Alternative Polyadenylation of Malic Enzyme 1 Is Essential for Accelerated Adipogenesis

脂肪生成 基因亚型 聚腺苷酸 非翻译区 荧光素酶 三素数非翻译区 细胞生物学 化学 生物 生物化学 基因 基因表达 转染 信使核糖核酸
作者
Xuyong Qin,Chaoqun Meng,Chengping Li,Wei Zhao,Shizhong Ren,Shujun Cao,Guoli Zhou
出处
期刊:Journal of Agricultural and Food Chemistry [American Chemical Society]
卷期号:71 (51): 20815-20825
标识
DOI:10.1021/acs.jafc.3c06289
摘要

Understanding the mechanism of adipogenesis is an important basis for improving meat quality traits of livestock. Alternative polyadenylation (APA) is a vital mechanism to regulate the expression of eukaryotic genes. However, how the individual APA functions in adipogenesis remains elusive. This study was intended to investigate the effect of malic enzyme 1 (ME1) APA on adipogenesis. Here, intracellular lipid droplets were stained using Oil red O. 3' RACE was used to verify APA events of the ME1 gene. Interactions between ME1 3' untranslated region (3' UTR)-APA isoforms and miRNAs, as well as differential expression of isoforms, were examined using dual-luciferase reporter and molecular experiments. The mechanism of ME1 APA on adipogenesis was explored by gain and loss of function assays. In this study, two ME1 isoforms with different 3' UTR lengths were detected during adipogenesis. Moreover, the ME1 isoform with a short 3' UTR was significantly upregulated compared with the one with a long 3' UTR. Mechanistically, only the long ME1 isoform was targeted by miR-153-3p to attenuate adipogenesis, while the short one escaped the regulation of miR-153-3p to accelerate adipogenesis. Our results reveal a novel mechanism of ME1 APA in regulating adipogenesis.
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