Institut für Pharmazeutische Chemie, Philipps-Universität Marburg, Marburg, Germany.
Zentrum für Synthetische Mikrobiologie, Philipps-Universität Marburg, Marburg, Germany.
PLoS Pathog. 2021 Oct 26;17(10):e1010002. doi: 10.1371/journal.ppat.1010002. eCollection 2021 Oct.
Transcription of non-segmented negative sense (NNS) RNA viruses follows a stop-start mechanism and is thought to be initiated at the genome's very 3'-end. The synthesis of short abortive leader transcripts (leaderRNAs) has been linked to transcription initiation for some NNS viruses. Here, we identified the synthesis of abortive leaderRNAs (as well as trailer RNAs) that are specifically initiated opposite to (anti)genome nt 2; leaderRNAs are predominantly terminated in the region of nt ~ 60-80. LeaderRNA synthesis requires hexamer phasing in the 3'-leader promoter. We determined a steady-state NP mRNA:leaderRNA ratio of ~10 to 30-fold at 48 h after Ebola virus (EBOV) infection, and this ratio was higher (70 to 190-fold) for minigenome-transfected cells. LeaderRNA initiation at nt 2 and the range of termination sites were not affected by structure and length variation between promoter elements 1 and 2, nor the presence or absence of VP30. Synthesis of leaderRNA is suppressed in the presence of VP30 and termination of leaderRNA is not mediated by cryptic gene end (GE) signals in the 3'-leader promoter. We further found different genomic 3'-end nucleotide requirements for transcription versus replication, suggesting that promoter recognition is different in the replication and transcription mode of the EBOV polymerase. We further provide evidence arguing against a potential role of EBOV leaderRNAs as effector molecules in innate immunity. Taken together, our findings are consistent with a model according to which leaderRNAs are abortive replicative RNAs whose synthesis is not linked to transcription initiation. Rather, replication and transcription complexes are proposed to independently initiate RNA synthesis at separate sites in the 3'-leader promoter, i.e., at the second nucleotide of the genome 3'-end and at the more internally positioned transcription start site preceding the first gene, respectively, as reported for Vesicular stomatitis virus.
非节段负义(NNS)RNA 病毒的转录遵循一种停止-启动机制,据认为起始于基因组的非常 3'末端。一些 NNS 病毒的转录起始与短的中止先导转录物(leaderRNAs)的合成有关。在这里,我们鉴定了在与(反)基因组 nt 2 相反的位置起始的中止先导 RNA(以及 trailer RNA)的合成;leaderRNAs 主要在 nt~60-80 区域终止。leaderRNA 的合成需要在 3'-leader 启动子中六聚体相位。在埃博拉病毒(EBOV)感染后 48 小时,我们确定了稳定状态的 NP mRNA:leaderRNA 比值约为 10 至 30 倍,而 minigenome 转染细胞的比值更高(70 至 190 倍)。nt 2 处的 leaderRNA 起始和终止位点不受启动子元件 1 和 2 之间的结构和长度变化以及 VP30 的存在或不存在的影响。VP30 的存在抑制了 leaderRNA 的合成,并且 leaderRNA 的终止不是由 3'-leader 启动子中的隐蔽基因末端(GE)信号介导的。我们进一步发现,转录和复制对基因组 3'末端核苷酸的要求不同,这表明 EBOV 聚合酶的复制和转录模式中的启动子识别不同。我们进一步提供了证据,证明 EBOV leaderRNAs 不太可能作为先天免疫中的效应分子。总之,我们的研究结果与一种模型一致,即 leaderRNAs 是中止性复制 RNA,其合成与转录起始无关。相反,复制和转录复合物被提议分别在 3'-leader 启动子的不同位点独立起始 RNA 合成,即在基因组 3'末端的第二个核苷酸处,以及在更内部的转录起始位点处,分别在 Vesicular stomatitis virus 中报道。