The cooperative regulatory effect of the miRNA-130 family on milk fat metabolism in dairy cows
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Objective: There is a strong relationship between the content of beneficial fatty acids in milk and milk fat metabolic activity in the mammary gland. To improve milk quality, it is therefore necessary to study fatty acid metabolism in bovine mammary gland tissue. In adipose tissue, peroxisome proliferator-activated receptor gamma (<i>PPARG</i>), the core transcription factor, regulates the fatty acid metabolism gene network and determines fatty acid deposition. However, its regulatory effects on mammary gland fatty acid metabolism during lactation have rarely been reported.Methods: Transcriptome sequencing was performed during the prelactation period and the peak lactation period to examine mRNA expression. The significant upregulation of <i>PPARG</i> drew our attention and led us to conduct further research.Results: According to bioinformatics prediction, dual-luciferase reporter system detection, real-time quantitative reverse transcription polymerase chain reaction and Western blotting, miR-130a and miR-130b could directly target <i>PPARG</i> and inhibit its expression. Furthermore, triglyceride and oil red O staining proved that miR-130a and miR-130b inhibited milk fat metabolism in bovine mammary epithelial cells (BMECs), while <i>PPARG</i> promoted this metabolism. In addition, we also found that the coexpression of miR-130a and miR-130b significantly enhanced their ability to regulate milk fat metabolism.Conclusion: In conclusion, our findings indicated that miR-130a and miR-130b could target and repress PPARG and that they also have a functional superposition effect. miR-130a and miR-130b seem to synergistically regulate lipid catabolism via the control of PPARG in BMECs. In the long-term, these findings might be helpful in developing practical means to improve high-quality milk.
Abstract
Objective: There is a strong relationship between the content of beneficial fatty acids in milk and milk fat metabolic activity in the mammary gland. To improve milk quality, it is therefore necessary to study fatty acid metabolism in bovine mammary gland tissue. In adipose tissue, peroxisome proliferator-activated receptor gamma (PPARG), the core transcription factor, regulates the fatty acid metabolism gene network and determines fatty acid deposition. However, its regulatory effects on mammary gland fatty acid metabolism during lactation have rarely been reported. Methods: Transcriptome sequencing was performed during the prelactation period and the peak lactation period to examine mRNA expression. The significant upregulation of PPARG drew our attention and led us to conduct further research. Results: According to bioinformatics prediction, dual-luciferase reporter system detection, real-time quantitative reverse transcription polymerase chain reaction and Western blotting, miR-130a and miR-130b could directly target PPARG and inhibit its expression. Furthermore, triglyceride and oil red O staining proved that miR-130a and miR-130b inhibited milk fat metabolism in bovine mammary epithelial cells (BMECs), while PPARG promoted this metabolism. In addition, we also found that the coexpression of miR-130a and miR-130b significantly enhanced their ability to regulate milk fat metabolism. Conclusion: In conclusion, our findings indicated that miR-130a and miR-130b could target and repress PPARG and that they also have a functional superposition effect. miR130a and miR-130b seem to synergistically regulate lipid catabolism via the control of PPARG in BMECs. In the long-term, these findings might be helpful in developing practical means to improve high-quality milk.
참고문헌 (35)
- Chen Z, "Circ007071 Inhibits unsaturated fatty acid synthesis by Interacting with miR-103-5p to enhance PPARγ expression in the dairy goat mammary gland", J Agric Food Chem, 70, pp.13719~13729 (2022)[DOI]
- Chen Z, "circ01592 regulates unsaturated fatty acid metabolism through adsorbing miR-218 in bovine mammary epithelial cells", Food Funct, 12, pp.12047~12058 (2021)[DOI]
- Wang MQ, "Lipopolysaccharide inhibits triglyceride synthesis in dairy cow mammary epithelial cells by upregulating miR-27a-3p, which targets the PPARG gene", J Dairy Sci, 104, pp.989~1001 (2021)[DOI]
- Wilson HE, "Breast cancer-associated skeletal muscle mitochondrial dysfunction and lipid accumulation is reversed by PPARG", Am J Physiol Cell Physiol, 320, pp.C577~C590 (2021)[DOI]
- Pham DV, "Autophagy activation and SREBP-1 induction contribute to fatty acid metabolic reprogramming by leptin in breast cancer cells", Mol Oncol, 15, pp.657~678 (2021)[DOI]
- Zhao Q, "Targeting SREBP-1-mediated lipogenesis as potential strategies for cancer", Front Oncol, 12, pp.952371~ (2022)[DOI]
- Peterson DG, "The inhibitory effect of trans-10, cis-12 CLA on lipid synthesis in bovine mammary epithelial cells involves reduced proteolytic activation of the transcription factor SREBP-1", J Nutr, 134, pp.2523~2527 (2004)[DOI]
- Lu Q, "The overlooked transformation mechanisms of VLCFAs : peroxisomal β-oxidation", Agriculture, 12, pp.947~ (2022)[DOI]
- Chen GH, "SREBP1, PPARG and AMPK pathways mediated the Cu-induced change in intestinal lipogenesis and lipid transport of yellow catfish Pelteobagrus fulvidraco", Food Chem, 269, pp.595~602 (2018)[DOI]
- Mu T, "Regulation of key genes for milk fat synthesis in ruminants", Front Nutr, 8, pp.765147~ (2021)[DOI]
- Zaidi N, "Lipogenesis and lipolysis : the pathways exploited by the cancer cells to acquire fatty acids", Prog Lipid Res, 52, pp.585~589 (2013)[DOI]
- Bionaz M, "Gene networks driving bovine mammary protein synthesis during the lactation cycle", Bioinform Biol Insights (2011)[DOI]
- Chen Z, "miR-497 regulates fatty acid synthesis via LATS2 in bovine mammary epithelial cells", Food Funct, 11, pp.8625~8636 (2020)[DOI]
- Sempere LF, "microRNA-based diagnostic and therapeutic applications in cancer medicine", Wiley Interdiscip Rev RNA, 12, pp.e1662~ (2021)[DOI]
- Lu Q, "Progress on the regulation of ruminant milk fat by noncoding RNAs and ceRNAs", Front Genet, 12, pp.733925~ (2021)[DOI]
- Chen Z, "Circ11103 interacts with miR128", PPARGC1A to regulate milk fat metabolism in dairy cows, 2021, pp.69, 4490~4500
- Monoe Y, "Pharmacological inhibition of miR-130 family suppresses bladder tumor growth by targeting various oncogenic pathways via PTPN1", Int J Mol Sci, 22, pp.4751~ (2021)[DOI]
- Zhang HD, "The role of miR130a in cancer", Breast Cancer, 24, pp.521~527 (2017)[DOI]
- Wei MC, "miR-130a-mediated KLF3can inhibit the growth of lung cancer cells", Cancer Manag Res, 13, pp.2995~3004 (2021)[DOI]
- Egawa H, "The miR-130 family promotes cell migration and invasion in bladder cancer through FAK and Akt phosphorylation by regulating PTEN", Sci Rep, 6, pp.20574~ (2016)[DOI]
- Nisenblat V, "Blood biomarkers for the non-invasive diagnosis of endometriosis", Cochrane Database Syst Rev, 2016, pp.CD012179~ (2016)[DOI]
- Zhou Q, "MicroRNAs as potential biomarkers for the diagnosis of glioma : a systematic review and meta-analysis", Cancer Sci, 109, pp.2651~2659 (2018)[DOI]
- Kamity R, "MicroRNA-mediated control of inflammation and tolerance in pregnancy", Front Immunol, 10, pp.718~ (2019)[DOI]
- Wang L, "A microRNA linking human positive selection and metabolic disorders", Cell, 183, pp.684~701 (2020)[DOI]
- Lee YS, "MicroRNAs in cancer", Annu Rev Pathol, 4, pp.199~227 (2009)[DOI]
- Chen Z, "MiR-183 regulates milk fat metabolism via MST1 in goat mammary epithelial cells", Gene, 646, pp.12~19 (2018)[DOI]
- Chen Z, "miR-30e-5p and miR-15a synergistically regulate fatty acid metabolism in goat mammary epithelial cells via LRP6 and YAP1", Int J Mol Sci, 17, pp.1909~ (2016)[DOI]
- Tang KQ, "miR-27a controls triacylglycerol synthesis in bovine mammary epithelial cells by targeting peroxisome proliferator-activated receptor gamma", J Dairy Sci, 100, pp.4102~4112 (2017)[DOI]
- Alarcón CR, "N6-methyladenosine marks primary microRNAs for processing", Nature, 519, pp.482~485 (2015)[DOI]
- Lu TX, "MicroRNA", J Allergy Clin Immunol, 141, pp.1202~1207 (2018)[DOI]
- Ma S, "A transcriptional regulatory loop of master regulator transcription factors, PPARG, and fatty acid synthesis promotes esophageal adenocarcinoma", Cancer Res, 81, pp.1216~1229 (2021)[DOI]
- Zheng JS, "Replication of a gene-diet interaction at CD36, NOS3 and PPARG in response to Omega-3 fatty acid supplements on blood lipids : a doubleblind randomized controlled trial", EBioMedicine, 31, pp.150~156 (2018)[DOI]
- Jing Y, "Circadian gene PER2 silencing downregulates PPARG and SREBF1 and suppresses lipid synthesis in bovine mammary epithelial cells", Biology, 10, pp.1226~ (2021)[DOI]
- Bionaz M, "Gene networks driving bovine milk fat synthesis during the lactation cycle", BMC Genomics, 9, pp.366~ (2008)[DOI]
- Bionaz M, "Identification of reference genes for quantitative real-time PCR in the bovine mammary gland during the lactation cycle", Physiol Genomics, 29, pp.312~319 (2007)[DOI]
