circMEF2D Negatively Regulated by HNRNPA1 Inhibits Proliferation and Differentiation of Myoblasts via miR-486-PI3K/AKT Axis

选择性拼接 RNA剪接 外显子 细胞生物学 PI3K/AKT/mTOR通路 生物 肌发生 基因 蛋白激酶B 基因表达 核糖核酸 信号转导 遗传学 心肌细胞
作者
Xiaoyan Zhang,Shuling Yang,Zihong Kang,Wenxiu Ru,Xuemei Shen,Meng Li,Xianyong Lan,Hong Chen
出处
期刊:Journal of Agricultural and Food Chemistry [American Chemical Society]
卷期号:70 (26): 8145-8163 被引量:16
标识
DOI:10.1021/acs.jafc.2c01888
摘要

Circular RNA (circRNA) is a form of endogenous RNA that can regulate gene expression and participate in the regulation of myogenesis. However, the molecular mechanisms and potential roles of circRNAs in bovine muscle development remain largely unknown. Nevertheless, the RNA splicing factors regulating the biogenesis of bovine circRNA have not yet been characterized. In this study, we identified a novel circRNA, circMEF2D, formed by back-splicing of constitutive exons (exons 5-7) of the bovine MEF2D gene. Functional assays showed that circMEF2D inhibited the proliferation and differentiation of bovine myoblasts. Importantly, we showed that circMEF2D regulated the PI3K-AKT signaling pathway through direct and competitive binding to miR-486. Furthermore, to explore the formation mechanism of circMEF2D, we explored the MEF2D gene alternative splicing progress. Four alternative linear variants of MEF2D were found. Due to its role in alternative splicing, the RNA-binding protein HNRNPA1 was selected for further study and the modulation of HNRNPA1 levels showed that it negatively regulated both back-splicing and linear splicing of MEF2D gene. Overall, in addition to the characterization of bovine circRNAs, these findings revealed the crucial role of HNRNPA1 in MEF2D gene alternative splicing and demonstrated a regulatory circMEF2D-miR-486-PI3K-AKT axis.
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