Zhang Xiao-fei, Song He, Liu Jing, Zhang Wen-jian, Yan Xiao-hong, Li Hui, Wang Ning
1. Key Laboratory of Chicken Genetics and Breeding, Ministry of Agriculture, Harbin 150030, China; 2. Key Laboratory of Animal Genetics, Breeding and Reproduction, Education Department of Heilongjiang Province, Harbin 150030, China; 3. College of Animal Science and Technology, Northeast Agricultural University, Harbin 150030, China.
Yi Chuan. 2017 Apr 20;39(4):333-345. doi: 10.16288/j.yczz.16-425.
The miR-17-92 cluster plays important roles in a variety of physiological and pathological processes in mammals. Previously, we showed that miR-17-92 cluster promotes chicken preadipocyte proliferation; however, the mechanism for its action is unknown. In order to explore the mechanism by which miR-17-92 cluster promotes chicken preadipocyte proliferation, CCK8 proliferation assay was performed to determine the effect of ZFPM2 knockdown on chicken preadipocyte proliferation. The results showed that ZFPM2 knockdown significantly promoted chicken preadipocyte proliferation (P<0.01). Consistent with the CCK8 results, the mRNA levels of cell proliferation marker genes, i.e., Cyclin D1, PCNA and Ki67, were markedly increased in the si-ZFPM2-transfected preadipocytes (P<0.01 or P<0.05). Bioinformatics analysis showed that there were two potential miRNA binding sites for the four individual members of miR-17-92 cluster in the ZFPM2 3'UTR, one for miR-17-5p and miR-20a and the other for miR-19a and miR-19b. To test whether ZFPM2 is a target for the miR-17-92 cluster, the ZFPM2 3'UTR reporter (psi-CHECK2-ZFPM2-3'UTR-WT) and its mutant reporter (psi-CHECK2-ZFPM2-3'UTR-MUT) were constructed. Reporter assays showed that overexpression of miR-17-92 cluster significantly inhibited the luciferase reporter activity of psi-CHECK2-ZFPM2-3'UTR-WT (P<0.01), as compared with control vector (empty pcDNA3.1). Transfection of miR-17-5p, miR-19a and miR-20a inhibitors increased the reporter activities of psi-CHECK2-ZFPM2-3'UTR-WT (P<0.01 or P<0.05). In contrast, transfection of miR-17-5p, miR-19a, and miR-20a inhibitors had no obvious effect on reporter activity of psi-CHECK2-ZFPM2-3'UTR-MUT. Further qRT-PCR analysis showed that miR-17-5p, miR-20a and miR-19a inhibitors significantly elevated the endogenous ZFPM2 mRNA expression (P<0.01 or P<0.05). Cotransfection of either miR-17-5p or miR-19a inhibitor and siZFPM2 showed that both inhibitors tended to reduce only slightly the promoting effect of siZFPM2 on chicken preadipocyte proliferation. Taken together, these data demonstrated that ZFPM2 is a target of miR-17-5p, miR-20a, miR-19a, and miR-19b, and that miR-17-92 cluster promotes chicken preadipocyte proliferation at least in part by targeting ZFPM2 and inhibiting its expression.
miR-17-92簇在哺乳动物的多种生理和病理过程中发挥着重要作用。此前,我们发现miR-17-92簇可促进鸡前脂肪细胞增殖;然而,其作用机制尚不清楚。为了探究miR-17-92簇促进鸡前脂肪细胞增殖的机制,进行了CCK8增殖试验以确定敲低ZFPM2对鸡前脂肪细胞增殖的影响。结果表明,敲低ZFPM2可显著促进鸡前脂肪细胞增殖(P<0.01)。与CCK8结果一致,在转染了si-ZFPM2的前脂肪细胞中,细胞增殖标记基因Cyclin D1、PCNA和Ki67的mRNA水平显著升高(P<0.01或P<0.05)。生物信息学分析表明,在ZFPM2的3'UTR中,miR-17-92簇的四个单独成员有两个潜在的miRNA结合位点,一个是miR-17-5p和miR-20a的结合位点,另一个是miR-19a和miR-19b的结合位点。为了检测ZFPM2是否是miR-17-92簇的靶标,构建了ZFPM2 3'UTR报告基因(psi-CHECK2-ZFPM2-3'UTR-WT)及其突变报告基因(psi-CHECK2-ZFPM2-3'UTR-MUT)。报告基因试验表明,与对照载体(空的pcDNA3.1)相比,miR-17-92簇的过表达显著抑制了psi-CHECK2-ZFPM2-3'UTR-WT的荧光素酶报告基因活性(P<0.01)。转染miR-17-5p、miR-19a和miR-20a抑制剂可增加psi-CHECK2-ZFPM2-3'UTR-WT的报告基因活性(P<0.01或P<0.05)。相反,转染miR-17-5p、miR-19a和miR-20a抑制剂对psi-CHECK2-ZFPM2-3'UTR-MUT的报告基因活性没有明显影响。进一步的qRT-PCR分析表明,miR-17-5p、miR-20a和miR-19a抑制剂显著提高了内源性ZFPM2 mRNA的表达(P<0.01或P<0.05)。共转染miR-17-5p或miR-19a抑制剂与siZFPM2表明,两种抑制剂仅略微降低了siZFPM2对鸡前脂肪细胞增殖的促进作用。综上所述,这些数据表明ZFPM2是miR-17-5p、miR-20a、miR-19a和miR-19b的靶标,并且miR-17-92簇至少部分地通过靶向ZFPM2并抑制其表达来促进鸡前脂肪细胞增殖。