Unknown

Dataset Information

0

Population-genetic properties of differentiated copy number variations in cattle.


ABSTRACT: While single nucleotide polymorphism (SNP) is typically the variant of choice for population genetics, copy number variation (CNV) which comprises insertion, deletion and duplication of genomic sequence, is an informative type of genetic variation. CNVs have been shown to be both common in mammals and important for understanding the relationship between genotype and phenotype. However, CNV differentiation, selection and its population genetic properties are not well understood across diverse populations. We performed a population genetics survey based on CNVs derived from the BovineHD SNP array data of eight distinct cattle breeds. We generated high resolution results that show geographical patterns of variations and genome-wide admixture proportions within and among breeds. Similar to the previous SNP-based studies, our CNV-based results displayed a strong correlation of population structure and geographical location. By conducting three pairwise comparisons among European taurine, African taurine, and indicine groups, we further identified 78 unique CNV regions that were highly differentiated, some of which might be due to selection. These CNV regions overlapped with genes involved in traits related to parasite resistance, immunity response, body size, fertility, and milk production. Our results characterize CNV diversity among cattle populations and provide a list of lineage-differentiated CNVs.

SUBMITTER: Xu L 

PROVIDER: S-EPMC4804293 | biostudies-literature | 2016 Mar

REPOSITORIES: biostudies-literature

altmetric image

Publications

Population-genetic properties of differentiated copy number variations in cattle.

Xu Lingyang L   Hou Yali Y   Bickhart Derek M DM   Zhou Yang Y   Hay El Hamidi Abdel el HA   Song Jiuzhou J   Sonstegard Tad S TS   Van Tassell Curtis P CP   Liu George E GE  

Scientific reports 20160323


While single nucleotide polymorphism (SNP) is typically the variant of choice for population genetics, copy number variation (CNV) which comprises insertion, deletion and duplication of genomic sequence, is an informative type of genetic variation. CNVs have been shown to be both common in mammals and important for understanding the relationship between genotype and phenotype. However, CNV differentiation, selection and its population genetic properties are not well understood across diverse pop  ...[more]

Similar Datasets

| S-EPMC4909312 | biostudies-literature
| S-EPMC3059424 | biostudies-literature
2011-02-01 | GSE26450 | GEO
| S-EPMC6988284 | biostudies-literature
| S-EPMC5962699 | biostudies-literature
| S-EPMC3053260 | biostudies-literature
| S-EPMC10647706 | biostudies-literature
| S-EPMC2588508 | biostudies-other
| S-EPMC2816609 | biostudies-literature
| S-EPMC2860171 | biostudies-literature