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RNA 聚合酶 III 的通用转录因子 TFIIIB 和 TFIIIC 以及 MAF1 蛋白对 tRNA 合成的调控。

Regulation of tRNA synthesis by the general transcription factors of RNA polymerase III - TFIIIB and TFIIIC, and by the MAF1 protein.

机构信息

Institute of Biochemistry and Biophysics, Polish Academy of Sciences, Pawińskiego 5a, 02-106 Warsaw, Poland.

Institute of Biochemistry and Biophysics, Polish Academy of Sciences, Pawińskiego 5a, 02-106 Warsaw, Poland.

出版信息

Biochim Biophys Acta Gene Regul Mech. 2018 Apr;1861(4):320-329. doi: 10.1016/j.bbagrm.2018.01.011. Epub 2018 Feb 6.

Abstract

The synthesis of transfer RNA (tRNA) is directed by RNA polymerase III (Pol III) specialized in high-level transcription of short DNA templates. Pol III recruitment to tRNA genes is controlled by two general initiation factors, TFIIIB and TFIIIC. They are multi-protein complexes regulated at the level of expression of individual subunits, as well as through phosphorylation and interaction with partner proteins. Here, we describe particular aspects of TFIIIB and TFIIIC control in yeast and human cells. Under stress conditions, tRNA synthesis is negatively regulated by the MAF1 protein, which interacts directly with Pol III. Sequence and function of MAF1 are conserved among eukaryotic organisms from yeast to humans. MAF1 is a phosphoprotein which mediates diverse regulatory signals to Pol III. Interestingly, there is a subset of housekeeping tRNA genes, both in the yeast and human genome, which are less sensitive to MAF1-dependent repression. The possible mechanisms responsible for this differential regulation of tRNA synthesis by MAF1 are discussed.

摘要

转移 RNA(tRNA) 的合成由专门用于短 DNA 模板高水平转录的 RNA 聚合酶 III (Pol III) 指导。Pol III 募集到 tRNA 基因受到两种通用起始因子 TFIIIB 和 TFIIIC 的控制。它们是多蛋白复合物,在个体亚基的表达水平以及通过磷酸化和与伴侣蛋白相互作用进行调节。在这里,我们描述了酵母和人类细胞中 TFIIIB 和 TFIIIC 控制的特定方面。在应激条件下,tRNA 的合成受到 MAF1 蛋白的负调控,该蛋白与 Pol III 直接相互作用。MAF1 的序列和功能在从酵母到人类的真核生物中是保守的。MAF1 是一种磷酸化蛋白,可将多种调节信号转导至 Pol III。有趣的是,酵母和人类基因组中都有一组看家 tRNA 基因,它们对 MAF1 依赖性抑制的敏感性较低。讨论了 MAF1 对 tRNA 合成的这种差异调节的可能机制。

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