MicroRNA‐2285f regulates milk fat metabolism by targeting MAP2K2 in bovine mammary epithelial cells

Abstract

AbstractIn this study, Holstein dairy cows raised in Ningxia were selected as the research object. Mammary epithelial cells (BMECs) were extracted from the milk of eight Holstein cows with significantly different milk fat expression rates and transcribed for sequencing. Bioinformatics analysis was used to analyse the correlation of fat milk percentage, and the critical miR‐2285f regulating milk fat was screened out. The target gene binding sites were predicted, and 293T cells and mammary epithelial cells were used as miRNA and target gene models for functional verification in vitro. The tissue difference of miR‐2285f Holstein cows was quantitatively analysed by transfecting miR‐2285f mimic and inhibitor. Assay (dual luciferase reporter gene assay) and quantitative real‐time PCR (quantitative real‐time PCR, qRT‐PCR), triglyceride (TAG) detection, oil red O detection of lipid droplets, Western Blot assay, Edu and Flow cytometry, The molecular regulatory effects of miR‐2285f and target gene MAP2K2 on milk fat metabolism of Holstein dairy cows were studied. The wild‐type vector and mutant vector of map2k2‐3′utr were constructed, and double luciferase reporting experiments were conducted to verify that MAP2K2 was one of the target genes of miR‐2285f. According to qRT‐PCR and Western Blot analysis, miR‐2285f mainly regulates the expression of MAP2K2 protein in BMECs at the translation level. Bta‐miR‐2285f can promote cell proliferation and slow cell apoptosis by regulating MAP2K2. Bta‐miR‐2285f can promote triglyceride (TAG) and lipid droplet accumulation in mammary epithelial cells by targeting MAP2K2. Bta‐miR‐2285f can regulate protein levels of fat milk marker gene PPARG by targeting MAP2K2. In conclusion, miR‐2285f can target the expression of the MAP2K2 gene, promote the proliferation of dairy mammary epithelial cells, inhibit cell apoptosis and regulate the milk fat metabolism in dairy mammary epithelial cells. The results of this study revealed the function of miR‐2285f in regulating the differential expression of fat milk in Holstein dairy cows at the cellular level. They provided a theoretical and experimental basis for analysing the regulation network of milk fat synthesis of Holstein dairy cows and the molecular breeding of dairy cows.