College of Animal Science and Technology, Hebei Agricultural University, Lekai South Street, Baoding, 071001, China.
Hebei Animal Husbandry and Veterinary Institute, Baoding, 071000, China.
BMC Genet. 2020 Jul 9;21(1):72. doi: 10.1186/s12863-020-00882-y.
RNA-sequencing was performed to explore the bovine liver transcriptomes of Holstein cows to detect potential functional genes related to lactation and milk composition traits in dairy cattle. The bovine transcriptomes of the nine liver samples from three Holstein cows during dry period (50-d prepartum), early lactation (10-d postpartum), and peak of lactation (60-d postpartum) were sequenced using the Illumina HiSeq 2500 platform.
A total of 204, 147 and 81 differentially expressed genes (DEGs, p < 0.05, false discovery rate q < 0.05) were detected in early lactation vs. dry period, peak of lactation vs. dry period, and peak of lactation vs. early lactation comparison groups, respectively. Gene ontology and KEGG pathway analysis showed that these DEGs were significantly enriched in specific biological processes related to metabolic and biosynthetic and signaling pathways of PPAR, AMPK and p53 (p < 0.05). Ten genes were identified as promising candidates affecting milk yield, milk protein and fat traits in dairy cattle by using an integrated analysis of differential gene expression, previously reported quantitative trait loci (QTL), data from genome-wide association studies (GWAS), and biological function information. These genes were APOC2, PPP1R3B, PKLR, ODC1, DUSP1, LMNA, GALE, ANGPTL4, LPIN1 and CDKN1A.
This study explored the complexity of the liver transcriptome across three lactation periods in dairy cattle by performing RNA sequencing. Integrated analysis of DEGs and reported QTL and GWAS data allowed us to find ten key candidate genes influencing milk production traits.
为了探索荷斯坦奶牛肝脏的转录组,以检测与奶牛泌乳和乳成分性状相关的潜在功能基因,我们对来自三头荷斯坦奶牛的九个干奶期(产前 50 天)、泌乳早期(产后 10 天)和泌乳高峰期(产后 60 天)的肝脏样本进行了 RNA 测序,测序平台为 Illumina HiSeq 2500。
在泌乳早期与干奶期、泌乳高峰期与干奶期、泌乳高峰期与泌乳早期比较组中,分别检测到 204、147 和 81 个差异表达基因(DEGs,p<0.05,错误发现率 q<0.05)。GO 注释和 KEGG 通路分析表明,这些 DEGs 显著富集在与代谢和生物合成以及 PPAR、AMPK 和 p53 信号通路相关的特定生物学过程中(p<0.05)。通过差异基因表达、先前报道的数量性状位点(QTL)、全基因组关联研究(GWAS)数据和生物功能信息的综合分析,鉴定出 10 个候选基因,这些基因可能影响奶牛的产奶量、乳蛋白和乳脂性状,它们是 APOC2、PPP1R3B、PKLR、ODC1、DUSP1、LMNA、GALE、ANGPTL4、LPIN1 和 CDKN1A。
本研究通过 RNA 测序探索了奶牛三个泌乳期肝脏转录组的复杂性。DEGs 与先前报道的 QTL 和 GWAS 数据的综合分析,使我们找到了十个影响产奶性状的关键候选基因。