Li H F, Wang S H, Guo Y, Zhao H B, Li X Y, Wang X
College of Animal Science and Technology, Northwest A&F University, Yangling, Shaanxi, 712100, China.
Shandong Provincial Academy of Agricultural Sciences, Institute of Animal Science and Veterinary Medicine, Jinan, Shandong, 250100, China.
Anim Genet. 2017 Aug;48(4):455-458. doi: 10.1111/age.12550. Epub 2017 Mar 10.
It has been shown that the oxidized low density lipoprotein receptor 1 (OLR1) gene plays an important role in the degradation of oxidized low density lipoprotein. Previous studies found a SNP in the 3'-untranslated region (3'-UTR) of the OLR1 gene associated with milk production traits in different dairy cattle populations and with loin eye area and marbling depth in beef cattle. MicroRNAs can regulate gene expression by binding the 3'-UTR of target genes to degrade or to repress the translation of target genes. Bioinformatics have shown that there is a binding site of bta-miR-370 in the 3'-UTR of the OLR1 gene, and a previous luciferase reporter assay system showed that the A/C mutation occurring in the 3'-UTR of this gene caused the binding sites of bta-miR-370 to disappear in HEK293 cells. To further validate whether OLR1 was the target gene of bta-miR-370, the over-expression and interference expression of bta-miR-370 were determined by transfecting bta-miR-370 mimics and inhibitor supplementations into bovine adipocyte. The qRT-PCR result showed that the relative expression of OLR1 gene significantly decreased in the mimics group compared to the control, whereas the expression level in inhibitor group was higher than its control group. The above results were further verified by a Western blot at the protein level. In addition, lipid formation analysis of bovine adipocytes was performed via oil red O staining, and we found that cytoplasm lipid droplets in the inhibitor group showed a tendency to increase compared to the control group, whereas in the mimics group, we observed an obvious decrease of cytoplasm lipid droplets compared to the control and inhibitor groups. Taken together, our data here suggest that bta-miR-370 has a negative regulation role for OLR1 both at the gene expression and protein levels and bovine adipocytes cytoplasm lipid droplets formation, which provides a reference for illustrating how the OLR1 gene affects milk production and beef quality traits in cattle.
研究表明,氧化型低密度脂蛋白受体1(OLR1)基因在氧化型低密度脂蛋白的降解过程中发挥着重要作用。先前的研究发现,OLR1基因3'非翻译区(3'-UTR)中的一个单核苷酸多态性(SNP)与不同奶牛群体的产奶性状以及肉牛的眼肌面积和大理石花纹深度相关。微小RNA(MicroRNAs)可通过与靶基因的3'-UTR结合来调节基因表达,从而降解或抑制靶基因的翻译。生物信息学分析表明,OLR1基因的3'-UTR中存在bta-miR-370的结合位点,先前的荧光素酶报告基因检测系统显示,该基因3'-UTR中发生的A/C突变导致bta-miR-370的结合位点在HEK293细胞中消失。为进一步验证OLR1是否为bta-miR-370的靶基因,通过将bta-miR-370模拟物和抑制剂转染到牛脂肪细胞中,检测bta-miR-370的过表达和干扰表达情况。qRT-PCR结果显示,与对照组相比,模拟物组中OLR1基因的相对表达显著降低,而抑制剂组中的表达水平高于其对照组。上述结果在蛋白质水平上通过蛋白质印迹法进一步得到验证。此外,通过油红O染色对牛脂肪细胞进行脂质形成分析,我们发现,与对照组相比,抑制剂组中的细胞质脂滴呈现增加趋势,而在模拟物组中,与对照组和抑制剂组相比,我们观察到细胞质脂滴明显减少。综上所述,我们的数据表明,bta-miR-370在基因表达、蛋白质水平以及牛脂肪细胞细胞质脂滴形成方面对OLR1具有负调控作用,这为阐明OLR1基因如何影响牛的产奶量和牛肉品质性状提供了参考。