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作 者:XU Yuan ZHANG Ai-ling ZHANG Zhe YUAN Xiao-long CHEN Zan-mou ZHANG Hao LI Jia-qi
机构地区:[1]Guangdong Provincial Key Lab of Agro-Animal Genomics and Molecular Breeding,College of Animal Science,South China Agricultural University [2]College of Biological and Food Engineering,Guangdong University of Education
出 处:《Journal of Integrative Agriculture》2017年第9期2019-2028,共10页农业科学学报(英文版)
基 金:supported by the National Natural Science Foundation of China (31201771);the earmarked fund for the China Agriculture Research System (CARS-36)
摘 要:Granulosa cells(GCs) are somatic cells of ovary, the behaviors of GCs are important for ovarian function. MicroRNAs(miRNAs) are a class of endogenous 18–24 nucleotide(nt) non-coding RNAs, some of which have been shown to be important regulators of GCs function. miR-34c involved in the regulation of various biological processes and was identified to be a pro-apoptotic and anti-proliferative factor in many cell types. However, the roles of miR-34c in GCs function remain unknown. In this study, we used Annexin V-FITC and Ed U assays to demonstrate that miR-34c exerted pro-apoptotic and anti-proliferative effects in porcine GCs. Dual-luciferase reporter assays, quantitative real-time PCR(q RT-PCR) and Western blotting identified Forkhead box O3a(Fox O3a) as a direct target gene of miR-34c. The overexpression of FoxO3a rescued the phenotypic change caused by miR-34c in porcine GCs. In conclusion, miR-34c regulate the function of porcine GCs by targeting FoxO3a.Granulosa cells(GCs) are somatic cells of ovary, the behaviors of GCs are important for ovarian function. MicroRNAs(miRNAs) are a class of endogenous 18–24 nucleotide(nt) non-coding RNAs, some of which have been shown to be important regulators of GCs function. miR-34c involved in the regulation of various biological processes and was identified to be a pro-apoptotic and anti-proliferative factor in many cell types. However, the roles of miR-34c in GCs function remain unknown. In this study, we used Annexin V-FITC and Ed U assays to demonstrate that miR-34c exerted pro-apoptotic and anti-proliferative effects in porcine GCs. Dual-luciferase reporter assays, quantitative real-time PCR(q RT-PCR) and Western blotting identified Forkhead box O3a(Fox O3a) as a direct target gene of miR-34c. The overexpression of FoxO3a rescued the phenotypic change caused by miR-34c in porcine GCs. In conclusion, miR-34c regulate the function of porcine GCs by targeting FoxO3a.
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