Department of Chemistry and Biochemistry; University of Bern; Bern, Switzerland; Graduate School for Cellular and Biomedical Sciences; University of Bern; Bern, Switzerland.
Department of Chemistry and Biochemistry; University of Bern; Bern, Switzerland; Division of Genomics and RNomics; Medical University Innsbruck; Innsbruck, Austria.
RNA Biol. 2013 Dec;10(12):1798-806. doi: 10.4161/rna.27177. Epub 2013 Nov 21.
Post-transcriptional cleavage of RNA molecules to generate smaller fragments is a widespread mechanism that enlarges the structural and functional complexity of cellular RNomes. Substrates for such RNA fragmentations are coding as well as non-protein-coding RNAs. In particular, fragments derived from both precursor and mature tRNAs represent one of the rapidly growing classes of post-transcriptional RNA pieces. Importantly, these tRNA fragments possess distinct expression patterns, abundance, cellular localizations, or biological roles compared with their parental tRNA molecules. Here we review recent reports on tRNA cleavage and attempt to categorize tRNA pieces according to their origin and cellular function. The biological scope of tRNA-derived fragments ranges from translation control, over RNA silencing, to regulating apoptosis, and thus clearly enlarges the functional repertoire of ncRNA biology.
RNA 分子的转录后切割产生较小的片段是一种广泛存在的机制,它扩大了细胞 RNA 组的结构和功能复杂性。这种 RNA 片段化的底物包括编码和非编码蛋白的 RNA。特别是,来自前体和成熟 tRNA 的片段代表了一类快速增长的转录后 RNA 片段。重要的是,与它们的母体 tRNA 分子相比,这些 tRNA 片段具有不同的表达模式、丰度、细胞定位或生物学功能。在这里,我们回顾了最近关于 tRNA 切割的报道,并试图根据其起源和细胞功能对 tRNA 片段进行分类。tRNA 衍生片段的生物学范围从翻译控制,到 RNA 沉默,再到调节细胞凋亡,因此明显扩大了 ncRNA 生物学的功能范围。