Department of Biochemistry, Albert Einstein College of Medicine, Bronx, New York 10461, USA; email:
Department of Systems and Computational Biology, Albert Einstein College of Medicine, Bronx, New York 10461, USA.
Annu Rev Biochem. 2018 Jun 20;87:75-100. doi: 10.1146/annurev-biochem-062917-012624. Epub 2018 Jan 12.
RNA polymerase (Pol) III has a specialized role in transcribing the most abundant RNAs in eukaryotic cells, transfer RNAs (tRNAs), along with other ubiquitous small noncoding RNAs, many of which have functions related to the ribosome and protein synthesis. The high energetic cost of producing these RNAs and their central role in protein synthesis underlie the robust regulation of Pol III transcription in response to nutrients and stress by growth regulatory pathways. Downstream of Pol III, signaling impacts posttranscriptional processes affecting tRNA function in translation and tRNA cleavage into smaller fragments that are increasingly attributed with novel cellular activities. In this review, we consider how nutrients and stress control Pol III transcription via its factors and its negative regulator, Maf1. We highlight recent work showing that the composition of the tRNA population and the function of individual tRNAs is dynamically controlled and that unrestrained Pol III transcription can reprogram central metabolic pathways.
RNA 聚合酶 (Pol) III 在转录真核细胞中最丰富的 RNA(转移 RNA (tRNA))以及其他普遍存在的小非编码 RNA 方面发挥着特殊作用,其中许多具有与核糖体和蛋白质合成相关的功能。产生这些 RNA 的高能量成本以及它们在蛋白质合成中的核心作用,使得 Pol III 转录在受到生长调节途径的营养和应激影响时受到严格调控。Pol III 的下游,信号转导影响影响 tRNA 在翻译中的功能以及 tRNA 切割成较小片段的过程,这些片段越来越多地被赋予新的细胞活性。在这篇综述中,我们考虑了营养物质和应激如何通过其因子及其负调节剂 Maf1 来控制 Pol III 转录。我们强调了最近的工作表明,tRNA 群体的组成和单个 tRNA 的功能是动态控制的,不受限制的 Pol III 转录可以重新编程中心代谢途径。