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Genome-wide analysis of CNVs in three populations of Tibetan sheep using whole-genome resequencing
Copy number variation (CNV), an important source of genomic structural variation, can disturb genetic structure, dosage, regulation and expression, and is associated with phenotypic diversity and adaptation to local environments in mammals. In the present study, 24 resequencing datasets were used to...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9490000/ https://www.ncbi.nlm.nih.gov/pubmed/36160022 http://dx.doi.org/10.3389/fgene.2022.971464 |
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author | Hu, Linyong Zhang, Liangzhi Li, Qi Liu, Hongjin Xu, Tianwei Zhao, Na Han, Xueping Xu, Shixiao Zhao, Xinquan Zhang, Cunfang |
author_facet | Hu, Linyong Zhang, Liangzhi Li, Qi Liu, Hongjin Xu, Tianwei Zhao, Na Han, Xueping Xu, Shixiao Zhao, Xinquan Zhang, Cunfang |
author_sort | Hu, Linyong |
collection | PubMed |
description | Copy number variation (CNV), an important source of genomic structural variation, can disturb genetic structure, dosage, regulation and expression, and is associated with phenotypic diversity and adaptation to local environments in mammals. In the present study, 24 resequencing datasets were used to characterize CNVs in three ecotypic populations of Tibetan sheep and assess CNVs related to domestication and adaptation in Qinghai-Tibetan Plateau. A total of 87,832 CNV events accounting for 0.3% of the sheep genome were detected. After merging the overlapping CNVs, 2777 CNV regions (CNVRs) were obtained, among which 1098 CNVRs were shared by the three populations. The average length of these CNVRs was more than 3 kb, and duplication events were more frequent than deletions. Functional analysis showed that the shared CNVRs were significantly enriched in 56 GO terms and 18 KEGG pathways that were mainly concerned with ABC transporters, olfactory transduction and oxygen transport. Moreover, 188 CNVRs overlapped with 97 quantitative trait loci (QTLs), such as growth and carcass QTLs, immunoglobulin QTLs, milk yield QTLs and fecal egg counts QTLs. PCDH15, APP and GRID2 overlapped with body weight QTLs. Furthermore, Vst analysis showed that RUNX1, LOC101104348, LOC105604082 and PAG11 were highly divergent between Highland-type Tibetan Sheep (HTS) and Valley-type Tibetan sheep (VTS), and RUNX1 and LOC101111988 were significantly differentiated between VTS and Oura-type Tibetan sheep (OTS). The duplication of RUNX1 may facilitate the hypoxia adaptation of OTS and HTS in Qinghai-Tibetan Plateau, which deserves further research in detail. In conclusion, for the first time, we represented the genome-wide distribution characteristics of CNVs in Tibetan sheep by resequencing, and provided a valuable genetic variation resource, which will facilitate the elucidation of the genetic basis underlying the distinct phenotypic traits and local adaptation of Tibetan sheep. |
format | Online Article Text |
id | pubmed-9490000 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-94900002022-09-22 Genome-wide analysis of CNVs in three populations of Tibetan sheep using whole-genome resequencing Hu, Linyong Zhang, Liangzhi Li, Qi Liu, Hongjin Xu, Tianwei Zhao, Na Han, Xueping Xu, Shixiao Zhao, Xinquan Zhang, Cunfang Front Genet Genetics Copy number variation (CNV), an important source of genomic structural variation, can disturb genetic structure, dosage, regulation and expression, and is associated with phenotypic diversity and adaptation to local environments in mammals. In the present study, 24 resequencing datasets were used to characterize CNVs in three ecotypic populations of Tibetan sheep and assess CNVs related to domestication and adaptation in Qinghai-Tibetan Plateau. A total of 87,832 CNV events accounting for 0.3% of the sheep genome were detected. After merging the overlapping CNVs, 2777 CNV regions (CNVRs) were obtained, among which 1098 CNVRs were shared by the three populations. The average length of these CNVRs was more than 3 kb, and duplication events were more frequent than deletions. Functional analysis showed that the shared CNVRs were significantly enriched in 56 GO terms and 18 KEGG pathways that were mainly concerned with ABC transporters, olfactory transduction and oxygen transport. Moreover, 188 CNVRs overlapped with 97 quantitative trait loci (QTLs), such as growth and carcass QTLs, immunoglobulin QTLs, milk yield QTLs and fecal egg counts QTLs. PCDH15, APP and GRID2 overlapped with body weight QTLs. Furthermore, Vst analysis showed that RUNX1, LOC101104348, LOC105604082 and PAG11 were highly divergent between Highland-type Tibetan Sheep (HTS) and Valley-type Tibetan sheep (VTS), and RUNX1 and LOC101111988 were significantly differentiated between VTS and Oura-type Tibetan sheep (OTS). The duplication of RUNX1 may facilitate the hypoxia adaptation of OTS and HTS in Qinghai-Tibetan Plateau, which deserves further research in detail. In conclusion, for the first time, we represented the genome-wide distribution characteristics of CNVs in Tibetan sheep by resequencing, and provided a valuable genetic variation resource, which will facilitate the elucidation of the genetic basis underlying the distinct phenotypic traits and local adaptation of Tibetan sheep. Frontiers Media S.A. 2022-09-07 /pmc/articles/PMC9490000/ /pubmed/36160022 http://dx.doi.org/10.3389/fgene.2022.971464 Text en Copyright © 2022 Hu, Zhang, Li, Liu, Xu, Zhao, Han, Xu, Zhao and Zhang. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Genetics Hu, Linyong Zhang, Liangzhi Li, Qi Liu, Hongjin Xu, Tianwei Zhao, Na Han, Xueping Xu, Shixiao Zhao, Xinquan Zhang, Cunfang Genome-wide analysis of CNVs in three populations of Tibetan sheep using whole-genome resequencing |
title | Genome-wide analysis of CNVs in three populations of Tibetan sheep using whole-genome resequencing |
title_full | Genome-wide analysis of CNVs in three populations of Tibetan sheep using whole-genome resequencing |
title_fullStr | Genome-wide analysis of CNVs in three populations of Tibetan sheep using whole-genome resequencing |
title_full_unstemmed | Genome-wide analysis of CNVs in three populations of Tibetan sheep using whole-genome resequencing |
title_short | Genome-wide analysis of CNVs in three populations of Tibetan sheep using whole-genome resequencing |
title_sort | genome-wide analysis of cnvs in three populations of tibetan sheep using whole-genome resequencing |
topic | Genetics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9490000/ https://www.ncbi.nlm.nih.gov/pubmed/36160022 http://dx.doi.org/10.3389/fgene.2022.971464 |
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