Zhong Tao, Wang Cheng, Hu Jiangtao, Chen Xiaoyong, Niu Lili, Zhan Siyuan, Wang Linjie, Guo Jiazhong, Cao Jiaxue, Li Li, Zhang Hongping
Farm Animal Genetic Resources Exploration and Innovation Key Laboratory of Sichuan Province, College of Animal Science and Technology, Sichuan Agricultural University, Chengdu 611130, China.
College of Animal Science and Technology, Hebei Agricultural University, Baoding 071001, China.
Animals (Basel). 2020 Oct 23;10(11):1951. doi: 10.3390/ani10111951.
The rumen is an important digestive organ of ruminants. From the fetal to adult stage, the morphology, structure and function of the rumen change significantly. However, the knowledge of the intrinsic genetic regulation of these changes is still limited. We previously reported a genome-wide expression profile of miRNAs in pre-natal goat rumens. In this study, we combined and analyzed the transcriptomes of rumen miRNAs during pre-natal (E60 and E135) and post-natal (D30 and D150) stages. A total of 66 differentially expressed miRNAs (DEMs) were identified in the rumen tissues from D30 and D150 goats. Of these, 17 DEMs were consistently highly expressed in the rumens at the pre-weaning stages (E60, E135 and D30), while down-regulated at D150. Noteworthy, annotation analysis revealed that the target genes regulated by the DEMs were mainly enriched in MAPK signaling pathway, Jak-STAT signaling pathway and Ras signaling pathway. Interestingly, the expression of miR-148a-3p was significantly high in the embryonic stage and down-regulated at D150. The potential binding sites of miR-148a-3p in the 3'-UTR of were predicted by the TargetScan and verified by the dual luciferase report assay. The co-localization of miR-148a-3p and through in situ hybridization was observed in the rumen tissues but not in the intestinal tracts. Moreover, the expression of miR-148a-3p in the epithelium was significantly higher than that in the other layers of the rumen, suggesting that miR-148a-3p is involved in the development of the rumen epithelial cells by targeting . Subsequently, miR-148a-3p inhibitor was found to induce the proliferation of GES-1 cells. Taken together, our study identified DEMs involved in the development of the rumen and provides insights into the regulation mechanism of rumen development in goats.
瘤胃是反刍动物重要的消化器官。从胎儿期到成年期,瘤胃的形态、结构和功能发生显著变化。然而,关于这些变化的内在基因调控的知识仍然有限。我们之前报道了产前山羊瘤胃中miRNA的全基因组表达谱。在本研究中,我们对产前(E60和E135)和产后(D30和D150)阶段瘤胃miRNA的转录组进行了合并和分析。在D30和D150山羊的瘤胃组织中总共鉴定出66个差异表达的miRNA(DEM)。其中,17个DEM在断奶前阶段(E60、E135和D30)的瘤胃中持续高表达,而在D150时下调。值得注意的是,注释分析表明,受DEM调控的靶基因主要富集在MAPK信号通路、Jak-STAT信号通路和Ras信号通路中。有趣的是,miR-148a-3p在胚胎期表达显著高,在D150时下调。通过TargetScan预测了miR-148a-3p在[具体基因名称] 3'-UTR中的潜在结合位点,并通过双荧光素酶报告试验进行了验证。通过原位杂交在瘤胃组织中观察到miR-148a-3p与[具体基因名称]的共定位,但在肠道中未观察到。此外,miR-148a-3p在上皮中的表达显著高于瘤胃其他层,表明miR-148a-3p通过靶向[具体基因名称]参与瘤胃上皮细胞的发育。随后,发现miR-148a-3p抑制剂可诱导GES-1细胞增殖。综上所述,我们的研究鉴定了参与瘤胃发育的DEM,并为山羊瘤胃发育的调控机制提供了见解。