Genome-wide identification of candidate copy number polymorphism genes associated with complex traits of Tibetan-sheep
Copy number variation (CNV) is a genetic structural polymorphism important for phenotypic diversity and important economic traits of livestock breeds, and it plays an important role in the desired genetic variation. This study used whole genome sequencing to detect the CNV variation in the genome of...
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Veröffentlicht in: | Scientific reports 2023-10, Vol.13 (1), p.17283-17283, Article 17283 |
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Sprache: | eng |
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Zusammenfassung: | Copy number variation (CNV) is a genetic structural polymorphism important for phenotypic diversity and important economic traits of livestock breeds, and it plays an important role in the desired genetic variation. This study used whole genome sequencing to detect the CNV variation in the genome of 6 local Tibetan sheep groups. We detected 69,166 CNV events and 7230 copy number variable regions (CNVRs) after merging the overlapping CNVs, accounting for 2.72% of the reference genome. The CNVR length detected ranged from 1.1 to 1693.5 Kb, with a total length of 118.69 Mb and an average length of 16.42 Kb per CNVR. Functional GO cluster analysis showed that the CNVR genes were mainly involved in sensory perception systems, response to stimulus, and signal transduction. Through CNVR-based Vst analysis, we found that the
CACNA2D3
and
CTBP1
genes related to hypoxia adaptation, the
HTR1A
gene related to coat color, and the
TRNAS-GGA
and
PIK3C3
genes related to body weight were all strongly selected. The findings of our study will contribute novel insights into the genetic structural variation underlying hypoxia adaptation and economically important traits in Tibetan sheep. |
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ISSN: | 2045-2322 2045-2322 |
DOI: | 10.1038/s41598-023-44402-1 |