Ayllón María A, Gowda Siddarame, Satyanarayana Tatineni, Karasev Alexander V, Adkins Scott, Mawassi Munir, Guerri José, Moreno Pedro, Dawson William O
Department of Plant Pathology, University of Florida, Citrus Research and Education Center, Lake Alfred, Florida 33850, USA.
J Virol. 2003 Sep;77(17):9232-43. doi: 10.1128/jvi.77.17.9232-9243.2003.
Citrus tristeza virus (CTV), a member of the Closteroviridae, has a positive-sense RNA genome of about 20 kb organized into 12 open reading frames (ORFs). The last 10 ORFs are expressed through 3'-coterminal subgenomic RNAs (sgRNAs) regulated in both amounts and timing. Additionally, relatively large amounts of complementary sgRNAs are produced. We have been unable to determine whether these sgRNAs are produced by internal promotion from the full-length template minus strand or by transcription from the minus-stranded sgRNAs. Understanding the regulation of 10 sgRNAs is a conceptual challenge. In analyzing commonalities of a replicase complex in producing so many sgRNAs, we examined initiating nucleotides of the sgRNAs. We mapped the 5' termini of intermediate- (CP and p13) and low- (p18) produced sgRNAs that, like the two highly abundant sgRNAs (p20 and p23) previously mapped, all initiate with an adenylate. We then examined modifications of the initiation site, which has been shown to be useful in defining mechanisms of sgRNA synthesis. Surprisingly, mutation of the initiating nucleotide of the CTV sgRNAs did not prevent sgRNA accumulation. Based on our results, the CTV replication complex appears to initiate sgRNA synthesis with purines, preferably with adenylates, and is able to initiate synthesis using a nucleotide a few positions 5' or 3' of the native initiation nucleotide. Furthermore, the context of the initiation site appears to be a regulatory mechanism for levels of sgRNA production. These data do not support either of the established mechanisms for synthesis of sgRNAs, suggesting that CTV sgRNA production utilizes a different mechanism.
柑橘衰退病毒(CTV)是长线形病毒科的成员,具有约20 kb的正义RNA基因组,该基因组被组织成12个开放阅读框(ORF)。最后10个ORF通过在数量和时间上都受到调控的3' 共末端亚基因组RNA(sgRNA)进行表达。此外,还会产生相对大量的互补sgRNA。我们一直无法确定这些sgRNA是通过全长模板负链的内部启动产生的,还是通过负链sgRNA的转录产生的。理解10种sgRNA的调控是一个概念上的挑战。在分析复制酶复合体产生如此多sgRNA的共性时,我们检查了sgRNA的起始核苷酸。我们绘制了中等丰度(CP和p13)和低丰度(p18)产生的sgRNA的5' 末端图谱,这些sgRNA与之前绘制的两种高丰度sgRNA(p20和p23)一样,均以腺苷酸起始。然后,我们检查了起始位点的修饰情况,结果表明这有助于确定sgRNA合成的机制。令人惊讶的是,CTV sgRNA起始核苷酸的突变并未阻止sgRNA的积累。基于我们的结果,CTV复制复合体似乎以嘌呤,最好是以腺苷酸起始sgRNA的合成,并且能够使用天然起始核苷酸5' 或3' 几个位置处的核苷酸起始合成。此外,起始位点的背景似乎是sgRNA产生水平的一种调控机制。这些数据不支持已确立的sgRNA合成机制中的任何一种,这表明CTV sgRNA的产生利用了不同的机制。