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植物miRNA稳定性与降解的分子基础

郭梦玮, 樊友宏, 任国栋   

  1. 复旦大学生命科学学院,复杂性状的遗传调控全国重点实验室,上海200438


  • 收稿日期:2025-01-26 修回日期:2025-04-30 出版日期:2025-05-07 发布日期:2025-05-07
  • 基金资助:
    国家自然科学基金项目;上海市科学技术委员会项目

Molecular basis of microRNA stability and degradation in plants

Mengwei Guo,Youhong Fan,Guodong Ren   

  1. State Key Laboratory of Genetics and Development of Complex Phenotypes, School of Life Sciences, Fudan University, Shanghai 200438, China

  • Received:2025-01-26 Revised:2025-04-30 Published:2025-05-07 Online:2025-05-07

摘要:

miRNAmicroRNA)是一类由内源基因编码的、长度在20~24个核苷酸的小分子非编码RNAmiRNA主要在转录后水平调控基因表达,进而影响动植物生殖、发育和环境应答等各种生物学过程。miRNA在不同组织和细胞内的分布、稳态维持和动态调节受到多个层次调控,包括转录、加工生成稳定性调节以及靶向降解等。关于miRNA生物合成(包括转录和加工)的生化途径已经建立,对其调控的分子机制也有了较为深入的认识。本文系统综述植物miRNA生成后稳定性调节、周转和靶向降解的相关研究进展,并结合动物中的机制进行比较和讨论,旨在为深入阐明控制细胞内miRNA丰度的分子机制提供理论框架

关键词: miRNA, 稳定性, 降解, Argonaute, 甲基化, 尿苷化, 靶标RNA, 核酸酶

Abstract:

MicroRNAs (miRNAs) are a class of endogenous small non-coding RNAs with 20 to 24 nucleotides in length. They primarily regulate gene expression at the post-transcriptional level and influence numerous biological processes, including reproduction, development, and responses to environmental stimuli in both plants and animals. The spatiotemporal expression of miRNAs across organs, tissues, and cells is tightly regulated at multiple levels, encompassing transcription, processing, stability control, and targeted degradation. The biochemical pathway of miRNA biogenesis, including transcription and processing, has been established, and its regulatory mechanisms have also been extensively studied. In this review, we systematically summarize current advances in post-biogenesis regulation of miRNA stability, turnover, and targeted degradation in plants, with comparative analyses of similarities and differences in animal systems. By integrating these advances, this review seeks to provide a framework for further elucidating the molecular mechanisms controlling intracellular miRNA abundance. 

Key words: miRNA, stability, degradation, Argonaute, methylation, uridylation, target RNA, nucleases