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首页> 外文期刊>Biochimica et Biophysica Acta. Gene Regulatory Mechanisms >Regulation of tRNA synthesis by posttranslational modifications of RNA polymerase III subunits
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Regulation of tRNA synthesis by posttranslational modifications of RNA polymerase III subunits

机译:RNA聚合酶III亚基的后期修饰调节TRNA合成

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摘要

RNA polymerase III (RNAPIII) transcribes tRNA genes, 5S RNA as well as a number of other non-coding RNAs. Because transcription by RNAPIII is an energy-demanding process, its activity is tightly linked to the stress levels and nutrient status of the cell. Multiple signaling pathways control RNAPIII activity in response to environmental cues, but exactly how these pathways regulate RNAPIII is still poorly understood. One major target of these pathways is the transcriptional repressor Maf1, which inhibits RNAPIII activity under conditions that are detrimental to cell growth. However, recent studies have found that the cell can also directly regulate the RNAPIII machinery through phosphorylation and sumoylation of RNAPIII subunits. In this review we summarize post-translational modifications of RNAPIII subunits that mainly have been identified in large-scale proteomics studies, and we highlight several examples to discuss their relevance for regulation of RNAPIII.
机译:RNA聚合酶III(RNAPIII)转录TRNA基因,5S RNA以及许多其他非编码RNA。 因为RNAPIII的转录是一种能量要求苛刻的方法,因此其活性与细胞的应力水平和养分状态紧密相关。 多种信令途径控制RNAPIII活动以响应环境提示,但是这些途径如何调节RNAPIII仍然是不知识的。 这些途径的一个主要靶标是转录抑制因子MAF1,其在对细胞生长有害的条件下抑制RNAPIII活性。 然而,最近的研究发现该细胞还可以通过磷酸化和RNAPIII亚基的磷酸化直接调节RNAPIII机械。 在本次综述中,我们总结了主要在大型蛋白质组学研究中识别的RNAPIII亚基的翻译后修改,并且突出了几个例子来讨论其对RNAPIII调节的相关性。

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