a Department of Microbiology , The Ohio State University , Columbus , Ohio , USA.
b The Center for RNA Biology , The Ohio State University , Columbus , Ohio , USA.
RNA Biol. 2018;15(4-5):554-566. doi: 10.1080/15476286.2017.1371402. Epub 2017 Sep 26.
A signature of most eukaryotic cells is the presence of intricate membrane systems. Intracellular organization presumably evolved to provide order, and add layers for regulation of intracellular processes; compartmentalization also forcibly led to the appearance of sophisticated transport systems. With nucleus-encoded tRNAs, it led to the uncoupling of tRNA synthesis from many of the maturation steps it undergoes. It is now clear that tRNAs are actively transported across intracellular membranes and at any point, in any compartment, they can be post-transcriptionally modified; modification enzymes themselves may localize to any of the genome-containing compartments. In the following pages, we describe a number of well-known examples of how intracellular compartmentalization of tRNA processing and modification activities impact the function and fate of tRNAs. We raise the possibility that rates of intracellular transport may influence the level of modification and as such increase the diversity of differentially modified tRNAs in cells.
大多数真核细胞的特征是存在复杂的膜系统。细胞内的组织可能是为了提供秩序而进化的,并为细胞内过程的调节增加了层次;分隔也强制导致了复杂的运输系统的出现。对于核编码的 tRNA 来说,它导致了 tRNA 合成与其所经历的许多成熟步骤的解耦。现在很清楚,tRNA 是在细胞内膜上被主动运输的,并且在任何时候,在任何隔室中,它们都可以进行转录后修饰;修饰酶本身可能定位于任何包含基因组的隔室中。在接下来的几页中,我们描述了一些众所周知的例子,说明 tRNA 加工和修饰活动的细胞内分隔如何影响 tRNA 的功能和命运。我们提出了这样一种可能性,即细胞内运输的速度可能会影响修饰的水平,并因此增加细胞中不同修饰的 tRNA 的多样性。