Division of Biosciences, Institute of Structural and Molecular Biology, University College London, London WC1E 6BT, UK.
Wellcome Trust Centre for Cell Biology, University of Edinburgh, Edinburgh EH9 3BF, UK.
Nat Commun. 2016 Nov 24;7:13595. doi: 10.1038/ncomms13595.
Little is known about how archaeal viruses perturb the transcription machinery of their hosts. Here we provide the first example of an archaeo-viral transcription factor that directly targets the host RNA polymerase (RNAP) and efficiently represses its activity. ORF145 from the temperate Acidianus two-tailed virus (ATV) forms a high-affinity complex with RNAP by binding inside the DNA-binding channel where it locks the flexible RNAP clamp in one position. This counteracts the formation of transcription pre-initiation complexes in vitro and represses abortive and productive transcription initiation, as well as elongation. Both host and viral promoters are subjected to ORF145 repression. Thus, ORF145 has the properties of a global transcription repressor and its overexpression is toxic for Sulfolobus. On the basis of its properties, we have re-named ORF145 RNAP Inhibitory Protein (RIP).
关于古菌病毒如何干扰宿主的转录机制,目前我们知之甚少。在这里,我们提供了第一个古菌病毒转录因子的例子,它可以直接靶向宿主 RNA 聚合酶(RNAP)并有效地抑制其活性。来自温和的 Acidianus two-tailed 病毒(ATV)的 ORF145 通过与 DNA 结合通道内的 RNAP 结合形成高亲和力复合物,从而将灵活的 RNAP 夹锁定在一个位置。这在体外阻止了转录起始复合物的形成,并抑制了转录起始的流产和产物,以及延伸。宿主和病毒启动子都受到 ORF145 的抑制。因此,ORF145 具有全局转录抑制剂的特性,其过表达对 Sulfolobus 是有毒的。基于其特性,我们重新命名 ORF145 为 RNAP 抑制蛋白(RIP)。