m[sup.6]A Methylation Mediates the Function of the circRNA-08436/miR-195/ELOVL6 Axis in Regards to Lipid Metabolism in Dairy Goat Mammary Glands

The synthesis and secretion of milk fat is a multifaceted biological process, prompting extensive research into the regulatory mechanisms governing milk fat production in regards to genetics and dairy science. Analyzing the regulation of milk fat metabolism in dairy goats provides insights for improving goat milk quality via molecular breeding strategies. Therefore, this research aims to design a series of molecular biological experiments to elucidate the molecular mechanism underlying the regulation of breast milk fat metabolism by the m[sup.6]A methylation mediated circRNA-08436/miR-195/ELOVL6 axis. The research findings of this study will enrich the existing theories regarding fatty acid metabolism in the mammary gland tissue of dairy goats, shed new light on the production of high-quality goat milk, and provide new ways to improve the dietary structure of residents. The nutritional value of goat milk is determined by the composition of its fatty acids, with particular importance placed on the role of unsaturated fatty acids in promoting human health. CircRNAs have been known to affect fatty acid metabolism through different pathways. In this study, high-throughput sequencing was employed to construct expression profiles of mammary tissue harvested during the dry period and peak lactation stages of dairy goats. Differentially expressed circRNAs and mRNAs were screened, revealing significantly higher expression levels of circRNA-08436 and ELOVL6 during the peak lactation period compared with the dry period. Thus, circRNA-08436 and ELOVL6 were chosen for subsequent studies. The findings demonstrated that circRNA-08436 not only promotes the synthesis of triglyceride (TAG) and cholesterol in goat mammary epithelial cells (GMECs), but also increases the concentrations of saturated fatty acids in the cells. Through the utilization of software prediction, the dual luciferase reporter system, and qRT-PCR, it was observed that circRNA-08436 binds to miR-195, with its overexpression reducing the expression levels of miR-195 and inhibiting TAG synthesis. In addition, circRNA-08436 upregulated the expression levels of the miR-195 target gene ELOVL6. The data also revealed that YTHDC1 facilitated the transport of circRNA-08436 from the nucleus to the cytoplasm, while YTHDC2 in the cytoplasm functioned as a “reader” to identify and degrade circRNA-08436. Taken together, these findings contribute to a better understanding of the molecular regulation of fatty acid meta