TY - JOUR
T1 - Detection of copy number variations and their effects in Chinese bulls
AU - Zhang, Liangzhi
AU - Jia, Shangang
AU - Yang, Mingjuan
AU - Xu, Yao
AU - Li, Congjun
AU - Sun, Jiajie
AU - Huang, Yongzhen
AU - Lan, Xianyong
AU - Lei, Chuzhao
AU - Zhou, Yang
AU - Zhang, Chunlei
AU - Zhao, Xin
AU - Chen, Hong
N1 - KAUST Repository Item: Exported on 2020-10-01
PY - 2014/6/17
Y1 - 2014/6/17
N2 - Background: Copy number variations (CNVs) are a main source of genomic structural variations underlying animal evolution and production traits. Here, with one pure-blooded Angus bull as reference, we describe a genome-wide analysis of CNVs based on comparative genomic hybridization arrays in 29 Chinese domesticated bulls and examined their effects on gene expression and cattle growth traits.Results: We identified 486 copy number variable regions (CNVRs), covering 2.45% of the bovine genome, in 24 taurine (Bos taurus), together with 161 ones in 2 yaks (Bos grunniens) and 163 ones in 3 buffaloes (Bubalus bubalis). Totally, we discovered 605 integrated CNVRs, with more " loss" events than both " gain" and " both" ones, and clearly clustered them into three cattle groups. Interestingly, we confirmed their uneven distributions across chromosomes, and the differences of mitochondrion DNA copy number (gain: taurine, loss: yak & buffalo). Furthermore, we confirmed approximately 41.8% (253/605) and 70.6% (427/605) CNVRs span cattle genes and quantitative trait loci (QTLs), respectively. Finally, we confirmed 6 CNVRs in 9 chosen ones by using quantitative PCR, and further demonstrated that CNVR22 had significantly negative effects on expression of PLA2G2D gene, and both CNVR22 and CNVR310 were associated with body measurements in Chinese cattle, suggesting their key effects on gene expression and cattle traits.Conclusions: The results advanced our understanding of CNV as an important genomic structural variation in taurine, yak and buffalo. This study provides a highly valuable resource for Chinese cattle's evolution and breeding researches. 2014 Zhang et al.; licensee BioMed Central Ltd.
AB - Background: Copy number variations (CNVs) are a main source of genomic structural variations underlying animal evolution and production traits. Here, with one pure-blooded Angus bull as reference, we describe a genome-wide analysis of CNVs based on comparative genomic hybridization arrays in 29 Chinese domesticated bulls and examined their effects on gene expression and cattle growth traits.Results: We identified 486 copy number variable regions (CNVRs), covering 2.45% of the bovine genome, in 24 taurine (Bos taurus), together with 161 ones in 2 yaks (Bos grunniens) and 163 ones in 3 buffaloes (Bubalus bubalis). Totally, we discovered 605 integrated CNVRs, with more " loss" events than both " gain" and " both" ones, and clearly clustered them into three cattle groups. Interestingly, we confirmed their uneven distributions across chromosomes, and the differences of mitochondrion DNA copy number (gain: taurine, loss: yak & buffalo). Furthermore, we confirmed approximately 41.8% (253/605) and 70.6% (427/605) CNVRs span cattle genes and quantitative trait loci (QTLs), respectively. Finally, we confirmed 6 CNVRs in 9 chosen ones by using quantitative PCR, and further demonstrated that CNVR22 had significantly negative effects on expression of PLA2G2D gene, and both CNVR22 and CNVR310 were associated with body measurements in Chinese cattle, suggesting their key effects on gene expression and cattle traits.Conclusions: The results advanced our understanding of CNV as an important genomic structural variation in taurine, yak and buffalo. This study provides a highly valuable resource for Chinese cattle's evolution and breeding researches. 2014 Zhang et al.; licensee BioMed Central Ltd.
UR - http://hdl.handle.net/10754/325244
UR - http://bmcgenomics.biomedcentral.com/articles/10.1186/1471-2164-15-480
UR - http://www.scopus.com/inward/record.url?scp=84902302515&partnerID=8YFLogxK
U2 - 10.1186/1471-2164-15-480
DO - 10.1186/1471-2164-15-480
M3 - Article
C2 - 24935859
SN - 1471-2164
VL - 15
SP - 480
JO - BMC Genomics
JF - BMC Genomics
IS - 1
ER -