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Role of an SNP in Alternative Splicing of Bovine NCF4 and Mastitis Susceptibility
Neutrophil cytosolic factor 4 (NCF4) is component of the nicotinamide dinucleotide phosphate oxidase complex, a key factor in biochemical pathways and innate immune responses. In this study, splice variants and functional single-nucleotide polymorphism (SNP) of NCF4 were identified to determine the...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4658021/ https://www.ncbi.nlm.nih.gov/pubmed/26600390 http://dx.doi.org/10.1371/journal.pone.0143705 |
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author | Ju, Zhihua Wang, Changfa Wang, Xiuge Yang, Chunhong Sun, Yan Jiang, Qiang Wang, Fei Li, Mengjiao Zhong, Jifeng Huang, Jinming |
author_facet | Ju, Zhihua Wang, Changfa Wang, Xiuge Yang, Chunhong Sun, Yan Jiang, Qiang Wang, Fei Li, Mengjiao Zhong, Jifeng Huang, Jinming |
author_sort | Ju, Zhihua |
collection | PubMed |
description | Neutrophil cytosolic factor 4 (NCF4) is component of the nicotinamide dinucleotide phosphate oxidase complex, a key factor in biochemical pathways and innate immune responses. In this study, splice variants and functional single-nucleotide polymorphism (SNP) of NCF4 were identified to determine the variability and association of the gene with susceptibility to bovine mastitis characterized by inflammation. A novel splice variant, designated as NCF4-TV and characterized by the retention of a 48 bp sequence in intron 9, was detected in the mammary gland tissues of infected cows. The expression of the NCF4-reference main transcript in the mastitic mammary tissues was higher than that in normal tissues. A novel SNP, g.18174 A>G, was also found in the retained 48 bp region of intron 9. To determine whether NCF4-TV could be due to the g.18174 A>G mutation, we constructed two mini-gene expression vectors with the wild-type or mutant NCF4 g.18174 A>G fragment. The vectors were then transiently transfected into 293T cells, and alternative splicing of NCF4 was analyzed by reverse transcription-PCR and sequencing. Mini-gene splicing assay demonstrated that the aberrantly spliced NCF4-TV with 48 bp retained fragment in intron 9 could be due to g.18174 A>G, which was associated with milk somatic count score and increased risk of mastitis infection in cows. NCF4 expression was also regulated by alternative splicing. This study proposes that NCF4 splice variants generated by functional SNP are important risk factors for mastitis susceptibility in dairy cows. |
format | Online Article Text |
id | pubmed-4658021 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-46580212015-12-02 Role of an SNP in Alternative Splicing of Bovine NCF4 and Mastitis Susceptibility Ju, Zhihua Wang, Changfa Wang, Xiuge Yang, Chunhong Sun, Yan Jiang, Qiang Wang, Fei Li, Mengjiao Zhong, Jifeng Huang, Jinming PLoS One Research Article Neutrophil cytosolic factor 4 (NCF4) is component of the nicotinamide dinucleotide phosphate oxidase complex, a key factor in biochemical pathways and innate immune responses. In this study, splice variants and functional single-nucleotide polymorphism (SNP) of NCF4 were identified to determine the variability and association of the gene with susceptibility to bovine mastitis characterized by inflammation. A novel splice variant, designated as NCF4-TV and characterized by the retention of a 48 bp sequence in intron 9, was detected in the mammary gland tissues of infected cows. The expression of the NCF4-reference main transcript in the mastitic mammary tissues was higher than that in normal tissues. A novel SNP, g.18174 A>G, was also found in the retained 48 bp region of intron 9. To determine whether NCF4-TV could be due to the g.18174 A>G mutation, we constructed two mini-gene expression vectors with the wild-type or mutant NCF4 g.18174 A>G fragment. The vectors were then transiently transfected into 293T cells, and alternative splicing of NCF4 was analyzed by reverse transcription-PCR and sequencing. Mini-gene splicing assay demonstrated that the aberrantly spliced NCF4-TV with 48 bp retained fragment in intron 9 could be due to g.18174 A>G, which was associated with milk somatic count score and increased risk of mastitis infection in cows. NCF4 expression was also regulated by alternative splicing. This study proposes that NCF4 splice variants generated by functional SNP are important risk factors for mastitis susceptibility in dairy cows. Public Library of Science 2015-11-24 /pmc/articles/PMC4658021/ /pubmed/26600390 http://dx.doi.org/10.1371/journal.pone.0143705 Text en © 2015 Ju et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Ju, Zhihua Wang, Changfa Wang, Xiuge Yang, Chunhong Sun, Yan Jiang, Qiang Wang, Fei Li, Mengjiao Zhong, Jifeng Huang, Jinming Role of an SNP in Alternative Splicing of Bovine NCF4 and Mastitis Susceptibility |
title | Role of an SNP in Alternative Splicing of Bovine NCF4 and Mastitis Susceptibility |
title_full | Role of an SNP in Alternative Splicing of Bovine NCF4 and Mastitis Susceptibility |
title_fullStr | Role of an SNP in Alternative Splicing of Bovine NCF4 and Mastitis Susceptibility |
title_full_unstemmed | Role of an SNP in Alternative Splicing of Bovine NCF4 and Mastitis Susceptibility |
title_short | Role of an SNP in Alternative Splicing of Bovine NCF4 and Mastitis Susceptibility |
title_sort | role of an snp in alternative splicing of bovine ncf4 and mastitis susceptibility |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4658021/ https://www.ncbi.nlm.nih.gov/pubmed/26600390 http://dx.doi.org/10.1371/journal.pone.0143705 |
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