4.6 Article

Genome-wide analysis of CNVs in three populations of Tibetan sheep using whole-genome resequencing

Journal

FRONTIERS IN GENETICS
Volume 13, Issue -, Pages -

Publisher

FRONTIERS MEDIA SA
DOI: 10.3389/fgene.2022.971464

Keywords

copy number variations; Tibetan sheep; whole genome resequencing; adaptation; domestication

Funding

  1. Second Tibetan Plateau Scientific Expedition and Research (STEP) program
  2. Key R & D Project of Qinghai Province
  3. Basic Applied Study of Qinghai Province
  4. [2019QZKK0302]
  5. [2020-NK-166]
  6. [2014-ZJ-710]

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This study characterized copy number variations (CNVs) in Tibetan sheep using resequencing data and found a large number of CNVs that are associated with genetic structure, dosage regulation, and expression in the sheep genome. The shared CNV regions (CNVRs) were found to be significantly enriched in various pathways and GO terms related to transporters, sensory perception, and oxygen transport. Several CNVRs were also found to overlap with quantitative trait loci (QTLs) related to growth, body weight, and other traits. Vst analysis revealed significant divergence of certain genes between different ecotypic populations of Tibetan sheep. These findings provide valuable genetic variation resources for further elucidating the genetic basis of distinct phenotypic traits and local adaptation in Tibetan sheep.
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.

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