NWIPB OpenIR
Dysregulated m6A modification promotes lipogenesis and development of non-alcoholic fatty liver disease and hepatocellular carcinoma
Yang, YM; Cai, JS; Yang, X; Wang, KF; Sun, KX; Yang, ZL; Zhang, L; Yang, L; Gu, C; Huang, X; Wang, ZY; Zhu, XJ
2022
发表期刊MOLECULAR THERAPY
卷号30期号:6页码:2342
摘要Type 2 diabetes mellitus (DM2) is associated closely with non-alcoholic fatty liver disease (NAFLD) by affecting lipid metabolism, which may lead to non-alcoholic steatohepatitis (NASH), fibrosis, and hepatocellular carcinoma (HCC). N6-methyladenosine (m6A) RNA methylation is an important epigenetic regulation for gene expression and is related to HCC development. We developed a new NAFLD model oriented from DM2 mouse, which spontaneously progressed to histological features of NASH, fibrosis, and HCC with high incidence. By RNA sequencing, protein expression and methylated RNA immunoprecipitation (MeRIP)-qPCR analysis, we found that enhanced expression of ACLY and SCD1 in this NAFLD model and human HCC samples was due to excessive m6A modification, but not elevation of mature SREBP1. Moreover, targeting METTL3/14 in vitro increases protein level of ACLY and SCD1 as well as triglyceride and cholesterol production and accumulation of lipid droplets. m6A sequencing analysis revealed that overexpressed METTL14 binds to mRNA of ACLY and SCD1 and alters their expression pattern. Our findings demonstrate a new NAFLD mouse model that provides a study platform for DM2-related NAFLD and reveals a unique epitranscriptional regulating mechanism for lipid metabolism via m6A-modified protein expression of ACLY and SCD1.
收录类别SCIE
文献类型期刊论文
条目标识符http://210.75.249.4/handle/363003/61202
专题中国科学院西北高原生物研究所
推荐引用方式
GB/T 7714
Yang, YM,Cai, JS,Yang, X,et al. Dysregulated m6A modification promotes lipogenesis and development of non-alcoholic fatty liver disease and hepatocellular carcinoma[J]. MOLECULAR THERAPY,2022,30(6):2342.
APA Yang, YM.,Cai, JS.,Yang, X.,Wang, KF.,Sun, KX.,...&Zhu, XJ.(2022).Dysregulated m6A modification promotes lipogenesis and development of non-alcoholic fatty liver disease and hepatocellular carcinoma.MOLECULAR THERAPY,30(6),2342.
MLA Yang, YM,et al."Dysregulated m6A modification promotes lipogenesis and development of non-alcoholic fatty liver disease and hepatocellular carcinoma".MOLECULAR THERAPY 30.6(2022):2342.
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