNA polymerase delta subunit 2-like (POLD2) gene, are located in the same NW_003779909 contig as NK-lysin, and were thus indirectly mapped to chromosome 22 as well. Previously, we reported a functionally significant SNP at position 271 of the NK-lysin coding sequence in two different chicken breeds. Here, we examined this SNP and found that the A allele appears to be more common than the G allele in these heritage breeds and inbred lines. CONCLUSIONS: The chicken NK-lysin gene mapped to the distal end of chromosome 22. Two additional genes, AEBP1 and POLD2, were indirectly mapped to chromosome 22 also. SNP analyses revealed that the A allele, which encodes a peptide with a higher antimicrobial activity, is more common than the G allele in our tested inbred lines and heritage breeds. BioMed Central 2014-07-07 /pmc/articles/PMC4120735/ /pubmed/25001618 http://dx.doi.org/10.1186/1297-9686-46-43 Text en Copyright © 2014 Lee et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Lee, Mi Ok
Yang, Ence
Morisson, Mireille
Vignal, Alain
Huang, Yong-Zhen
Cheng, Hans H
Muir, William M
Lamont, Susan J
Lillehoj, Hyun Soon
Lee, Sung Hyen
Womack, James E
Mapping and genotypic analysis of the NK-lysin gene in chicken
title Mapping and genotypic analysis of the NK-lysin gene in chicken
title_full Mapping and genotypic analysis of the NK-lysin gene in chicken
title_fullStr Mapping and genotypic analysis of the NK-lysin gene in chicken
title_full_unstemmed Mapping and genotypic analysis of the NK-lysin gene in chicken
title_short Mapping and genotypic analysis of the NK-lysin gene in chicken
title_sort mapping and genotypic analysis of the nk-lysin gene in chicken
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4120735/
https://www.ncbi.nlm.nih.gov/pubmed/25001618
http://dx.doi.org/10.1186/1297-9686-46-43
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