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miR-17-3p靶向KCTD15调控延边黄牛前体脂肪细胞分化
引用本文:邵静,张珈溯,尹宝珍,张洛萌,夏广军. miR-17-3p靶向KCTD15调控延边黄牛前体脂肪细胞分化[J]. 畜牧兽医学报, 2020, 51(11): 2689-2698. DOI: 10.11843/j.issn.0366-6964.2020.11.008
作者姓名:邵静  张珈溯  尹宝珍  张洛萌  夏广军
作者单位:1. 延边大学农学院, 延吉 133002;2. 东北寒区肉牛科技创新教育部工程研究中心, 延吉 133002
基金项目:吉林省科技发展计划重点研发项目(20200402053NC);高等学校学科创新引智计划(D20034)
摘    要:旨在探究miR-17-3p是否可以通过靶向KCTD15调节延边黄牛前体脂肪细胞的分化。本研究使用生物信息学软件鉴定miR-17-3p的同源性,预测miR-17-3p的靶基因;通过在延边黄牛的前体脂肪细胞中转染miR-17-3p mimic或miR-17-3p inhibitor及阴性对照实现细胞内miR-17-3p过表达或抑制表达;采用双荧光素酶报告基因检测系统确定miR-17-3p与KCTD15的靶标关系;使用qRT-PCR和Western blot技术在mRNA和蛋白水平上检测miR-17-3p对KCTD15基因以及脂代谢标志基因PPARγC/EBPα表达水平的影响。结果表明,生物信息学软件预测KCTD15可作为miR-17-3p的靶基因,且miR-17-3p在哺乳动物中具有较高的同源性;转染miR-17-3p mimic后脂代谢标志基因PPARγC/EBPα的mRNA和蛋白表达量显著或极显著高于转染NC-mimic的对照组(P<0.05或P<0.01);抑制miR-17-3p的表达后,PPARγC/EBPα的表达量则显著或极显著低于对照组(P<0.05或P<0.01);双荧光素酶报告基因验证分析显示,过表达miR-17-3p极显著抑制了含有KCTD15 3'UTR片段的载体的荧光活性(P<0.01);过表达miR-17-3p也会显著或极显著抑制候选靶基因KCTD15 mRNA和蛋白质的表达量(P<0.05或P<0.01);而抑制miR-17-3p的表达则会显著提高靶基因KCTD15的mRNA和蛋白质的表达量(P<0.05)。这些结果说明,miR-17-3p可能通过抑制KCTD15的表达促进延边黄牛前体脂肪细胞分化。

关 键 词:miR-17-3p  延边黄牛  前体脂肪细胞分化  KCTD15  
收稿时间:2020-05-28

miR-17-3p Regulates Preadipocyte Differentiation by Targeting KCTD15 in Yanbian Yellow Cattle
SHAO Jing,ZHANG Jiasu,YIN Baozhen,ZHANG Luomeng,XIA Guangjun. miR-17-3p Regulates Preadipocyte Differentiation by Targeting KCTD15 in Yanbian Yellow Cattle[J]. Chinese Journal of Animal and Veterinary Sciences, 2020, 51(11): 2689-2698. DOI: 10.11843/j.issn.0366-6964.2020.11.008
Authors:SHAO Jing  ZHANG Jiasu  YIN Baozhen  ZHANG Luomeng  XIA Guangjun
Affiliation:1. Agriculture College of Yanbian University, Yanji 133002, China;2. Engineering Research Center of North-East Cold Region Beef Cattle Science & Technology Innovation, Yanji 133002, China
Abstract:The aim of this study was to explore whether miR-17-3p could target KCTD15 to regulate the preadipocytes differentiation of Yanbian Yellow cattle. Bioinformatics softwares were used to identify homology and predict target genes of miR-17-3p. miR-17-3p mimic or miR-17-3p inhibitor and their negative control were transfected into bovine preadipocytes to overexpress or inhibit the expression of miR-17-3p. The binding sites of miR-17-3p to KCTD15 were verified via double luciferase report system. qRT-PCR and Western blot were used to detect the effect of miR-17-3p on the expressions of PPARγ, C/EBPα and KCTD15 both at mRNA and protein levels. Bioinformatics software prediction showed that KCTD15 was the target gene of miR-17-3p, and miR-17-3p had high homology in mammals. The mRNA and protein expressions of adipogenic marker genes PPARγ and C/EBPα after transfection of miR-17-3p mimic were significantly or extremely significantly higher than those of the control group transfected with NC-mimic (P<0.05 or P<0.01). After the expression of miR-17-3p was inhibited, the expressions of PPARγ and C/EBPα were significantly or extremely significantly lower than that in the control group (P<0.05 or P<0.01). Through the dual-luciferase reporter assay verification, the overexpression of miR-17-3p extremely significantly inhibited the fluorescent activity of the luciferase reporter gene vector containing the 3'UTR fragment of KCTD15 (P<0.01). Overexpression of miR-17-3p could also significantly or extremely significantly inhibit the expression of KCTD15 mRNA and protein(P<0.05 or P<0.01). However, inhibition of miR-17-3p expression could significantly increase the expression of KCTD15 mRNA and protein(P<0.05). These results suggest that miR-17-3p may regulate the differentiation of preadipocytes in Yanbian Yellow cattle by inhibiting the expression of KCTD15.
Keywords:miR-17-3p  Yanbian Yellow cattle  preadipocyte differentiation  KCTD15  
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