College of Animal and Veterinary Sciences, Southwest Minzu University, Chengdu 610041, China.
Key Laboratory of Qinghai-Tibetan Plateau Animal Genetic Resource Reservation and Utilization, Ministry of Education, Southwest Minzu University, Chengdu 610041, China.
Int J Mol Sci. 2024 Nov 20;25(22):12466. doi: 10.3390/ijms252212466.
The goat breeding industry on the Tibetan Plateau faces strong selection pressure to enhance fertility. Consequently, there is an urgent need to develop goat lines with higher fertility and adaptability. The ovary, as a key organ determining reproductive performance, is regulated by a complex transcriptional network involving numerous protein-coding and non-coding genes. However, the molecular mechanisms of the key mRNA-miRNA-lncRNA regulatory network in goat ovaries remain largely unknown. This study focused on the histology and differential mRNA/miRNA/lncRNA between Chuanzhong black goat (CBG, high productivity, multiple births) and Tibetan goat (TG, strong adaptability, single birth) ovaries. Histomorphological analysis showed that the medulla proportion in CBG ovaries was significantly reduced compared to TG. RNA-Seq and small RNA-Seq analysis identified 1218 differentially expressed (DE) mRNAs, 100 DE miRNAs, and 326 DE lncRNAs, which were mainly enriched in ovarian steroidogenesis, oocyte meiosis, biosynthesis of amino acids and protein digestion, and absorption signaling pathways. Additionally, five key mRNA-miRNA-lncRNA interaction networks regulating goat reproductive performance were identified, including -novel68_mature-ENSCHIT00000010023, -novel475_mature-ENSCHIT00000003176, -novel68_mature-XR_001919123.1, -novel65_star-TCONS_00013850, and -novel71_mature-XR_001919911.1. Further analyses showed that these networks mainly affected ovarian function and reproductive performance by regulating biological processes such as germ cell development and oocyte development, which also affected the plateau adaptive capacity of the ovary by participating in the individual immune and metabolic capacities. In conclusion, we identified numerous mRNA-miRNA-lncRNA interaction networks involved in regulating ovarian function and reproductive performance in goats. This discovery offers new insights into the molecular breeding of Tibetan Plateau goats and provides a theoretical foundation for developing new goat lines with high reproductive capacity and strong adaptability to the plateau environment.
青藏高原的山羊养殖产业面临着提高繁殖力的强大选择压力。因此,迫切需要开发出具有更高繁殖力和适应性的山羊品系。卵巢作为决定繁殖性能的关键器官,受到涉及众多蛋白质编码和非编码基因的复杂转录网络的调节。然而,山羊卵巢中关键 mRNA-miRNA-lncRNA 调控网络的分子机制在很大程度上仍然未知。本研究聚焦于 Chuanzhong 黑山羊(CBG,高生产力,多胎)和藏山羊(TG,强适应性,单胎)卵巢之间的组织学差异以及差异表达的 mRNA/miRNA/lncRNA。组织形态学分析表明,与 TG 相比,CBG 卵巢的髓质比例显著降低。RNA-Seq 和小 RNA-Seq 分析鉴定了 1218 个差异表达(DE)mRNA、100 个 DE miRNA 和 326 个 DE lncRNA,这些基因主要富集在卵巢甾体生成、卵母细胞减数分裂、氨基酸和蛋白质消化与吸收信号通路中。此外,还鉴定出了 5 个调控山羊繁殖性能的关键 mRNA-miRNA-lncRNA 互作网络,包括-novel68_mature-ENSCHIT00000010023.1、-novel475_mature-ENSCHIT00000003176、-novel68_mature-XR_001919123.1、-novel65_star-TCONS_00013850 和-novel71_mature-XR_001919911.1。进一步分析表明,这些网络主要通过调节生殖细胞发育和卵母细胞发育等生物学过程来影响卵巢功能和繁殖性能,同时通过参与个体免疫和代谢能力来影响卵巢的高原适应能力。综上所述,本研究鉴定出了许多参与调控山羊卵巢功能和繁殖性能的 mRNA-miRNA-lncRNA 互作网络。这一发现为青藏高原山羊的分子育种提供了新的见解,并为开发具有高繁殖力和对高原环境强适应性的新山羊品系提供了理论基础。