Department of Biochemistry, University of Turku, FIN-20014 Turku, Finland.
Department of Chemistry, University of Turku, FIN-20014 Turku, Finland.
Nucleic Acids Res. 2019 Nov 4;47(19):10296-10312. doi: 10.1093/nar/gkz782.
Oxazinomycin is a C-nucleoside antibiotic that is produced by Streptomyces hygroscopicus and closely resembles uridine. Here, we show that the oxazinomycin triphosphate is a good substrate for bacterial and eukaryotic RNA polymerases (RNAPs) and that a single incorporated oxazinomycin is rapidly extended by the next nucleotide. However, the incorporation of several successive oxazinomycins or a single oxazinomycin in a certain sequence context arrested a fraction of the transcribing RNAP. The addition of Gre RNA cleavage factors eliminated the transcriptional arrest at a single oxazinomycin and shortened the nascent RNAs arrested at the polythymidine sequences suggesting that the transcriptional arrest was caused by backtracking of RNAP along the DNA template. We further demonstrate that the ubiquitous C-nucleoside pseudouridine is also a good substrate for RNA polymerases in a triphosphorylated form but does not inhibit transcription of the polythymidine sequences. Our results collectively suggest that oxazinomycin functions as a Trojan horse substrate and its inhibitory effect is attributable to the oxygen atom in the position corresponding to carbon five of the uracil ring.
氧嗪霉素是一种由吸水链霉菌产生的 C-核苷抗生素,与尿嘧啶非常相似。在这里,我们表明氧嗪霉素三磷酸酯是细菌和真核 RNA 聚合酶 (RNAP) 的良好底物,并且单个掺入的氧嗪霉素可被下一个核苷酸迅速延伸。然而,几个连续的氧嗪霉素或在特定序列环境中单个氧嗪霉素的掺入会阻止一部分转录的 RNAP。添加 Gre RNA 切割因子可消除单个氧嗪霉素的转录停滞,并缩短在多聚胸苷序列中停滞的新生 RNA,这表明转录停滞是由 RNAP 沿着 DNA 模板回溯引起的。我们进一步证明,普遍存在的 C-核苷假尿嘧啶在三磷酸化形式下也是 RNA 聚合酶的良好底物,但不会抑制多聚胸苷序列的转录。我们的结果共同表明,氧嗪霉素作为一种特洛伊木马底物发挥作用,其抑制作用归因于尿嘧啶环的碳五位置的氧原子。