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Comparative iTRAQ proteomics revealed proteins associated with horn development in yak
BACKGROUND: The practice of dehorning yak raises animal safety concerns, which have been addressed by selective breeding to obtain genetically hornless yak. The POLLED locus in yak has been studied extensively; however, little is known regarding the proteins that regulate horn bud development. METHO...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6056918/ https://www.ncbi.nlm.nih.gov/pubmed/30061793 http://dx.doi.org/10.1186/s12953-018-0141-9 |
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author | Li, Mingna Wu, Xiaoyun Guo, Xian Bao, Pengjia Ding, Xuezhi Chu, Min Liang, Chunnian Yan, Ping |
author_facet | Li, Mingna Wu, Xiaoyun Guo, Xian Bao, Pengjia Ding, Xuezhi Chu, Min Liang, Chunnian Yan, Ping |
author_sort | Li, Mingna |
collection | PubMed |
description | BACKGROUND: The practice of dehorning yak raises animal safety concerns, which have been addressed by selective breeding to obtain genetically hornless yak. The POLLED locus in yak has been studied extensively; however, little is known regarding the proteins that regulate horn bud development. METHODS: A differential proteomic analysis was performed to compare the skin from the horn bud region of polled yak fetuses and the horn bud tissue of horned yak fetuses using isobaric tags for relative and absolute quantitation (iTRAQ) technology coupled with 2D LC-MS/MS. RESULTS: One hundred differentially abundant proteins (DAPs) were identified. Of these, 29 were up-regulated and 71 were down-regulated in skin from the horn bud region of polled fetuses when compared to the horn bud tissue of horned fetuses. Bioinformatics analyses showed that the up-regulated DAPs were mainly associated with metabolic activities, while the down-regulated DAPs were significantly enriched in cell adhesion and cell movement activities. CONCLUSIONS: We concluded that some important proteins were associated with cell adhesion, cell motility, keratinocyte differentiation, cytoskeleton organization, osteoblast differentiation, and fatty acid metabolism during horn bud development. These results advance our understanding of the molecular mechanisms underlying horn development. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12953-018-0141-9) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-6056918 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-60569182018-07-30 Comparative iTRAQ proteomics revealed proteins associated with horn development in yak Li, Mingna Wu, Xiaoyun Guo, Xian Bao, Pengjia Ding, Xuezhi Chu, Min Liang, Chunnian Yan, Ping Proteome Sci Research BACKGROUND: The practice of dehorning yak raises animal safety concerns, which have been addressed by selective breeding to obtain genetically hornless yak. The POLLED locus in yak has been studied extensively; however, little is known regarding the proteins that regulate horn bud development. METHODS: A differential proteomic analysis was performed to compare the skin from the horn bud region of polled yak fetuses and the horn bud tissue of horned yak fetuses using isobaric tags for relative and absolute quantitation (iTRAQ) technology coupled with 2D LC-MS/MS. RESULTS: One hundred differentially abundant proteins (DAPs) were identified. Of these, 29 were up-regulated and 71 were down-regulated in skin from the horn bud region of polled fetuses when compared to the horn bud tissue of horned fetuses. Bioinformatics analyses showed that the up-regulated DAPs were mainly associated with metabolic activities, while the down-regulated DAPs were significantly enriched in cell adhesion and cell movement activities. CONCLUSIONS: We concluded that some important proteins were associated with cell adhesion, cell motility, keratinocyte differentiation, cytoskeleton organization, osteoblast differentiation, and fatty acid metabolism during horn bud development. These results advance our understanding of the molecular mechanisms underlying horn development. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12953-018-0141-9) contains supplementary material, which is available to authorized users. BioMed Central 2018-07-24 /pmc/articles/PMC6056918/ /pubmed/30061793 http://dx.doi.org/10.1186/s12953-018-0141-9 Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. 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 Li, Mingna Wu, Xiaoyun Guo, Xian Bao, Pengjia Ding, Xuezhi Chu, Min Liang, Chunnian Yan, Ping Comparative iTRAQ proteomics revealed proteins associated with horn development in yak |
title | Comparative iTRAQ proteomics revealed proteins associated with horn development in yak |
title_full | Comparative iTRAQ proteomics revealed proteins associated with horn development in yak |
title_fullStr | Comparative iTRAQ proteomics revealed proteins associated with horn development in yak |
title_full_unstemmed | Comparative iTRAQ proteomics revealed proteins associated with horn development in yak |
title_short | Comparative iTRAQ proteomics revealed proteins associated with horn development in yak |
title_sort | comparative itraq proteomics revealed proteins associated with horn development in yak |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6056918/ https://www.ncbi.nlm.nih.gov/pubmed/30061793 http://dx.doi.org/10.1186/s12953-018-0141-9 |
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