MicroRNA-Mediated Gene Regulation of Secondary Metabolism in Plants

被引:11
作者
Jiang, Shan [1 ,2 ]
Cui, Jin-Long [1 ]
Li, Xiao-ke [1 ,2 ]
机构
[1] Shanxi Univ, Inst Appl Chem, Taiyuan, Peoples R China
[2] Shanxi Univ, Modern Res Ctr Tradit Chinese Med, Key Lab Chem Biol & Mol Engn, Minist Educ, Taiyuan, Peoples R China
基金
中国国家自然科学基金;
关键词
MicroRNAs (miRNAs); post-transcriptional regulation; regulatory modules; secondary metabolites; targets; CAMELLIA-SINENSIS; ANTHOCYANIN ACCUMULATION; FLAVONOID BIOSYNTHESIS; DIFFERENT ORGANS; LIGNIN CONTENT; MIRNAS; ARABIDOPSIS; PATHWAY; TARGETS; IDENTIFICATION;
D O I
10.1080/07352689.2022.2031674
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Plant microRNAs (miRNAs), a class of about 21-nucleotide-long small noncoding RNAs (ncRNAs), generally act as key regulators of their target genes by guiding mRNA cleavage or translational repression. Recent researches have reported that miRNAs can interact with pathway-related structural genes, transcription factors (TFs) and noncoding RNAs (ncRNAs) to form regulatory network in secondary metabolite (SM) biosynthetic pathways. The validated interactions can better reflect the real regulatory mechanism of miRNA and convert miRNAs into more efficient tools to control the production of precious SMs. However, there is no systematic review available on this topic especially in plants, particularly model plants and crops. Here, we firstly overviewed the critical secondary metabolic pathways in plants, especially those biosynthetic pathways related structural genes which were well-studied and representative SMs, including phenylpropanoids, terpenoids, alkaloids. Principally, we summarized miRNAs involved in the biosynthesis of SMs, miRNA-target modules and their regulation on the mentioned pathways in the last decade. Significantly, the modules included miRNA-structural gene, miRNA-TF, miRNA-ncRNA interaction pairs carried out by target validation or functional confirmation. This knowledge will promote understanding the sophisticated miRNA-mediated gene regulatory network of SM biosynthesis, and drive the development of synthetic biology.
引用
收藏
页码:459 / 478
页数:20
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