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METTL3 regulates Leydig cell proliferation via miR-145-PCK1 mediated gluconeogenesis in goats
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作者 Wen Tang Maosheng Cao +6 位作者 Fengxin Qiao Jinhong Luo Yonghong Ju Xiaodong Wang pengchen an Wei Sun Xiang Chen 《Journal of Animal Science and Biotechnology》 2026年第2期768-785,共18页
Background Normal testicular development is essential for maintaining male fertility and reproductive performance in livestock.Leydig cells(LCs)play a central role in testicular physiology;however,the epigenetic mecha... Background Normal testicular development is essential for maintaining male fertility and reproductive performance in livestock.Leydig cells(LCs)play a central role in testicular physiology;however,the epigenetic mechanisms regulating their development remain largely unclear.Methyltransferase-like 3(METTL3),a key m^(6)A methylation enzyme,and micro RNAs are increasingly recognised as critical regulators of this process.Results METTL3 expression in goat LCs markedly decreased during testicular development.This downregulation reduced m^(6)A modification on pri-miR-145,impairing Di George syndrome critical region 8-mediated processing and resulting in decreased levels of mature mi R-145-3p.This reduction in mi R-145-3p increased the expression of phosphoenolpyruvate carboxykinase 1(PCK1),which activated gluconeogenesis,increased intracellular glucose levels,and increased mitochondrial membrane potential.Consequently,this metabolic shift upregulated cell cyclerelated genes(cyclin B1 and cyclin E2),promoting LC proliferation and testicular growth.Conclusions Our findings demonstrate that the METTL3/mi R-145-3p/PCK1 axis is a key regulatory pathway linking epigenetic modification to the metabolic activity and proliferation of LCs.This mechanism provides novel insights into the molecular control of testicular development in male goats and may offer new targets for improving male reproductive capacity in livestock. 展开更多
关键词 Leydig cells Methyltransferase like 3 MiR-145-3p PCK1 Testicular development
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