Department of Genetics and Microbiology, Faculty of Science, Charles University, Prague, Czech Republic.
Institute of Microbiology, Academy of Sciences of the Czech Republic, Prague, Czech Republic.
PLoS Pathog. 2018 Oct 22;14(10):e1007377. doi: 10.1371/journal.ppat.1007377. eCollection 2018 Oct.
Extrachromosomal hereditary elements such as organelles, viruses, and plasmids are important for the cell fitness and survival. Their transcription is dependent on host cellular RNA polymerase (RNAP) or intrinsic RNAP encoded by these elements. The yeast Kluyveromyces lactis contains linear cytoplasmic DNA virus-like elements (VLEs, also known as linear plasmids) that bear genes encoding putative non-canonical two-subunit RNAP. Here, we describe the architecture and identify the evolutionary origin of this transcription machinery. We show that the two RNAP subunits interact in vivo, and this complex interacts with another two VLE-encoded proteins, namely the mRNA capping enzyme and a putative helicase. RNAP, mRNA capping enzyme and the helicase also interact with VLE-specific DNA in vivo. Further, we identify a promoter sequence element that causes 5' mRNA polyadenylation of VLE-specific transcripts via RNAP slippage at the transcription initiation site, and structural elements that precede the termination sites. As a result, we present a first model of the yeast virus-like element transcription initiation and intrinsic termination. Finally, we demonstrate that VLE RNAP and its promoters display high similarity to poxviral RNAP and promoters of early poxviral genes, respectively, thereby pointing to their evolutionary origin.
染色体外遗传元件,如细胞器、病毒和质粒,对细胞的适应性和存活很重要。它们的转录依赖于宿主细胞的 RNA 聚合酶 (RNAP) 或这些元件编码的内在 RNAP。酵母 Kluyveromyces lactis 含有线性细胞质 DNA 病毒样元件 (VLEs,也称为线性质粒),它们携带编码假定非规范二亚基 RNAP 的基因。在这里,我们描述了这个转录机制的结构并确定了它的进化起源。我们表明,两个 RNAP 亚基在体内相互作用,并且这个复合物与另两个 VLE 编码的蛋白质相互作用,即 mRNA 加帽酶和一个假定的解旋酶。RNAP、mRNA 加帽酶和解旋酶也与体内 VLE 特异性 DNA 相互作用。此外,我们确定了一个启动子序列元件,该元件通过在转录起始位点处 RNAP 滑动导致 VLE 特异性转录物的 5' mRNA 多聚腺苷酸化,并确定了终止位点之前的结构元件。因此,我们提出了酵母病毒样元件转录起始和内在终止的第一个模型。最后,我们证明了 VLE RNAP 及其启动子与痘病毒 RNAP 和早期痘病毒基因的启动子具有高度相似性,从而指出了它们的进化起源。