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Table3_MiRNA-Seq reveals key MicroRNAs involved in fat metabolism of sheep liver.XLSX

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frontiersin.figshare.com2023-06-04 更新2025-01-15 收录
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https://frontiersin.figshare.com/articles/dataset/Table3_MiRNA-Seq_reveals_key_MicroRNAs_involved_in_fat_metabolism_of_sheep_liver_XLSX/22242643/1
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There is a genetic difference between Hu sheep (short/fat-tailed sheep) and Tibetan sheep (short/thin-tailed sheep) in tail type, because of fat metabolism. Previous studies have mainly focused directly on sheep tail fat, which is not the main organ of fat metabolism. The function of miRNAs in sheep liver fat metabolism has not been thoroughly elucidated. In this study, miRNA-Seq was used to identify miRNAs in the liver tissue of three Hu sheep (short/fat-tailed sheep) and three Tibetan sheep (short/thin-tailed sheep) to characterize the differences in fat metabolism of sheep. In our study, Hu sheep was in a control group, we identified 11 differentially expressed miRNAs (DE miRNAs), including six up-regulated miRNAs and five down-regulated miRNAs. Miranda and RNAhybrid were used to predict the target genes of DE miRNAs, obtaining 3,404 target genes. A total of 115 and 67 GO terms as well as 54 and 5 KEGG pathways were significantly (padj < 0.05) enriched for predicted 3,109 target genes of up-regulated and 295 target genes of down-regulated miRNAs, respectively. oar-miR-432 was one of the most up-regulated miRNAs between Hu sheep and Tibetan sheep. And SIRT1 is one of the potential target genes of oar-miR-432. Furthermore, functional validation using the dual-luciferase reporter assay indicated that the up-regulated miRNA; oar-miR-432 potentially targeted sirtuin 1 (SIRT1) expression. Then, the oar-miR-432 mimic transfected into preadipocytes resulted in inhibited expression of SIRT1. This is the first time reported that the expression of SIRT1 gene was regulated by oar-miR-432 in fat metabolism of sheep liver. These results could provide a meaningful theoretical basis for studying the fat metabolism of sheep.

本研究所涉及的胡羊(短尾肥羊)与藏绵羊(短尾瘦羊)之间,在尾型方面存在遗传差异,此差异源于脂肪代谢。以往的研究主要直接关注羊尾脂肪,而羊尾脂肪并非脂肪代谢的主要器官。关于miRNA在羊肝脏脂肪代谢中的功能尚未得到充分阐明。本研究采用miRNA测序技术,对三只胡羊(短尾肥羊)和三只藏绵羊(短尾瘦羊)的肝脏组织进行测序,以表征羊脂肪代谢的差异。在本研究中,胡羊作为对照组,我们鉴定出11种差异表达miRNA(DE miRNA),包括6种上调miRNA和5种下调miRNA。Miranda和RNAhybrid被用于预测DE miRNA的目标基因,共获得3,404个目标基因。针对上调miRNA预测的3,109个目标基因和下调miRNA预测的295个目标基因,分别富集了115个和67个GO术语,以及54个和5个KEGG通路,显著(padj < 0.05)。在胡羊与藏绵羊之间,oar-miR-432是上调miRNA中最为显著的一种。SIRT1是oar-miR-432的潜在靶基因之一。此外,通过双荧光素酶报告基因检测的功能验证表明,上调的miRNA oar-miR-432可能靶向沉默信息调节因子1(SIRT1)的表达。随后,将oar-miR-432模拟物转染至前脂肪细胞中,导致SIRT1表达受抑制。这是首次报道SIRT1基因的表达在羊肝脏脂肪代谢过程中受到oar-miR-432的调控。这些研究结果可为研究羊的脂肪代谢提供有意义的理论依据。
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