Integrated analysis of lncRNA, miRNA and mRNA reveals novel insights into the fertility regulation of large white sows

BMC Genomics

Bo Zhou¹  Jianzhong Xi¹  Huiyan Hu¹  Zhiqiang Li¹  Qing Jia² 

[1] Department of Animal Genetics, Breeding and Reproduction, College of Animal Science and Technology, Hebei Agricultural University, Lekai South Street No. 2596, 071000, Baoding, Hebei, China;Department of Animal Genetics, Breeding and Reproduction, College of Animal Science and Technology, Hebei Agricultural University, Lekai South Street No. 2596, 071000, Baoding, Hebei, China;Engineering Research Center for Agriculture in Hebei Mountainous Areas, 071000, Baoding, Hebei, China;

关键词: Pigs;    Fertility;    Ovary;    Follicular and luteal phases;    Competing endogenous RNAs;    Regulation networks;   

DOI  :  10.1186/s12864-020-07055-2

来源: Springer

【 摘 要 】

BackgroundImproving sow fertility is extremely important as it can lead to increased reproductive efficiency and thus profitability for swine producers. There are considerable differences in fertility rates among individual animals, but the underlying molecular mechanisms remain unclear. In this study, by using different types of RNA libraries, we investigated the complete transcriptome of ovarian tissue during the luteal (L) and follicular (F) phases of the estrous cycle in Large White pigs with high (H) and low (L) fecundity, and performed a comprehensive analysis of long noncoding RNAs (lncRNAs), mRNAs and micro RNAs (miRNAs) from 16 samples by combining RNA sequencing (RNA-seq) with bioinformatics.ResultsIn total, 24,447 lncRNAs, 27,370 mRNAs, and 216 known miRNAs were identified in ovarian tissues. The genomic features of lncRNAs, such as length distribution and number of exons, were further analyzed. We selected a threshold of P < 0.05 and |log2 (fold change)| ≥ 1 to obtain the differentially expressed lncRNAs, miRNAs and mRNAs by pairwise comparison (LH vs. LL, FH vs. FL). Bioinformatics analysis of these differentially expressed RNAs revealed multiple significantly enriched pathways (P < 0.05) that were closely involved in the reproductive process, such as ovarian steroidogenesis, lysosome, steroid biosynthesis, and the estrogen and GnRH signaling pathways. Moreover, bioinformatics screening of differentially expressed miRNAs that share common miRNA response elements (MREs) with lncRNAs and their downstream mRNA targets were performed. Finally, we constructed lncRNA–miRNA–mRNA regulation networks. The key genes in these networks were verified by Reverse Transcription Real-time Quantitative PCR (RT-qRCR), which were consistent with the results from RNA-Seq data.ConclusionsThese results provide further insights into the fertility of pigs andcan contribute to further experimental investigation of the functions of these genes.

【 授权许可】

CC BY