Kravchenko Julia E, Rogozin Igor B, Koonin Eugene V, Chumakov Peter M
Lerner Research Institute, The Cleveland Clinic Foundation, Cleveland, Ohio 44195, USA.
Nature. 2005 Aug 4;436(7051):735-9. doi: 10.1038/nature03848.
Transcription of eukaryotic genes is performed by three nuclear RNA polymerases, of which RNA polymerase II is thought to be solely responsible for the synthesis of messenger RNAs. Here we show that transcription of some mRNAs in humans and rodents is mediated by a previously unknown single-polypeptide nuclear RNA polymerase (spRNAP-IV). spRNAP-IV is expressed from an alternative transcript of the mitochondrial RNA polymerase gene (POLRMT). The spRNAP-IV lacks 262 amino-terminal amino acids of mitochondrial RNA polymerase, including the mitochondrial-targeting signal, and localizes to the nucleus. Transcription by spRNAP-IV is resistant to the RNA polymease II inhibitor alpha-amanitin but is sensitive to short interfering RNA specific for the POLRMT gene. The promoters for spRNAP-IV differ substantially from those used by RNA polymerase II, do not respond to transcriptional enhancers and contain a common functional sequence motif.
真核基因的转录由三种细胞核RNA聚合酶完成,其中RNA聚合酶II被认为是唯一负责信使RNA合成的酶。我们在此表明,人类和啮齿动物中某些mRNA的转录是由一种先前未知的单多肽细胞核RNA聚合酶(spRNAP-IV)介导的。spRNAP-IV由线粒体RNA聚合酶基因(POLRMT)的一个可变转录本表达。spRNAP-IV缺少线粒体RNA聚合酶的262个氨基末端氨基酸,包括线粒体靶向信号,并定位于细胞核。spRNAP-IV介导的转录对RNA聚合酶II抑制剂α-鹅膏蕈碱具有抗性,但对POLRMT基因特异性的小干扰RNA敏感。spRNAP-IV的启动子与RNA聚合酶II使用的启动子有很大差异,对转录增强子无反应,且包含一个共同的功能序列基序。