Gmyl Anatoly P, Korshenko Sergey A, Belousov Evegny V, Khitrina Elena V, Agol Vadim I
M.P. Chumakov Institute of Poliomyelitis & Viral Encephalitides, Russian Academy of Medical Sciences, Moscow 142782, Russia.
RNA. 2003 Oct;9(10):1221-31. doi: 10.1261/rna.5111803.
Biologically important joining of RNA pieces in cells, as exemplified by splicing and some classes of RNA editing, is posttranscriptional, whereas in RNA viruses it is generally believed to occur during viral RNA polymerase-dependent RNA synthesis. Here, we demonstrate the assembly of precise genome of an RNA virus (poliovirus) from its cotransfected fragments, which does not require specific RNA sequences, takes place before generation of the viral RNA polymerase, and occurs in different ways: Apparently unrestricted ligation of the terminal nucleotides, joining of any one of the two entire fragments with the relevant internal nucleotide of its partner, or internal crossovers within the overlapping sequence. Incorporation of the entire 5' or 3' partners into the recombinant RNA is activated by the presence of terminal 3'-phosphate and 5'-OH, respectively. Such postreplicative reactions, fundamentally differing from the known site-specific and structurally demanding cellular RNA rearrangements, might contribute to the origin and evolution of RNA viruses and could generate new RNA species during all stages of biological evolution.
细胞中RNA片段的生物学重要连接,如剪接和某些类型的RNA编辑,是在转录后进行的,而在RNA病毒中,通常认为这种连接发生在依赖病毒RNA聚合酶的RNA合成过程中。在此,我们证明了一种RNA病毒(脊髓灰质炎病毒)的精确基因组可从其共转染的片段组装而成,这种组装不需要特定的RNA序列,发生在病毒RNA聚合酶产生之前,并且以不同方式进行:末端核苷酸明显不受限制的连接、两个完整片段中的任何一个与其伙伴的相关内部核苷酸的连接,或重叠序列内的内部交换。分别通过末端3'-磷酸和5'-羟基的存在,将整个5'或3'伙伴掺入重组RNA中。这种复制后反应与已知的位点特异性和结构要求严格的细胞RNA重排根本不同,可能有助于RNA病毒的起源和进化,并可能在生物进化的所有阶段产生新的RNA种类。