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Comparisons of lung and gluteus transcriptome profiles between yaks at different ages

The yak, Bos grunniens, is the only large mammal in the Qinghai-Tibet Plateau and has been bred to provide meat, milk, and transportation. Previous studies indicate that the immune system contributes to the yak’s adaptation to high-altitude environments. In order to further investigate changes in im...

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Autores principales: Xin, Jin-Wei, Chai, Zhi-Xin, Zhang, Cheng-Fu, Zhang, Qiang, Zhu, Yong, Cao, Han-Wen, Ji, Qiu-Mei, Zhong, Jin-Cheng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6775228/
https://www.ncbi.nlm.nih.gov/pubmed/31578356
http://dx.doi.org/10.1038/s41598-019-50618-x
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author Xin, Jin-Wei
Chai, Zhi-Xin
Zhang, Cheng-Fu
Zhang, Qiang
Zhu, Yong
Cao, Han-Wen
Ji, Qiu-Mei
Zhong, Jin-Cheng
author_facet Xin, Jin-Wei
Chai, Zhi-Xin
Zhang, Cheng-Fu
Zhang, Qiang
Zhu, Yong
Cao, Han-Wen
Ji, Qiu-Mei
Zhong, Jin-Cheng
author_sort Xin, Jin-Wei
collection PubMed
description The yak, Bos grunniens, is the only large mammal in the Qinghai-Tibet Plateau and has been bred to provide meat, milk, and transportation. Previous studies indicate that the immune system contributes to the yak’s adaptation to high-altitude environments. In order to further investigate changes in immune function during yak development, we compared the transcriptome profiles of gluteus and lung tissues among yaks at 6, 30, 60, and 90 months of age. Analyses of significantly differentially expressed genes (DEGs) in lung tissues revealed that immune function was more activated at 6-months and less activated at 90-months than in the 30 and 60-month-old animals. DEG exploration in gluteal tissues revealed that immune functions were more highly activated at both 6 and 90-months, compared with 30 and 60-months. Immune system activation in the muscle and lung tissues of 30-month-old yaks may increase their resistance to infections, while decreased may be due to aging. Furthermore, the higher immune activation status in the gluteal tissues in 90-month-old yaks could be due to muscle injury and subsequent regeneration, which is supported by the fact that 5 unigenes related with muscle injury and 3 related to muscle regeneration displayed greater expression levels at 90-months than at 30 and 60-months. Overall, the present study highlights the important role of the immune system in yak development, which will facilitate future investigations.
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spelling pubmed-67752282019-10-09 Comparisons of lung and gluteus transcriptome profiles between yaks at different ages Xin, Jin-Wei Chai, Zhi-Xin Zhang, Cheng-Fu Zhang, Qiang Zhu, Yong Cao, Han-Wen Ji, Qiu-Mei Zhong, Jin-Cheng Sci Rep Article The yak, Bos grunniens, is the only large mammal in the Qinghai-Tibet Plateau and has been bred to provide meat, milk, and transportation. Previous studies indicate that the immune system contributes to the yak’s adaptation to high-altitude environments. In order to further investigate changes in immune function during yak development, we compared the transcriptome profiles of gluteus and lung tissues among yaks at 6, 30, 60, and 90 months of age. Analyses of significantly differentially expressed genes (DEGs) in lung tissues revealed that immune function was more activated at 6-months and less activated at 90-months than in the 30 and 60-month-old animals. DEG exploration in gluteal tissues revealed that immune functions were more highly activated at both 6 and 90-months, compared with 30 and 60-months. Immune system activation in the muscle and lung tissues of 30-month-old yaks may increase their resistance to infections, while decreased may be due to aging. Furthermore, the higher immune activation status in the gluteal tissues in 90-month-old yaks could be due to muscle injury and subsequent regeneration, which is supported by the fact that 5 unigenes related with muscle injury and 3 related to muscle regeneration displayed greater expression levels at 90-months than at 30 and 60-months. Overall, the present study highlights the important role of the immune system in yak development, which will facilitate future investigations. Nature Publishing Group UK 2019-10-02 /pmc/articles/PMC6775228/ /pubmed/31578356 http://dx.doi.org/10.1038/s41598-019-50618-x Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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 images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Xin, Jin-Wei
Chai, Zhi-Xin
Zhang, Cheng-Fu
Zhang, Qiang
Zhu, Yong
Cao, Han-Wen
Ji, Qiu-Mei
Zhong, Jin-Cheng
Comparisons of lung and gluteus transcriptome profiles between yaks at different ages
title Comparisons of lung and gluteus transcriptome profiles between yaks at different ages
title_full Comparisons of lung and gluteus transcriptome profiles between yaks at different ages
title_fullStr Comparisons of lung and gluteus transcriptome profiles between yaks at different ages
title_full_unstemmed Comparisons of lung and gluteus transcriptome profiles between yaks at different ages
title_short Comparisons of lung and gluteus transcriptome profiles between yaks at different ages
title_sort comparisons of lung and gluteus transcriptome profiles between yaks at different ages
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6775228/
https://www.ncbi.nlm.nih.gov/pubmed/31578356
http://dx.doi.org/10.1038/s41598-019-50618-x
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