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Long read genome assemblies complemented by single cell RNA-sequencing reveal genetic and cellular mechanisms underlying the adaptive evolution of yak

Wild yak (Bos mutus) and domestic yak (Bos grunniens) are adapted to high altitude environment and have ecological, economic, and cultural significances on the Qinghai-Tibetan Plateau (QTP). Currently, the genetic and cellular bases underlying adaptations of yak to extreme conditions remains elusive...

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Autores principales: Gao, Xue, Wang, Sheng, Wang, Yan-Fen, Li, Shuang, Wu, Shi-Xin, Yan, Rong-Ge, Zhang, Yi-Wen, Wan, Rui-Dong, He, Zhen, Song, Ren-De, Zhao, Xin-Quan, Wu, Dong-Dong, Yang, Qi-En
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9448747/
https://www.ncbi.nlm.nih.gov/pubmed/36068211
http://dx.doi.org/10.1038/s41467-022-32164-9
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author Gao, Xue
Wang, Sheng
Wang, Yan-Fen
Li, Shuang
Wu, Shi-Xin
Yan, Rong-Ge
Zhang, Yi-Wen
Wan, Rui-Dong
He, Zhen
Song, Ren-De
Zhao, Xin-Quan
Wu, Dong-Dong
Yang, Qi-En
author_facet Gao, Xue
Wang, Sheng
Wang, Yan-Fen
Li, Shuang
Wu, Shi-Xin
Yan, Rong-Ge
Zhang, Yi-Wen
Wan, Rui-Dong
He, Zhen
Song, Ren-De
Zhao, Xin-Quan
Wu, Dong-Dong
Yang, Qi-En
author_sort Gao, Xue
collection PubMed
description Wild yak (Bos mutus) and domestic yak (Bos grunniens) are adapted to high altitude environment and have ecological, economic, and cultural significances on the Qinghai-Tibetan Plateau (QTP). Currently, the genetic and cellular bases underlying adaptations of yak to extreme conditions remains elusive. In the present study, we assembled two chromosome-level genomes, one each for wild yak and domestic yak, and screened structural variants (SVs) through the long-read data of yak and taurine cattle. The results revealed that 6733 genes contained high-FST SVs. 127 genes carrying special type of SVs were differentially expressed in lungs of the taurine cattle and yak. We then constructed the first single-cell gene expression atlas of yak and taurine cattle lung tissues and identified a yak-specific endothelial cell subtype. By integrating SVs and single-cell transcriptome data, we revealed that the endothelial cells expressed the highest proportion of marker genes carrying high-FST SVs in taurine cattle lungs. Furthermore, we identified pathways which were related to the medial thickness and formation of elastic fibers in yak lungs. These findings provide new insights into the high-altitude adaptation of yak and have important implications for understanding the physiological and pathological responses of large mammals and humans to hypoxia.
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spelling pubmed-94487472022-09-08 Long read genome assemblies complemented by single cell RNA-sequencing reveal genetic and cellular mechanisms underlying the adaptive evolution of yak Gao, Xue Wang, Sheng Wang, Yan-Fen Li, Shuang Wu, Shi-Xin Yan, Rong-Ge Zhang, Yi-Wen Wan, Rui-Dong He, Zhen Song, Ren-De Zhao, Xin-Quan Wu, Dong-Dong Yang, Qi-En Nat Commun Article Wild yak (Bos mutus) and domestic yak (Bos grunniens) are adapted to high altitude environment and have ecological, economic, and cultural significances on the Qinghai-Tibetan Plateau (QTP). Currently, the genetic and cellular bases underlying adaptations of yak to extreme conditions remains elusive. In the present study, we assembled two chromosome-level genomes, one each for wild yak and domestic yak, and screened structural variants (SVs) through the long-read data of yak and taurine cattle. The results revealed that 6733 genes contained high-FST SVs. 127 genes carrying special type of SVs were differentially expressed in lungs of the taurine cattle and yak. We then constructed the first single-cell gene expression atlas of yak and taurine cattle lung tissues and identified a yak-specific endothelial cell subtype. By integrating SVs and single-cell transcriptome data, we revealed that the endothelial cells expressed the highest proportion of marker genes carrying high-FST SVs in taurine cattle lungs. Furthermore, we identified pathways which were related to the medial thickness and formation of elastic fibers in yak lungs. These findings provide new insights into the high-altitude adaptation of yak and have important implications for understanding the physiological and pathological responses of large mammals and humans to hypoxia. Nature Publishing Group UK 2022-09-06 /pmc/articles/PMC9448747/ /pubmed/36068211 http://dx.doi.org/10.1038/s41467-022-32164-9 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Gao, Xue
Wang, Sheng
Wang, Yan-Fen
Li, Shuang
Wu, Shi-Xin
Yan, Rong-Ge
Zhang, Yi-Wen
Wan, Rui-Dong
He, Zhen
Song, Ren-De
Zhao, Xin-Quan
Wu, Dong-Dong
Yang, Qi-En
Long read genome assemblies complemented by single cell RNA-sequencing reveal genetic and cellular mechanisms underlying the adaptive evolution of yak
title Long read genome assemblies complemented by single cell RNA-sequencing reveal genetic and cellular mechanisms underlying the adaptive evolution of yak
title_full Long read genome assemblies complemented by single cell RNA-sequencing reveal genetic and cellular mechanisms underlying the adaptive evolution of yak
title_fullStr Long read genome assemblies complemented by single cell RNA-sequencing reveal genetic and cellular mechanisms underlying the adaptive evolution of yak
title_full_unstemmed Long read genome assemblies complemented by single cell RNA-sequencing reveal genetic and cellular mechanisms underlying the adaptive evolution of yak
title_short Long read genome assemblies complemented by single cell RNA-sequencing reveal genetic and cellular mechanisms underlying the adaptive evolution of yak
title_sort long read genome assemblies complemented by single cell rna-sequencing reveal genetic and cellular mechanisms underlying the adaptive evolution of yak
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9448747/
https://www.ncbi.nlm.nih.gov/pubmed/36068211
http://dx.doi.org/10.1038/s41467-022-32164-9
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