The Institute of Cancer Research, London SW7 3RP, UK.
The Institute of Cancer Research, London SW7 3RP, UK.
Biochim Biophys Acta Gene Regul Mech. 2018 Apr;1861(4):285-294. doi: 10.1016/j.bbagrm.2017.11.005. Epub 2017 Nov 15.
RNA polymerase III catalyses the synthesis of tRNAs in eukaryotic organisms. Through combined biochemical and structural characterisation, multiple auxiliary factors have been identified alongside RNA Polymerase III as critical in both facilitating and regulating transcription. Together, this machinery forms dynamic multi-protein complexes at tRNA genes which are required for polymerase recruitment, DNA opening and initiation and elongation of the tRNA transcripts. Central to the function of these complexes is their ability to undergo multiple conformational changes and rearrangements that regulate each step. Here, we discuss the available biochemical and structural data on the structural plasticity of multi-protein complexes involved in RNA Polymerase III transcriptional initiation and facilitated re-initiation during tRNA synthesis. Increasingly, structural information is becoming available for RNA polymerase III and its functional complexes, allowing for a deeper understanding of tRNA transcriptional initiation. This article is part of a Special Issue entitled: SI: Regulation of tRNA synthesis and modification in physiological conditions and disease edited by Dr. Boguta Magdalena.
RNA 聚合酶 III 催化真核生物中 tRNA 的合成。通过结合生化和结构特征,已经鉴定出多种辅助因子与 RNA 聚合酶 III 一起,在促进和调节转录中至关重要。这些酶共同在 tRNA 基因处形成动态的多蛋白复合物,这对于聚合酶募集、DNA 打开以及 tRNA 转录物的起始和延伸都是必需的。这些复合物的功能核心是它们能够进行多次构象变化和重排,从而调节每个步骤。在这里,我们讨论了有关参与 RNA 聚合酶 III 转录起始以及在 tRNA 合成过程中辅助重新起始的多蛋白复合物的结构可塑性的现有生化和结构数据。越来越多的 RNA 聚合酶 III 及其功能复合物的结构信息正在变得可用,这使得我们能够更深入地了解 tRNA 转录起始。本文是由 Magdalena Boguta 博士编辑的题为“生理条件和疾病下 tRNA 合成和修饰的调控”的特刊的一部分。