Pegler Joseph L, Oultram Jackson M J, Mann Christopher W G, Carroll Bernard J, Grof Christopher P L, Eamens Andrew L
Centre for Plant Science, School of Environmental and Life Sciences, College of Engineering, Science and Environment, University of Newcastle, Callaghan, NSW 2308, Australia.
School of Chemistry and Molecular Biosciences, The University of Queensland, St. Lucia, QLD 4072, Australia.
Plants (Basel). 2023 Mar 1;12(5):1101. doi: 10.3390/plants12051101.
Angiosperms form the largest phylum within the Plantae kingdom and show remarkable genetic variation due to the considerable difference in the nuclear genome size of each species. Transposable elements (TEs), mobile DNA sequences that can amplify and change their chromosome position, account for much of the difference in nuclear genome size between individual angiosperm species. Considering the dramatic consequences of TE movement, including the complete loss of gene function, it is unsurprising that the angiosperms have developed elegant molecular strategies to control TE amplification and movement. Specifically, the RNA-directed DNA methylation (RdDM) pathway, directed by the repeat-associated small-interfering RNA (rasiRNA) class of small regulatory RNA, forms the primary line of defense to control TE activity in the angiosperms. However, the miniature inverted-repeat transposable element (MITE) species of TE has at times avoided the repressive effects imposed by the rasiRNA-directed RdDM pathway. MITE proliferation in angiosperm nuclear genomes is due to their preference to transpose within gene-rich regions, a pattern of transposition that has enabled MITEs to gain further transcriptional activity. The sequence-based properties of a MITE results in the synthesis of a noncoding RNA (ncRNA), which, after transcription, folds to form a structure that closely resembles those of the precursor transcripts of the microRNA (miRNA) class of small regulatory RNA. This shared folding structure results in a MITE-derived miRNA being processed from the MITE-transcribed ncRNA, and post-maturation, the MITE-derived miRNA can be used by the core protein machinery of the miRNA pathway to regulate the expression of protein-coding genes that harbor homologous MITE insertions. Here, we outline the considerable contribution that the MITE species of TE have made to expanding the miRNA repertoire of the angiosperms.
被子植物是植物界中最大的门,由于每个物种的核基因组大小存在显著差异,它们表现出显著的遗传变异。转座元件(TEs)是可以扩增并改变其染色体位置的移动DNA序列,在被子植物个体之间核基因组大小的差异中占很大一部分。考虑到TE移动的巨大后果,包括基因功能的完全丧失,被子植物已经开发出精妙的分子策略来控制TE的扩增和移动也就不足为奇了。具体而言,由重复相关小干扰RNA(rasiRNA)这类小调控RNA指导的RNA定向DNA甲基化(RdDM)途径,构成了控制被子植物中TE活性的主要防线。然而,TE的微型反向重复转座元件(MITE)有时会避开rasiRNA指导的RdDM途径施加的抑制作用。MITE在被子植物核基因组中的增殖是由于它们倾向于在富含基因的区域内转座,这种转座模式使MITE能够获得进一步的转录活性。MITE基于序列的特性导致非编码RNA(ncRNA)的合成,转录后,该ncRNA折叠形成一种结构,与小调控RNA中的微小RNA(miRNA)类前体转录本的结构非常相似。这种共同的折叠结构导致从MITE转录的ncRNA中加工出MITE衍生的miRNA,成熟后,MITE衍生的miRNA可被miRNA途径的核心蛋白质机制用于调节含有同源MITE插入的蛋白质编码基因的表达。在这里,我们概述了TE的MITE种类对扩大被子植物miRNA库所做出的重大贡献。