Abo-Ismail Mohammed K, Brito Luiz F, Miller Stephen P, Sargolzaei Mehdi, Grossi Daniela A, Moore Steve S, Plastow Graham, Stothard Paul, Nayeri Shadi, Schenkel Flavio S
Department of Animal Biosciences, Centre for Genetic Improvement of Livestock, University of Guelph, Guelph, ON, Canada.
Department of Animal and Poultry Production, Damanhour University, Damanhour, Egypt.
Genet Sel Evol. 2017 Nov 7;49(1):82. doi: 10.1186/s12711-017-0356-8.
Our aim was to identify genomic regions via genome-wide association studies (GWAS) to improve the predictability of genetic merit in Holsteins for 10 calving and 28 body conformation traits. Animals were genotyped using the Illumina Bovine 50 K BeadChip and imputed to the Illumina BovineHD BeadChip (HD). GWAS were performed on 601,717 real and imputed single nucleotide polymorphism (SNP) genotypes using a single-SNP mixed linear model on 4841 Holstein bulls with breeding value predictions and followed by gene identification and in silico functional analyses. The association results were further validated using five scenarios with different numbers of SNPs.
Seven hundred and eighty-two SNPs were significantly associated with calving performance at a genome-wise false discovery rate (FDR) of 5%. Most of these significant SNPs were on chromosomes 18 (71.9%), 17 (7.4%), 5 (6.8%) and 7 (2.4%) and mapped to 675 genes, among which 142 included at least one significant SNP and 532 were nearby one (100 kbp). For body conformation traits, 607 SNPs were significant at a genome-wise FDR of 5% and most of them were located on chromosomes 5 (30%), 18 (27%), 20 (13%), 6 (6%), 7 (5%), 14 (5%) and 13 (3%). SNP enrichment functional analyses for calving traits at a FDR of 1% suggested potential biological processes including musculoskeletal movement, meiotic cell cycle, oocyte maturation and skeletal muscle contraction. Furthermore, pathway analyses suggested potential pathways associated with calving performance traits including tight junction, oxytocin signaling, and MAPK signaling (P < 0.10). The prediction ability of the 1206 significant SNPs was between 78 and 83% of the prediction ability of the BovineSNP50 SNPs for calving performance traits and between 35 and 79% for body conformation traits.
Various SNPs that are significantly associated with calving performance are located within or nearby genes with potential roles in tight junction, oxytocin signaling, and MAPK signaling. Combining the significant SNPs or SNPs within or nearby gene(s) from the HD panel with the BovineSNP50 panel yielded a marginal increase in the accuracy of prediction of genomic estimated breeding values for all traits compared to the use of the BovineSNP50 panel alone.
我们的目标是通过全基因组关联研究(GWAS)来识别基因组区域,以提高荷斯坦奶牛10个产犊性状和28个体型性状遗传价值的预测能力。使用Illumina牛50K芯片对动物进行基因分型,并推算至Illumina牛HD芯片(HD)。对4841头具有育种值预测的荷斯坦公牛的601,717个真实和推算的单核苷酸多态性(SNP)基因型,采用单SNP混合线性模型进行GWAS分析,随后进行基因鉴定和计算机功能分析。使用五种不同SNP数量的情景对关联结果进行进一步验证。
在全基因组错误发现率(FDR)为5%时,有782个SNP与产犊性能显著相关。这些显著SNP大多位于18号染色体(71.9%)、17号染色体(7.4%)、5号染色体(6.8%)和7号染色体(2.4%)上,共映射到675个基因,其中142个基因至少包含一个显著SNP,532个基因位于其附近(100kbp)。对于体型性状,在全基因组FDR为5%时,有607个SNP显著,其中大部分位于5号染色体(30%)、18号染色体(27%)、20号染色体(13%)、6号染色体(6%)、7号染色体(5%)、14号染色体(5%)和13号染色体(3%)上。在FDR为1%时对产犊性状进行SNP富集功能分析,提示了包括肌肉骨骼运动、减数分裂细胞周期、卵母细胞成熟和骨骼肌收缩等潜在生物学过程。此外,通路分析提示了与产犊性能性状相关的潜在通路,包括紧密连接、催产素信号传导和MAPK信号传导(P<0.10)。1206个显著SNP对产犊性能性状的预测能力为BovineSNP50芯片预测能力的78%至83%,对体型性状的预测能力为35%至79%。
与产犊性能显著相关的各种SNP位于紧密连接、催产素信号传导和MAPK信号传导中具有潜在作用的基因内部或附近。与单独使用BovineSNP50芯片相比,将HD芯片中显著SNP或基因内部或附近的SNP与BovineSNP50芯片相结合,可使所有性状的基因组估计育种值预测准确性略有提高。